TW201306799A - Method and device of identification with characteristics of sleep apnea, cough and asthma - Google Patents

Method and device of identification with characteristics of sleep apnea, cough and asthma Download PDF

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TW201306799A
TW201306799A TW100127468A TW100127468A TW201306799A TW 201306799 A TW201306799 A TW 201306799A TW 100127468 A TW100127468 A TW 100127468A TW 100127468 A TW100127468 A TW 100127468A TW 201306799 A TW201306799 A TW 201306799A
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signal
identification
wrist
seconds
lung sound
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TWI442904B (en
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Ming-Feng Wu
Chih-Yu Wen
Jeng-Yuan Hsu
Wei-Chang Huang
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Nat Univ Chung Hsing
Taichung Veterans General Hospital
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Abstract

This invention relates to the method and device of identification with characteristics of sleep apnea, cough and asthma. About the method, it includes (1) preparing step, (2) body detecting step, (3) signal processing step, (4) signal analyzing step, and (5) finishing step. This device includes a voice detector, an abdomen detector, and a wrist detector for detecting a lung sound signal, an abdomen breath signal, and a wrist movement signal respectively. This device also includes three fuzzy logic systems so as to analyze the characteristics of sleep apnea, cough and asthma based on these three detected signals. Then, it can judge which event is occurred or not. Thus, this invention can precisely analyze the events times and happening time of sleep apnea, cough and asthma. In addition, its wireless detecting design can effectuate a long period of detection time under a static or dynamic status.

Description

辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置Method and device for identifying features of sleep apnea, cough and asthma

本發明係有關一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置,尤指一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置,其兼具利用特徵進行模糊邏輯辨識氣喘事件及睡眠呼吸中止事件與咳嗽事件相當準確、可判別氣喘事件及睡眠呼吸中止事件與咳嗽事件發生之次數與時間,以及無線感測設計可同時在靜態與動態下進行長時間檢測等功效。The invention relates to a method and a device for identifying the characteristics of sleep breathing, cough and asthma, in particular to a method and device for identifying characteristics of sleep breathing, coughing and asthma, and the utility model has the characteristics of fuzzy logic to identify asthma. The events and sleep-dissipation events and coughing events are quite accurate, and the number and timing of asthmatic events and sleep-disordering events and coughing events can be identified, and the wireless sensing design can perform long-term detection in both static and dynamic conditions.

睡眠時呼吸道的徵象,是許多疾病控制的指標,如氣喘、睡眠呼吸中止或是咳嗽等。其中,睡眠呼吸中止根據不同標準需求,已有許多檢查與監控的產品,傳統檢測方法及裝置共分四級,其分別產生以下問題:The signs of respiratory tract during sleep are indicators of many disease control, such as asthma, sleep breathing or coughing. Among them, sleep breathing is suspended according to different standard requirements, there are many products for inspection and monitoring. The traditional detection methods and devices are divided into four levels, which respectively produce the following problems:

[1] 應用範圍受限。第一級為全頻道標準檢查,在醫院使用;就治療睡眠呼吸中止(如陽壓呼吸器、手術或牙套等)之成效的評估,以長時間觀察變化最為理想。到醫院做確認雖然最準確,但仍需做排程等候;並無法讓行動不便者或沒有時間到醫院就診者即時進行檢查,僅限制在醫院使用。[1] The scope of application is limited. The first level is the full-channel standard examination, which is used in hospitals; the evaluation of the effectiveness of the treatment of sleep-disorder (such as positive pressure breathing apparatus, surgery or braces, etc.) is most ideal for long-term observation. Although it is most accurate to go to the hospital for confirmation, it still needs to be scheduled to wait; it is not possible for people with mobility problems or those who do not have time to go to the hospital for immediate examination, and is restricted to hospital use.

[2] 使用不便。睡眠第二級為全頻道在非醫護人員場合下使用;第三級為胸腹帶、呼吸氣流與血氧濃度等四項作為篩檢與治療評估;以第二、第三級方式來監控雖然是替代的方法,但可能必需小心活動時拉扯到相關的感測線,長期使用相當不便。[2] Inconvenient to use. The second level of sleep is for all channels in non-medical personnel; the third level is for chest and abdomen, respiratory airflow and blood oxygen concentration as screening and treatment evaluation; monitoring in the second and third levels It is an alternative method, but it may be necessary to carefully pull the relevant sensing line when the activity is active, which is quite inconvenient for long-term use.

[3] 檢測較不準確。睡眠第四級為血氧濃度偵測,為單純篩檢血氧狀態進而推論呼吸情形,與第三級之睡眠檢查皆無睡眠偵測訊號,在估測睡眠呼吸中止上錯誤率相對較高。至於傳統偵測氣喘或偵測咳嗽之裝置(例如中華民國發明專利公開第200704391號之『貼片式生理監測裝置、系統及網路』)亦無辨識睡眠功能,無法準確辨識氣喘或咳嗽是否在睡眠發生之問題。而攜帶式結構(例如中華民國發明專利第I294280號之『可攜式氣喘肺音監測系統』)同樣無法區分檢測到的訊號是發生於清醒或睡眠,檢測較不準確。另外,亦有利用個人錄製之肺音資料庫作辨識之裝置,然而每個人在不同疾病都有不同表現,此裝置亦會產生誤差。[3] Detection is less accurate. The fourth level of sleep is the detection of blood oxygen concentration. It is a simple screening of blood oxygen status and further inference of respiratory conditions. There is no sleep detection signal in the third stage sleep examination. The error rate is relatively high in estimating sleep breathing. As for the traditional device for detecting asthma or detecting cough (for example, the "Spot Physiological Monitoring Device, System and Network" of the Republic of China Invention Patent Publication No. 200704391), there is no recognition of sleep function, and it is impossible to accurately identify whether asthma or cough is present. The problem of sleep. The portable structure (for example, the "portable asthma lung sound monitoring system" of the Republic of China invention patent No. I294280) is also incapable of distinguishing whether the detected signal occurs in waking or sleeping, and the detection is less accurate. In addition, there are also devices that use the personally recorded lung sound database for identification. However, each person has different performances in different diseases, and this device also produces errors.

[4]有線設計使用不便。傳統偵測氣喘或偵測咳嗽之裝置(例如中華民國發明專利公開第200704391號之『貼片式生理監測裝置、系統及網路』)仍以有線方式來支援感測,使待測者不論在行動上或是躺在病床上,都增加自然活動時之拉扯的機會,有線設計使用不便。[4] Wired design is inconvenient to use. Conventional devices for detecting asthma or detecting cough (for example, "SMD-type physiological monitoring devices, systems, and networks" in the Republic of China Invention Patent Publication No. 200704391) still support sensing in a wired manner, so that the test subject is In action or lying on a hospital bed, it increases the chance of pulling during natural activities, and the cable design is inconvenient to use.

有鑑於此,必需研發出可解決上述習用缺點之技術。In view of this, it is necessary to develop a technique that can solve the above disadvantages.

本發明之目的,在於提供一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置,其兼具利用特徵進行模糊邏輯辨識氣喘事件及睡眠呼吸中止事件與咳嗽事件相當準確、可判別氣喘事件及睡眠呼吸中止事件與咳嗽事件發生之次數與時間,以及無線感測設計可同時在靜態與動態下進行長時間檢測之優點。特別是,本發明所欲解決之問題包括:應用範圍受限、使用不便、檢測較不準確與有線設計使用不便等問題。The object of the present invention is to provide a method and a device for identifying characteristics of sleep breathing, coughing and wheezing, which have the characteristics of using fuzzy logic to identify an asthmatic event, a sleep breathing abort event and a coughing event, and can identify an asthmatic event. And the number and timing of sleep apnea events and coughing events, and the advantages of wireless sensing design for long-term detection both statically and dynamically. In particular, the problems to be solved by the present invention include: limited application range, inconvenient use, inaccurate detection, and inconvenient use of wired designs.

解決上述問題之技術手段係提供一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置,其方法部份係包括下列步驟:The technical means for solving the above problems is to provide a method for identifying characteristics of sleep breathing, coughing and wheezing, and a device thereof, the method comprising the following steps:

一.準備步驟;One. Preparation steps

二.人體偵測步驟;two. Human body detection step;

三.訊號處理步驟;three. Signal processing step;

四.訊號辨識步驟;及four. Signal identification step; and

五.完成步驟。Fives. Complete the steps.

其裝置部份係包括:一聲音感測裝置,係用以即時偵測一待測者而產生一肺音訊號,並傳送至該偵測識別裝置;一腹部感測裝置,係用以即時偵測該待測者之腹部呼吸起伏過程,而產生一腹部呼吸運動訊號,並傳送至該偵測識別裝置;一腕部感測裝置,係用以即時偵測該待測者而產生一腕部活動訊號,並傳送至該偵測識別裝置;一偵測識別裝置,係具有一第一模糊邏輯系統、一第二模糊邏輯系統、一第三模糊邏輯系統及一估測辨識裝置;該偵測識別裝置用以接收該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號;先對該肺音訊號進行快速傅立葉轉換而得到頻率,並對該肺音訊號及該腹部呼吸運動訊號進行訊號切割處理;藉此,以該偵測識別裝置配合該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號進行下列三種辨識作業:The device part comprises: a sound sensing device for detecting a patient to be detected and generating a lung sound signal and transmitting the signal to the detection and identification device; and an abdominal sensing device for detecting Measuring the abdominal breathing process of the test subject, and generating a abdominal respiratory motion signal, and transmitting to the detection and identification device; a wrist sensing device for detecting the test subject to generate a wrist The activity signal is transmitted to the detection and identification device; a detection and identification device has a first fuzzy logic system, a second fuzzy logic system, a third fuzzy logic system and an estimation identification device; The identification device is configured to receive the lung sound signal, the abdominal respiratory motion signal and the wrist activity signal; first perform fast Fourier transform on the lung sound signal to obtain a frequency, and signal the lung sound signal and the abdominal respiratory motion signal Cutting processing; thereby, the detection identification device cooperates with the lung sound signal, the abdominal respiratory motion signal and the wrist activity signal to perform the following three identification operations:

[a] 氣喘辨識:該偵測識別裝置以該第一模糊邏輯系統進行辨識;而氣喘發作之特徵為哮鳴;當該肺音訊號之頻率達到一頻率標準值,其係介於200Hz~600Hz之間,且該頻率標準值持續一第一辨識時間,其係介於250毫秒~500毫秒之間;則辨識為哮鳴,並定義為該待測者發生氣喘事件;[a] Asthma identification: the detection and recognition device is identified by the first fuzzy logic system; and the asthma attack is characterized by wheezing; when the frequency of the lung sound signal reaches a frequency standard value, the system is between 200 Hz and 600 Hz And the frequency standard value continues for a first identification time, which is between 250 milliseconds and 500 milliseconds; and is recognized as wheezing, and is defined as an asthmatic event of the test subject;

[b] 睡眠呼吸中止辨識:該偵測識別裝置以該第二模糊邏輯系統進行辨識;當該相鄰之肺音訊號間隔持續一第二辨識時間;其係介於10秒~90秒之間;並該相鄰之腹部呼吸運動訊號同樣間隔持續該第二辨識時間;且由該腕部活動訊號判別該待測者為睡眠狀態;則定義為該待測者發生睡眠呼吸中止事件;[b] sleep breathing abort identification: the detection and recognition device is identified by the second fuzzy logic system; when the adjacent lung sound signal interval continues for a second identification time; the system is between 10 seconds and 90 seconds And the adjacent abdominal respiratory motion signal continues to be separated by the second identification time; and the wrist activity signal determines that the test subject is in a sleep state; and is defined as a sleep breathing suspension event of the test subject;

[c] 咳嗽辨識:該偵測識別裝置以該第三模糊邏輯系統進行辨識;當該每一肺音訊號之呼氣相位持續一呼氣相位時間,其係介於0.3秒~1秒之間;且該相鄰之肺音訊號彼此間隔一第三辨識時間,其係介於3秒~6秒之間;則定義為該待測者發生咳嗽事件;[c] Cough recognition: the detection and recognition device is identified by the third fuzzy logic system; when the expiratory phase of each lung sound signal continues for an expiratory phase time, the system is between 0.3 seconds and 1 second. And the adjacent lung sound signals are spaced apart from each other by a third identification time, which is between 3 seconds and 6 seconds; and is defined as a coughing event of the test subject;

最後,該估測辨識裝置依氣喘事件、睡眠呼吸中止事件、咳嗽事件之順序,於該第一、該第二與該第三辨識時間之重疊時間內,比對去模糊化數值,辨識發生機率最大之事件,並判別其為該待測者發生之事件。Finally, the estimation and identification device compares the defuzzification value and identifies the probability of occurrence according to the sequence of the asthmatic event, the sleep breathing abort event, and the cough event in the overlapping time of the first, the second, and the third identification time. The largest event, and identify it as the event of the person to be tested.

本發明之上述目的與優點,不難從下述所選用實施例之詳細說明與附圖中,獲得深入瞭解。The above objects and advantages of the present invention will be readily understood from the following detailed description of the preferred embodiments illustrated herein.

