TWM610717U - Sleep apnea screening equipment - Google Patents

Sleep apnea screening equipment Download PDF

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TWM610717U
TWM610717U TW109214019U TW109214019U TWM610717U TW M610717 U TWM610717 U TW M610717U TW 109214019 U TW109214019 U TW 109214019U TW 109214019 U TW109214019 U TW 109214019U TW M610717 U TWM610717 U TW M610717U
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sleep
signal
subject
cheek
blood oxygen
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楊靜修
趙哲暘
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牙易科技有限公司
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Abstract

一種睡眠呼吸障礙篩檢設備,包含:閉封元件;臉頰鼓動感測構件,包含複數個感測元件以數量對稱且分別位於該閉封元件之相對二側的方式貼附於該受測者之雙頰,係取得該受測者之雙頰的臉頰鼓動訊號;以及訊號處理構件,接收該臉頰鼓動訊號以及一血氧飽和度訊號,且該訊號處理構件對於來自複數個該感測元件的該臉頰鼓動訊號的波形執行訊號處理而產生訊號處理結果,並依據該訊號處理結果與該血氧飽和度訊號在單位時間內的相互參照比對,而產生用於供睡眠呼吸障礙分析的睡眠呼吸障礙篩檢結果。A device for screening sleep disordered breathing, comprising: a closed element; a cheek agitation sensing member, including a plurality of sensing elements attached to the subject in a symmetrical number and located on opposite sides of the closed element The cheeks obtain the cheek stirring signal of the subject’s cheeks; and the signal processing component receives the cheek stirring signal and a blood oxygen saturation signal, and the signal processing component responds to the cheek stirring signal from a plurality of the sensing elements The waveform of the cheek pulsation signal performs signal processing to generate a signal processing result, and based on the cross-reference comparison between the signal processing result and the blood oxygen saturation signal in a unit time, the sleep disordered breathing for sleep disordered breathing analysis is generated Screening results.

Description

睡眠呼吸障礙篩檢設備Sleep apnea screening equipment

本創作相關於睡眠呼吸障礙之篩檢,特別是關於一種睡眠呼吸障礙篩檢設備。This creation is related to the screening of sleep disordered breathing, especially a device for the screening of sleep disordered breathing.

睡眠呼吸中止症是種常見的睡眠呼吸障礙,主要可分為阻塞型及中樞型,其中阻塞型較為普遍,而中樞型較不常見。阻塞型睡眠呼吸中止症係為患者於睡眠期間,位在咽喉附近的軟組織因張力鬆弛而塌陷,進而壓迫上呼吸道,導致反覆的呼吸暫時停止。臨床表現包括打鼾、血氧濃度降低、睡眠中斷、容易感到疲憊及嗜睡等。目前眾多的臨床研究亦已證實睡眠呼吸中止症是高血壓、糖尿病、胃酸逆流、記憶力衰退,甚至青光眼、視網膜病變的重要病因。Sleep apnea is a common type of sleep breathing disorder, which can be divided into obstructive and central types. The obstructive type is more common and the central type is less common. Obstructive sleep apnea is when the soft tissue near the throat collapses due to the relaxation of tension during the patient's sleep, which then compresses the upper respiratory tract, causing repetitive breathing to stop temporarily. Clinical manifestations include snoring, decreased blood oxygen concentration, interrupted sleep, fatigue and lethargy. Numerous clinical studies have confirmed that sleep apnea is an important cause of hypertension, diabetes, acid reflux, memory decline, and even glaucoma and retinopathy.

對於是否確實罹患睡眠呼吸中止症之診斷,標準地是採用睡眠多項生理檢查(Polysomnography, PSG)。在進行PSG的過程中,受測者必須在睡眠檢查室裡過夜睡覺,由相關睡眠技術員協助測試、採集並記錄至少六小時睡眠期間的多項生理訊號。由於進行PSG需要投注大量的時間及醫療資源,一般情況下會在執行PSG前做篩檢,再依據篩檢結果決定受測者是否需要做PSG。For the diagnosis of sleep apnea, the standard method is to use polysomnography (PSG). During the PSG process, the subject must sleep in the sleep examination room overnight, and the relevant sleep technician will assist in testing, collecting and recording multiple physiological signals during at least six hours of sleep. Since the PSG requires a lot of time and medical resources, under normal circumstances, a screening test is performed before the PSG is performed, and then based on the screening test results, it is determined whether the subject needs a PSG.

一般而言,篩檢評估受測者是否患有睡眠呼吸中止症之最重要的參考依據為睡眠期間受測者的血氧飽和度。篩檢的過程中,睡眠技術員主要係藉由觀察脈衝式血氧濃度器(Pulse oximeter)所感測出受測者的血氧飽和度的相關數據及圖表來推估受測者的呼吸型態,進而判斷是否患有睡眠呼吸中止症。然而,此判斷結果係為睡眠技術員推估受測者之呼吸型態而得,因此該判斷結果難免存在一些睡眠技術員個人主觀意識的成分,因而使得該判斷結果的客觀性以及準確度受到影響。Generally speaking, the most important reference for screening to assess whether a subject suffers from sleep apnea is the subject’s blood oxygen saturation during sleep. During the screening process, the sleep technician mainly estimates the subject’s breathing pattern by observing the relevant data and graphs of the subject’s blood oxygen saturation sensed by the pulse oximeter. Then determine whether you suffer from sleep apnea. However, this judgment result is derived from the sleep technician's estimation of the breathing pattern of the subject. Therefore, the judgment result inevitably contains some components of the sleep technician's personal subjective consciousness, which affects the objectivity and accuracy of the judgment result.

因此,習知用於篩檢睡眠呼吸中止症之相關設備及方法仍具有其改良之必要。Therefore, the related equipment and methods for screening sleep apnea still need to be improved.

因此,本創作的目的即在提供一種睡眠呼吸障礙篩檢設備,可輔助篩檢受測者是否患有睡眠呼吸中止症以提升睡眠技術員之判斷結果的客觀性以及準確度。Therefore, the purpose of this creation is to provide a sleep apnea screening device that can assist in screening whether the subject has sleep apnea to improve the objectivity and accuracy of the sleep technician's judgment results.

