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The operative report is dictated right after a surgical procedure and later transcribed into the patient's record. The operative report includes preoperative and postoperative diagnoses, patient condition after surgery, all medications used in association with the procedure, pertinent medical history (Hx) , physical examination (PE), consent ...
A logbook (or log book) is a record used to record states, events, or conditions applicable to complex machines or the personnel who operate them.Logbooks are commonly associated with the operation of aircraft, nuclear plants, particle accelerators, and ships (among other applications).
This surgical equipment is usually found inside the surgery room of a hospital. [2] A specialized type of operating table, called a surgical fracture table (or trauma table), is designed to allow an orthopedic surgeon to perform common orthopedic procedures such as hip fractures , pelvic fractures , tibial fractures , fibula fractures , and ...
The World Health Organization (WHO) published the WHO Surgical Safety Checklist in 2008 in order to increase the safety of patients undergoing surgery. [1] The checklist serves to remind the surgical team of important items to be performed before and after the surgical procedure in order to reduce adverse events such as surgical site infections or retained instruments. [1]
Admissions to a hospital not associated with a surgery are also sometimes included here, though admissions associated with childbirth are often described in a distinct section. For example, an "OB/GYN" section may be included, including language such as " G3P2 , menarche at age 14, LMP 2 weeks ago, regular".
The Surgical Council on Resident Education (SCORE®) is the national curriculum for general surgery and its associated subspecialties, housed within the American Board of Surgery. It was originally founded as a nonprofit consortium in 2004 by seven organizations involved in U.S. surgical education.
Image credits: Vast_Sweet_1221 #8. In my car, I always keep a lighter, canned/bottled water, a change of clothes, an old (but functional) pair of shoes, and a phone charging cord.
The FDA provides a database for reporting of adverse medical device events called the Manufacturer and User Facility Device Experience Database (MAUDE)[1]. The data consist of voluntary reports since June 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August 1996, and is open for public view.