茲以下列實施例並配合圖式詳細說明本發明於後:The invention will be described in detail in the following examples in conjunction with the drawings:

本發明係為一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法及其裝置,參閱第一圖,其方法部份包括下列步驟:The present invention is a method and apparatus for identifying characteristics of sleep apnea, cough and wheezing. Referring to the first figure, the method portion includes the following steps:

一.準備步驟11:參閱第二圖,預先準備一聲音感測裝置20、一腹部感測裝置30、一腕部感測裝置40及一偵測識別裝置50,該偵測識別裝置50具有一第一模糊邏輯系統51、一第二模糊邏輯系統52、一第三模糊邏輯系統53及一估測辨識裝置54;One. Preparation Step 11: Referring to the second figure, a sound sensing device 20, an abdominal sensing device 30, a wrist sensing device 40, and a detection and recognition device 50 are prepared in advance. The detection and recognition device 50 has a first a fuzzy logic system 51, a second fuzzy logic system 52, a third fuzzy logic system 53 and an estimation and identification device 54;

二.人體偵測步驟12:該聲音感測裝置20用以即時偵測一待測者91而產生一肺音訊號20A,並傳送至該偵測識別裝置50;該腹部感測裝置30用以即時偵測該待測者91之腹部呼吸起伏過程,而產生一腹部呼吸運動訊號30A,並傳送至該偵測識別裝置50;該腕部感測裝置40用以即時偵測該待測者91而產生一腕部活動訊號40A,並傳送至該偵測識別裝置50;two. The human body detecting device 12 is configured to detect a test subject 91 and generate a lung sound signal 20A and transmit the same to the detection and recognition device 50. The abdominal sensing device 30 is used for instant detection. The abdominal respiratory motion of the test subject 91 is measured, and a abdominal respiratory motion signal 30A is generated and transmitted to the detection and recognition device 50. The wrist sensing device 40 is configured to detect the tester 91 in real time. a wrist activity signal 40A, and transmitted to the detection and identification device 50;

三.訊號處理步驟13:該偵測識別裝置50先將該肺音訊號20A進行快速傅立葉轉換(Fast Fourier Transform,英文簡稱FFT)而得到頻率(參閱第四圖),並對該肺音訊號20A及該腹部呼吸運動訊號30A進行訊號切割(Segmentation)處理;three. Signal processing step 13: The detection and recognition device 50 first performs a Fast Fourier Transform (FFT) for the lung sound signal 20A to obtain a frequency (refer to the fourth figure), and the lung sound signal 20A and the Abdominal respiratory motion signal 30A performs signal segmentation processing;

四.訊號辨識步驟14:該偵測識別裝置50以該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A進行下列三種辨識作業(參閱第三圖):four. The signal recognition step 14: the detection and recognition device 50 performs the following three identification operations using the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist activity signal 40A (see the third figure):

[a] 氣喘辨識:該偵測識別裝置50以該第一模糊邏輯系統51進行辨識;而氣喘發作之特徵為哮鳴;當該肺音訊號20A之頻率達到一頻率標準值,其係介於200Hz~600Hz之間(參閱第四圖(以「中」等頻率表示),且該頻率標準值持續一第一辨識時間T1,其係介於250毫秒~500毫秒之間(參閱第五圖,以「長」表示。);則辨識為哮鳴,並定義為該待測者91發生氣喘事件;[a] Asthma recognition: the detection and recognition device 50 is identified by the first fuzzy logic system 51; and the asthma attack is characterized by wheezing; when the frequency of the lung sound signal 20A reaches a frequency standard value, the system is interposed Between 200 Hz and 600 Hz (refer to the fourth figure (indicated by "medium" and other frequencies), and the frequency standard value continues for a first identification time T1, which is between 250 milliseconds and 500 milliseconds (see the fifth figure, It is expressed as "long".); it is recognized as wheezing, and is defined as the asthmatic event of the test subject 91;

[b] 睡眠呼吸中止辨識:該偵測識別裝置50以該第二模糊邏輯系統52進行辨識;當該相鄰之肺音訊號20A間隔持續一第二辨識時間T2;其係介於10秒~90秒之間(參閱第六圖,以「長」表示。);並該相鄰之腹部呼吸運動訊號30A同樣間隔持續該第二辨識時間T2(參閱第七圖,以「長」表示。);且由該腕部活動訊號40A判別該待測者91為睡眠狀態;則定義為該待測者91發生睡眠呼吸中止事件;[b] sleep breathing abort identification: the detection and recognition device 50 is identified by the second fuzzy logic system 52; when the adjacent lung sound signal 20A is separated by a second identification time T2; the system is between 10 seconds~ Between 90 seconds (refer to the sixth figure, indicated by "long"); and the adjacent abdominal respiratory motion signal 30A continues at the same interval for the second identification time T2 (refer to the seventh figure, indicated by "long".) And determining, by the wrist activity signal 40A, the test subject 91 is in a sleep state; then defining that the test subject 91 has a sleep breathing suspension event;

[c] 咳嗽辨識:該偵測識別裝置50以該第三模糊邏輯系統53進行辨識;當該每一肺音訊號20A之呼氣相位持續一呼氣相位時間T31(參閱第八A、第八B、第八C、第八D圖),其係介於0.3秒~1秒之間;且該相鄰之肺音訊號20A彼此間隔一第三辨識時間T32,其係介於3秒~6秒之間;則定義為該待測者91發生咳嗽事件;[c] Cough recognition: the detection and recognition device 50 recognizes the third fuzzy logic system 53; when the expiratory phase of each lung sound signal 20A continues for an expiratory phase time T31 (see eighth, eighth, eighth) B, eighth C, and eighth D), the system is between 0.3 seconds and 1 second; and the adjacent lung sound signals 20A are spaced apart from each other by a third identification time T32, which is between 3 seconds and 6 seconds. Between seconds; it is defined as the occurrence of a coughing event in the test subject 91;

最後,該估測辨識裝置54依氣喘事件、睡眠呼吸中止事件、咳嗽事件之順序,於該第一、該第二與該第三辨識時間T1、T2與T32之重疊時間內,比對去模糊化數值,辨識發生機率最大之事件,並判別其為該待測者91發生之事件;五.完成步驟15:完成辨識氣喘事件、睡眠呼吸中止事件與咳嗽事件。Finally, the estimation and identification device 54 performs deblurring in the overlapping time of the first, second, and third identification times T1, T2, and T32 according to an asthmatic event, a sleep breathing abort event, and a coughing event. The numerical value is used to identify the event with the highest probability of occurrence, and it is determined that it is the event of the tester 91; Complete step 15: Complete identification of asthmatic events, sleep breathing abortion events, and coughing events.

實務上,該肺音訊號20A之頻率標準值可以400Hz為最佳值。In practice, the frequency standard value of the lung sound signal 20A can be 400 Hz as the optimum value.

該第一辨識時間T1係可介於100毫秒~500毫秒之間。The first identification time T1 can be between 100 milliseconds and 500 milliseconds.

該第二辨識時間T2係可介於10秒~120秒之間。The second identification time T2 can be between 10 seconds and 120 seconds.

該呼氣相位時間T31,係可介於0.12秒~2.5秒之間。The expiratory phase time T31 can be between 0.12 seconds and 2.5 seconds.

該第三辨識時間T32係可介於2秒~10秒之間。The third identification time T32 can be between 2 seconds and 10 seconds.

該聲音感測裝置20係包括:一第一固定部21、一第一殼體22、一聲音感測元件23、一第一記憶體24、一第一微處理器25、一第一無線射頻元件26及一第一電池27;該第一固定部21與該第一殼體22為相互結合(舉凡可相互連結之技術手段皆可為之)之結構,且該第一固定部21用以將該第一殼體22固定於該待測者91之胸口(原則上是平貼於胸口之皮膚上,接近肺之位置,以供長時間檢測之用);該聲音感測元件23(可為公知之微麥風。例如:中華民國發明專利第I268115號之『矽微麥克風之振膜晶片及其製造方法』)用以感測該待測者91之肺音訊號20A;該第一記憶體24用以記憶並將該肺音訊號20A傳送至該第一微處理器25,該第一微處理器25用以控制該第一無線射頻元件26將該肺音訊號20A傳送出去;該第一電池27係供應前述相關元件所需之電力。The sound sensing device 20 includes a first fixing portion 21, a first housing 22, an acoustic sensing component 23, a first memory 24, a first microprocessor 25, and a first radio frequency. The first fixing portion 21 and the first housing portion 22 are configured to be coupled to each other (the technical means can be connected to each other), and the first fixing portion 21 is used for Fixing the first housing 22 to the chest of the test subject 91 (in principle, it is flat on the skin of the chest, close to the position of the lung for long-term detection); the sound sensing component 23 ( For example, the "Micro-microphone diaphragm film and its manufacturing method" of the Republic of China invention patent No. I268115 is used to sense the lung sound signal 20A of the test subject 91; the first memory The body 24 is configured to transmit the lung audio signal 20A to the first microprocessor 25, and the first microprocessor 25 is configured to control the first radio frequency component 26 to transmit the lung audio signal 20A; A battery 27 supplies the power required by the aforementioned associated components.

該腹部感測裝置30係包括:一第二固定部31、一第二殼體32、一第一加速度感測器33、一第二記憶體34、一第二微處理器35、一第二無線射頻元件36及一第二電池37;該第二固定部31與該第二殼體32為相互結合(舉凡可相互連結之技術手段皆可為之)之結構,且該第二固定部31用以將該第二殼體32固定於該待測者91之腹部(原則上是接近腹部之皮膚,以供長時間檢測之用);該第一加速度感測器33用以感測該待測者91之腹部於呼吸過程之起伏狀態,並產生電壓變化,電壓變化可轉換為該腹部呼吸運動訊號30A;該第二記憶體34用以記憶並將該腹部呼吸運動訊號30A傳送至該第二微處理器35,該第二微處理器35用以控制該第二無線射頻元件36將該腹部呼吸運動訊號30A傳送出去;該第二電池37係供應前述相關元件所需之電力。The abdominal sensing device 30 includes a second fixing portion 31, a second housing 32, a first acceleration sensor 33, a second memory 34, a second microprocessor 35, and a second The radio frequency component 36 and the second battery 37; the second fixing portion 31 and the second casing 32 are combined with each other (the technical means can be connected to each other), and the second fixing portion 31 For fixing the second casing 32 to the abdomen of the test subject 91 (in principle, the skin close to the abdomen for long-term detection); the first acceleration sensor 33 is used to sense the waiting The abdomen of the tester 91 is in an undulating state of the breathing process, and a voltage change is generated, and the voltage change can be converted into the abdominal respiratory motion signal 30A; the second memory 34 is used to memorize and transmit the abdominal respiratory motion signal 30A to the first The second microprocessor 35 is configured to control the second radio frequency component 36 to transmit the abdominal respiratory motion signal 30A; the second battery 37 is to supply the power required by the related components.

該腕部感測裝置40係包括:一腕部固定帶41、一第三殼體42、一第二加速度感測器43、一第三記憶體44、一第三微處理器45、一第三無線射頻元件46、一第三電池47、一按鍵組48及一螢幕49;該腕部固定帶41用以將該第三殼體42固定該待測者91之腕部;該第二加速度感測器43用以感測該待測者91之腕部肌肉張力的變化(隨之產生電壓變化,並可設定電壓呈減少時,肌肉張力變小→待測者91呈睡眠。電壓呈增加時,肌肉張力變大→待測者91呈清醒。);電壓變化轉換為該腕部活動訊號40A,該第三記憶體44用以記憶該腕部活動訊號40A,並設一多工器441將接收之該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A多工傳送至該第三微處理器45,該第三微處理器45用以控制該第三無線射頻元件46,將該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A傳送出去;該第三電池47係供應前述相關元件所需之電力;該按鍵組48包括一選擇鍵481、一確認鍵482及一電源鍵483;該選擇鍵481用以選擇要進行之功能;該確認鍵482用以確認所選擇之功能;該電源鍵483用以啟、閉該腕部感測裝置40;該螢幕49用以顯示該腕部感測裝置40之訊號或相關之檢測結果。The wrist sensing device 40 includes a wrist fixing strap 41, a third housing 42, a second acceleration sensor 43, a third memory 44, a third microprocessor 45, and a first a third radio frequency component 46, a third battery 47, a button group 48 and a screen 49; the wrist fixing strap 41 is used to fix the third housing 42 to the wrist of the test subject 91; the second acceleration The sensor 43 is configured to sense a change in the muscle tension of the wrist of the test subject 91 (there is a voltage change, and when the set voltage is decreased, the muscle tension becomes small → the test subject 91 sleeps. The voltage increases. When the muscle tension becomes large, the test subject 91 is awake. The voltage change is converted into the wrist activity signal 40A, and the third memory 44 is used to memorize the wrist activity signal 40A, and a multiplexer 441 is provided. The received lung sound signal 20A, the abdominal respiratory motion signal 30A, and the wrist activity signal 40A are multiplexed to the third microprocessor 45, and the third microprocessor 45 is configured to control the third wireless RF component. 46, the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist activity signal 40A are transmitted The third battery 47 is supplied with power required by the aforementioned related components; the button group 48 includes a selection button 481, a confirmation button 482 and a power button 483; the selection button 481 is used to select a function to be performed; the confirmation button 482 is used to confirm the selected function; the power button 483 is used to open and close the wrist sensing device 40; the screen 49 is used to display the signal of the wrist sensing device 40 or related detection results.