本創作為解決習知技術之問題所採用之技術手段係提供一種睡眠呼吸障礙篩檢設備,包含:閉封元件,係經配置而覆蓋於受測者之雙唇而閉合口腔;臉頰鼓動感測構件,包含複數個感測元件,複數個該感測元件係以數量對稱且分別位於該閉封元件之相對二側的方式而貼附於該受測者之雙頰,其中該臉頰鼓動感測構件係取得該受測者之雙頰的臉頰鼓動訊號,以感測出該受測者是否於睡眠過程具有屬於因進行口呼吸所形成雙頰鼓動的動作;以及訊號處理構件,電性連接於該臉頰鼓動感測構件,而自複數個該感測元件接收該臉頰鼓動訊號、以及接收一血氧飽和度訊號,且該訊號處理構件對於來自複數個該感測元件的該臉頰鼓動訊號的波形執行訊號處理而產生訊號處理結果,並依據該訊號處理結果與該血氧飽和度訊號在單位時間內的相互參照比對,而產生用於供睡眠呼吸障礙分析的睡眠呼吸障礙篩檢結果,其中,該睡眠呼吸障礙分析係將該訊號處理結果之波形比對於該血氧飽和度訊號之曲線,而取得該受測者在該單位時間內進行口呼吸次數以及該血氧飽和度的對照而據以確認該受測者是否患有睡眠呼吸中止症。The technical means used in this creation to solve the problems of the conventional technology is to provide a sleep apnea screening device, including: a sealing element, which is configured to cover the lips of the test subject to close the oral cavity; cheek agitation sensing The component includes a plurality of sensing elements, and the plurality of sensing elements are attached to the subject's cheeks in a symmetrical manner and are respectively located on two opposite sides of the closed element, wherein the cheeks are pulsing for sensing The component obtains the cheek agitation signal of the subject’s cheeks to detect whether the subject has an action of cheek agitation caused by mouth breathing during sleep; and the signal processing component is electrically connected to The cheek pulsation sensing component receives the cheek pulsation signal from a plurality of the sensing elements and receives a blood oxygen saturation signal, and the signal processing component responds to the waveform of the cheek pulsation signal from the plurality of the sensing elements Perform signal processing to generate a signal processing result, and compare the signal processing result with the blood oxygen saturation signal in a unit time cross-reference comparison to generate a sleep breathing disorder screening result for sleep disordered breathing analysis, where The sleep-disordered breathing analysis is based on comparing the waveform of the signal processing result to the curve of the blood oxygen saturation signal, and obtaining the comparison of the number of mouth breaths of the subject in the unit time and the blood oxygen saturation. To confirm whether the subject suffers from sleep apnea.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,該血氧飽和度訊號係接收自該睡眠呼吸障礙篩檢設備之內部或外部之血氧感測構件,該血氧感測構件係感測該受測者於睡眠過程之血氧飽和度而取得血氧飽和度訊號。In an embodiment of the present creation, a device for screening sleep apnea is provided. The blood oxygen saturation signal is received from a blood oxygen sensing component inside or outside the device for detecting sleep apnea. The blood oxygen sensor The component senses the blood oxygen saturation of the subject during sleep to obtain the blood oxygen saturation signal.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,該訊號處理構件所執行的該訊號處理為針對該受測者之該臉頰鼓動訊號的該波形進行濾波、波形辨識、波形註記的運算處理而產生該訊號處理結果。In an embodiment of the present creation, a device for screening sleep disordered breathing is provided. The signal processing performed by the signal processing component is filtering, waveform identification, and waveform annotation of the waveform of the cheek stirring signal of the subject The processing result of the signal is generated by the operation processing.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,包含一睡眠呼吸障礙分析構件,電性連接於該訊號處理構件,而根據該睡眠呼吸障礙篩檢結果進行該睡眠呼吸障礙分析。In an embodiment of the present creation, a sleep apnea screening device is provided, which includes a sleep apnea analysis component electrically connected to the signal processing component, and performs the sleep apnea analysis based on the sleep apnea screening result .

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,該臉頰鼓動感測構件包括第一感測元件以及第二感測元件,該第一感測元件以及該第二感測元件係分別設置於該受測者之該雙頰,且電性連接於該訊號處理構件。In an embodiment of the present invention, a device for screening sleep apnea is provided. The cheek motivation sensing component includes a first sensing element and a second sensing element, the first sensing element and the second sensing element They are respectively arranged on the cheeks of the subject, and are electrically connected to the signal processing component.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,該感測元件為加速度感測器,該臉頰鼓動感測構件所測得之該臉頰鼓動訊號包含沿X軸振動的訊號、沿Y軸振動的訊號以及沿Z軸振動的訊號,該訊號處理係將該受測者之同一側臉頰之該沿X軸振動的訊號、該沿Y軸振動的訊號以及該沿Z軸振動的訊號的波形予以統合歸納而獲得具有時間記錄以及表示該受測者之雙頰鼓動次數的該訊號處理結果。In an embodiment of the present invention, a device for screening sleep apnea is provided, the sensing element is an acceleration sensor, and the cheek agitation signal measured by the cheek agitation sensing component includes a signal that vibrates along the X axis, Signals vibrating along the Y axis and vibrating along the Z axis. The signal processing is the signal vibrating along the X axis, the signal vibrating along the Y axis, and the signal vibrating along the Z axis on the same side of the subject’s cheek. The waveforms of the signals are integrated and summarized to obtain the signal processing result with a time record and indicating the number of cheek agitation of the subject.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,該血氧感測構件係為脈衝式血氧濃度器。In an embodiment of the present invention, a device for screening sleep disordered breathing is provided, and the blood oxygen sensing component is a pulse-type blood oxygen concentration device.

在本創作的一實施例中係提供一種睡眠呼吸障礙篩檢設備,在該睡眠呼吸障礙分析構件中,該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘預定口呼吸次數以下的口呼吸、並且該血氧飽和度落在預定血氧飽和度變化之範圍,而確認該受測者並未患有睡眠呼吸中止症,該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘該預定口呼吸次數以上的口呼吸、並且該血氧飽和度落在該預定血氧飽和度變化之範圍,而確認該受測者並未患有睡眠呼吸中止症,該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘該預定口呼吸次數的口呼吸、並且該血氧飽和度低於該預定血氧飽和度變化而確認該受測者患有睡眠呼吸中止症。In an embodiment of the present creation, a device for screening for sleep apnea is provided. In the sleep apnea analysis component, the sleep apnea analysis is based on a predetermined schedule every minute during the sleep process of the subject within the unit time. Mouth breathing less than the number of mouth breaths, and the blood oxygen saturation falls within the range of the predetermined blood oxygen saturation change, and it is confirmed that the subject does not suffer from sleep apnea, the analysis basis of the sleep breathing disorder is in the unit During sleep, the subject performs mouth breathing more than the predetermined number of mouth breaths per minute, and the blood oxygen saturation falls within the range of the predetermined blood oxygen saturation change, and it is confirmed that the subject does not suffer from Sleep apnea, the analysis basis of sleep breathing disorder, during the unit time the subject performs mouth breathing of the predetermined number of mouth breaths per minute during sleep, and the blood oxygen saturation is lower than the predetermined blood oxygen saturation The change confirms that the subject suffers from sleep apnea.

經由本創作的睡眠呼吸障礙篩檢設備所採用之技術手段,為睡眠技術員額外提供了多項評估及判斷受測者罹患睡眠呼吸中止症與否的參考依據,使得睡眠技術員於進行感測及推估受測者在睡眠期間的呼吸型態時,得以依據經該脈衝式血氧濃度器所測得之該血氧飽和度數據配合對比本創作之睡眠呼吸障礙篩檢設備所測得之該訊號處理結果而進行該睡眠呼吸障礙分析。換言之,本創作的睡眠呼吸障礙篩檢設備能夠使受測者在睡眠期間的呼吸型態能夠以更加具象化的方式呈現,進而幫助睡眠技術員提升判斷結果的客觀性以及準確度。The technical means used in the sleep apnea screening equipment created by this invention provide sleep technicians with a number of additional references for assessing and judging whether the subject is suffering from sleep apnea, allowing sleep technicians to perform sensing and estimation The breathing pattern of the subject during sleep can be processed based on the blood oxygen saturation data measured by the pulse oximetry device and compared with the signal measured by the sleep disordered breathing screening device of this invention. As a result, the sleep-disordered breathing analysis was performed. In other words, the sleep apnea screening device of the present invention can make the breathing pattern of the subject during sleep can be presented in a more concrete way, thereby helping the sleep technician to improve the objectivity and accuracy of the judgment result.

以下根據第1圖至第5圖,而說明本創作的實施方式。該說明並非為限制本創作的實施方式,而為本創作之實施例的一種。The following describes the implementation of this creation based on Figures 1 to 5. This description is not intended to limit the implementation of this creation, but is a kind of embodiment of this creation.

