CN111540435A - Management method and system based on woman medication data - Google Patents
Management method and system based on woman medication data Download PDFInfo
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- CN111540435A CN111540435A CN202010373231.2A CN202010373231A CN111540435A CN 111540435 A CN111540435 A CN 111540435A CN 202010373231 A CN202010373231 A CN 202010373231A CN 111540435 A CN111540435 A CN 111540435A
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
- G16H10/60—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
Abstract
The invention provides a management method and a system based on medicine data of women, which can realize the consistency and the perfection of detecting and checking related medicines and the like by comprehensively and dynamically recording the female detection and detection files and the medicine files in real time, particularly for the groups of women who are ready for pregnancy, lactation, climacteric and the like, thereby ensuring the comprehensiveness of the health files of women; meanwhile, relevant medication based on inspection, examination and the like is monitored, reasonable medication suggestions and guidance are provided for women with pregnancy preparation, pregnancy, lactation and climacteric period, and personalized medication adjustment is given in time; meanwhile, the method can also be used for screening by combining the data of the women population according to the early-stage inspection and inspection results, particularly tracking, follow-up, induction and analysis are carried out on the medication outcome to obtain the data of the influence of different drugs on the women at different stages, so that more evidence-based evidences are provided for reasonable medication, and the method has very important practical and instructive significance.
Description
Technical Field
The invention belongs to the technical field of medicines, and particularly relates to a method and a system for managing medication data based on women.
Background
In the prior art, on one hand, reasonable administration is a major problem all over the world, and how to carry out reasonable administration while ensuring high-efficiency treatment on patients is urgently needed to be solved, especially for women in different physiological stages. On one hand, the existing hospitals and even different departments are respectively responsible for different departments, so that unified and efficient inspection and examination cannot be realized, the imperfect and non-unified medical records of examination of women in different physiological stages are caused, data statistical analysis cannot be effectively carried out, and a reasonable medicine guidance scheme is provided for patients. On the other hand, in the prior art, no good tracking method for the medication of women in special stages exists, which causes medication errors or personal behavior errors of women in different physiological stages due to large-scale and specific medication, even more serious consequences are generated, and the happy lives of individuals and families are seriously influenced.
Therefore, it is necessary to provide a technical solution to solve the above technical problems.
Disclosure of Invention
In view of the above, the embodiment of the invention provides a method and a system for managing medication data based on women.
In a first aspect, an embodiment of the present invention provides a data management method based on medication for women, where the data management method includes:
establishing a medication file, a check file and an inspection file of the woman, wherein the medication file comprises at least one of a category of taken medicines, a category of recommended medicines, a category of new medicines and a category of contraindicated medicines; the examination and check-up archive comprises at least one of a first general physical examination, a first examination and check-up item, a first examination and check-up time, a first examination and check-up image, and a first examination and check-up diagnosis result;
determining a first medication regimen based on said woman's custom project, said inspection and review profile, said class of medications taken;
wherein the self-defined project comprises at least one of a pregnancy preparation project, a pregnancy project, a lactation project and a climacteric project;
the first medication regimen includes at least one of a first medication category, first medication production information, a first medication amount, a first usage amount, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
A second aspect of an embodiment of the present invention provides a data management system for medication for women, the data management system comprising:
the medicine file module is used for establishing a medicine file of the woman, wherein the medicine file comprises at least one of a medicine category which is taken, a medicine category which is suggested to be taken, a new medicine category and a medicine category which is contraindicated to be taken;
a check and examination archive module for creating a check and examination archive including at least one of a first general physical examination, a first check and examination item, a first check and examination time, a first check and examination image, a first check and examination diagnostic result;
a customization module for customizing a project for the woman; the self-defined item comprises at least one of a pregnancy preparation item, a pregnancy item, a lactation item and a climacteric item;
a recommended medication module for determining a first medication regimen based on the woman's customized items, the inspection and review profile, and the categories of medications taken; the first medication regimen includes at least one of a first medication category, first medication production information, a first usage amount, a first medication time, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
Compared with the prior art, the embodiment of the invention has the following beneficial effects: the invention realizes the continuity and the perfection of relevant medicine application and the like of the detection and the inspection by comprehensively and dynamically recording the woman detection and inspection results and the medicine application file in real time, particularly for the groups of women who are ready for pregnancy, lactation and climacteric, thereby ensuring the comprehensiveness of the woman health file; meanwhile, a guidance suggestion is provided for the reasonable medication of women in pregnancy, pregnancy and lactation periods; on the basis, related medicines based on inspection, examination and the like are monitored, reasonable medicine application suggestions and guidance are provided for women with pregnancy preparation, pregnancy, lactation and climacteric, and personalized medicine application adjustment is given in time; meanwhile, the data of groups of people for pregnancy, lactation, climacteric women and the like can be regularly screened according to the results of the early-stage examination and in combination with the medication of patients, and the pregnancy medication fate is tracked, followed, induced and analyzed to obtain the human data of different drugs influencing the embryo in different stages of pregnancy, so that more evidence-based bases are provided for the reasonable medication of the national pregnancy, and the method has very important practical and instructive significance.