該第一及該第二固定部21與31皆用以平貼於皮膚表面較不容易脫落,並當流汗或其他因素造成脫落亦可進行簡單置換。The first and the second fixing portions 21 and 31 are used for flattening on the surface of the skin, and are not easily detached, and can be easily replaced when sweating or other factors cause detachment.

該偵測識別裝置50可設於該腕部感測裝置40內(利於隨身24小時攜帶使用),並該聲音感測裝置20、該腹部感測裝置30與該腕部感測裝置40可透過該第一、該第二、該第三無線射頻元件26、36與46構成無線感測網路系統,以該第三無線射頻元件46為叢集頭(Cluster head)調配網路傳輸架構;當有外部裝置(如電腦或嵌入型處理器)等即可下載資料;亦可直接設於外部電腦或嵌入型處理器等,進行原始資料(RAW Data)分析。The detection and recognition device 50 can be disposed in the wrist sensing device 40 (used to be carried around for 24 hours), and the sound sensing device 20, the abdominal sensing device 30 and the wrist sensing device 40 can be permeable. The first, the second, and the third radio frequency components 26, 36, and 46 constitute a wireless sensing network system, and the third radio frequency component 46 is configured as a cluster head to configure a network transmission architecture; External devices (such as computers or embedded processors) can download data; they can also be directly connected to external computers or embedded processors for RAW Data analysis.

參閱第二及第三圖,該偵測識別裝置50又包括:一訊號處理模組50A,係用以從該多工器441接收該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A;該訊號處理模組50A設有:一快速傅立葉轉換單元501,係用以將該肺音訊號20A(此時為時域訊號)經傅立葉轉換(FFT)(進行在離散時間非週期之訊號之計算)變成頻域訊號20A(f);其處理方式係經下列公式:進行運算(公知技術,恕不贅述。);其中:x[n]為取樣後之訊號,Ω為單位(徑度);離散時間傅立葉轉換是有關區間-π<Ω≦π的頻率分佈。Referring to the second and third figures, the detection and identification device 50 further includes a signal processing module 50A for receiving the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist from the multiplexer 441. The signal processing module 50A is provided with a fast Fourier transform unit 501 for performing Fourier transform (FFT) on the lung sound signal 20A (in this case, a time domain signal) (for discrete time aperiodic The calculation of the signal becomes a frequency domain signal 20A(f); its processing is based on the following formula: The calculation is performed (known techniques are not described here); wherein: x[n] is the signal after sampling, Ω is the unit (diameter); the discrete-time Fourier transform is the frequency distribution of the interval -π<Ω≦π.

一非線性能量運算單元502,係用以對該肺音訊號20A(概呈時域訊號)、該腹部呼吸運動訊號30A(概呈時域訊號)、該腕部活動訊號40A(概呈時域訊號)及該頻域訊號20A(f)進行訊號切割,再傳送至該第一、該第二與該第三模糊邏輯系統51、52與53;其處理方式係經下列公式:輸入訊號x(n)=Acos(ωn+)+w(n)進行運算;其中:w(n)表示白高斯之通道效應;A為輸入訊號的振幅;ω為輸入訊號的頻率;至於非線性能量運算可應用下列公式:Ψ[x(n)]=x(n-1)2-x(n)x(n-2)進行運算。A non-linear energy operation unit 502 is configured for the lung sound signal 20A (general time domain signal), the abdominal respiratory motion signal 30A (general time domain signal), and the wrist activity signal 40A (general time domain) The signal and the frequency domain signal 20A(f) perform signal cutting, and then transmit to the first, second and third fuzzy logic systems 51, 52 and 53; the processing method is as follows: input signal x ( n )= A cos( ωn + + w ( n ) performs the operation; where: w ( n ) represents the channel effect of white Gauss; A is the amplitude of the input signal; ω is the frequency of the input signal; as for the nonlinear energy operation, the following formula can be applied: Ψ[x( n)]=x(n-1) 2 -x(n)x(n-2) is operated.

一資料儲存部55(參閱第二及第二十二圖),用以儲存該估測辨識裝置54處理後之訊號及結果。A data storage unit 55 (see FIGS. 2 and 22) for storing the signals and results processed by the estimation and identification device 54.

於該訊號辨識步驟14中:當進行[a]氣喘辨識時,可進一步配合該腕部活動訊號40A(由於每人之肌肉張力均不同,此點依實際測量之基準值為準)之數值判別該待測者91為睡眠/清醒(同理,咳嗽辨識亦可依此類推判別該待測者91為睡眠/清醒)。In the signal identification step 14, when the [a] asthma recognition is performed, the wrist activity signal 40A can be further matched (as the muscle tension of each person is different, and the point is based on the actual measurement reference value) The test subject 91 is sleep/awake (same reason, the cough recognition can also be determined by the push to determine that the test subject 91 is sleep/awake).

在此先說明模糊邏輯,自然界中有許多現象是無法用有或無等明確的二元方式來界定。而模糊邏輯則提供解決之道;以身高為例,例如180公分為“高”,大於180為很高,小於160為低,其中可設定歸屬度為0到1。如描述「很高」,大於180公分歸屬度為1,160公分為0;描述「矮」,則165公分之歸屬度可能為0.7;此一模糊化依設定之函數(member function)而定。當輸入的值經過模糊化後,透過邏輯規則推論最後以去模糊化而得到最佳解。Here we first explain fuzzy logic. There are many phenomena in nature that cannot be defined by a clear binary method with or without. Fuzzy logic provides a solution; for example, height is 180 cm "high", greater than 180 is high, and less than 160 is low, and the degree of attribution can be set to 0 to 1. If the description is "very high", the degree of attribution greater than 180 cm is 1,160 cm 0; for the description of "short", the degree of attribution of 165 cm may be 0.7; this fuzzification depends on the member function. When the input value is blurred, the logical solution is inferred and finally defuzzified to get the best solution.

以該第一模糊邏輯系統51進行氣喘辨識為例,預先設定氣喘事件之肺音訊號20A的頻率為400Hz,而正常之肺音訊號20A的頻率為100~200Hz(以100 Hz為基準);當進行氣喘辨識時,則400Hz之歸屬度為1,100Hz的歸屬度為0,參閱第九圖,圖中所示之六個肺音訊號20A之頻率皆達到頻率標準值(400Hz)(歸屬度為1),且頻率標準值持續第一辨識時間T1(250毫秒),定義為氣喘事件,該估測辨識裝置54於該第一、該第二、該第三辨識時間T1、T2與T32之重疊時間內,判別該待測者91發生六次氣喘事件。Taking the first fuzzy logic system 51 as an example of asthma recognition, the frequency of the lung sound signal 20A of the asthma event is set to 400 Hz, and the frequency of the normal lung sound signal 20A is 100 to 200 Hz (based on 100 Hz); For asthma recognition, the attribution of 400Hz is 1,100Hz, and the attribution degree is 0. Referring to the ninth figure, the frequencies of the six lung sound signals 20A shown in the figure all reach the frequency standard value (400Hz) (the attribution is 1), and the frequency standard value continues for the first identification time T1 (250 milliseconds), defined as an asthma event, the estimation identification device 54 overlaps the first, second, and third identification times T1, T2, and T32 During the time, it is determined that the subject 91 has six asthmatic events.

當以該第二模糊邏輯系統52(設定過程與該第一模糊邏輯系統51同理,恕不贅述)進行睡眠呼吸中止辨識,參閱第十A及第十B圖(分別為肺音訊號20A與腹部呼吸運動訊號30A皆經切割處理後之波形圖),圖中顯示符合呼吸氣流暫停大於10秒鐘(圖中之第二辨識時間T2係為28秒)以上之波形(睡眠呼吸中止事件之參考特徵);定義為睡眠呼吸中止事件;該估測辨識裝置54於該第一、該第二、該第三辨識時間T1、T2與T32之重疊時間內,判別該待測者91發生一次睡眠呼吸中止事件。When the second fuzzy logic system 52 (the setting process is the same as the first fuzzy logic system 51, and will not be described later), the sleep breathing suspension identification is performed, refer to the tenth A and tenth B pictures (the lung sound signal 20A and the respectively Abdominal respiratory motion signal 30A is the waveform after cutting process), the figure shows the waveform above the respiratory airflow pause for more than 10 seconds (the second identification time T2 in the figure is 28 seconds) (reference for sleep breathing suspension event) a feature is defined as a sleep apnea event; the estimation and identification device 54 determines that the test subject 91 has a sleep breath during the overlap time of the first, second, and third identification times T1, T2, and T32. Suspend the incident.

當以該第三模糊邏輯系統53(設定過程與該第一模糊邏輯系統51同理,恕不贅述)進行咳嗽辨識,參閱第十一A及第十一B圖(分別為肺音訊號20A與腹部呼吸運動訊號30A皆經切割處理後之波形圖),圖中顯示共有四個呼氣相位符合呼氣相位時間T31(介於0.3秒~1秒之間),並間隔達第三辨識時間T32(介於3秒~6秒之間)之間隔;定義為咳嗽事件;該估測辨識裝置54於該第一、該第二、該第三辨識時間T1、T2與T32之重疊時間內,判別該待測者91發生四次咳嗽事件。When the third fuzzy logic system 53 (the setting process is the same as the first fuzzy logic system 51, and will not be described later), the cough identification is performed, refer to the 11th and 11th B pictures (the lung sound signal 20A and the respectively Abdominal respiratory motion signal 30A is the waveform after cutting.) The picture shows that there are four exhalation phases in accordance with the expiratory phase time T31 (between 0.3 seconds and 1 second), and the interval is up to the third identification time T32. (interval between 3 seconds and 6 seconds); defined as a coughing event; the estimation and identification device 54 discriminates between the first, second, and third identification times T1, T2, and T32 The subject 91 had four coughing events.

當該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A經該第一、該第二與該第三模糊邏輯系統51、52與53辨識,不符合氣喘事件、睡眠呼吸中止事件、咳嗽事件時;則該估測辨識裝置54判別為正常或雜訊,例如如十二A及第十二B圖所示,係分別為某一待測者91之肺音訊號20A與腹部呼吸運動訊號30A經切割處理後之波形圖,圖中顯示之波形的頻率未達“氣喘事件”之頻率標準值(400Hz),相鄰之肺音訊號20A與相鄰之腹部呼吸運動訊號30A其間隔持續時間均未達睡眠呼吸中止事件之第二辨識時間T2(10秒以上);每一肺音訊號20A之呼氣相位的呼氣相位時間T31與第三辨識時間T32均未達“咳嗽事件”之標準值,該估測辨識裝置54判別待測者91為正常呼吸狀態。When the lung sound signal 20A, the abdominal respiratory motion signal 30A, and the wrist activity signal 40A are recognized by the first, the second, and the third fuzzy logic systems 51, 52, and 53 , the asthmatic event and the sleep breathing stop are not met. In the case of an event or a coughing event, the estimation and identification device 54 determines that it is normal or noise. For example, as shown in FIG. 12A and FIG. 12B, the lung sound signal 20A and the abdomen of a certain subject 91 respectively. The waveform of the respiratory motion signal 30A after cutting, the frequency of the waveform shown in the figure is less than the frequency standard value (400 Hz) of the "anti-asthmatic event", the adjacent lung sound signal 20A and the adjacent abdominal respiratory motion signal 30A The duration of the interval did not reach the second identification time T2 of the sleep apnea event (10 seconds or more); the expiratory phase time T31 and the third identification time T32 of the expiratory phase of each lung sound signal 20A did not reach the "cough event" The standard value of the estimation means 54 determines that the subject 91 is in a normal breathing state.

