Overview Statement on Medical Records

PEDIATRICS ◽  
1975 ◽  
Vol 56 (2) ◽  
pp. 329-329 ◽  
Author(s):  
Hugh C. Thompson ◽  
Stanton J. Barron ◽  
John P. Connelly ◽  
Andrew Margileth ◽  
Richard Olmsted ◽  
...  

Historically, medical records have been maintamed by individual physicians to record specific information concerning patients. This information was often understandable only to the writer. The data were of outstanding events. This was thought to be sufficient documentation for patient care. Records are now read by others than the individual physicians. Groups of physicians working together often share the same patients and their records. Patients may have multiple sources of care. Our population has become more mobile which makes it necessary to transfer vast amounts of medical information. The medical record many times is the one instrument which gives a complete and continuous documentation of the patient's medical history. Third-party payers are requesting access to medical records to document services provided. Chart audit is being tested as a mechanism for evaluating physician performance. Records must reflect what the physician does in order to be useful in such an appraisal. Much clinical research on the delivery of health care depends on accurately kept records which are easily interpreted. A chart is also a legal document for the protection of the physician as well as the patient. Thus, records will be used in other than traditional ways. Proper confidentiality must be maintained when such uses are necessary. Physicians generally agree as to the essential content of a medical record. However, there is little unanimity as to the structure of the chart. No one system of keeping records is now appropriate for all situations. The maintenance of adequate charts requires additional cost in both time and money.

PEDIATRICS ◽  
1977 ◽  
Vol 59 (4) ◽  
pp. 636-636
Author(s):  
Nicholas Cunningham

The "Overview Statement on Medical Records," which appeared in the August 1975 issue, overlooks the needs of patients and parents. The Committee on Standards of Child Health Care has noted that patients may have multiple sources of care and that the population is more mobile. It seems not to have observed that people want to know and learn more about their state of health and care. The doctor, clinic, or any one institution that owns the medical record is unlikely ever to be "the one institution which gives a complete and continuous documentation of the patient's medical history."


Author(s):  
Omar Gutiérrez ◽  
Giordy Romero ◽  
Luis Pérez ◽  
Augusto Salazar ◽  
Marina Charris ◽  
...  

The current information systems for the registration and control of electronic medical records (EMR) present a series of problems in terms of the fragmentation, security, and privacy of medical information, since each health institution, laboratory, doctor, etc. has its own database and manages its own information, without the intervention of patients. This situation does not favor effective treatment and prevention of diseases for the population, due to potential information loss, misinformation, or data leaks related to a patient, which in turn may imply a direct risk for the individual and high public health costs for governments. One of the proposed solutions to this problem has been the creation of electronic medical record (EMR) systems using blockchain networks; however, most of them do not take into account the occurrence of connectivity failures, such as those found in various developing countries, which can lead to failures in the integrity of the system data. To address these problems, HealthyBlock is presented in this paper as an architecture based on blockchain networks, which proposes a unified electronic medical record system that considers different clinical providers, with resilience in data integrity during connectivity failure and with usability, security, and privacy characteristics. On the basis of the HealthyBlock architecture, a prototype was implemented for the care of patients in a network of hospitals. The results of the evaluation showed high efficiency in keeping the EMRs of patients unified, updated, and secure, regardless of the network clinical provider they consult.


1999 ◽  
Vol 25 (2-3) ◽  
pp. 203-231
Author(s):  
Helena Gail Rubinstein

There is little quarrel that access by medical and health policy researchers to medical records and claims data has spurred advances in quality and access to medical treatment. Nevertheless, dissatisfaction lingers with the regime used to regulate access to that information. The American regulatory regime on medical record access has politely been characterized as “fragmented” and less politely as a “black hole.” U.S. Senator Edward M. Kennedy asserts, “[t]oday, video rental records have greater protection than sensitive medical information.” At the center of this dissatisfaction is the question of how much say an individual should have in letting others—even those with legitimate need—look at and use an individual's records.