Drawings
In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed to be used in the embodiments or the prior art descriptions will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art to obtain other drawings based on these drawings without inventive exercise.
FIG. 1 is a schematic flow chart of an implementation of a method for managing medication data based on women according to an embodiment of the present invention;
fig. 2 is a schematic structural module diagram of a management method based on female medication data according to a second embodiment of the present invention.
Detailed Description
In the following description, for purposes of explanation and not limitation, specific details are set forth, such as particular system structures, techniques, etc. in order to provide a thorough understanding of the embodiments of the invention. It will be apparent, however, to one skilled in the art that the present invention may be practiced in other embodiments that depart from these specific details. In other instances, detailed descriptions of well-known systems, devices, circuits, and methods are omitted so as not to obscure the description of the present invention with unnecessary detail.
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are some, not all, embodiments of the present invention. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
It will be understood that the terms "comprises" and/or "comprising," when used in this specification and the appended claims, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof.
It should be further understood that the term "and/or" as used in this specification and the appended claims refers to and includes any and all possible combinations of one or more of the associated listed items.
In order to explain the technical means of the present invention, the following description will be given by way of specific examples.
Fig. 1 is a schematic flow chart illustrating an implementation of the management method based on medication data for women according to an embodiment of the present invention. As shown in FIG. 1, the method for managing medication data based on women can comprise the following steps:
s01: establishing a medication file, a check file and an inspection file of the woman, wherein the medication file comprises at least one of a category of taken medicines, a category of recommended medicines, a category of new medicines and a category of contraindicated medicines; the examination and check-up archive comprises at least one of a first general physical examination, a first examination and check-up item, a first examination and check-up time, a first examination and check-up image, and a first examination and check-up diagnosis result;
wherein, for women, especially for pregnant women, nursing women and climacteric women, a multi-time administration file, a check and examination file can be established according to the self needs or different stages. For example, for a woman, it may establish an inspection and examination profile during an unexpected pregnancy for teratogenic risk assessment and advice, pregnancy guidance, medication guidance, behavioral guidance, health education, and the like; meanwhile, a lactation-related inspection and examination file can be established at the postpartum lactation stage so as to conduct lactation guidance, medication guidance, behavior guidance and the like during physical recovery and lactation.
Preferably, in order to ensure the systematicness, continuity and comprehensiveness of personal inspection and examination, a medicine file, an inspection file and an examination file are preferably established, a multi-hospital and pharmacy fusion mode is adopted, and the uniformity and continuity of personal medicine administration, inspection and examination are realized, so that the comprehensiveness and continuity of personal inspection, inspection and examination and medicine administration are ensured, the physical condition of women and individuals can be effectively analyzed, physical diseases are prevented and treated, appropriate guidance suggestions are given, the inspection and examination cost born by individuals can be reduced, and hospital resources are saved.
Specifically, the new drug category in the drug file is the statistics and analysis of the second clinical drug administration, drug effect and late effect influence of the drug effect according to the targeted drugs appearing in the market, especially aiming at the situations that the drug effect and adverse reaction of women in a special physiological stage are not clear and the like.
Preferably, the check and test profile may be a check and test profile in a specific phase or may be all check and test profiles from the first time.
Specifically, the first examination and examination diagnosis result not only includes the medication scheme of the relevant times, but also includes all information related to the examination and examination, such as medical advice, image diagnosis result and the like, so that the follow-up doctor can make accurate medical record judgment and medication, health promotion and education and other guidance for the woman himself.