本發明之裝置部份係包括(參閱第二及第三圖):一聲音感測裝置20,係用以即時偵測一待測者91而產生一肺音訊號20A,並傳送至該偵測識別裝置50;一腹部感測裝置30,係用以即時偵測該待測者91之腹部呼吸起伏過程,而產生一腹部呼吸運動訊號30A,並傳送至該偵測識別裝置50;一腕部感測裝置40,係用以即時偵測該待測者91而產生一腕部活動訊號40A,並傳送至該偵測識別裝置50;一偵測識別裝置50,係具有一第一模糊邏輯系統51、一第二模糊邏輯系統52、一第三模糊邏輯系統53及一估測辨識裝置54;該偵測識別裝置50用以接收該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A;先對該肺音訊號20A進行快速傅立葉轉換(Fast Fourier Transform,英文簡稱FFT)而得到頻率(參閱第四圖),並對該肺音訊號20A及該腹部呼吸運動訊號30A進行訊號切割(Segmentation)處理;藉此,以該偵測識別裝置50配合該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A進行下列三種辨識作業(參閱第三圖):The device of the present invention includes (see the second and third figures): a sound sensing device 20 for detecting a test subject 91 and generating a lung sound signal 20A, and transmitting to the detection The identification device 50 is an abdominal sensing device 30 for detecting the abdominal breathing process of the test subject 91, and generating a abdominal respiratory motion signal 30A, and transmitting to the detection and recognition device 50; The sensing device 40 is configured to detect the subject 91 and generate a wrist activity signal 40A and transmit the motion signal to the detection device 50. The detection device 50 has a first fuzzy logic system. 51. A second fuzzy logic system 52, a third fuzzy logic system 53 and an estimation and identification device 54. The detection and identification device 50 is configured to receive the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist The activity signal 40A; firstly, the lung sound signal 20A is subjected to Fast Fourier Transform (FFT) to obtain the frequency (refer to the fourth figure), and the lung sound signal 20A and the abdominal respiratory motion signal 30A are signaled. Segmentation processing; borrowing To fit the 50 lung sound identification signal to the detecting means 20A, the signals 30A and abdominal respiratory movement of the arm 40A for the following three activities signal identification operation (see FIG third):

[a] 氣喘辨識:該偵測識別裝置50以該第一模糊邏輯系統51進行辨識;而氣喘發作之特徵為哮鳴;當該肺音訊號20A之頻率達到一頻率標準值,其係介於200Hz~600Hz之間(參閱第四圖(以「中」等頻率表示),且該頻率標準值持續一第一辨識時間T1,其係介於250毫秒~500毫秒之間(參閱第五圖,以「長」表示。);則辨識為哮鳴,並定義為該待測者91發生氣喘事件;[a] Asthma recognition: the detection and recognition device 50 is identified by the first fuzzy logic system 51; and the asthma attack is characterized by wheezing; when the frequency of the lung sound signal 20A reaches a frequency standard value, the system is interposed Between 200 Hz and 600 Hz (refer to the fourth figure (indicated by "medium" and other frequencies), and the frequency standard value continues for a first identification time T1, which is between 250 milliseconds and 500 milliseconds (see the fifth figure, It is expressed as "long".); it is recognized as wheezing, and is defined as the asthmatic event of the test subject 91;

[b] 睡眠呼吸中止辨識:該偵測識別裝置50以該第二模糊邏輯系統52進行辨識;當該相鄰之肺音訊號20A間隔持續一第二辨識時間T2;其係介於10秒~90秒之間(參閱第六圖,以「長」表示。);並該相鄰之腹部呼吸運動訊號30A同樣間隔持續該第二辨識時間T2(參閱第七圖,以「長」表示。);且由該腕部活動訊號40A判別該待測者91為睡眠狀態;則定義為該待測者91發生睡眠呼吸中止事件;[b] sleep breathing abort identification: the detection and recognition device 50 is identified by the second fuzzy logic system 52; when the adjacent lung sound signal 20A is separated by a second identification time T2; the system is between 10 seconds~ Between 90 seconds (refer to the sixth figure, indicated by "long"); and the adjacent abdominal respiratory motion signal 30A continues at the same interval for the second identification time T2 (refer to the seventh figure, indicated by "long".) And determining, by the wrist activity signal 40A, the test subject 91 is in a sleep state; then defining that the test subject 91 has a sleep breathing suspension event;

[c] 咳嗽辨識:該偵測識別裝置50以該第三模糊邏輯系統53進行辨識;當該每一肺音訊號20A之呼氣相位持續一呼氣相位時間T31(參閱第八A、第八B、第八C、第八D圖),其係介於0.3秒~1秒之間;且該相鄰之肺音訊號20A彼此間隔一第三辨識時間T32,其係介於3秒~6秒之間;則定義為該待測者91發生咳嗽事件;[c] Cough recognition: the detection and recognition device 50 recognizes the third fuzzy logic system 53; when the expiratory phase of each lung sound signal 20A continues for an expiratory phase time T31 (see eighth, eighth, eighth) B, eighth C, and eighth D), the system is between 0.3 seconds and 1 second; and the adjacent lung sound signals 20A are spaced apart from each other by a third identification time T32, which is between 3 seconds and 6 seconds. Between seconds; it is defined as the occurrence of a coughing event in the test subject 91;

最後,該估測辨識裝置54依氣喘事件、睡眠呼吸中止事件、咳嗽事件之順序,於該第一、該第二與該第三辨識時間T1、T2與T32之重疊時間內,比對去模糊化數值,辨識發生機率最大之事件,並判別其為該待測者91發生之事件。Finally, the estimation and identification device 54 performs deblurring in the overlapping time of the first, second, and third identification times T1, T2, and T32 according to an asthmatic event, a sleep breathing abort event, and a coughing event. The numerical value is used to identify the event with the highest probability of occurrence, and it is determined that it is an event occurring by the test subject 91.

實務上,該肺音訊號20A之頻率標準值可以400Hz為最佳值。In practice, the frequency standard value of the lung sound signal 20A can be 400 Hz as the optimum value.

該第一辨識時間T1係可介於100毫秒~500毫秒之間。The first identification time T1 can be between 100 milliseconds and 500 milliseconds.

該第二辨識時間T2係可介於10秒~120秒之間。The second identification time T2 can be between 10 seconds and 120 seconds.

該呼氣相位時間T31,係可介於0.12秒~2.5秒之間。The expiratory phase time T31 can be between 0.12 seconds and 2.5 seconds.

該第三辨識時間T32係可介於2秒~10秒之間。The third identification time T32 can be between 2 seconds and 10 seconds.

該聲音感測裝置20係包括:一第一固定部21、一第一殼體22、一聲音感測元件23、一第一記憶體24、一第一微處理器25、一第一無線射頻元件26及一第一電池27;該第一固定部21與該第一殼體22為相互結合(舉凡可相互連結之技術手段皆可為之)之結構,且該第一固定部21用以將該第一殼體22固定於該待測者91之胸口(原則上是平貼於胸口之皮膚上,接近肺之位置,以供長時間檢測之用);該聲音感測元件23(可為公知之微麥風。例如:中華民國發明專利第I268115號之『矽微麥克風之振膜晶片及其製造方法』)用以感測該待測者91之肺音訊號20A;該第一記憶體24用以記憶並將該肺音訊號20A傳送至該第一微處理器25,該第一微處理器25用以控制該第一無線射頻元件26將該肺音訊號20A傳送出去;該第一電池27係供應前述相關元件所需之電力。The sound sensing device 20 includes a first fixing portion 21, a first housing 22, an acoustic sensing component 23, a first memory 24, a first microprocessor 25, and a first radio frequency. The first fixing portion 21 and the first housing portion 22 are configured to be coupled to each other (the technical means can be connected to each other), and the first fixing portion 21 is used for Fixing the first housing 22 to the chest of the test subject 91 (in principle, it is flat on the skin of the chest, close to the position of the lung for long-term detection); the sound sensing component 23 ( For example, the "Micro-microphone diaphragm film and its manufacturing method" of the Republic of China invention patent No. I268115 is used to sense the lung sound signal 20A of the test subject 91; the first memory The body 24 is configured to transmit the lung audio signal 20A to the first microprocessor 25, and the first microprocessor 25 is configured to control the first radio frequency component 26 to transmit the lung audio signal 20A; A battery 27 supplies the power required by the aforementioned associated components.

該腹部感測裝置30係包括:一第二固定部31、一第二殼體32、一第一加速度感測器33、一第二記憶體34、一第二微處理器35、一第二無線射頻元件36及一第二電池37;該第二固定部31與該第二殼體32為相互結合(舉凡可相互連結之技術手段皆可為之)之結構,且該第二固定部31用以將該第二殼體32固定於該待測者91之腹部(原則上是接近腹部之皮膚,以供長時間檢測之用);該第一加速度感測器33用以感測該待測者91之腹部於呼吸過程之起伏狀態,並產生電壓變化,電壓變化可轉換為該腹部呼吸運動訊號30A;該第二記憶體34用以記憶並將該腹部呼吸運動訊號30A傳送至該第二微處理器35,該第二微處理器35用以控制該第二無線射頻元件36將該腹部呼吸運動訊號30A傳送出去;該第二電池37係供應前述相關元件所需之電力。The abdominal sensing device 30 includes a second fixing portion 31, a second housing 32, a first acceleration sensor 33, a second memory 34, a second microprocessor 35, and a second The radio frequency component 36 and the second battery 37; the second fixing portion 31 and the second casing 32 are combined with each other (the technical means can be connected to each other), and the second fixing portion 31 For fixing the second casing 32 to the abdomen of the test subject 91 (in principle, the skin close to the abdomen for long-term detection); the first acceleration sensor 33 is used to sense the waiting The abdomen of the tester 91 is in an undulating state of the breathing process, and a voltage change is generated, and the voltage change can be converted into the abdominal respiratory motion signal 30A; the second memory 34 is used to memorize and transmit the abdominal respiratory motion signal 30A to the first The second microprocessor 35 is configured to control the second radio frequency component 36 to transmit the abdominal respiratory motion signal 30A; the second battery 37 is to supply the power required by the related components.

該腕部感測裝置40係包括:一腕部固定帶41、一第三殼體42、一第二加速度感測器43、一第三記憶體44、一第三微處理器45、一第三無線射頻元件46、一第三電池47、一按鍵組48及一螢幕49;該腕部固定帶41用以將該第三殼體42固定該待測者91之腕部;該第二加速度感測器43用以感測該待測者91之腕部肌肉張力的變化(隨之產生電壓變化,並可設定電壓呈減少時,肌肉張力變小→待測者91呈睡眠。電壓呈增加時,肌肉張力變大→待測者91呈清醒。);電壓變化轉換為該腕部活動訊號40A,該第三記憶體44用以記憶該腕部活動訊號40A,並設一多工器441將接收之該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A多工傳送至該第三微處理器45,該第三微處理器45用以控制該第三無線射頻元件46,將該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A傳送出去;該第三電池47係供應前述相關元件所需之電力;該按鍵組48包括一選擇鍵481、一確認鍵482及一電源鍵483;該選擇鍵481用以選擇要進行之功能;該確認鍵482用以確認所選擇之功能;該電源鍵483用以啟、閉該腕部感測裝置40;該螢幕49用以顯示該腕部感測裝置40之訊號或相關之檢測結果。The wrist sensing device 40 includes a wrist fixing strap 41, a third housing 42, a second acceleration sensor 43, a third memory 44, a third microprocessor 45, and a first a third radio frequency component 46, a third battery 47, a button group 48 and a screen 49; the wrist fixing strap 41 is used to fix the third housing 42 to the wrist of the test subject 91; the second acceleration The sensor 43 is configured to sense a change in the muscle tension of the wrist of the test subject 91 (there is a voltage change, and when the set voltage is decreased, the muscle tension becomes small → the test subject 91 sleeps. The voltage increases. When the muscle tension becomes large, the test subject 91 is awake. The voltage change is converted into the wrist activity signal 40A, and the third memory 44 is used to memorize the wrist activity signal 40A, and a multiplexer 441 is provided. The received lung sound signal 20A, the abdominal respiratory motion signal 30A, and the wrist activity signal 40A are multiplexed to the third microprocessor 45, and the third microprocessor 45 is configured to control the third wireless RF component. 46, the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist activity signal 40A are transmitted The third battery 47 is supplied with power required by the aforementioned related components; the button group 48 includes a selection button 481, a confirmation button 482 and a power button 483; the selection button 481 is used to select a function to be performed; the confirmation button 482 is used to confirm the selected function; the power button 483 is used to open and close the wrist sensing device 40; the screen 49 is used to display the signal of the wrist sensing device 40 or related detection results.

該第一及該第二固定部21與31皆用以平貼於皮膚表面較不容易脫落,並當流汗或其他因素造成脫落亦可進行簡單置換。The first and the second fixing portions 21 and 31 are used for flattening on the surface of the skin, and are not easily detached, and can be easily replaced when sweating or other factors cause detachment.

該偵測識別裝置50可設於該腕部感測裝置40內(利於隨身24小時攜帶使用),並該聲音感測裝置20、該腹部感測裝置30與該腕部感測裝置40可透過該第一、該第二、該第三無線射頻元件26、36與46構成無線感測網路系統,以該第三無線射頻元件46為叢集頭(Cluster head)調配網路傳輸架構;當有外部裝置(如電腦或嵌入型處理器)等即可下載資料;亦可直接設於外部電腦或嵌入型處理器等,進行原始資料(RAW Data)分析。The detection and recognition device 50 can be disposed in the wrist sensing device 40 (used to be carried around for 24 hours), and the sound sensing device 20, the abdominal sensing device 30 and the wrist sensing device 40 can be permeable. The first, the second, and the third radio frequency components 26, 36, and 46 constitute a wireless sensing network system, and the third radio frequency component 46 is configured as a cluster head to configure a network transmission architecture; External devices (such as computers or embedded processors) can download data; they can also be directly connected to external computers or embedded processors for RAW Data analysis.