2020 ◽  
Vol 20 ◽  
pp. 59-80
Author(s):  
Juhan Maiste

In the article, the author examines one of the most outstanding andproblematic periods in the art history of Tallinn as a Hanseatic city,which originated, on the one hand, in the Hanseatic tradition andthe medieval approach to Gothic transcendental realism, and onthe other, in the approach typical of the new art cities of Flanders,i.e. to see a reflection of the new illusory reality in the pictures. Acloser examination is made of two works of art imported to Tallinnin the late 15th century, i.e. the high altar in the Church of the HolySpirit by Bernt Notke and the altarpiece of Holy Mary, whichwas originally commissioned by the Brotherhood of Blackheadsfor the Dominican Monastery and is now in St Nicholas’ Church.Despite the differences in the iconography and style of the twoworks, their links to tradition and artistic geography, which in thisarticle are conditionally defined as the Hanse canon, are apparentin both of them.The methods and rules for classifying the transition from theMiddle Ages to the Modern Era were not critical nor exclusive.Rather they included a wide range of phenomena on the outskirtsof the major art centres starting from the clients and ending with the semantic significance of the picture, and the attributes that wereemployed to the individual experiences of the different masters,who were working together in the large workshops of Lübeck, andsomewhat later, in Bruges and Brussels.When ‘reading’ the Blackheads’ altar, a question arises of threedifferent styles, all of them were united by tradition and the waythat altars were produced in the large workshops for the extensiveart market that stretched from one end of the continent to the other,and even further from Lima to Narva. Under the supervision ofthe leading master and entrepreneur (Hans Memling?) two othermasters were working side by side in Bruges – Michel Sittow, whowas born in Tallinn, and the Master of the Legend of Saint Lucywere responsible for executing the task.In this article, the author has highlighted new points of reference,which on the one hand explain the complex issues of attributionof the Tallinn Blackheads’ altar, and on the other hand, placethe greatest opus in the Baltics in a broader context, where, inaddition to aesthetic ambitions, both the client and the workshopthat completed the order, played an extensive role. In this way,identifying a specific artist from among the others would usuallyremain a matter of discussion. Tallinn was a port and a wealthycommercial city at the foregates of the East where it took decadesfor the spirit of the Renaissance to penetrate and be assimilated.Instead of an unobstructed view we are offered uncertain andoften mixed values based on what we perceive through the veil ofsemantic research.


2021 ◽  
Vol 2 (1) ◽  
pp. 1
Author(s):  
Ahmad Muchlis ◽  
Rifa Aulia Ramadhanty

Background: Completeness of patient medical information in medical records is one indicator in assessing the quality of health services. Complete and accurate medical records contribute to the accuracy of medical staff in making a diagnosis so that they can determine the correct diagnosis code according to the ICD-10 guidelines. A good medical record shows that a doctor or other medical staff has carried out their duties by the demands of their profession as stated in the Medical Practice Law No.29 of 2004. Purposes: To find out there is or not a correlation between the medical information completeness and the accuracy of the diagnosis code for upper respiratory tract infection and hypertension based on the ICD-10 in the medical record documents of outpatients at the Cibening Health Center in 2019. Method: The method used in this study is observational analytic with a cross-sectional study design. The population of this study was outpatient medical records with a diagnosis of upper respiratory tract infection and hypertension at the Cibening Health Center in 2019. The sampling technique used a simple random sampling technique with a sample size of 100. Results: Out of obtained 71 complete medical record (71%) filling in medical records, 64 medical records (64%) were accurate in giving ICD-10 codes, 63 medical records (88.7%) with complete medical information had accurate diagnosis codes in comparison with 8 medical records (11.3%) which were complete but inaccurate diagnosis code. Conclusion: With a p-value of 0.000, there is a significant correlation between the completeness of medical information and the accuracy of the diagnosis code for Upper Respiratory Tract Infection and Hypertension based on ICD-10.


2021 ◽  
Vol 1 (1) ◽  
pp. 1-8
Author(s):  
Almas Ummi Fatharina ◽  
Sri Sugiarsi ◽  
Trismianto Asmo Sutrisno