S02: determining a first medication regimen based on said woman's custom project, said inspection and review profile, said class of medications taken;
wherein the self-defined project comprises at least one of a pregnancy preparation project, a pregnancy project, a lactation project and a climacteric project;
the first medication regimen includes at least one of a first medication category, first medication production information, a first usage amount, a first medication time, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
The customized project of the woman is targeted according to the stage requirements of the woman, particularly the pregnancy preparation stage, the pregnancy stage, the lactation stage, the climacteric stage and the like, and meanwhile, the customized project also comprises basic situation information and the like of the woman, such as age, other medical history, allergic situation, family genetic history and other basic situations.
The self-defining project is implemented according to specific and significant stages in the whole life stage of the woman, and is more beneficial to the diagnosis and treatment of the woman in different physiological stages by the medical system. Meanwhile, the self-defined project is also an important technical characteristic of the invention aiming at the effective research that the effective and unified diagnosis and treatment scheme for women in specific physiological stages is not available in the prior art.
The first medicine scheme not only combines the medicine taking file, the inspection and examination file, but also needs the class of the taken medicines, reasonably and accurately gives out relevant medicine information and medical advice under the diagnosis of a doctor, and also gives out instructive suggestions, including replaceable medicines, contraindication medicines, medicines with compatibility and contraindication, and the like, so that the medicine taking suggestions are more comprehensively and accurately provided for women.
The method provides inspection and examination guidance, a medication scheme and follow-up behavior guidance by combining the current stage requirements or the follow-up stage requirements of the women, realizes reasonable dispensing, reasonable inspection and examination, reasonable body health guidance and the like of the women, reduces the influence of unnecessary medicaments on follow-up bodies, reduces unnecessary inspection and examination, and simultaneously can reduce the cost of the women in the aspects of inspection and examination, medication and the like.
Specifically, according to the customized unexpected pregnancy stage of a woman, the age, occupation, menstrual cycle, other medical history, bad contact history, bad pregnancy history, allergic conditions, family genetic history and the like of the woman, and the medication history, medicines with uncertain safety and teratogenesis medicines can be safely used in different stages of pregnancy, and related inspection and examination, adjustment of a medication scheme, notification of teratogenesis risks and the like are required to be carried out in time.
Preferably, in an embodiment of the present invention, the data management method further includes:
updating the medication file periodically;
the periodically updating the medication profile may include: regularly fusing first medicine purchasing information, corresponding first medicine taking information and first order information of the woman in each grade hospital and pharmacy;
the first medicine purchasing information comprises at least one of a first medicine purchasing medicine name, first medicine purchasing medicine production information, a first medicine purchasing medicine usage amount, a first medicine purchasing time, a first medicine purchasing medicine duration, a same-sex related medicine category and a reverse-sex related medicine category.
The medicine file is updated regularly, especially aiming at prescription medicine management, medicine tracking, follow-up and management can be carried out on women in special stages, and more reasonable and timely medicine guide can be given by combining the previous medicine of the women.
For example, according to the customized unexpected pregnancy stage of the woman, and the age, occupation, medication history, menstrual cycle, other medical history, bad contact history, bad pregnancy history, allergic condition, family genetic history and the like of the woman, medication teratogenicity risk assessment and suggestion are carried out, and the method provides the required medicine taking, the unnecessary medicine taking, the impossible medicine taking, the inspection and the inspection which need to be carried out in time, the health propaganda and education scheme and the like in different stages of the pregnancy. Even according to the high teratogenicity medicine taken before pregnancy, a risk assessment suggestion, a compensatory medicine suggestion and the like are given.
Preferably, in an embodiment of the present invention, the check-up and inspection profile is updated periodically;
said periodically updating said inspection and review profile comprises: and fusing examination and examination medical records of all levels of hospitals of the women at regular time.
In view of the fact that women can carry out examination and check in different hospitals, even take medicine in different places and the like, the method provided by the invention can update the examination and check files, meanwhile, the examination and check of hospitals of all levels on the woman are integrated, the uniformity, the continuity and the non-repeatability of the examination and check on the woman are realized, and the method is also beneficial to providing more accurate medical record judgment and reasonable medicine taking for the woman in combination with the examination and check before, the related medical advice, the related third medicine scheme and the like by a subsequent doctor, and improves the rationality and the accuracy of diagnosis and medicine taking while reducing repeated examination and check.
Meanwhile, detection and examination of different hospitals and different departments are integrated, so that the internal unification of the medical system is realized, and the medical system is more beneficial to medical treatment and treatment of patients, women and the like.