參閱第二及第三圖,該偵測識別裝置50又包括:一訊號處理模組50A,係用以從該多工器441接收該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A;該訊號處理模組50A設有:一快速傅立葉轉換單元501,係用以將該肺音訊號20A(此時為時域訊號)經傅立葉轉換(FFT)(進行在離散時間非週期之訊號之計算)變成頻域訊號20A(f);其處理方式係經下列公式:進行運算(公知技術,恕不贅述。);其中:x[n]為取樣後之訊號,Ω為單位(徑度);離散時間傅立葉轉換是有關區間-π<Ω≦π的頻率分佈。Referring to the second and third figures, the detection and identification device 50 further includes a signal processing module 50A for receiving the lung sound signal 20A, the abdominal respiratory motion signal 30A and the wrist from the multiplexer 441. The signal processing module 50A is provided with a fast Fourier transform unit 501 for performing Fourier transform (FFT) on the lung sound signal 20A (in this case, a time domain signal) (for discrete time aperiodic The calculation of the signal becomes a frequency domain signal 20A(f); its processing is based on the following formula: The calculation is performed (known techniques are not described here); wherein: x[n] is the signal after sampling, Ω is the unit (diameter); the discrete-time Fourier transform is the frequency distribution of the interval -π<Ω≦π.

一非線性能量運算單元502,係用以對該肺音訊號20A(概呈時域訊號)、該腹部呼吸運動訊號30A(概呈時域訊號)、該腕部活動訊號40A(概呈時域訊號)及該頻域訊號20A(f)進行訊號切割,再傳送至該第一、該第二與該第三模糊邏輯系統51、52與53;其處理方式係經下列公式:輸入訊號x(n)=Acos(ωn+)+w(n)進行運算;其中:w(n)表示白高斯之通道效應;A為輸入訊號的振幅;ω為輸入訊號的頻率;至於非線性能量運算可應用下列公式:Ψ[x(n)]=x(n-1)2-x(n)x(n-2)進行運算。A non-linear energy operation unit 502 is configured for the lung sound signal 20A (general time domain signal), the abdominal respiratory motion signal 30A (general time domain signal), and the wrist activity signal 40A (general time domain) The signal and the frequency domain signal 20A(f) perform signal cutting, and then transmit to the first, second and third fuzzy logic systems 51, 52 and 53; the processing method is as follows: input signal x ( n )= A cos( ωn + + w ( n ) performs the operation; where: w ( n ) represents the channel effect of white Gauss; A is the amplitude of the input signal; ω is the frequency of the input signal; as for the nonlinear energy operation, the following formula can be applied: Ψ[x( n)]=x(n-1) 2 -x(n)x(n-2) is operated.

一資料儲存部55(參閱第二及第二十二圖),用以儲存該估測辨識裝置54處理後之訊號及結果。A data storage unit 55 (see FIGS. 2 and 22) for storing the signals and results processed by the estimation and identification device 54.

至於模糊運算應用的部份,以公知洗衣機之洗衣時間設計為例:As for the part of the fuzzy computing application, the laundry time design of the known washing machine is taken as an example:

以欲清洗之衣物「污泥程度」與「油污程度」做為輸入條件,清洗時間為輸出,其模糊函數分別如第十三、第十四及第十五圖所示,模糊規則請參閱表一:For the clothing to be cleaned, the "sludge degree" and the "degree of oil stain" are used as input conditions, and the cleaning time is output. The fuzzy functions are shown in the thirteenth, fourteenth and fifteenth figures, respectively. One:

「衣物污泥:中;油污:中,清洗時間:長時間」。"Clothing sludge: medium; oil: medium, cleaning time: long time."

「衣物污泥:中,油污:大,清洗時間:長時間」。"Clothing sludge: medium, oil stain: large, cleaning time: long time."

「衣物污泥:高,油污:中,清洗時間:長時間」。"Clothing sludge: high, oil: medium, cleaning time: long time."

「衣物污泥:高,油污:大,清洗時間:很長時間」。"Clothing sludge: high, oily: large, cleaning time: very long time."

其模糊推論:Its fuzzy inference:

假設污泥為120,油污為140。Suppose the sludge is 120 and the oil is 140.

則得到污泥歸屬度”中”=0.8,“高”=0.2。Then, the sludge ownership degree is "in" = 0.8, and "high" = 0.2.

油污歸屬度”中”=0.6,”大”=0.4。Oil pollution attribution "in" = 0.6, "large" = 0.4.

經min運算:By min operation:

Min(中、中)=min(0.8、0.6)=0.6;min(中、大)=min(0.8、0.4)=0.4。Min (medium, middle) = min (0.8, 0.6) = 0.6; min (medium, large) = min (0.8, 0.4) = 0.4.

Min(高、中)=min(0.2、0.6)=0.2;min(高、大)=min(0.2、0.4)=0.2。Min (high, medium) = min (0.2, 0.6) = 0.2; min (high, large) = min (0.2, 0.4) = 0.2.

將min運算結果之數值再進行max運算:The value of the min operation result is further subjected to the max operation:

Max(0.6、0.4、0.2)=0.6(長);Max(0.2)=0.2(很長)。Max (0.6, 0.4, 0.2) = 0.6 (long); Max (0.2) = 0.2 (long).

再進行(例如以重心法解模糊化)模糊化為(13+23)/2=18(即為洗衣時間)。Then proceed (for example, to solve the blurring by the center of gravity method) and blur it to (13+23)/2=18 (that is, the washing time).

當應用於本發明時:When applied to the present invention:

[a] 以辨識氣喘事件為例:參閱第十六圖,係擷取總檢測時間(假設為一天24小時)中之120分鐘的波形,以第一個肺音訊號20A為例,其頻率為200Hz(參閱第四圖),且肺音訊號20A經切割後維持該第一辨識時間T1為250ms(參閱第五圖),其min-max運算如下表二:[a] Take the identification of asthmatic events as an example: refer to the sixteenth figure, which is a waveform of 120 minutes in the total detection time (assumed to be 24 hours a day), taking the first lung sound signal 20A as an example, the frequency is 200Hz (refer to the fourth figure), and the lung sound signal 20A is cut to maintain the first identification time T1 is 250ms (refer to the fifth figure), the min-max operation is as follows:

經min運算:By min operation:

MIN(極短,高)=(0,0)=0;MIN(極短,中)=(0,0)=0;MIN(極短,低)=(1,0)=0;MIN(短,高)=(0,0)=0;MIN(短,中)=(0,0)=0;MIN(短,低)=(1,0)=0;MIN(中,高)=(0,0)=0;MIN(中,中)=(0,0)=0;MIN(中,低)=(1,0)=0;MIN(長,高)=(0,1)=0;MIN(長,中)=(0,1)=0;MIN(長,低)=(1,1)=1。MIN (very short, high) = (0, 0) = 0; MIN (very short, medium) = (0, 0) = 0; MIN (very short, low) = (1, 0) = 0; MIN ( Short, high) = (0, 0) = 0; MIN (short, medium) = (0, 0) = 0; MIN (short, low) = (1, 0) = 0; MIN (medium, high) = (0,0)=0;MIN(medium,middle)=(0,0)=0;MIN(medium,low)=(1,0)=0;MIN(long,high)=(0,1) =0; MIN (long, medium) = (0, 1) = 0; MIN (long, low) = (1, 1) = 1.

由於該第一模糊邏輯系統51辨識氣喘事件係設定頻率為“中”;且維持第一辨識時間T1為“長”之配合要件為“辨識度高”,其餘皆為“辨識度低”。而MIN(長,中)=(0,1)=0,於第十七圖之辨識度“高”為0,至於辨識度“低”之最大值為1,於第十七圖之歸屬度為1,最後構成氣喘辨識線段L1,去模糊化值為25%,並可設定20%(亦可設定50%為判定標準)為判別氣喘之標準,若是設定為20%,則25%判定為氣喘,或是設定為50%,則25%判定未達氣喘標準,全依實際需求而定。The first fuzzy logic system 51 recognizes that the set frequency of the asthmatic event is "medium"; and the matching requirement that the first identification time T1 is "long" is "high recognition", and the rest are "low recognition". And MIN (long, medium) = (0, 1) = 0, the recognition degree "high" in the seventeenth figure is 0, and the maximum value of the recognition "low" is 1, the degree of attribution in the seventeenth figure 1 is the last to form the asthma recognition line segment L1, the defuzzification value is 25%, and 20% can be set (50% can also be set as the criterion for judging). If it is set to 20%, 25% is judged as Asthma, or set to 50%, 25% of the judgment does not meet the asthma standard, all depending on actual needs.

[b] 以辨識睡眠呼吸中止事件為例:參閱第十八圖,同樣擷取總檢測時間(假設為一天24小時)中之120分鐘的波形,並設定第一個肺音訊號20A經切割後間隔維持第二辨識時間T2(參閱第六圖,例如為50秒),且腹部呼吸運動訊號30A經切割後間隔同樣維持第二辨識時間T2(參閱第七圖,例如為50秒),其min-max運算如下表三:[b] For example, to identify the sleep breathing abort event: Refer to Figure 18, and take the waveform of 120 minutes in the total detection time (assumed to be 24 hours a day), and set the first lung sound signal 20A after cutting. The interval maintains the second identification time T2 (refer to the sixth figure, for example, 50 seconds), and the abdominal respiratory motion signal 30A also maintains the second identification time T2 after the cutting interval (refer to the seventh figure, for example, 50 seconds), and its min The -max operation is shown in Table 3 below:

經min運算:By min operation:

MIN(很長,很長)=(0,0)=0;MIN(很長,長)=(0,0)=0;MIN(很長,短)=(0,0)=0;MIN(長,很長)=(1,1)=1;MIN(長,長)=(1,1)=1;MIN(長,短)=(1,1)=1;MIN(短,很長)=(0,0)=0;MIN(短,長)=(0,0)=0;MIN(短,短)=(0,0)=0。MIN (very long, very long) = (0, 0) = 0; MIN (very long, long) = (0, 0) = 0; MIN (very long, short) = (0, 0) = 0; MIN (long, very long) = (1, 1) = 1; MIN (long, long) = (1, 1) = 1; MIN (long, short) = (1, 1) = 1; MIN (short, very Long) = (0, 0) = 0; MIN (short, long) = (0, 0) = 0; MIN (short, short) = (0, 0) = 0.

由於該第二模糊邏輯系統52辨識睡眠呼吸中止事件係設定該肺音訊號20A經切割後之間隔的第二辨識時間T2間隔為「長」,且該腹部呼吸運動訊號30A經切割後之間隔的第二辨識時間T2為「長」,則睡眠呼吸中止事件辨識度為高;其餘組合辨識度為低。The second fuzzy logic system 52 recognizes that the sleep apnea event is set to set the second identification time T2 interval of the interval after the lung sound signal 20A is cut to be "long", and the interval of the abdominal respiratory motion signal 30A is cut. When the second identification time T2 is "long", the recognition of the sleep breathing abort event is high; the remaining combination recognition is low.

而MIN(長,長)=(1,1)=1,於第十九圖之辨識度“高”為1,辨識度“低”為0,最後構成睡眠呼吸中止辨識線段L2,去模糊化值為75%。And MIN (long, long) = (1, 1) = 1, in the nineteenth figure, the recognition "high" is 1, the recognition "low" is 0, and finally constitutes the sleep breathing abort identification line segment L2, defuzzification The value is 75%.

[3] 以辨識咳嗽事件為例:參閱第二十圖,擷取總檢測時間(假設為一天24小時)中之120分鐘的波形,以第一個肺音訊號20A為例,該肺音訊號20A切割後維持第一辨識時間T1為200ms(參閱第五圖),且相鄰之該肺音訊號20A間隔維持第二辨識時間T2(參閱第六圖,例如為4秒),其min-max運算如下表四:[3] Take the identification of coughing event as an example: Refer to the 20th figure and take the waveform of 120 minutes in the total detection time (assumed to be 24 hours a day). Take the first lung sound signal 20A as an example. After the 20A cutting, the first identification time T1 is maintained for 200ms (refer to the fifth figure), and the adjacent lung sound signal 20A is maintained at the second identification time T2 (refer to the sixth figure, for example, 4 seconds), and its min-max The operation is as follows in Table 4:

經min運算:By min operation:

MIN(短,極短)=(1,0)=0;MIN(長,極短)=(0,0)=0;MIN(很長,極短)=(0,0)=0;MIN(短,短)=(1,0)=0;MIN(長,短)=(0,0)=0;MIN(很長,短)=(0,0)=0;MIN(短,中)=(1,0.3)=0.3;MIN(長,中)=(0,0.3)=0;MIN(很長,中)=(0,0.3)=0;MIN(短,長)=(1,0.5)=0.5;MIN(長,長)=(0,0.5)=0;MIN(很長,長)=(0,0.5)=0。MIN (short, very short) = (1, 0) = 0; MIN (long, very short) = (0, 0) = 0; MIN (very long, very short) = (0, 0) = 0; MIN (short, short) = (1, 0) = 0; MIN (long, short) = (0, 0) = 0; MIN (very long, short) = (0, 0) = 0; MIN (short, medium ) = (1, 0.3) = 0.3; MIN (long, medium) = (0, 0.3) = 0; MIN (very long, medium) = (0, 0.3) = 0; MIN (short, long) = (1 , 0.5) = 0.5; MIN (long, long) = (0, 0.5) = 0; MIN (very long, long) = (0, 0.5) = 0.