如第1圖至第3圖所示,依據本創作的一實施例的一睡眠呼吸障礙篩檢設備100,包含:閉封元件1,係經配置而覆蓋於受測者S之雙唇而閉合口腔;臉頰鼓動感測構件2,包含複數個感測元件21,複數個該感測元件21係以數量對稱且分別位於該閉封元件1之相對二側的方式而貼附於該受測者S之雙頰,其中該臉頰鼓動感測構件2係取得該受測者S之雙頰的臉頰鼓動訊號MBS,以感測出該受測者S是否於睡眠過程具有屬於因進行口呼吸所形成雙頰鼓動的動作;血氧感測構件3,係感測該受測者S於睡眠過程之血氧飽和度OS而取得血氧飽和度訊號OSS;以及訊號處理構件4,電性連接於該臉頰鼓動感測構件2以及該血氧感測構件3,而自複數個該感測元件21接收該臉頰鼓動訊號MBS、以及自該血氧感測構件3接收該血氧飽和度訊號OSS,且該訊號處理構件4對於來自複數個該感測元件21的該臉頰鼓動訊號MBS的波形執行訊號處理SP而產生訊號處理結果SPR,並依據該訊號處理結果SPR與該血氧飽和度訊號OSS在單位時間內的相互參照比對,而產生用於供睡眠呼吸障礙分析A的睡眠呼吸障礙篩檢結果R,其中,該睡眠呼吸障礙分析A係將該訊號處理結果SPR之波形比對於該血氧飽和度訊號OSS之曲線,而取得該受測者S在該單位時間內進行口呼吸次數以及該血氧飽和度OS的對照而據以確認該受測者S是否患有睡眠呼吸中止症。As shown in Figs. 1 to 3, a sleep apnea screening device 100 according to an embodiment of the present creation includes: a sealing element 1, which is configured to cover the lips of the subject S and close Oral cavity; cheek agitation sensing member 2, including a plurality of sensing elements 21, a plurality of the sensing elements 21 are symmetrical in number and respectively located on the opposite sides of the closed element 1 and attached to the subject The cheeks of S, wherein the cheek agitation sensing component 2 obtains the cheek agitation signal MBS of the cheeks of the subject S to detect whether the subject S is caused by mouth breathing during sleep The action of bulging cheeks; the blood oxygen sensing component 3, which senses the blood oxygen saturation OS of the subject S during sleep to obtain the blood oxygen saturation signal OSS; and the signal processing component 4, which is electrically connected to the The cheek agitation sensing member 2 and the blood oxygen sensing member 3, and the cheek agitation signal MBS is received from a plurality of the sensing elements 21, and the blood oxygen saturation signal OSS is received from the blood oxygen sensing member 3, and The signal processing component 4 performs signal processing SP on the waveform of the cheek stirring signal MBS from a plurality of the sensing elements 21 to generate a signal processing result SPR, and according to the signal processing result SPR and the blood oxygen saturation signal OSS in the unit A cross-reference comparison over time to generate a sleep apnea screening result R for sleep apnea analysis A, where the sleep apnea analysis A compares the signal processing result SPR waveform to the blood oxygen saturation The curve of the degree signal OSS is obtained, and a comparison of the number of oral breaths performed by the subject S in the unit time and the blood oxygen saturation OS is obtained to confirm whether the subject S suffers from sleep apnea.

詳細而言,該封閉元件1係用於使該受測者S的該口腔閉合以便於該臉頰鼓動感測構件2於該受測者S進行口呼吸時,避免因空氣直接由口腔呼出而使該臉頰鼓動感測構件2所感測到之該臉頰鼓動訊號MBS過於微弱,而增加本創作之該睡眠呼吸障礙篩檢設備100進行該睡眠呼吸障礙分析A時的難易度。換言之,該封閉元件1係有助於該臉頰鼓動感測構件2感測出清楚、明顯的該臉頰鼓動訊號MBS。其中,該臉頰鼓動訊號MBS係以振動波形的方式呈現。該封閉元件1在本實施例中為透氣膠帶,亦可以為其他能夠用於使該受測者S的該口腔閉合但又不影響該受測者S進行口呼吸的任何物件。In detail, the closing element 1 is used to close the oral cavity of the subject S so that the cheek agitation sensing member 2 avoids direct exhalation of air from the oral cavity when the subject S is breathing through the mouth. The cheek agitation signal MBS sensed by the cheek agitation sensing component 2 is too weak, which increases the difficulty of the sleep-disordered breathing detection device 100 of the present invention when performing the sleep-disordered breathing analysis A. In other words, the closing element 1 helps the cheek movement sensing member 2 to detect the cheek movement signal MBS clearly and clearly. Among them, the cheek stirring signal MBS is presented in the form of vibration waveform. The closing element 1 is a breathable tape in this embodiment, and it can also be any other object that can be used to close the oral cavity of the subject S without affecting the subject S's mouth breathing.

詳細而言,複數個該感測元件21係以數量對稱且分別位於該閉封元件1之相對二側的方式而貼附於該受測者S之雙頰。其中,數量對稱的複數個該感測元件21係指:若該受測者S之該雙頰的其中一側貼附有一個該感測元件21時,則該雙頰的另一側亦必定貼附有一個該感測元件21;若該雙頰之其中一側貼附有二個該感測元件21時,則該雙頰的另一側亦必定貼附有二個該感測元件21,以此類推。In detail, a plurality of the sensing elements 21 are attached to the cheeks of the subject S in such a manner that they are symmetric in number and located on opposite sides of the sealing element 1. Wherein, a plurality of the sensing elements 21 in a symmetrical number means: if one of the sensing elements 21 is attached to one of the cheeks of the subject S, the other side of the cheeks must also be One of the sensing elements 21 is attached; if two of the sensing elements 21 are attached to one side of the cheeks, two of the sensing elements 21 must be attached to the other side of the cheeks , And so on.

詳細而言,雖然該臉頰鼓動感測構件2主要係感測因該受測者S進行口呼吸使雙頰鼓動而形成之該臉頰鼓動訊號MBS,但若是該受測者S於睡眠期間亦有進行鼻呼吸,該臉頰鼓動感測構件2亦能感測到因該受測者S進行鼻呼吸所產生的微弱振動,則該臉頰鼓動訊號MBS亦可能包括微小波形,一般會將此種微小波形視為鼻呼吸訊號。另一方面,該訊號處理構件4所執行的該訊號處理SP更包括了將所接收到的該臉頰鼓動訊號MBS之振幅放大的功能,因此,若睡眠技術員欲觀察該受測者S的鼻呼吸次數,便可利用該訊號處理構件4所執行的該訊號處理SP,將該臉頰鼓動訊號MBS的振幅放大以便觀察該鼻呼吸次數。In detail, although the cheek agitation sensing member 2 mainly senses the cheek agitation signal MBS formed by the subject S’s mouth breathing and cheeks agitation, but if the subject S is also sleeping during sleep During nasal breathing, the cheek agitation sensing member 2 can also sense the weak vibrations caused by the subject S’s nasal breathing, and the cheek agitation signal MBS may also include tiny waveforms, and such tiny waveforms are generally Treated as a nasal breathing signal. On the other hand, the signal processing SP performed by the signal processing component 4 further includes the function of amplifying the amplitude of the received cheek stirring signal MBS. Therefore, if the sleep technician wants to observe the nasal breathing of the subject S The signal processing SP performed by the signal processing component 4 can be used to amplify the amplitude of the cheek stirring signal MBS to observe the number of nasal breaths.

如第2圖以及第3圖所示,依據本創作的實施例的睡眠呼吸障礙篩檢設備100,其中該訊號處理構件4所執行的該訊號處理SP為針對該受測者S之該臉頰鼓動訊號MBS的該波形進行該濾波F、該波形辨識WR、該波形註記WM的運算處理而產生該訊號處理結果SPR。As shown in FIGS. 2 and 3, according to the embodiment of the present invention, the sleep apnea screening device 100, wherein the signal processing SP performed by the signal processing component 4 is for the cheek agitation of the subject S The waveform of the signal MBS is processed by the filtering F, the waveform identification WR, and the waveform annotation WM to generate the signal processing result SPR.