The check and check files may be check and check files in a specific phase, or may be all check and check files from the first time.
Specifically, the first examination and examination diagnosis result not only includes the medication scheme of the relevant times, but also includes all information related to the examination and examination, such as medical advice, image diagnosis result and the like, so that the follow-up doctor can make accurate medical record judgment and medication, health promotion and education and other guidance for the woman himself.
Preferably, in an embodiment of the present invention, a pharmacist regularly tracks and feeds back the physical health and medication related information of the woman according to the medication file to obtain the influence factors of different medications on the woman of different self-defined items.
The method comprises the steps of regularly carrying out medication process and ending tracking, follow-up and induction on data of special populations such as women with pregnancy, lactation and climacteric period and the like, and screening populations of women in various physiological stages to obtain the influence of different drugs on the women in different physiological stages, even the influence of different combined drugs on the women in different physiological stages. Can well define the medication influence factors and provide accurate and scientific basis for the subsequent medication of women.
Preferably, in an embodiment of the present invention, the categories of the medicines taken include names of the medicines taken, name production information of the medicines taken, name usage amount of the medicines taken, name time of the medicines taken, and name duration time of the medicines taken;
the recommended medicine category comprises a recommended medicine name, a recommended medicine usage amount, a recommended medicine taking time and a recommended medicine taking duration;
the new medicine category comprises a new medicine name, new medicine production information, a new medicine usage amount, a new medicine medication time and a new medicine duration;
the contraindicated medicine category comprises a name of a contraindicated medicine, and the duration time of the contraindicated medicine is determined according to the time node of the custom item.
The invention realizes the continuity and the perfection of relevant medicine application and the like of the detection and the inspection by comprehensively and dynamically recording the woman detection and inspection results and the medicine application file in real time, particularly for the groups of women who are ready for pregnancy, lactation and climacteric, thereby ensuring the comprehensiveness of the woman health file; meanwhile, the pharmacist provides guidance suggestions for reasonable medication of the women in the pregnancy, pregnancy and lactation periods; on the basis, related medicines based on inspection, examination and the like are monitored, reasonable medicine application suggestions and guidance are provided for women with pregnancy preparation, pregnancy, lactation and climacteric, and personalized medicine application adjustment is given in time; meanwhile, according to the results of the early-stage examination and examination, a pharmacist can regularly screen the data of groups of people such as women who are ready for pregnancy, lactation and climacteric period by combining the medication of the patient, and particularly, the pregnancy medication fate is tracked, followed, induced and analyzed to obtain the human data of different drugs influencing the embryo in different stages of pregnancy, so that more evidence-based bases are provided for the reasonable medication of the national pregnancy, and the practical guiding significance is very important.
Referring to fig. 2, a schematic block diagram of a system for managing medication data based on women according to a second embodiment of the present invention is shown. As shown in FIG. 2, the system for managing medication data based on women may comprise:
the medicine file module is used for establishing a medicine file of the woman, wherein the medicine file comprises at least one of a medicine category which is taken, a medicine category which is suggested to be taken, a new medicine category and a medicine category which is contraindicated to be taken;
a check and examination archive module for creating a check and examination archive including at least one of a first general physical examination, a first check and examination item, a first check and examination time, a first check and examination image, a first check and examination diagnostic result;
a customization module for customizing a project for the woman; the self-defined item comprises at least one of a pregnancy preparation item, a pregnancy item, a lactation item and a climacteric item;
a recommended medication module for determining a first medication regimen based on the woman's customized items, the inspection and review profile, and the categories of medications taken; the first medication regimen includes at least one of a first medication category, first medication production information, a first medication amount, a first medication time, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
Wherein, for women, especially for pregnant women, nursing women and climacteric women, a multi-time administration file, a check and examination file can be established according to the self needs or different stages. For example, for a woman, it may establish an inspection and examination profile during an unexpected pregnancy for teratogenic risk assessment and advice, pregnancy guidance, medication guidance, behavioral guidance, health education, and the like; meanwhile, a lactation-related inspection and examination file can be established at the postpartum lactation stage so as to conduct lactation guidance, medication guidance, behavior guidance and the like during physical recovery and lactation.