由於該第三模糊邏輯系統53辨識咳嗽事件係設定維持第一辨識時間T1為“中”,且第二辨識時間T2為“短”為“辨識度高”之要件,其餘組合皆為“辨識度低”,而MIN(短,中)=(1,0.3)=0.3(辨識度高),至於辨識度低(短,長)=(1,0.5)=0.5。於第二十一圖;取max則辨識度低為(18,32),辨識度高為(60,100),進行去模糊化採重心法則為(60+100)/2=80%。Since the third fuzzy logic system 53 recognizes that the coughing event is set to maintain the first identification time T1 as "medium" and the second identification time T2 is "short" to "high recognition", the remaining combinations are all "identification". Low", while MIN (short, medium) = (1, 0.3) = 0.3 (high recognition), as the recognition is low (short, long) = (1, 0.5) = 0.5. In the twenty-first figure; the max is low (18,32), the high degree of recognition is (60,100), and the defuzzification method is (60+100)/2=80%.

關於該估測辨識裝置54之動作過程:該多工器441(參閱第三圖)輸入之三個訊號(包括該肺音訊號20A、該腹部呼吸運動訊號30A及該腕部活動訊號40A),經該一、該第二及該第三模糊邏輯系統51、52與53得到去模糊化值,即進入該估測辨識裝置54先後進行閾值判別(參閱第二十二圖)、時間序列分析以及重複性比較。其中閾值可依嚴格度設定,如50%之辨識度方能進入分析;時間序列分析為固定時間(如每1秒)移動之固定長度(如120秒)為計算單位,若單位內發生不同事件則做重複性比較。舉例來講,假設t1-t2時間(120分鐘)發生之訊號為25%,在閾值(假設為50%)判斷為拒絕訊號。在t2-t3之120分鐘發生之訊號為87.5%,閾值假設為80%,則通過閾值後,經時間序列分析為同單位時間發生即以重複性比較估測為一次「睡眠呼吸中止事件」。然若數值一樣,則以氣喘>睡眠呼吸中止>咳嗽來判別。完成後即可顯示於該螢幕49,或儲存於該資料儲存部55。The operation process of the estimation and identification device 54 is: three signals input by the multiplexer 441 (refer to the third figure) (including the lung sound signal 20A, the abdominal respiratory motion signal 30A, and the wrist activity signal 40A), The first and second fuzzy logic systems 51, 52, and 53 obtain deblurring values, that is, enter the estimation and identification device 54 to perform threshold determination (see FIG. 22), time series analysis, and Repeatability comparison. The threshold can be set according to the strictness, for example, 50% of the recognition can enter the analysis; the time series analysis is a fixed time (such as 120 seconds) of the fixed time (such as every 1 second) is the calculation unit, if different events occur within the unit Then do a repetitive comparison. For example, suppose the signal generated by t1-t2 time (120 minutes) is 25%, and the threshold (assumed to be 50%) is judged as a rejection signal. The signal generated at 120 minutes of t2-t3 is 87.5%, and the threshold is assumed to be 80%. After passing the threshold, the time series analysis is the same unit time, that is, the repeat comparison is estimated as a "sleep breathing stop event". However, if the values are the same, it is judged by asthma > sleep breathing suspension > cough. After completion, it can be displayed on the screen 49 or stored in the data storage unit 55.

參閱第二十三圖,關於該估測辨識裝置54之估測辨識過程,於開始後可包括下列步驟:Referring to the twenty-third figure, the estimation and identification process of the estimation and identification device 54 may include the following steps after the start:

步驟A(61):輸入去模糊化之肺音訊號、腹部呼吸運動訊號及腕部活動訊號。Step A (61): Input the defuzzified lung sound signal, abdominal respiratory motion signal and wrist activity signal.

步驟B(62):判別訊號是否大於閾值?若判別結果為“是”(以第一模糊邏輯系統辨識氣喘事件為例,假設閾值為20%,若辨識氣喘事件得到之訊號為25%,則可通過閾值。),則進行下一步驟。若判別結果為“否”(假設為18%),則拒絕訊號。Step B (62): Is the discrimination signal greater than the threshold? If the result of the discrimination is "Yes" (take the first fuzzy logic system to identify the asthmatic event as an example, assume that the threshold is 20%, and if the signal obtained by identifying the asthma event is 25%, the threshold can be passed.), the next step is performed. If the result of the discrimination is "No" (assumed to be 18%), the signal is rejected.

步驟C(63):對訊號進行時間序列分析,將同單位時間發生之事件進行重複性比較,若數值一樣,則以氣喘>睡眠呼吸中止>咳嗽來判別。Step C (63): Perform a time series analysis on the signal, and repeat the comparison with the events occurring in the unit time. If the values are the same, the asthma is determined by asthma > sleep breathing suspension > cough.

步驟D(64):完成判別後,將訊號儲存或顯示以供參考。Step D (64): After the discrimination is completed, the signal is stored or displayed for reference.

本發明之優點及功效可歸納如下:The advantages and effects of the present invention can be summarized as follows:

[1] 利用特徵進行模糊邏輯辨識氣喘事件、睡眠呼吸中止事件與咳嗽事件相當準確。本發明預先測得人體於睡眠或清醒時,對於產生氣喘事件(哮鳴聲)、睡眠呼吸中止事件與咳嗽事件等現象時之各種最大特徵之集合,分別用以預先設定辨識氣喘事件、睡眠呼吸中止事件與咳嗽事件之三個模糊邏輯系統,當將任一待測者之肺音訊號、腹部呼吸運動訊號及腕部活動訊號分別輸入此三個模糊邏輯系統,即可配合估測辨識裝置,準確判別待測者是否於睡眠或清醒時,發生氣喘事件、睡眠呼吸中止事件與咳嗽事件等現象。[1] The use of features for fuzzy logic to identify asthma events, sleep breathing abortion events and coughing events is quite accurate. The invention pre-measures a set of various maximum features for a phenomenon of an asthmatic event (wrying sound), a sleep breathing abort event and a coughing event when the human body sleeps or wakes up, respectively, for presetting the identification of an asthmatic event and a sleep breathing, respectively. The three fuzzy logic systems of the suspension event and the coughing event, when the lung sound signal, the abdominal respiratory motion signal and the wrist activity signal of any test subject are respectively input into the three fuzzy logic systems, the estimation and identification device can be matched. Accurately discriminating whether the subject is asleep or awake, an asthmatic event, a sleep-disordering event, and a coughing event occur.

[2] 可判別氣喘事件、睡眠呼吸中止事件與咳嗽事件事件發生之次數與時間。本發明不僅可由三個模糊邏輯系統準確辨識氣喘事件、睡眠呼吸中止事件與咳嗽事件,並可由估測辨識裝置判別發生的次數與時間;供控制疾病判別之用較精確。[2] The number and timing of asthmatic events, sleep-disordering events, and coughing events can be identified. The invention can not only accurately identify the asthma event, the sleep breathing abort event and the cough event by three fuzzy logic systems, but also can determine the number and time of occurrence by the estimation and identification device; the use for controlling disease identification is more accurate.

[3] 無線感測設計可同時在靜態與動態下進行長時間檢測。本發明為無線感測設計,利於待測者隨身(長時間檢測)攜帶(動態)進行檢測,且不會影響生活作息中的動作,若供躺在病床上(靜態)之待測者使用,則讓待測者可輕鬆翻身不用耽心壓到感測線。故,無線設計同時利於在靜態與動態下進行長時間檢測。[3] The wireless sensing design allows for long-term detection both statically and dynamically. The invention is designed for wireless sensing, which is convenient for the person to be tested to carry (dynamic) detection with the body (long-time detection), and does not affect the action in the daily work and rest, if used for the person to be tested lying on the bed (static), Then let the person to be tested can easily turn over without touching the sensor line. Therefore, the wireless design is also conducive to long-term detection under static and dynamic conditions.

以上僅是藉由較佳實施例詳細說明本發明,對於該實施例所做的任何簡單修改與變化,皆不脫離本發明之精神與範圍。The present invention has been described in detail with reference to the preferred embodiments of the present invention, without departing from the spirit and scope of the invention.

11...準備步驟11. . . Preparation step

12...人體偵測步驟12. . . Human detection step

13...訊號處理步驟13. . . Signal processing step

14...訊號辨識步驟14. . . Signal identification step

15...完成步驟15. . . Complete the steps

20...聲音感測裝置20. . . Sound sensing device

20A...肺音訊號20A. . . Lung sound signal

20A(f)...頻域訊號20A(f). . . Frequency domain signal

21...第一固定部twenty one. . . First fixed part

22...第一殼體twenty two. . . First housing

23...聲音感測元件twenty three. . . Sound sensing component

24...第一記憶體twenty four. . . First memory

25...第一微處理器25. . . First microprocessor

26...第一無線射頻元件26. . . First radio frequency component

27...第一電池27. . . First battery

30...腹部感測裝置30. . . Abdominal sensing device

30A...腹部呼吸運動訊號30A. . . Abdominal respiratory motion signal

31...第二固定部31. . . Second fixed part

32...第二殼體32. . . Second housing

33...第一加速度感測器33. . . First acceleration sensor

34...第二記憶體34. . . Second memory

35...第二微處理器35. . . Second microprocessor

36...第二無線射頻元件36. . . Second radio frequency component

37...第二電池37. . . Second battery

40...腕部感測裝置40. . . Wrist sensing device

40A...腕部活動訊號40A. . . Wrist activity signal

41...腕部固定帶41. . . Wrist strap

42...第三殼體42. . . Third housing

43...第二加速度感測器43. . . Second acceleration sensor

44...第三記憶體44. . . Third memory

441...多工器441. . . Multiplexer

45...第三微處理器45. . . Third microprocessor

46...第三無線射頻元件46. . . Third wireless RF component

47...第三電池47. . . Third battery

48...按鍵組48. . . Button set

481...選擇鍵481. . . Selection button

482...確認鍵482. . . Enter

483...電源鍵483. . . Power button

49...螢幕49. . . Screen

50...偵測識別裝置50. . . Detection and identification device

50A...訊號處理模組50A. . . Signal processing module

501...傅立葉轉換單元501. . . Fourier transform unit

502...非線性能量運算單元502. . . Nonlinear energy unit

51...第一模糊邏輯系統51. . . First fuzzy logic system

52...第二模糊邏輯系統52. . . Second fuzzy logic system

53...第三模糊邏輯系統53. . . Third fuzzy logic system

54...估測辨識裝置54. . . Estimation identification device

55...資料儲存部55. . . Data storage department

61...步驟A61. . . Step A

62...步驟B62. . . Step B

63...步驟C63. . . Step C

64...步驟D64. . . Step D

91...待測者91. . . Subject to be tested

T1...第一辨識時間T1. . . First identification time

T2...第二辨識時間T2. . . Second identification time

T31...呼氣相位時間T31. . . Expiratory phase time

T32...第三辨識時間T32. . . Third identification time

L1...氣喘辨識線段L1. . . Asthma identification line segment

L2...睡眠呼吸中止辨識線段L2. . . Sleep breathing abort identification line segment

第一圖係本發明之方法之流程圖The first figure is a flow chart of the method of the present invention

第二圖係本發明之裝置示意圖The second figure is a schematic view of the device of the present invention

第三圖係本發明之裝置的系統方塊圖The third figure is a system block diagram of the device of the present invention.

第四圖係本發明之肺音訊號經快速傅立葉轉換後之訊號切割頻率模糊歸屬函數圖The fourth figure is a fuzzy attribution function diagram of the signal cutting frequency after the fast Fourier transform of the lung sound signal of the present invention

第五圖係本發明之肺音訊號經訊號切割後之事件維持時間(ms)模糊歸屬函數圖The fifth figure is the event retention time (ms) fuzzy attribution function graph of the lung sound signal of the present invention after signal cutting

第六圖係本發明之肺音訊號經訊號切割後之事件維持時間(s)模糊歸屬函數圖The sixth figure is the event retention time (s) fuzzy attribution function graph of the lung sound signal of the present invention after signal cutting

第七圖係本發明之腹部呼吸運動訊號經訊號切割後之事件維持時間模糊歸屬函數圖The seventh figure is the fuzzy time-dependent function of the event maintenance time after the abdominal respiratory motion signal of the present invention is cut by the signal

第八A、第八B、第八C及第八D圖係分別為本發明之經訊號切割處理後之肺音訊號與辨識時間皆符合辨識為咳嗽事件之波形圖The eighth, eighth, eighth, eighth, and eighth D drawings are respectively waveforms of the lung sound signal and the identification time after the signal cutting process of the present invention are consistent with the waveform identified as a cough event.

第九圖係本發明之判別待測者發生六次氣喘事件之波形圖The ninth graph is a waveform diagram of the six asthmatic events in the present invention.