Abstract Release of medical information must be subject to applicable procedures and must be with the patient's consent. Patients must make a stamped written statement that has authorized a third party to request medical data from a doctor. The purpose of this study is to determine the policy of releasing medical information and the flow of procedures for releasing medical information to the insurer. The research method in this study is to use a literature review design, namely research that examines research articles on the release of medical information to insurance parties by comparing, summarizing, and drawing conclusions. The search strategy used keywords and operator bundles used in this study, namely "medical records" or "information release" or "insurers". The result of the research is that a hospital is in the process of releasing medical information using policies in the form of SOPs, cooperation agreements with insurance parties, and orally. In addition, there are hospitals that have different procedures for releasing medical information because they do not only serve one insurance party, but there are several insurance parties that are served such as BPJS, Jasa Raharja, and Askes. However, in the process of releasing medical information, there are hospitals that are not yet in accordance with the flow of medical information release procedures that have been determined by the Hospital. Therefore, the hospital conducts outreach on the flow of procedures for releasing medical information so that the officer in charge has a better understanding of the release of medical information. Keyword : medical records, information release, insurers Abstrak Pelepasan informasi medis harus mengacu pada prosedur yang berlaku dan harus dengan persetujuan pasien. Pasien harus membuat pernyataan tertulis bermaterai bahwa telah memberi kuasa kepada pihak ketiga untuk meminta data medis dari dokter. Tujuan penelitian ini adalah untuk mengetahui kebijakan pelepasan informasi medis dan alur prosedur pelepasan informasi medis kepada pihak asuransi. Metode penelitian dalam penelitian ini adalah menggunakan desain literature review yaitu penelitian yang mengkaji artikel-artikel penelitian tentang Pelepasan Informasi Medis Kepada Pihak Asuransi dengan cara membandingkan, meringkas, dan mengambil kesimpulan. Strategi pencarian menggunakan keyword dan booelan operator yang digunakan dalam penelitian ini yaitu “rekam medis” or “pelepasan informasi” or “pihak asuransi”. Hasil penelitian terdapat Rumah Sakit yang dalam proses pelepasan informasi medis menggunakan kebijakan dalam bentuk SOP, perjanjian kerjasama dengan pihak asuransi, dan secara lisan. Selain itu terdapat Rumah Sakit memiliki alur prosedur pelepasan informasi medis yang berbeda-beda karena tidak hanya melayani satu pihak asuransi saja, tetapi ada beberapa pihak asuransi yang dilayani seperti BPJS, Jasa Raharja, dan Askes. Akan tetapi dalam proses pelepasan informasi medis terdapat Rumah Sakit yang belum sesuai dengan alur prosedur pelepasan informasi medis yang telah ditentukan oleh Rumah Sakit. Oleh karena itu pihak Rumah Sakit melakukan sosialisasi mengenai alur prosedur pelepasan informasi medis agar petugas yang bertanggungjawab lebih paham mengenai pelepasan informasi medis.


2008 ◽  
Vol 47 (03) ◽  
pp. 235-240 ◽  
Author(s):  
D. Weerasinghe ◽  
K. Elmufti ◽  
V. Rakocevic ◽  
M. Rajarajan

Summary Objective: The objective of this study is to develop a solution to preserve security and privacy in a healthcare environment where health-sensitive information will be accessed by many parties and stored in various distributed databases. The solution should maintain anonymous medical records and it should be able to link anonymous medical information in distributed databases into a single patient medical record with the patient identity. Methods: In this paper we present a protocol that can be used to authenticate and authorize patients to healthcare services without providing the patient identification. Healthcare service can identify the patient using separate temporary identities in each identification session and medical records are linked to these temporary identities. Temporary identities can be used to enable record linkage and reverse track real patient identity in critical medical situations. Results: The proposed protocol provides main security and privacy services such as user anonymity, message privacy, message confidentiality, user authentication, user authorization and message replay attacks. The medical environment validates the patient at the healthcare service as a real and registered patient for the medical services. Using the proposed protocol, the patient anonymous medical records at different healthcare services can be linked into one single report and it is possible to securely reverse track anonymous patient into the real identity. Conclusion: The protocol protects the patient privacy with a secure anonymous authentication to healthcare services and medical record registries according to the European and the UK legislations, where the patient real identity is not disclosed with the distributed patient medical records.