Preferably, in order to ensure the systematicness, continuity and comprehensiveness of personal inspection and examination, a medicine file, an inspection file and an examination file are preferably established, a multi-hospital and pharmacy fusion mode is adopted, and the uniformity and continuity of personal medicine use, inspection and examination are realized, so that the comprehensiveness and continuity of personal inspection, inspection and examination and medicine use are ensured, the physical condition of women and individuals can be effectively analyzed, diseases are prevented and treated, guiding suggestions are given, the inspection and examination cost born by the individuals can be reduced, and the hospital resources are saved.
Specifically, the new drug category in the drug file is the statistics and analysis of the second clinical drug administration, drug effect and late effect influence of the drug effect according to the targeted drugs appearing in the market, especially aiming at the situation that the drug effect and risk of women in a special stage are not clear.
Preferably, the check and test profile may be a check and test profile in a specific phase or may be all check and test profiles from the first time.
Specifically, the first examination and examination diagnosis result not only includes the medication scheme of the relevant times, but also includes all information related to the examination and examination, such as medical advice, image diagnosis result and the like, so that the follow-up doctor can make accurate medical record judgment and medication, health promotion and education and other guidance for the woman himself.
The customized project of the woman is targeted according to the stage requirements of the woman, particularly the pregnancy preparation stage, the pregnancy stage, the lactation stage, the climacteric stage and the like, and meanwhile, the customized project also comprises basic situation information and the like of the woman, such as age, other medical history, allergic situation, family genetic history and other basic situations.
The self-defining project is implemented according to specific and significant stages in the whole life stage of the woman, and is more beneficial to the diagnosis and treatment of the woman in different stages by the medical system. Meanwhile, the self-defined project is also an important technical characteristic of the invention aiming at the effective research that the effective and unified diagnosis and treatment scheme for the women at a specific stage is not available in the prior art.
The first medicine scheme is combined with the medicine file, the inspection file and the inspection file, the class of the medicine to be taken is needed, relevant medicine information and medical advice are reasonably and accurately given under the diagnosis of a doctor, meanwhile, guiding suggestions are given by a pharmacist, the guidance suggestions comprise replaceable medicines, contraindication medicines, compatibility contraindication medicines and the like, and the medicine suggestions are more comprehensively and accurately provided for women.
The method provides inspection and examination guidance, a medication scheme and follow-up behavior guidance by combining the current stage requirements or the follow-up stage requirements of the women, realizes reasonable dispensing, reasonable inspection and examination, reasonable body health guidance and the like of the women, reduces the influence of unnecessary medicaments on follow-up bodies, reduces unnecessary inspection and examination, and simultaneously can reduce the cost of the women in the aspects of inspection and examination, medication and the like.
Specifically, according to the self-defined unexpected pregnancy stage of the woman, and the age, occupation, medication history, menstrual cycle, other medical history, bad contact history, bad pregnancy history, allergic conditions, family genetic history and the like of the woman, medication teratogenesis risk assessment and suggestion are carried out, and the method provides the inspection and examination, health propaganda and education scheme and the like which are required to take medicines, do not need to take medicines, cannot take medicines, need to be carried out in time in different stages of pregnancy.
Preferably, in an embodiment of the present invention, the data management system further includes a medication profile update module: the medication file updating module is used for regularly fusing first medication purchasing information, corresponding first medication taking information and first order information of the woman in each grade hospital and pharmacy;
the first medicine purchasing information comprises at least one of a first medicine purchasing medicine name, first medicine purchasing medicine production information, a first medicine purchasing medicine usage amount, a first medicine purchasing time, a first medicine purchasing medicine duration, a same-sex related medicine category and a reverse-sex related medicine category.
The medicine file is updated regularly, especially aiming at prescription medicine management, medicine tracking, follow-up and management can be carried out on women in special stages, and more reasonable and timely medicine guide can be given by combining the previous medicine of the women.
For example, according to the customized unexpected pregnancy stage of the woman, and the age, occupation, medication history, menstrual cycle, other medical history, bad contact history, bad pregnancy history, allergic condition, family genetic history and the like of the woman, medication teratogenicity risk assessment and suggestion are carried out, and the method provides the required medicine taking, the unnecessary medicine taking, the impossible medicine taking, the inspection and the inspection which need to be carried out in time, the health propaganda and education scheme and the like in different stages of the pregnancy. Even according to the high teratogenicity medicine taken before pregnancy, a risk assessment suggestion, a compensatory medicine suggestion and the like are given.
Preferably, in an embodiment of the present invention, the data management system further includes a checking and checking archive updating module:
the examination and check file updating module is used for fusing examination and check medical records of all levels of hospitals of the women at regular time.