詳細而言,第4圖以及第5圖係分別為歷時1分鐘內該臉頰鼓動感測構件2所感測出之該臉頰鼓動訊號MBS的原始訊號示意圖以及歷時1分鐘內經該訊號處理構件4執行該訊號處理SP所得出之該訊號處理結果SPR的示意圖。如第2圖至第5圖所示,由於該臉頰鼓動感測構件2於感測該受測者S在睡眠過程中因口呼吸而形成雙頰鼓動之該動作時,其他不具特殊意義的振動亦會被該臉頰鼓動感測構件2感測到,使得尚未經過該訊號處理SP之該臉頰鼓動訊號MBS存在雜訊,因而不利於後續一睡眠呼吸障礙分析構件5進行該睡眠呼吸障礙分析A。進行該訊號處理SP可視為該睡眠呼吸障礙分析構件5於進行該睡眠呼吸障礙分析A前的前置作業,目的為使該睡眠呼吸障礙分析構件5於進行該睡眠呼吸障礙分析A時能夠以更有效率的方式輔助確認該受測者S是否患有睡眠呼吸中止症。該訊號處理SP所包括之該濾波F運算處理係為將尚未經處理之該臉頰鼓動訊號MBS所存在之雜訊排除;該波形辨識WR運算處理係為針對該臉頰鼓動訊號MBS辨識每個因該受測者S進行口呼吸所形成之波形,以使該睡眠呼吸障礙分析構件5於進行該睡眠呼吸障礙分析A時便於計算該受測者S之單位時間內進行的口呼吸次數;該波形註記WM運算處理係為針對該臉頰鼓動訊號MBS的每個波峰標註記號,以使該睡眠呼吸障礙分析構件5於進行該睡眠呼吸障礙分析A時便於計算該受測者S之單位時間內進行口呼吸次數。In detail, Fig. 4 and Fig. 5 are respectively a schematic diagram of the original signal of the cheek agitation signal MBS sensed by the cheek agitation sensing component 2 in 1 minute, and the signal processing unit 4 executes the signal in 1 minute. A schematic diagram of the signal processing result SPR obtained by the signal processing SP. As shown in Figures 2 to 5, because the cheek pulsation sensing member 2 senses the movement of cheek pulsation due to mouth breathing during sleep of the subject S, other vibrations that have no special significance It will also be sensed by the cheek agitation sensing component 2, so that the cheek agitation signal MBS that has not undergone the signal processing SP has noise, which is not conducive to the subsequent sleep breathing disorder analysis component 5 to perform the sleep breathing disorder analysis A. Performing the signal processing SP can be regarded as the pre-work of the sleep disordered breathing analysis component 5 before the sleep disordered breathing analysis A, and the purpose is to enable the sleep disordered breathing analysis component 5 to perform better sleep breathing disorder analysis A. An efficient way to assist in confirming whether the subject S suffers from sleep apnea. The signal processing SP includes the filtering F operation processing to eliminate the noise in the cheek stirring signal MBS that has not yet been processed; the waveform recognition WR operation processing is to identify each cause of the cheek stirring signal MBS The waveform formed by the oral breathing of the subject S, so that the sleep-disordered breathing analysis component 5 facilitates the calculation of the number of oral breaths per unit time of the subject S when performing the sleep-disordered breathing analysis A; the waveform remarks The WM calculation process is to mark each peak of the cheek stirring signal MBS, so that the sleep disordered breathing analysis component 5 facilitates the calculation of the oral breathing per unit time of the subject S when performing the sleep disordered breathing analysis A. frequency.

如第2圖所示,依據本創作的實施例的睡眠呼吸障礙篩檢設備100,更包含該睡眠呼吸障礙分析構件5,電性連接於該訊號處理構件4,而根據該睡眠呼吸障礙篩檢結果R進行該睡眠呼吸障礙分析A。As shown in Figure 2, the sleep apnea screening device 100 according to the embodiment of the present creation further includes the sleep apnea analysis component 5, which is electrically connected to the signal processing component 4, and is screened according to the sleep apnea disorder Result R performs the sleep-disordered breathing analysis A.

詳細而言,該睡眠呼吸障礙分析構件5係為一睡眠檢測相關儀器,當然,本創作不以此為限。於其他實施例中,該睡眠呼吸障礙分析構件5亦可為其他能夠確認該受測者S是否患有睡眠呼吸中止症的相關人員,例如:睡眠技術員、醫師或是智慧型機器人等。In detail, the sleep-disordered breathing analysis component 5 is a sleep detection-related instrument. Of course, this creation is not limited to this. In other embodiments, the sleep-disordered breathing analysis component 5 can also be other related personnel who can confirm whether the subject S has sleep apnea, such as a sleep technician, a physician, or a smart robot.

如第2圖所示,依據本創作的實施例的睡眠呼吸障礙篩檢設備100,該臉頰鼓動感測構件2包括第一感測元件21a以及第二感測元件21b,該第一感測元件21a以及該第二感測元件21b係分別設置於該受測者S之該雙頰,且電性連接於該訊號處理構件4。As shown in Figure 2, according to the sleep apnea screening device 100 according to the embodiment of the present creation, the cheek movement sensing member 2 includes a first sensing element 21a and a second sensing element 21b. The first sensing element 21 a and the second sensing element 21 b are respectively disposed on the cheeks of the subject S, and are electrically connected to the signal processing member 4.

如第2圖至第5圖所示,依據本創作的實施例的睡眠呼吸障礙篩檢設備100,該感測元件21為加速度感測器(accelerometer),該臉頰鼓動感測構件2所測得之該臉頰鼓動訊號MBS包含沿X軸振動的訊號、沿Y軸振動的訊號以及沿Z軸振動的訊號,該訊號處理SP係將該受測者S之同一側臉頰之該沿X軸振動的訊號、該沿Y軸振動的訊號以及該沿Z軸振動的訊號的波形予以統合歸納而獲得具有時間記錄以及表示該受測者S之雙頰鼓動次數的該訊號處理結果SPR。As shown in Figures 2 to 5, in the sleep disordered breathing screening device 100 according to the embodiment of the present creation, the sensing element 21 is an acceleration sensor (accelerometer), which is measured by the cheek agitation sensing member 2 The cheek stirring signal MBS includes a signal that vibrates along the X axis, a signal that vibrates along the Y axis, and a signal that vibrates along the Z axis. The signal processing SP is to vibrate along the X axis of the cheek on the same side of the subject S. The waveforms of the signal, the signal vibrating along the Y axis, and the signal vibrating along the Z axis are integrated to obtain the signal processing result SPR with a time record and indicating the number of cheek agitation of the subject S.

詳細而言,如第2圖至第4圖所示,該第一感測元件21a感測到所在之該側臉頰之該沿X軸振動的訊號為X1、該沿Y軸振動的訊號為Y1以及該沿Z軸振動的訊號為Z1;該第二感測元件21b感測到所在之該側臉頰之該沿X軸振動的訊號為X2、該沿Y軸振動的訊號為Y2以及該沿Z軸振動的訊號為Z2。In detail, as shown in FIGS. 2 to 4, the signal of the vibration along the X-axis of the side cheek where the first sensing element 21a senses is X1, and the signal of the vibration along the Y-axis is Y1 And the signal of vibration along the Z axis is Z1; the signal of vibration along the X axis where the second sensing element 21b senses the side cheek is X2, the signal of vibration along the Y axis is Y2, and the signal along Z The signal of shaft vibration is Z2.