2018 ◽  
Vol 7 (4) ◽  
pp. 60
Author(s):  
Hanen Ghorbel ◽  
Sirine Farjallah

The meta-modeling of medical records helps standardize and capitalize the expert’s knowledge domain. It promotes the interoperability knowledge and the reuse of clinical concepts, i.e., archetypes. It also promotes high quality electronic medical record system (EMRS) design, which helps provide better care service delivery. As a result, different standards of medical informatics use the dual model to support interoperability between Medical Information Systems. We particularly quote ISO/EN 13606 and OpenEHR. However, the use of these standards still presents challenges. Apart from political reasons, the main obstacles to the adoption of these standards include: (1) a lack of guides and methodological tools to facilitate the construction of EMRS using two conceptual levels. Designers must have languages, approaches and tools to assist them in the modeling of archetypal EMRS; (2) a lack of methodologies for semantic activities on the content of electronic health records in the semantic web environment; (3) and a lack of management of uncertainties and inaccuracies that may exist in the medical field. Theconstruction of an approach to modeling EMRS according to the dual model approach, considering the uncertainties, inaccuracies and semantics of these systems, is a difficult task, given the challenges to emancipate. In literature, we don’t find such an approach. We, therefore, defined one in this paper. Our goal is to guide the designer in all stages of developing a new generation of EMRS, from analysis and specification of requirements to implementation. To achieve this goal, we have created an approach to support the following activities: (1) clinical concepts and information management and meta-modeling in accordance with the openEHR standard, (2) integration of the semantic dimension into EMRS considered to enable the execution of semantic activities in the semantic web environment; and (3) integration of the fuzzy dimension into electronic medical record data structures. As a contribution, we defined an approach called Fuzzy SemanticOpenEHR allowing the integration of semantic and fuzzy dimensions into EMRS modeled using the openEHR standard. Fuzzy SemanticOpenEHR intends to help and equip the designer during the different phases of creating a fuzzy ontology. Thanks to the mechanisms offered by this approach, we have been able to obtain a fuzzy ontological basis that can serve as a knowledge base that can support the semantic interoperability between EMRS, the deduction of new knowledge and the taking of knowledge’s clinical decision. To test our contribution, we proceeded to the realization of a prototype of tools realized for the pediatric neurology service of the university hospital “Hédi Chaker Sfax - Tunisia” and the association of the handicapped persons safeguard of Sfax. This prototype is a framework called “XML 2 FuzzyOWL”. Then, we tested this framework using a case of a disease which is “Cerebral Palsy”.


2018 ◽  
Author(s):  
Audrey Ozols ◽  
Eugene Luskin ◽  
Paul Buehrens

BACKGROUND Patient medical records contain important information for healthcare professionals to make the right decisions that provide efficient care and optimize quality patient outcomes. Electronic health record (EHR) systems are now the standard to document patient health information. However, the exchange of patient protected health information remains a challenge due to the lack of connectivity across hundreds of different EHR systems. OBJECTIVE The aim of the study is to describe the implementation of a secure and EHR-agnostic portable patient medical record technology, and to describe initial user experiences. METHODS We developed the VYRTY solution, a HIPPA compliant and secure medical record card and reader that allows for user authentication, patient authentication, data capture, data storage, and documentation sharing that works with any EHR system. Storage of all patient medical records is encrypted on the VYRTY card allowing safe patient transportation of medical records. Physician activation was phased in over the first 5 months of the one-year pilot. Patient enrollment was voluntary and was complete within 8 months from start of the pilot. Physicians uploaded medical record documents from their EHR by using the print function. Patients that were referred shared their VYRTY card with the receiving physician for downloading of medical records. The exchange of medical records was recorded by the VYRTY system and personal interviews were conducted and recorded to assess user experience. RESULTS One hundred and ninety-four patients participated out of 200 enrolled, while 23 physicians actively participated out of 45 enrolled. Patients utilized their VYRTY cards 49% of the time, and physicians downloaded documents 51% of the time during the 1-year pilot period. Participating physicians found VYRTY easy to use and their patients were very satisfied with the convenient portability of their medical records. CONCLUSIONS VYRTY was implemented successfully and found to be easy to use by physicians and patients. Using the VYRTY system gave patients their own medical records to share with other providers, which effectively solved the problem of exchanging health information between different EHR systems.


2021 ◽  
Vol 8 (2) ◽  
pp. 15-25
Author(s):  
Narcisa Galeș ◽  
Dumitrița Florea

When referring to children, we must admit that they are not just physical existences whose stages of development participate in determining the concept of legal capacity. Children are natural persons who, until the age of majority, are protected by the law, precisely because of their insufficient psychological maturity. In particular, we are referring to legal protection of the child in civil matters, subject to civil law, but also to legal protection of the child in general, which goes beyond the civil support given to the individual, legally called a natural person, within the general legal framework which safeguards the fundamental social values of the individual, by including a special legal protection regime on the child. Therefore, the child is no longer an identity substitute for the parents, but needs to be treated according to what it is and not what it will become, as he is the holder of his or her own rights, having a legal status in his or her own right, while also interacting with the rights and obligations of others (extended nuclear family or third-party relationships), as well as society as a whole, which has structured the status of the child according to its values. This is the ideology of the rights of the child, as a result of its development, centered on the recognition of the child as holder of related rights of indivisibility, interdependence and interrelation, the respect, protection and enforcement of which are bound by the States signatory to the Convention on the Rights of the Child. This legal instrument is a probable consequence of the equalitarian dynamics of human rights, on the one hand, and, on the other, based on the discovery of psychology by highlighting children's ability to understand and feel.


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