In view of the fact that women can carry out examination and check in different hospitals, even take medicine in different places and the like, the method provided by the invention can update the examination and check files, meanwhile, the examination and check of hospitals of all levels on the woman are integrated, the uniformity, the continuity and the non-repeatability of the examination and check on the woman are realized, and the method is also beneficial to providing more accurate medical record judgment and reasonable medicine taking for the woman in combination with the examination and check before, the related medical advice, the related third medicine scheme and the like by a subsequent doctor, and improves the rationality and the accuracy of diagnosis and medicine taking while reducing repeated examination and check.
Meanwhile, detection and examination of different hospitals and different departments are integrated, so that the internal unification of the medical system is realized, and the medical system is more beneficial to medical treatment and treatment of patients, women and the like.
The check and check files may be check and check files in a specific phase, or may be all check and check files from the first time.
Specifically, the first examination and examination diagnosis result not only includes the medication scheme of the relevant times, but also includes all information related to the examination and examination, such as medical advice, image diagnosis result and the like, so that the follow-up doctor can make accurate medical record judgment and medication, health promotion and education and other guidance for the woman himself.
Preferably, in an embodiment of the present invention, the data management system further includes a tracking module:
the tracking module is used for a pharmacist to track and feed back the body health and medication related information of the woman at regular time to obtain influence factors of different medications on the woman of different self-defined items.
Wherein, the medicine process, the ending tracking, the follow-up, the induction and the screening of the women in each physiological stage are carried out on the data of special populations such as women in pregnancy, lactation and climacteric period at regular intervals, so as to obtain the influence of different medicines on the women in different physiological stages, even the influence of different combined medicines on the women in different physiological stages. Can well define the medication influence factors and provide accurate and scientific basis for the subsequent medication of women.
Preferably, in an embodiment of the present invention, the categories of the medicines taken include names of the medicines taken, name production information of the medicines taken, name usage amount of the medicines taken, name time of the medicines taken, and name duration time of the medicines taken;
the recommended medicine category comprises a recommended medicine name, a recommended medicine usage amount, a recommended medicine taking time and a recommended medicine taking duration;
the new medicine category comprises a new medicine name, new medicine production information, a new medicine usage amount, a new medicine medication time and a new medicine duration;
the contraindicated medicine category comprises a name of a contraindicated medicine, and the duration time of the contraindicated medicine is determined according to the time node of the custom item.
The invention realizes the continuity and the perfection of relevant medicine application and the like of the detection and the inspection by comprehensively and dynamically recording the woman detection and inspection results and the medicine application file in real time, particularly for the groups of women who are ready for pregnancy, lactation and climacteric, thereby ensuring the comprehensiveness of the woman health file; meanwhile, a guidance suggestion is provided for the reasonable medication of women in pregnancy, pregnancy and lactation periods; on the basis, related medicines based on inspection, examination and the like are monitored, reasonable medicine application suggestions and guidance are provided for women with pregnancy preparation, pregnancy, lactation and climacteric, and personalized medicine application adjustment is given in time; meanwhile, the data of groups of people for pregnancy, lactation, climacteric women and the like can be regularly screened according to the results of the early-stage examination and in combination with the medication of patients, and the pregnancy medication fate is tracked, followed, induced and analyzed to obtain the human data of different drugs influencing the embryo in different stages of pregnancy, so that more evidence-based bases are provided for the reasonable medication of the national pregnancy, and the method has very important practical and instructive significance.
The above-mentioned embodiments are only used for illustrating the technical solutions of the present invention, and not for limiting the same; although the present invention has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; such modifications and substitutions do not substantially depart from the spirit and scope of the embodiments of the present invention, and are intended to be included within the scope of the present invention.