第十A及第十B圖係分別為本發明之判別待測者發生一次睡眠呼吸中止事件之波形圖The tenth A and Xth B diagrams are waveform diagrams of a sleep breathing abort event in the discriminating test subject of the present invention, respectively.

第十一A及第十一B圖係分別為本發明之判別待測者發生四次咳嗽事件之波形圖The eleventh A and eleventh B diagrams are waveform diagrams for discriminating four times of coughing events in the present invention.

第十二A及第十二B圖係分別為本發明之判別待測者呈正常呼吸之波形圖The twelfth A and twelfth B diagrams are waveform diagrams for determining the normal breathing of the subject to be tested according to the present invention, respectively.

第十三、第十四及第十五圖係分別為本發明之污泥程度、油污程度與清洗時間之模糊邏輯函數之示意圖The thirteenth, fourteenth and fifteenth drawings are schematic diagrams of the fuzzy logic function of the degree of sludge, the degree of oil stain and the cleaning time of the present invention, respectively.

第十六及第十七圖係分別為本發明應用於氣喘事件辨識之肺音訊號振幅與歸屬度之示意圖The sixteenth and seventeenth figures are schematic diagrams showing the amplitude and attribution of the lung sound signal for the identification of asthmatic events according to the present invention.

第十八及第十九圖係分別為本發明之應用於睡眠呼吸中止事件之腹部呼吸運動訊號振幅與歸屬度之示意圖The eighteenth and nineteenth figures are schematic diagrams showing the amplitude and attribution of the abdominal respiratory motion signal applied to the sleep breathing stop event of the present invention, respectively.

第二十及第二十一圖係分別為本發明之應用於咳嗽事件之肺音訊號振幅與歸屬度之示意圖The twentieth and twenty-first figures are schematic diagrams showing the amplitude and attribution of the lung sound signal applied to the cough event of the present invention, respectively.

第二十二圖係本發明之估測辨識裝置之系統方塊圖The twenty-second figure is a system block diagram of the estimation and identification device of the present invention

第二十三圖係第二十二圖之動作流程圖The twenty-third figure is the action flow chart of the twenty-second figure

11...準備步驟11. . . Preparation step

12...人體偵測步驟12. . . Human detection step

13...訊號處理步驟13. . . Signal processing step

14...訊號辨識步驟14. . . Signal identification step

15...完成步驟15. . . Complete the steps

Claims (8)

