12 hours ago Yes. Under HIPAA, a case report is an activity to develop information to be shared for medical/educational purposes. Although the use of protected health information to prepare the paper does not require IRB review, the author of a case report must comply with HIPAA. Ideally, the author of the article will obtain the signed authorization of the ... >> Go To The Portal
Does the case report provide information about the patient's age, sex, ethnicity, race, employment status, social situation, medical history, diagnosis, prognosis, previous treatments, past and current diagnostic test results, medications, psychological tests, clinical and functional assessments, and current intervention?
Q: What constitutes a “case report”? A case report for IRB purposes is a retrospective analysis of one, two, or three clinical cases. If more than three cases are involved in the analytical activity, the activity will constitute “research.” Please review the JHM Organization Policy on Single Case Reports and Case Series (Policy No. 102.3) .
The patient should be described in detail, allowing others to identify patients with similar characteristics.
III. Patient case presentationDescribe the case in a narrative form.Provide patient demographics (age, sex, height, weight, race, occupation).Avoid patient identifiers (date of birth, initials).Describe the patient's complaint.List the patient's present illness.List the patient's medical history.More items...•
You should include: • A brief summary (1-2 lines) of the patient, the reason for admission, and your likely diagnosis. This should also include information regarding the patient's clinical stability. While it can be similar to your opener, it should not be identical.
Case reports should encompass the following five sections: an abstract, an introduction with a literature review, a description of the case report, a discussion that includes a detailed explanation of the literature review, and a brief summary of the case and a conclusion.
A case report is a detailed report of the symptoms, signs, diagnosis, treatment, and follow-up of an individual patient. Case reports usually describe an unusual or novel occurrence and as such, remain one of the cornerstones of medical progress and provide many new ideas in medicine.
Case Presentation. The case report should be chronological and detail the history, physical findings, and investigations followed by the patient's course. At this point, you may wish to include more details than you might have time to present, prioritizing the content later.
Highlighted in this chapter are the essential components of the presentation: the chief complaint, the history of present illness (HPI), the past medical history, the family and social history, the review of systems, and finally, the physical examination findings.
First, we describe the complaint that brought the patient to us. It is often useful to use the patient's own words. Next, we introduce the important information that we obtained from our history-taking. We don't need to include every detail – just the information that helped us to settle on our diagnosis.
First, you want to introduce the topic not discuss the actual case. Therefore, you should not include details about your client until the case description section. The introduction should only give the background on why this case report was written and some background on the condition of interest.
Strength: The case study gives researchers the possibility to investigate cases which could not be set up in research laboratories. Strength: Case studies may contradict established theory and helps to develop new theories.
A case report is a medical/educational activity that does not meet the DHHS definition of “research”, which is: "a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge.".
Yes. Under HIPAA, a case report is an activity to develop information to be shared for medical/educational purposes. Although the use of protected health information to prepare the paper does not require IRB review, the author of a case report must comply with HIPAA.
Tuberculosis (TB) and HIV/AIDS are the 2 most common causes of death from infectious diseases across the world. [1] In China, the total estimated number of people living with HIV/AIDS rose to 780,000 in 2011.
We performed a cross-sectional study in the HIV/AIDS clinic of the Guigang City People's Hospital. Guigang City People's Hospital is a public hospital in Guigang City, which serves patients residing in Guigang City and nearby counties.
The response rate for the study was 150/194 (77.3%). Table 1 presents the descriptive statistics.
With the increase of HIV and TB burden in China, it is important to have a clearer understanding of the potential health care needs of patients coinfected with HIV and TB.
The format for individual case safety reports includes provisions for transmitting all the relevant data elements useful to assess an individual adverse drug reaction or adverse event report. The data elements are sufficiently comprehensive to cover complex reports from most sources, different data sets, and transmission situations or requirements; therefore, not every data element will be available for every transmission. In many, if not most instances, a substantial number of the data elements will not be known and therefore not included in the transmission. Where it was deemed important, provisions for unknown or not applicable were included (e.g., outcome, route of administration). However, since the transmission is intended to be electronic, it was thought to be unnecessary to include provisions to assign values of unknown for all data elements. Different ways of including the same data have been provided to cope with differing information contents (e.g., age information can be sent as date of birth and date of reaction or event, age at the time of reaction or event, or patient age group according to the available information; see section B.1.2 and the respective user guidance). In this example, age should be provided by using the most precise available data element rather than by including multiple elements of redundant data.
The objectives of the working group are to standardize the data elements for transmission of individual case safety reports by identifying, and where necessary or advisable, by defining the data elements for the transmission of all types of individual case safety reports , regardless of source and destination. This includes case safety reports for both pre and postapproval periods and covers both adverse drug reaction and adverse event reports. It is not intended that this format be used for cases in the integrated safety summary of a marketing license application dossier. For adverse reactions
The figure provides an example of how one would populate the fields relevant to identifying cases and their reports. Patient XX suffers three separate adverse events (AE1, AE2, AE3) spaced over a time period.