Claims (10)
1. The management method based on the medicine taking data of women is characterized by comprising the following steps:
establishing a medication file, a check file and an inspection file of the woman, wherein the medication file comprises at least one of a category of taken medicines, a category of recommended medicines, a category of new medicines and a category of contraindicated medicines; the examination and check-up archive comprises at least one of a first general physical examination, a first examination and check-up item, a first examination and check-up time, a first examination and check-up image, and a first examination and check-up diagnosis result;
determining a first medication regimen based on said woman's custom project, said inspection and review profile, said class of medications taken;
wherein the self-defined project comprises at least one of a pregnancy preparation project, a pregnancy project, a lactation project and a climacteric project;
the first medication regimen includes at least one of a first medication category, first medication production information, a first usage amount, a first medication time, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
2. The method for managing data based on female medication use of claim 1, wherein: the data management method further comprises:
updating the medication file periodically;
the periodically updating the medication profile may include: regularly fusing first medicine purchasing information, corresponding first medicine taking information and first order information of the woman in each grade hospital and pharmacy;
the first medicine purchasing information comprises at least one of a first medicine purchasing medicine name, first medicine purchasing medicine production information, a first medicine purchasing medicine usage amount, a first medicine purchasing time, a first medicine purchasing medicine duration, a same-sex related medicine category and a reverse-sex related medicine category.
3. The method for managing data based on female medication use of claim 1, wherein: the data management method further comprises:
updating the inspection and review profile periodically;
said periodically updating said inspection and review profile comprises: and fusing examination and examination medical records of all levels of hospitals of the women at regular time.
4. The method for managing data based on female medication use of claim 1, wherein: the data management method further comprises:
and tracking and feeding back the body health and medication related information of the woman regularly according to the medication file to obtain influence factors of different medications on the woman of different self-defining items.
5. The method for managing data on female medication according to any of claims 1 to 4, wherein:
the class of the taken medicines comprises names of the taken medicines, name production information of the taken medicines, name usage amount of the taken medicines, name time of the taken medicines and name duration time of the taken medicines;
the recommended medicine category comprises a recommended medicine name, a recommended medicine usage amount, a recommended medicine taking time and a recommended medicine taking duration;
the new medicine category comprises a new medicine name, new medicine production information, a new medicine usage amount, a new medicine medication time and a new medicine duration;
the contraindicated medicine category comprises a name of a contraindicated medicine, and the duration time of the contraindicated medicine is determined according to the time node of the custom item.
6. A system for managing medication data for women, said system comprising:
the medicine file module is used for establishing a medicine file of the woman, wherein the medicine file comprises at least one of a medicine category which is taken, a medicine category which is suggested to be taken, a new medicine category and a medicine category which is contraindicated to be taken;
a check and examination archive module for creating a check and examination archive including at least one of a first general physical examination, a first check and examination item, a first check and examination time, a first check and examination image, a first check and examination diagnostic result;
a customization module for customizing a project for the woman; the self-defined item comprises at least one of a pregnancy preparation item, a pregnancy item, a lactation item and a climacteric item;
a recommended medication module for determining a first medication regimen based on the woman's customized items, the inspection and review profile, and the categories of medications taken; the first medication regimen includes at least one of a first medication category, first medication production information, a first usage amount, a first medication time, a first medication duration, a contraindication medication category, a like nature coherent medication category, an opposite nature coherent medication category.
7. The system for women medication-based data management of claim 6, wherein the data management system further comprises a medication profile update module:
the medication file updating module is used for regularly fusing first medication purchasing information, corresponding first medication taking information and first order information of the woman in each grade hospital and pharmacy;
the first medicine purchasing information comprises at least one of a first medicine purchasing medicine name, first medicine purchasing medicine production information, a first medicine purchasing medicine usage amount, a first medicine purchasing time, a first medicine purchasing medicine duration, a same-sex related medicine category and a reverse-sex related medicine category.
8. The system for women medication data management in accordance with claim 6, wherein the data management system further comprises a verification and review profile update module:
the examination and check file updating module is used for fusing examination and check medical records of all levels of hospitals of the women at regular time.
9. The system for women medication data management based on claim 6, wherein the data management system further comprises a tracking module:
the tracking module is used for tracking and feeding back the body health and medication related information of the woman in a timing mode to obtain influence factors of different medications on the woman of different self-defining items.
10. The system for managing data on female medication according to any one of claims 6 to 9, wherein:
the class of the taken medicines comprises names of the taken medicines, name production information of the taken medicines, name usage amount of the taken medicines, name time of the taken medicines and name duration time of the taken medicines;
the recommended medicine category comprises a recommended medicine name, a recommended medicine usage amount, a recommended medicine taking time and a recommended medicine taking duration;
the new medicine category comprises a new medicine name, new medicine production information, a new medicine usage amount, a new medicine medication time and a new medicine duration;
the contraindicated medicine category comprises a name of a contraindicated medicine, and the duration time of the contraindicated medicine is determined according to the time node of the custom item.
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