一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法,係包括下列步驟:一.準備步驟:預先準備一聲音感測裝置、一腹部感測裝置、一腕部感測裝置及一偵測識別裝置,該偵測識別裝置具有一第一模糊邏輯系統、一第二模糊邏輯系統、一第三模糊邏輯系統及一估測辨識裝置;二.人體偵測步驟:該聲音感測裝置用以即時偵測一待測者而產生一肺音訊號,並傳送至該偵測識別裝置;該腹部感測裝置用以即時偵測該待測者之腹部呼吸起伏過程,而產生一腹部呼吸運動訊號,並傳送至該偵測識別裝置;該腕部感測裝置用以即時偵測該待測者而產生一腕部活動訊號,並傳送至該偵測識別裝置;三.訊號處理步驟:該偵測識別裝置先將該肺音訊號進行快速傅立葉轉換而得到頻率,並對該肺音訊號及該腹部呼吸運動訊號進行訊號切割處理;四.訊號辨識步驟:該偵測識別裝置以該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號進行下列三種辨識作業:[a] 氣喘辨識:該偵測識別裝置以該第一模糊邏輯系統進行辨識;而氣喘發作之特徵為哮鳴;當該肺音訊號之頻率達到一頻率標準值,其係介於200Hz~600Hz之間,且該頻率標準值持續一第一辨識時間,其係介於250毫秒~500毫秒之間;則辨識為哮鳴,並定義為該待測者發生氣喘事件;[b] 睡眠呼吸中止辨識:該偵測識別裝置以該第二模糊邏輯系統進行辨識;當該相鄰之肺音訊號間隔持續一第二辨識時間;其係介於10秒~90秒之間;並該相鄰之腹部呼吸運動訊號同樣間隔持續該第二辨識時間;且由該腕部活動訊號判別該待測者為睡眠狀態;則定義為該待測者發生睡眠呼吸中止事件;[c] 咳嗽辨識:該偵測識別裝置以該第三模糊邏輯系統進行辨識;當該每一肺音訊號之呼氣相位持續一呼氣相位時間,其係介於0.3秒~1秒之間;且該相鄰之肺音訊號彼此間隔一第三辨識時間,其係介於3秒~6秒之間;則定義為該待測者發生咳嗽事件;最後,該估測辨識裝置依氣喘事件、睡眠呼吸中止事件、咳嗽事件之順序,於該第一、該第二與該第三辨識時間之重疊時間內,比對去模糊化數值,辨識發生機率最大之事件,並判別其為該待測者發生之事件;五.完成步驟:完成辨識氣喘事件、睡眠呼吸中止事件與咳嗽事件。A method for identifying characteristics of sleep breathing, coughing, and wheezing includes the following steps: The preparation step is: preparing a sound sensing device, an abdominal sensing device, a wrist sensing device and a detecting and identifying device, wherein the detecting and identifying device has a first fuzzy logic system, a second fuzzy logic system, a third fuzzy logic system and an estimation and identification device; The human body detecting step is configured to detect a person to be tested and generate a lung sound signal and transmit the signal to the detecting and identifying device; the abdominal sensing device is configured to detect the test subject immediately The abdominal breathing process generates a abdominal respiratory motion signal and transmits it to the detection and identification device; the wrist sensing device is configured to instantly detect the test subject to generate a wrist activity signal and transmit the motion signal to the detective Measuring and identifying device; three. Signal processing step: the detection and recognition device first performs fast Fourier transform on the lung sound signal to obtain a frequency, and performs signal cutting processing on the lung sound signal and the abdominal respiratory motion signal; The signal recognition step: the detection and recognition device performs the following three identification operations using the lung sound signal, the abdominal respiratory motion signal, and the wrist activity signal: [a] asthma recognition: the detection recognition device uses the first fuzzy logic system Identification is performed; and the asthma attack is characterized by wheezing; when the frequency of the lung sound signal reaches a frequency standard value, the system is between 200 Hz and 600 Hz, and the frequency standard value continues for a first identification time. Between 250 milliseconds and 500 milliseconds; it is recognized as wheezing and is defined as an asthmatic event in the subject; [b] sleep breathing abort identification: the detection and recognition device is identified by the second fuzzy logic system; The adjacent lung sound signal interval continues for a second identification time; the system is between 10 seconds and 90 seconds; and the adjacent abdominal respiratory motion signal is equally spaced for the second identification time; and the wrist is The activity signal determines that the subject is in a sleep state; it is defined as a sleep apnea event of the subject; [c] cough recognition: the detection and recognition device is identified by the third fuzzy logic system; The expiratory phase of each lung sound signal continues for an expiratory phase time, which is between 0.3 seconds and 1 second; and the adjacent lung sound signals are spaced apart from each other by a third identification time, which is between 3 seconds. Between ~6 seconds; it is defined as the occurrence of a coughing event in the subject; finally, the estimation and identification device is in the order of the asthmatic event, the sleep breathing abort event, and the coughing event, in the first, the second and the third During the overlap time of the identification time, the value is defuzzified to identify the event with the highest probability of occurrence, and the event is determined to be the event of the test subject; Complete the steps: complete the identification of asthmatic events, sleep breathing suspension events and coughing events. 如申請專利範圍第1項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法,其中:該肺音訊號之頻率標準值係以400Hz為最佳值;該第一辨識時間係介於100毫秒~500毫秒之間;該第二辨識時間係介於10秒~120秒之間;該呼氣相位時間係介於0.12秒~2.5秒之間;該第三辨識時間係介於2秒~10秒之間。A method for identifying characteristics of sleep apnea, cough, and wheezing as described in claim 1, wherein: the frequency standard value of the lung sound signal is 400 Hz as an optimum value; and the first identification time is between 100 Between milliseconds and 500 milliseconds; the second identification time is between 10 seconds and 120 seconds; the exhalation phase time is between 0.12 seconds and 2.5 seconds; the third identification time is between 2 seconds~ Between 10 seconds. 如申請專利範圍第1項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法,其中:該聲音感測裝置係包括:一第一固定部、一第一殼體、一聲音感測元件、一第一記憶體、一第一微處理器、一第一無線射頻元件及一第一電池;該第一固定部與該第一殼體為相互結合之結構,且該第一固定部用以將該第一殼體固定於該待測者之胸口;該聲音感測元件用以感測該待測者之肺音訊號;該第一記憶體用以記憶並將該肺音訊號傳送至該第一微處理器,該第一微處理器用以控制該第一無線射頻元件將該肺音訊號傳送出去;該第一電池係供應前述相關元件所需之電力;該腹部感測裝置係包括:一第二固定部、一第二殼體、一第一加速度感測器、一第二記憶體、一第二微處理器、一第二無線射頻元件及一第二電池;該第二固定部與該第二殼體為相互結合之結構,且該第二固定部用以將該第二殼體固定於該待測者之腹部;該第一加速度感測器用以感測該待測者之腹部於呼吸過程之起伏狀態,並產生電壓變化,電壓變化可轉換為該腹部呼吸運動訊號;該第二記憶體用以記憶並將該腹部呼吸運動訊號傳送至該第二微處理器,該第二微處理器用以控制該第二無線射頻元件將該腹部呼吸運動訊號傳送出去;該第二電池係供應前述相關元件所需之電力;該腕部感測裝置係包括:一腕部固定帶、一第三殼體、一第二加速度感測器、一第三記憶體、一第三微處理器、一第三無線射頻元件、一第三電池、一按鍵組及一螢幕;該腕部固定帶用以將該第三殼體固定該待測者之腕部;該第二加速度感測器用以感測該待測者之腕部肌肉張力的變化;電壓變化轉換為該腕部活動訊號,該第三記憶體用以記憶該腕部活動訊號,並設一多工器將接收之該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號多工傳送至該第三微處理器,該第三微處理器用以控制該第三無線射頻元件,將該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號傳送出去;該第三電池係供應前述相關元件所需之電力;該按鍵組包括一選擇鍵、一確認鍵及一電源鍵;該選擇鍵用以選擇要進行之功能;該確認鍵用以確認所選擇之功能;該電源鍵用以啟、閉該腕部感測裝置;該螢幕用以顯示該腕部感測裝置之訊號或相關之檢測結果。The method for identifying the characteristics of sleep apnea, cough and wheezing as described in claim 1, wherein the sound sensing device comprises: a first fixing portion, a first housing, and an acoustic sensing component a first memory, a first microprocessor, a first radio frequency component, and a first battery; the first fixing portion and the first housing are combined with each other, and the first fixing portion is used for Fixing the first housing to the chest of the test subject; the sound sensing component is configured to sense the lung sound signal of the test subject; the first memory is used to memorize and transmit the lung sound signal to The first microprocessor is configured to control the first radio frequency component to transmit the lung audio signal; the first battery system supplies power required by the related component; the abdominal sensing device includes a second fixing portion, a second housing, a first acceleration sensor, a second memory, a second microprocessor, a second radio frequency component, and a second battery; the second fixing The second housing and the second housing are combined with each other, and The second fixing portion is configured to fix the second housing to the abdomen of the subject; the first acceleration sensor is configured to sense the undulating state of the abdomen of the subject in the breathing process, and generate a voltage change. The voltage change can be converted into the abdominal respiratory motion signal; the second memory is used to memorize and transmit the abdominal respiratory motion signal to the second microprocessor, and the second microprocessor is configured to control the second wireless RF component to be The abdominal respiratory motion signal is transmitted; the second battery is supplied with power required by the related component; the wrist sensing device includes: a wrist fixing strap, a third housing, and a second acceleration sensor a third memory, a third microprocessor, a third radio frequency component, a third battery, a button set, and a screen; the wrist fixing strap is used to fix the third housing to be tested The second acceleration sensor is configured to sense a change in the muscle tension of the wrist of the subject; the voltage change is converted into the wrist activity signal, and the third memory is used to memorize the wrist activity signal. And set up a multiplex Transmitting the received lung sound signal, the abdominal respiratory motion signal and the wrist activity signal to the third microprocessor, the third microprocessor is configured to control the third wireless RF component, and the lung sound signal The abdominal respiratory motion signal and the wrist activity signal are transmitted; the third battery is supplied with power required by the related component; the button group includes a selection button, a confirmation button and a power button; the selection button is used for Selecting the function to be performed; the confirmation button is used to confirm the selected function; the power button is used to activate and close the wrist sensing device; the screen is used to display the signal of the wrist sensing device or the related detection result . 如申請專利範圍第1項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的方法,其中,該偵測識別裝置又包括:一訊號處理模組,係用以從該多工器接收該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號;該訊號處理模組設有:一快速傅立葉轉換單元,係用以將該肺音訊號經傅立葉轉換變成頻域訊號;一非線性能量運算單元,係用以對該肺音訊號、該腹部呼吸運動訊號、該腕部活動訊號及該頻域訊號進行訊號切割,再傳送至該第一、該第二與該第三模糊邏輯系統進行運算;一資料儲存部,用以儲存該估測辨識裝置處理後之訊號及結果。The method for identifying characteristics of sleep apnea, cough, and wheezing as described in claim 1, wherein the detection and recognition device further includes: a signal processing module for receiving the lung from the multiplexer The audio signal, the abdominal respiratory motion signal and the wrist activity signal; the signal processing module is provided with: a fast Fourier transform unit for transforming the lung sound signal into a frequency domain signal by Fourier transform; a nonlinear energy operation The unit is configured to perform signal cutting on the lung sound signal, the abdominal respiratory motion signal, the wrist activity signal and the frequency domain signal, and then transmit the signal to the first, second and third fuzzy logic systems for calculation a data storage unit for storing the signals and results processed by the estimation and identification device. 一種辨識睡眠呼吸中止、咳嗽與氣喘之特徵的裝置,係包括:一聲音感測裝置,係用以即時偵測一待測者而產生一肺音訊號,並傳送至該偵測識別裝置;一腹部感測裝置,係用以即時偵測該待測者之腹部呼吸起伏過程,而產生一腹部呼吸運動訊號,並傳送至該偵測識別裝置;一腕部感測裝置,係用以即時偵測該待測者而產生一腕部活動訊號,並傳送至該偵測識別裝置;一偵測識別裝置,係具有一第一模糊邏輯系統、一第二模糊邏輯系統、一第三模糊邏輯系統及一估測辨識裝置;該偵測識別裝置用以接收該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號;先對該肺音訊號進行快速傅立葉轉換而得到頻率,並對該肺音訊號及該腹部呼吸運動訊號進行訊號切割處理;藉此,以該偵測識別裝置配合該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號進行下列三種辨識作業:[a] 氣喘辨識:該偵測識別裝置以該第一模糊邏輯系統進行辨識;而氣喘發作之特徵為哮鳴;當該肺音訊號之頻率達到一頻率標準值,其係介於200Hz~600Hz之間,且該頻率標準值持續一第一辨識時間,其係介於250毫秒~500毫秒之間;則辨識為哮鳴,並定義為該待測者發生氣喘事件;[b] 睡眠呼吸中止辨識:該偵測識別裝置以該第二模糊邏輯系統進行辨識;當該相鄰之肺音訊號間隔持續一第二辨識時間;其係介於10秒~90秒之間;並該相鄰之腹部呼吸運動訊號同樣間隔持續該第二辨識時間;且由該腕部活動訊號判別該待測者為睡眠狀態;則定義為該待測者發生睡眠呼吸中止事件;[c] 咳嗽辨識:該偵測識別裝置以該第三模糊邏輯系統進行辨識;當該每一肺音訊號之呼氣相位持續一呼氣相位時間,其係介於0.3秒~1秒之間;且該相鄰之肺音訊號彼此間隔一第三辨識時間,其係介於3秒~6秒之間;則定義為該待測者發生咳嗽事件;最後,該估測辨識裝置依氣喘事件、睡眠呼吸中止事件、咳嗽事件之順序,於該第一、該第二與該第三辨識時間之重疊時間內,比對去模糊化數值,辨識發生機率最大之事件,並判別其為該待測者發生之事件。A device for recognizing the characteristics of sleep breathing, coughing, and wheezing includes: a sound sensing device for detecting a patient to be detected to generate a lung sound signal and transmitting the signal to the detecting and identifying device; The abdominal sensing device is configured to instantly detect the abdominal undulation process of the test subject, and generate a abdominal respiratory motion signal and transmit the same to the detection and identification device; a wrist sensing device is used for instant detection Measuring the subject to generate a wrist activity signal and transmitting the signal to the detection and identification device; a detection and identification device having a first fuzzy logic system, a second fuzzy logic system, and a third fuzzy logic system And an estimation device for receiving the lung sound signal, the abdominal respiratory motion signal and the wrist activity signal; performing fast Fourier transform on the lung sound signal to obtain a frequency, and the lung The signal signal and the abdominal respiratory motion signal are subjected to signal cutting processing; thereby, the detection and identification device cooperates with the lung sound signal, the abdominal respiratory motion signal and the wrist activity signal Three types of identification operations are listed: [a] Asthma identification: the detection and recognition device is identified by the first fuzzy logic system; and the asthma attack is characterized by wheezing; when the frequency of the lung sound signal reaches a frequency standard value, the system Between 200 Hz and 600 Hz, and the standard value of the frequency continues for a first identification time, which is between 250 milliseconds and 500 milliseconds; it is recognized as wheezing and is defined as an asthmatic event of the test subject; b] sleep breathing abort identification: the detection and recognition device is identified by the second fuzzy logic system; when the adjacent lung sound signal interval continues for a second identification time; the system is between 10 seconds and 90 seconds; And the adjacent abdominal respiratory motion signal continues to be separated by the second identification time; and the wrist activity signal determines that the test subject is in a sleep state; and is defined as a sleep breathing suspension event of the test subject; [c] Cough recognition: the detection and recognition device is identified by the third fuzzy logic system; when the expiratory phase of each lung sound signal continues for an expiratory phase time, the system is between 0.3 seconds and 1 second; and the Adjacent lung audio The third identification time is separated from each other by 3 seconds to 6 seconds; it is defined as the occurrence of a coughing event in the test subject; finally, the estimated identification device is based on an asthmatic event, a sleep breathing stop event, and a coughing event. In the sequence, during the overlapping time of the first, the second, and the third identification time, the deblurring value is compared, and the event with the highest probability of occurrence is identified, and the event is determined to be an event of the test subject. 如申請專利範圍第5項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的裝置,其中:該肺音訊號之頻率標準值係以400Hz為最佳值;該第一辨識時間係介於100毫秒~500毫秒之間;該第二辨識時間係介於10秒~120秒之間;該呼氣相位時間係介於0.12秒~2.5秒之間;該第三辨識時間係介於2秒~10秒之間。The device for identifying the characteristics of sleep apnea, cough and asthma as described in claim 5, wherein: the frequency standard value of the lung sound signal is 400 Hz as an optimum value; the first identification time is between 100 Between milliseconds and 500 milliseconds; the second identification time is between 10 seconds and 120 seconds; the exhalation phase time is between 0.12 seconds and 2.5 seconds; the third identification time is between 2 seconds~ Between 10 seconds. 如申請專利範圍第5項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的裝置,其中:該聲音感測裝置係包括:一第一固定部、一第一殼體、一聲音感測元件、一第一記憶體、一第一微處理器、一第一無線射頻元件及一第一電池;該第一固定部與該第一殼體為相互結合之結構,且該第一固定部用以將該第一殼體固定於該待測者之胸口;該聲音感測元件用以感測該待測者之肺音訊號;該第一記憶體用以記憶並將該肺音訊號傳送至該第一微處理器,該第一微處理器用以控制該第一無線射頻元件將該肺音訊號傳送出去;該第一電池係供應前述相關元件所需之電力;該腹部感測裝置係包括:一第二固定部、一第二殼體、一第一加速度感測器、一第二記憶體、一第二微處理器、一第二無線射頻元件及一第二電池;該第二固定部與該第二殼體為相互結合之結構,且該第二固定部用以將該第二殼體固定於該待測者之腹部;該第一加速度感測器用以感測該待測者之腹部於呼吸過程之起伏狀態,並產生電壓變化,電壓變化可轉換為該腹部呼吸運動訊號;該第二記憶體用以記憶並將該腹部呼吸運動訊號傳送至該第二微處理器,該第二微處理器用以控制該第二無線射頻元件將該腹部呼吸運動訊號傳送出去;該第二電池係供應前述相關元件所需之電力;該腕部感測裝置係包括:一腕部固定帶、一第三殼體、一第二加速度感測器、一第三記憶體、一第三微處理器、一第三無線射頻元件、一第三電池、一按鍵組及一螢幕;該腕部固定帶用以將該第三殼體固定該待測者之腕部;該第二加速度感測器用以感測該待測者之腕部肌肉張力的變化;電壓變化轉換為該腕部活動訊號,該第三記憶體用以記憶該腕部活動訊號,並設一多工器將接收之該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號多工傳送至該第三微處理器,該第三微處理器用以控制該第三無線射頻元件,將該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號傳送出去;該第三電池係供應前述相關元件所需之電力;該按鍵組包括一選擇鍵、一確認鍵及一電源鍵;該選擇鍵用以選擇要進行之功能;該確認鍵用以確認所選擇之功能;該電源鍵用以啟、閉該腕部感測裝置;該螢幕用以顯示該腕部感測裝置之訊號或相關之檢測結果。The device for identifying the characteristics of sleep apnea, cough and asthma as described in claim 5, wherein the sound sensing device comprises: a first fixing portion, a first housing, and an acoustic sensing component a first memory, a first microprocessor, a first radio frequency component, and a first battery; the first fixing portion and the first housing are combined with each other, and the first fixing portion is used for Fixing the first housing to the chest of the test subject; the sound sensing component is configured to sense the lung sound signal of the test subject; the first memory is used to memorize and transmit the lung sound signal to The first microprocessor is configured to control the first radio frequency component to transmit the lung audio signal; the first battery system supplies power required by the related component; the abdominal sensing device includes a second fixing portion, a second housing, a first acceleration sensor, a second memory, a second microprocessor, a second radio frequency component, and a second battery; the second fixing The second housing and the second housing are combined with each other, and The second fixing portion is configured to fix the second housing to the abdomen of the subject; the first acceleration sensor is configured to sense the undulating state of the abdomen of the subject in the breathing process, and generate a voltage change. The voltage change can be converted into the abdominal respiratory motion signal; the second memory is used to memorize and transmit the abdominal respiratory motion signal to the second microprocessor, and the second microprocessor is configured to control the second wireless RF component to be The abdominal respiratory motion signal is transmitted; the second battery is supplied with power required by the related component; the wrist sensing device includes: a wrist fixing strap, a third housing, and a second acceleration sensor a third memory, a third microprocessor, a third radio frequency component, a third battery, a button set, and a screen; the wrist fixing strap is used to fix the third housing to be tested The second acceleration sensor is configured to sense a change in the muscle tension of the wrist of the subject; the voltage change is converted into the wrist activity signal, and the third memory is used to memorize the wrist activity signal. And set up a multiplex Transmitting the received lung sound signal, the abdominal respiratory motion signal and the wrist activity signal to the third microprocessor, the third microprocessor is configured to control the third wireless RF component, and the lung sound signal The abdominal respiratory motion signal and the wrist activity signal are transmitted; the third battery is supplied with power required by the related component; the button group includes a selection button, a confirmation button and a power button; the selection button is used for Selecting the function to be performed; the confirmation button is used to confirm the selected function; the power button is used to activate and close the wrist sensing device; the screen is used to display the signal of the wrist sensing device or the related detection result . 如申請專利範圍第5項所述之辨識睡眠呼吸中止、咳嗽與氣喘之特徵的裝置,其中,該偵測識別裝置又包括:一訊號處理模組,係用以從該多工器接收該肺音訊號、該腹部呼吸運動訊號及該腕部活動訊號;該訊號處理模組設有:一快速傅立葉轉換單元,係用以將該肺音訊號經傅立葉轉換變成頻域訊號;一非線性能量運算單元,係用以對該肺音訊號、該腹部呼吸運動訊號、該腕部活動訊號及該頻域訊號進行訊號切割,再傳送至該第一、該第二與該第三模糊邏輯系統進行運算;一資料儲存部,用以儲存該估測辨識裝置處理後之訊號及結果。The device for identifying the characteristics of sleep apnea, cough and wheezing as described in claim 5, wherein the detection and recognition device further comprises: a signal processing module for receiving the lung from the multiplexer The audio signal, the abdominal respiratory motion signal and the wrist activity signal; the signal processing module is provided with: a fast Fourier transform unit for transforming the lung sound signal into a frequency domain signal by Fourier transform; a nonlinear energy operation The unit is configured to perform signal cutting on the lung sound signal, the abdominal respiratory motion signal, the wrist activity signal and the frequency domain signal, and then transmit the signal to the first, second and third fuzzy logic systems for calculation a data storage unit for storing the signals and results processed by the estimation and identification device.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103690168A (en) * 2013-12-31 2014-04-02 中国科学院深圳先进技术研究院 Method and system for detecting obstructive sleep apnea syndrome
TWI562761B (en) * 2014-05-22 2016-12-21 Apex Medical Corp
TWI642025B (en) * 2017-08-11 2018-11-21 國立中興大學 Method of fast evaluation for the moderate to severe obstructive sleep apnea

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103690168A (en) * 2013-12-31 2014-04-02 中国科学院深圳先进技术研究院 Method and system for detecting obstructive sleep apnea syndrome
CN103690168B (en) * 2013-12-31 2015-04-22 中国科学院深圳先进技术研究院 Method and system for detecting obstructive sleep apnea syndrome
TWI562761B (en) * 2014-05-22 2016-12-21 Apex Medical Corp
TWI642025B (en) * 2017-08-11 2018-11-21 國立中興大學 Method of fast evaluation for the moderate to severe obstructive sleep apnea

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