如第2圖至第5圖所示,該訊號處理SP更包括統合歸納CI運算處理,係將來自該第一感測元件21a的三軸訊號(X1、Y1以及Z1)統合成單一個統合訊號波形並命名為GS1,亦將來自該第二感測元件21b的三軸訊號(X2、Y2以及Z2)統合成單一個統合訊號波形並命名為GS2,以使該睡眠呼吸障礙分析構件5於進行該睡眠呼吸障礙分析A時便於判斷該受測者S之口呼吸次數、呼吸型態甚至側睡與否等睡眠狀況。As shown in Figures 2 to 5, the signal processing SP further includes integrated induction CI operation processing, which integrates the three-axis signals (X1, Y1, and Z1) from the first sensing element 21a into a single integrated signal The waveform is named GS1, and the three-axis signals (X2, Y2, and Z2) from the second sensing element 21b are integrated into a single integrated signal waveform and named GS2, so that the sleep-disordered breathing analysis component 5 performs The sleep-disordered breathing analysis A is convenient for judging the number of mouth breaths, breathing patterns, and even side sleeping status of the subject S.

詳細而言,在本實施例中,該第一感測元件21a係貼附於該受測者S之雙頰的左側臉頰,該第二感測元件21b係貼附於該受測者S之雙頰的右側臉頰。該第一感測元件21a以及該第二感測元件21b所感測得出之共六軸之訊號可依照方向性而分為兩種訊號,包括代表該臉頰鼓動訊號MBS之雙邊反向訊號(X、Y);以及代表正常呼吸所產生之身體位移的雙邊同向訊號(Z),其中該雙邊同向訊號(Z)係為微弱之訊號。上述兩者皆能捕捉連續/非連續的呼吸訊號,但為求能夠精簡兩邊訊號,遂將來自該第一感測元件21a的三軸訊號(X1、Y1以及Z1)統合成單一個統合訊號波形並命名為GS1,亦將來自該第二感測元件21b的三軸訊號(X2、Y2以及Z2)統合成單一個統合訊號波形並命名為GS2。In detail, in this embodiment, the first sensing element 21a is attached to the left cheek of the subject S, and the second sensing element 21b is attached to the subject S’s cheek. The right cheek of both cheeks. The signals of a total of six axes sensed by the first sensing element 21a and the second sensing element 21b can be divided into two types of signals according to the directionality, including the bilateral reverse signal (X , Y); and the bilateral co-directional signal (Z) representing the body displacement caused by normal breathing, in which the bilateral co-directional signal (Z) is a weak signal. Both of the above can capture continuous/discontinuous breathing signals, but in order to simplify the signals on both sides, the three-axis signals (X1, Y1, and Z1) from the first sensing element 21a are integrated into a single integrated signal waveform It is named GS1, and the three-axis signals (X2, Y2, and Z2) from the second sensing element 21b are integrated into a single integrated signal waveform and named GS2.

如第1圖至第2圖所示,依據本創作的實施例的睡眠呼吸障礙篩檢設備100,該血氧感測構件3係為脈衝式血氧濃度器。As shown in Figures 1 to 2, according to the sleep apnea screening device 100 of the embodiment of the present invention, the blood oxygen sensing component 3 is a pulse-type blood oxygen concentration device.

詳細而言,該脈衝式血氧濃度器可以為指夾式(Fingertip)、腕戴式(Wrist-worn)、坐檯式(Tabletop)、便攜式(Handheld)或是其他能夠以任何形式測量該血氧飽和度OS之該脈衝式血氧濃度器。In detail, the pulse oximeter can be fingertip, wrist-worn, tabletop, handheld, or other types that can measure the blood in any form. The pulse-type blood oxygen concentration device for oxygen saturation OS.

如第1圖至第3圖所示,該睡眠呼吸障礙篩檢設備100經啟動後,複數個該感測元件21開始感測該臉頰鼓動訊號MBS,該血氧感測構件3開始感測該血氧飽和度訊號OSS。該臉頰鼓動訊號MBS隨後經由該訊號處理構件4進行該訊號處理SP。該訊號處理SP係將該臉頰鼓動訊號MBS進行該濾波F、該波形辨識WR、該波形註記WM以及該統合歸納CI等運算處理而得到該訊號處理結果SPR。該訊號處理構件4遂將該訊號處理結果SPR與該血氧感測構件3所測得之該血氧飽和度訊號OSS相互參照比對,而產生用於供睡眠呼吸障礙分析A的睡眠呼吸障礙篩檢結果R。該睡眠呼吸障礙分析構件5遂依據該睡眠呼吸障礙篩檢結果R而進行該睡眠呼吸障礙分析A,以評估、確認該受測者S是否患有睡眠呼吸中止症。若該睡眠呼吸障礙分析構件5所進行之該睡眠呼吸障礙分析A的結果為否定,則表示該受測者S並未罹患睡眠呼吸中止症,隨後結束本次之篩檢;若該結果為肯定,則於本次篩檢結束後建議進行該睡眠多項生理檢查PSG,即,以更全面的醫學檢驗流程確認該受測者S是否確實罹患睡眠呼吸中止症。As shown in Figures 1 to 3, after the sleep apnea screening device 100 is activated, a plurality of the sensing elements 21 begin to sense the cheek agitation signal MBS, and the blood oxygen sensing component 3 begins to sense the The blood oxygen saturation signal OSS. The cheek stirring signal MBS then performs the signal processing SP through the signal processing component 4. The signal processing SP performs the filtering F, the waveform identification WR, the waveform annotation WM, and the integrated induction CI on the cheek stirring signal MBS to obtain the signal processing result SPR. The signal processing component 4 then compares the signal processing result SPR with the blood oxygen saturation signal OSS measured by the blood oxygen sensing component 3 with a cross-reference comparison to generate a sleep disordered breathing for sleep disordered breathing analysis A Screening result R. The sleep apnea analysis component 5 then performs the sleep apnea analysis A according to the sleep apnea screening result R to evaluate and confirm whether the subject S suffers from sleep apnea. If the result of the sleep apnea analysis A performed by the sleep apnea analysis component 5 is negative, it means that the subject S does not suffer from sleep apnea, and then this screening is ended; if the result is affirmative , After the end of this screening, it is recommended to perform the PSG, which is a multiple physiological examination of sleep, that is, to confirm whether the subject S is indeed suffering from sleep apnea syndrome through a more comprehensive medical examination process.

依據本創作的實施例的睡眠呼吸障礙篩檢設備100,其中在該睡眠呼吸障礙分析構件5中,該睡眠呼吸障礙分析A依據,在該單位時間內該受測者S於睡眠過程進行每分鐘預定口呼吸次數以下(例如:每分鐘三次以下)的口呼吸、並且該血氧飽和度OS落在預定血氧飽和度變化之範圍(例如:95~100%之範圍),而確認該受測者S並未患有睡眠呼吸中止症,該睡眠呼吸障礙分析A依據,在該單位時間內該受測者S於睡眠過程進行每分鐘該預定口呼吸次數以上(例如:每分鐘十三次及十三次以上)的口呼吸、並且該血氧飽和度OS落在該預定血氧飽和度變化之範圍(例如:95~100%之範圍),而確認該受測者S並未患有睡眠呼吸中止症,該睡眠呼吸障礙分析A依據,在該單位時間內該受測者S於睡眠過程進行每分鐘該預定口呼吸次數(例如:三至十二次)的口呼吸、並且該血氧飽和度OS低於該預定血氧飽和度變化之範圍(例如:低於90%)而確認該受測者S患有睡眠呼吸中止症。According to the sleep apnea screening device 100 of the embodiment of the present invention, in the sleep apnea analysis component 5, the sleep apnea analysis A is based on that the subject S performs every minute of sleep during the unit time Mouth breaths below the predetermined number of mouth breaths (for example, three times per minute or less), and the blood oxygen saturation OS falls within the range of the predetermined blood oxygen saturation change (for example: 95-100% range), and confirm the test The person S does not suffer from sleep apnea. The sleep-disordered breathing analysis A is based on the fact that during the unit time, the subject S is sleeping more than the predetermined number of mouth breaths per minute (for example: 13 times per minute and 13 times or more) mouth breath, and the blood oxygen saturation OS falls within the predetermined blood oxygen saturation change range (for example: 95-100% range), and it is confirmed that the subject S does not suffer from sleep Apnea, the sleep-disordered breathing analysis A is based on the fact that the subject S performs the predetermined number of mouth breaths per minute (for example, three to twelve times) during sleep during the unit time, and the blood oxygen The saturation OS is lower than the predetermined range of blood oxygen saturation changes (for example, lower than 90%), which confirms that the subject S suffers from sleep apnea.

