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Under the comparative effectiveness program, the Department of Health and Human Services and two agencies under it —the National Institutes of Health and the Agency for Healthcare Research and Quality — will finance studies that will look at various treatments and will pay for the development of information-gathering tools, like databases of patients being treated for a certain condition.
In a paper in The Journal of the American Medical Association last year, the psychiatrists Dr. Donald Klein of Columbia University and Dr. Charles O'Brien of the University of Pennsylvania argued that the best way to study the risk of rare side effects was to establish large, linked databases of patients, including medical records and prescription histories.
With this aim in mind, we convened a multinational investigator meeting to explore merging individual patient data from multiple clinical trials and observational databases of patients with SAH and to create an agreement under which such a group of investigators could submit data and collaborate.
For this retrospective study, patients injured as a result of contact with law enforcement personnel were identified using ICD-9 external cause of injury codes from medical record databases of patients treated in all hospitals and trauma units in Illinois between 2000 and 2009.
The USRDS is one of the largest databases of patients with ESRD.
A retrospective multicenter study was carried out by examining the medical records (computer databases) of patients followed in an outpatient setting and in hospital.
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Now such shoulder-rubbing is becoming a quaint memory — thanks to vast databases of patient and doctor information being used by pharmaceutical companies to market drugs.
Regarding sharing of information in medical databases, in [8] the authors discuss the effects of the American Recovery and Reinvestment Act of 2009 on medical research, namely the production of large-scale databases of patient data allowing better and larger studies.
And statisticians collaborate with medical and public health researchers on analyses of vast databases of patient information to uncover risk factors for disease, guide clinical practice, and generate new hypotheses.
They reviewed computer databases of patient files for patients' who were scheduled to soon attend primary care practices and outpatient clinics.
The government wants pharmacists to have access to the summary care record, the national database of patients' electronic records.
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