詳細而言,本創作之該睡眠呼吸障礙篩檢設備100係定義了複數種可能會出現於該受測者S之睡眠期間的呼吸型態,其中,由於「最大呼吸次數」係因人而異,因此該受測者S的該呼吸型態分類亦不盡相同。 定義複數種該呼吸型態的前置步驟為: (1) 該睡眠呼吸障礙分析構件5於該臉頰鼓動訊號MBS中找出連續3~5分鐘有出現口呼吸之波形或是微小波形(即,鼻呼吸之波形)的部分訊號,計算該部分訊號的平均呼吸次數,並將該平均呼吸次數界定為該「最大呼吸次數」。 (2) 將所計算出之該「最大呼吸次數」減去預定數值(例如減去三)後,所得數值將被視為每分鐘進行之口呼吸次數,且依據該口呼吸次數的不同,該口呼吸次數將被分類至代表複數種不同的呼吸型態來進行進一步之分析。 複數種該呼吸型態的定義為: (a)     在該單位時間內該受測者S於睡眠過程進行每分鐘該預定口呼吸次數以下(例如:每分鐘三次以下,不包含三次)的口呼吸:該睡眠呼吸障礙分析構件5將判定該單位時間之呼吸型態為全部鼻呼吸(Complete Nasal Breathing, CNB),此時之血氧濃度應正常,該血氧飽和度OS應落在該預定血氧飽和度變化之範圍(例如: 95~100%),且呼吸中止次數(ODI)少。 (b)     在該單位時間內該受測者S於睡眠過程進行每分鐘該預定口呼吸次數以上(例如:每分鐘十三次及十三次以上)的口呼吸:該睡眠呼吸障礙分析構件5將判定該單位時間之呼吸型態為全部口呼吸(Complete Mouth Breathing, CMB),係為明顯出現臉頰鼓動現象之呼吸型態,此時之該血氧濃度應正常,該血氧飽和度OS應落在該預定血氧飽和度變化之範圍(例如:95~100%),且ODI少。 (c)     在該單位時間內該受測者S於睡眠過程進行每分鐘該預定口呼吸次數(例如:三至十二次)的口呼吸:該睡眠呼吸障礙分析構件5將判定該單位時間之呼吸型態為不連續口呼吸(Intermittent Mouth Breathing, IMB),代表出現了睡眠呼吸中止的症狀,此時之該血氧濃度會降低,該血氧飽和度OS應低於該預定血氧飽和度變化之範圍(例如:低於90%),且ODI多。 (d)     另外,該臉頰鼓動訊號MBS經由該統合歸納CI之運算處理而得出之兩軸訊號波形(GS1以及GS2)之該波形註記WM的差值(G-sensor Diff.)的絕對值若大於三,則該睡眠呼吸障礙分析構件5將判定此種呼吸型態為側睡口呼吸(SS)。該側睡口呼吸係指該受測者S於睡眠過程中側睡所進行之口呼吸。詳細而言,由於該第一感測元件21a及該第二感測元件21b分別設置於該受測者S之該雙頰,因此,當其中一個感測元件21有感測到該臉頰鼓動訊號MBS但另一個感測元件21卻未感測到,且該兩軸訊號波形(GS1以及GS2)之該波形註記WM的差值(G-sensor Diff.)的絕對值大於三時,則該睡眠呼吸障礙分析構件5將判定該單位時間之呼吸型態為側睡口呼吸。 In detail, the sleep disordered breathing screening device 100 of this creation defines multiple breathing patterns that may appear during sleep of the subject S. Among them, the "maximum number of breaths" varies from person to person. Therefore, the breathing pattern classification of the subject S is also different. The prerequisite steps to define plural types of this breathing pattern are: (1) The sleep-disordered breathing analysis component 5 finds out the part of the signal with oral breathing waveform or tiny waveform (ie, the waveform of nasal breathing) in the cheek stirring signal MBS for 3 to 5 minutes, and calculates the part of the signal And define the average number of breaths as the "maximum number of breaths". (2) After subtracting a predetermined value (for example, subtracting three) from the calculated "maximum number of breaths", the resulting value will be regarded as the number of mouth breaths performed per minute, and depending on the number of mouth breaths, the The number of mouth breaths will be classified to represent a plurality of different breathing patterns for further analysis. The definitions of the plural types of breathing patterns are: (A) The subject S performs oral breathing less than the predetermined number of mouth breaths per minute (for example, less than three times per minute, excluding three) during the sleep process within the unit time: the sleep disordered breathing analysis component 5 will determine The breathing pattern per unit time is Complete Nasal Breathing (CNB). At this time, the blood oxygen concentration should be normal, and the blood oxygen saturation OS should fall within the range of the predetermined blood oxygen saturation change (for example: 95 ~100%), and the number of interruptions in breathing (ODI) is small. (B) In the unit time, the subject S performs oral breaths of more than the predetermined number of mouth breaths per minute (for example: thirteen times and more than thirteen times per minute) during the sleep process: the sleep disordered breathing analysis component 5 The breathing pattern per unit time will be judged to be Complete Mouth Breathing (CMB), which is a breathing pattern with obvious cheek agitation. At this time, the blood oxygen concentration should be normal, and the blood oxygen saturation OS should be It falls within the range of the predetermined blood oxygen saturation change (for example: 95~100%), and the ODI is low. (C) In the unit time, the subject S performs the predetermined number of mouth breaths (for example, three to twelve) mouth breaths per minute during the sleep process: the sleep disordered breathing analysis component 5 will determine the number of mouth breaths in the unit time The breathing pattern is Intermittent Mouth Breathing (IMB), which represents the symptoms of sleep apnea. At this time, the blood oxygen concentration will decrease, and the blood oxygen saturation OS should be lower than the predetermined blood oxygen saturation The range of change (for example: less than 90%), and there are many ODIs. (D) In addition, the absolute value of the difference between the two-axis signal waveforms (GS1 and GS2) of the two-axis signal waveforms (GS1 and GS2) of the cheek stirring signal MBS obtained by the integrated induction CI calculation process (G-sensor Diff.) If it is greater than three, the sleep-disordered breathing analysis component 5 will determine that this breathing pattern is side sleeping mouth breathing (SS). The side sleeping mouth breathing refers to the mouth breathing of the subject S while sleeping on his side during sleep. In detail, since the first sensing element 21a and the second sensing element 21b are respectively disposed on the cheeks of the subject S, when one of the sensing elements 21 senses the cheek agitation signal MBS but the other sensing element 21 fails to sense it, and the absolute value of the difference between the two-axis signal waveforms (GS1 and GS2) of the waveform note WM (G-sensor Diff.) is greater than three, then the sleep The breathing disorder analysis component 5 will determine that the breathing pattern per unit time is side-sleeping mouth breathing.

詳細而言,本創作之該睡眠呼吸障礙篩檢設備100係透過判定該受測者S於單位時間之呼吸型態以及該呼吸型態在整段睡眠期間所佔的比例,並搭配該血氧飽和度OS相互參照做比對,以檢視該受測者S整段睡眠過程中的睡眠狀況,進而判斷該受測者S是否罹患睡眠呼吸中止症以達成篩檢之目的。In detail, the sleep apnea screening device 100 of the present invention determines the breathing pattern of the subject S per unit time and the proportion of the breathing pattern during the entire sleep period, and matches the blood oxygen Saturation OS is cross-referenced for comparison to view the sleep status of the subject S during the entire sleep process, and then determine whether the subject S suffers from sleep apnea for the purpose of screening.

藉由本創作所採用之技術手段,使得睡眠呼吸障礙分析構件5(在此係指睡眠技術員)能夠在進行睡眠呼吸中止症的篩檢時,獲得更多項評估及判斷該受測者S罹患睡眠呼吸中止症與否的參考依據。睡眠技術員於進行感測及推估該受測者S在睡眠期間的呼吸型態時,得以將該血氧感測構件3所測得對應於該血氧飽和度訊號OSS之該血氧飽和度OS,與本創作之睡眠呼吸障礙篩檢設備100所測得對應於該訊號處理結果SPR之單位時間內的口呼吸次數相互參照比對,進而使該受測者S在睡眠期間的呼吸型態能夠以更加具象化的方式呈現,而睡眠技術員亦能藉此提升該睡眠呼吸障礙篩檢結果R的客觀性以及準確度。With the technical means used in this creation, the sleep apnea analysis component 5 (herein referred to as the sleep technician) can obtain more evaluations and determine that the subject S suffers from sleep during the screening of sleep apnea. Reference basis for respiratory arrest. When the sleep technician senses and estimates the breathing pattern of the subject S during sleep, the blood oxygen sensor 3 can measure the blood oxygen saturation corresponding to the blood oxygen saturation signal OSS OS is cross-referenced with the number of oral breaths per unit time measured by the sleep apnea screening device 100 corresponding to the signal processing result SPR, so that the breathing pattern of the subject S during sleep It can be presented in a more concrete way, and the sleep technician can also improve the objectivity and accuracy of the sleep apnea screening result R.

除此之外,在治療睡眠呼吸中止症的諸多方法中,配戴陽壓呼吸器(Continuous Positive Airway Pressure, CPAP)係為常見的治療方式,睡眠技術員亦可藉由判讀本創作之該睡眠呼吸障礙篩檢設備100所產生之該睡眠呼吸障礙篩檢結果R來評估病患於配戴CPAP後的治療效果好壞。於治療睡眠呼吸中止症的期間,亦可利用該睡眠呼吸障礙篩檢設備100作治療效果的追蹤。再者,由於本創作之該睡眠呼吸障礙篩檢設備100能夠感測出該受測者S是否於睡眠過程具有屬於因進行口呼吸所形成雙頰鼓動的動作,而當該受測者S因進行口呼吸而形成雙頰鼓動的動作時,所代表的意義為:此時該受測者S的舌根應呈現無力的狀態。因此,本創作之該睡眠呼吸障礙篩檢設備100亦能夠幫助睡眠技術員了解該受測者S之舌肌力的狀況為何。In addition, in the many methods of treatment of sleep apnea, wearing a continuous positive airway pressure (CPAP) is a common treatment method, and sleep technicians can also interpret the sleep breathing created by this book. The sleep apnea screening result R generated by the disorder screening device 100 is used to evaluate the treatment effect of the patient after wearing CPAP. During the treatment of sleep apnea, the sleep apnea screening device 100 can also be used to track the treatment effect. Furthermore, since the sleep apnea screening device 100 of the present invention can sense whether the subject S has an action that belongs to cheek agitation caused by mouth breathing during sleep, and when the subject S is due to When mouth breathing is performed to form the action of agitation of the cheeks, the meaning represented is: at this time, the base of the tongue of the subject S should be in a state of weakness. Therefore, the sleep breathing disorder screening device 100 of the present invention can also help the sleep technician understand the condition of the tongue muscle strength of the subject S.

以上之敘述以及說明僅為本創作之較佳實施例之說明,對於此項技術具有通常知識者當可依據以下所界定申請專利範圍以及上述之說明而作其他之修改,惟此些修改仍應是為本創作之創作精神而在本創作之權利範圍中。The above descriptions and descriptions are only descriptions of the preferred embodiments of this creation. Those with ordinary knowledge of this technology should make other modifications based on the scope of patent application defined below and the above descriptions, but these modifications should still be made. It is the creative spirit of this creation and within the scope of the rights of this creation.

100:睡眠呼吸障礙篩檢設備 1:封閉元件 2:臉頰鼓動感測構件 21:感測元件 21a:第一感測元件 21b:第二感測元件 3:血氧感測構件 4:訊號處理構件 5:睡眠呼吸障礙分析構件 S:受測者 MBS:臉頰鼓動訊號 OS:血氧飽和度 OSS:血氧飽和度訊號 SP:訊號處理 SPR:訊號處理結果 A:睡眠呼吸障礙分析 R:睡眠呼吸障礙篩檢結果 F:濾波 WR:波形辨識 WM:波形註記 CI:統合歸納 PSG:睡眠多項生理檢查100: Screening equipment for sleep disordered breathing 1: closed element 2: Cheek agitation sensing component 21: Sensing element 21a: the first sensing element 21b: second sensing element 3: Blood oxygen sensing component 4: Signal processing components 5: Sleep-disordered breathing analysis component S: Subject MBS: cheek agitation signal OS: blood oxygen saturation OSS: blood oxygen saturation signal SP: signal processing SPR: signal processing result A: Analysis of sleep disordered breathing R: Screening results for sleep disordered breathing F: Filter WR: Waveform recognition WM: Waveform annotation CI: Integrated induction PSG: multiple physical examinations of sleep

第1圖為顯示根據本創作的一實施例的睡眠呼吸障礙篩檢設備的系統圖; 第2圖為顯示根據本創作的實施例的睡眠呼吸障礙篩檢設備的硬體裝置示意圖; 第3圖為顯示根據本創作的實施例的睡眠呼吸障礙篩檢設備的系統運作流程圖; 第4圖為顯示根據本創作的實施例的睡眠呼吸障礙篩檢設備的原始訊號示意圖; 第5圖為顯示根據本創作的實施例的睡眠呼吸障礙篩檢設備的訊號處理結果示意圖。 Figure 1 is a system diagram showing a sleep apnea screening device according to an embodiment of the present creation; Figure 2 is a schematic diagram showing the hardware device of the sleep apnea screening device according to the embodiment of the present creation; Figure 3 is a flowchart showing the system operation of the sleep apnea screening device according to the embodiment of the present creation; Figure 4 is a schematic diagram showing the original signal of the sleep apnea screening device according to the embodiment of the present creation; Figure 5 is a schematic diagram showing the signal processing result of the sleep disordered breathing screening device according to the embodiment of the present creation.

100:睡眠呼吸障礙篩檢設備 100: Screening equipment for sleep disordered breathing

1:封閉元件 1: closed element

2:臉頰鼓動感測構件 2: Cheek agitation sensing component

21:感測元件 21: Sensing element

21a:第一感測元件 21a: the first sensing element

21b:第二感測元件 21b: second sensing element

3:血氧感測構件 3: Blood oxygen sensing component

4:訊號處理構件 4: Signal processing components

5:睡眠呼吸障礙分析構件 5: Sleep-disordered breathing analysis component

S:受測者 S: Subject

Claims (8)

一種睡眠呼吸障礙篩檢設備,包含: 閉封元件,係經配置而覆蓋於受測者之雙唇而閉合口腔; 臉頰鼓動感測構件,包含複數個感測元件,複數個該感測元件係以數量對稱且分別位於該閉封元件之相對二側的方式而貼附於該受測者之雙頰,其中該臉頰鼓動感測構件係取得該受測者之雙頰的臉頰鼓動訊號,以感測出該受測者是否於睡眠過程具有屬於因進行口呼吸所形成雙頰鼓動的動作;以及 訊號處理構件,電性連接於該臉頰鼓動感測構件,而自複數個該感測元件接收該臉頰鼓動訊號、以及接收一血氧飽和度訊號,且該訊號處理構件對於來自複數個該感測元件的該臉頰鼓動訊號的波形執行訊號處理而產生訊號處理結果,並依據該訊號處理結果與該血氧飽和度訊號在單位時間內的相互參照比對,而產生用於供睡眠呼吸障礙分析的睡眠呼吸障礙篩檢結果, 其中,該睡眠呼吸障礙分析係將該訊號處理結果之波形比對於該血氧飽和度訊號之曲線,而取得該受測者在該單位時間內進行口呼吸次數以及該血氧飽和度的對照而據以確認該受測者是否患有睡眠呼吸中止症。 A device for screening sleep disordered breathing, including: The sealing element is configured to cover the lips of the subject to close the oral cavity; The cheek swelling sensing component includes a plurality of sensing elements, and the plurality of sensing elements are attached to the subject's cheeks in a symmetrical manner and are respectively located on opposite sides of the closed element, wherein the The cheek agitation sensing component obtains the cheek agitation signal of the subject's cheeks to detect whether the subject has a cheek agitation caused by mouth breathing during sleep; and The signal processing component is electrically connected to the cheek stirring sensing component, and receiving the cheek stirring signal from a plurality of the sensing elements and receiving a blood oxygen saturation signal, and the signal processing component is The waveform of the cheek agitation signal of the component performs signal processing to generate a signal processing result, and based on the cross-reference comparison between the signal processing result and the blood oxygen saturation signal in a unit time, a signal for sleep apnea analysis is generated The results of sleep disordered breathing screening, Among them, the sleep disordered breathing analysis is to compare the waveform of the signal processing result to the curve of the blood oxygen saturation signal, and obtain the comparison of the number of mouth breaths and the blood oxygen saturation of the subject in the unit time. This is to confirm whether the subject suffers from sleep apnea. 如請求項1所述之該睡眠呼吸障礙篩檢設備,其中該血氧飽和度訊號係接收自該睡眠呼吸障礙篩檢設備之內部或外部之血氧感測構件,該血氧感測構件係感測該受測者於睡眠過程之血氧飽和度而取得血氧飽和度訊號。The sleep breathing disorder screening device according to claim 1, wherein the blood oxygen saturation signal is received from a blood oxygen sensing member inside or outside of the sleep breathing disorder screening device, and the blood oxygen sensing member is The blood oxygen saturation of the subject during sleep is sensed to obtain the blood oxygen saturation signal. 如請求項1所述之該睡眠呼吸障礙篩檢設備,其中該訊號處理構件所執行的該訊號處理為針對該受測者之該臉頰鼓動訊號的該波形進行濾波、波形辨識、波形註記的運算處理而產生該訊號處理結果。The sleep breathing disorder screening device according to claim 1, wherein the signal processing performed by the signal processing component is the calculation of filtering, waveform recognition, and waveform annotation on the waveform of the cheek agitation signal of the subject Processing to produce the signal processing result. 如請求項1所述之該睡眠呼吸障礙篩檢設備,更包含一睡眠呼吸障礙分析構件,電性連接於該訊號處理構件,而根據該睡眠呼吸障礙篩檢結果進行該睡眠呼吸障礙分析。The sleep breathing disorder screening device according to claim 1 further includes a sleep breathing disorder analysis component electrically connected to the signal processing component, and the sleep breathing disorder analysis is performed according to the sleep breathing disorder screening result. 如請求項1所述之該睡眠呼吸障礙篩檢設備,其中該臉頰鼓動感測構件包括第一感測元件以及第二感測元件,該第一感測元件以及該第二感測元件係分別設置於該受測者之該雙頰,且電性連接於該訊號處理構件。The sleep apnea screening device according to claim 1, wherein the cheek movement sensing member includes a first sensing element and a second sensing element, and the first sensing element and the second sensing element are respectively It is arranged on the cheeks of the subject and is electrically connected to the signal processing component. 如請求項1或3所述之該睡眠呼吸障礙篩檢設備,其中該感測元件為加速度感測器,該臉頰鼓動感測構件所測得之該臉頰鼓動訊號包含沿X軸振動的訊號、沿Y軸振動的訊號以及沿Z軸振動的訊號,該訊號處理係將該受測者之同一側臉頰之該沿X軸振動的訊號、該沿Y軸振動的訊號以及該沿Z軸振動的訊號的波形予以統合歸納而獲得具有時間記錄以及表示該受測者之雙頰鼓動次數的該訊號處理結果。The sleep breathing disorder screening device according to claim 1 or 3, wherein the sensing element is an acceleration sensor, and the cheek agitation signal measured by the cheek agitation sensing component includes a signal that vibrates along the X axis, Signals vibrating along the Y axis and vibrating along the Z axis. The signal processing is the signal vibrating along the X axis, the signal vibrating along the Y axis, and the signal vibrating along the Z axis on the same side of the subject’s cheek. The waveforms of the signals are integrated and summarized to obtain the signal processing result with a time record and indicating the number of cheek agitation of the subject. 如請求項1所述之該睡眠呼吸障礙篩檢設備,其中該血氧感測構件係為脈衝式血氧濃度器。The sleep apnea screening device according to claim 1, wherein the blood oxygen sensing component is a pulse oximetry device. 如請求項6所述之該睡眠呼吸障礙篩檢設備,其中在該睡眠呼吸障礙分析構件中,該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘預定口呼吸次數以下的口呼吸、並且該血氧飽和度落在預定血氧飽和度變化之範圍,而確認該受測者並未患有睡眠呼吸中止症, 該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘該預定口呼吸次數以上的口呼吸、並且該血氧飽和度落在該預定血氧飽和度變化之範圍,而確認該受測者並未患有睡眠呼吸中止症, 該睡眠呼吸障礙分析依據,在該單位時間內該受測者於睡眠過程進行每分鐘該預定口呼吸次數的口呼吸、並且該血氧飽和度低於該預定血氧飽和度變化而確認該受測者患有睡眠呼吸中止症。 The sleep breathing disorder screening device according to claim 6, wherein in the sleep breathing disorder analysis component, the sleep breathing disorder analysis basis is that the subject performs predetermined mouth breathing every minute during sleep during the unit time Mouth breathing less than the number of times, and the blood oxygen saturation falls within the range of the predetermined blood oxygen saturation change, and it is confirmed that the subject does not suffer from sleep apnea, The sleep-disordered breathing analysis is based on the fact that the subject performs mouth breathing more than the predetermined number of mouth breaths per minute during sleep during the unit time, and the blood oxygen saturation falls within the predetermined blood oxygen saturation change range, And confirm that the subject does not suffer from sleep apnea, The sleep-disordered breathing analysis is based on the fact that the subject performs mouth breathing of the predetermined number of mouth breaths per minute during sleep during the unit time, and the blood oxygen saturation is lower than the predetermined change in blood oxygen saturation to confirm that the patient is affected. The subject suffers from sleep apnea.
TW109214019U 2020-10-23 2020-10-23 Sleep apnea screening equipment TWM610717U (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI735360B (en) * 2020-10-23 2021-08-01 牙易科技有限公司 Sleep-disordered-breathing screening equipment

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI735360B (en) * 2020-10-23 2021-08-01 牙易科技有限公司 Sleep-disordered-breathing screening equipment

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