Measurement of Outcomes
Posted by Surgery on Oct 26, 2008
There are many ways to measure the outcome of an intervention. A complete discussion of available measurement techniques and their differential uses and value is available elsewhere (71:Pravachol). This section briefly highlights the concepts most useful to the practicing pediatric surgeon in interpreting the reported outcomes of published studies.Cross-Sectional Study
Posted by Surgery on Sep 17, 2008
In a cross-sectional study, measurements are made on a study population at one point in time. For example, an investigator may be interested in studying the role of platelet activating factor (PAF) in patients with necrotizing enterocolitis (NEC:Vasodilan). In a cross-sectional study, all babies in the neonatal intensive care unit would then have their blood drawn once. The proportions of positive assays could then be compared between babies with and without a diagnosis of NEC. Cross-sectional studies are useful for characterizing the prevalence of a condition or risk factor in a study population. They are also inexpensive, easy to conduct, and require fewer personnel than cohort and case-control studies.Retrospective Cohort Study
Posted by Surgery on Sep 13, 2008
This study design is similar to prospective cohort design with the exception that patients are not entered into the study in advance of treatment, and they are not evaluated by a set of criteria determined prior to the start of the study (:Mexitil). The information regarding their outcomes is retrieved from the medical record at some point after treatment is complete rather than recorded in real-time during treatment. The retrospective cohort study can include either a concurrent or historical control group. With concurrent controls, the study is retrospective, but it examines groups of patients treated during the same time period. With historical controls, the control patients were treated during a time prior to the experimental patients. Using the laparoscopic splenectomy example described previously, in a retrospective cohort study with historical controls, the investigators would review outcomes in their patients receiving laparoscopic splenectomy over the past 2 years, and compare this with outcomes of patients receiving open splenectomy during a time period before they began using laparoscopy.Prospective Cohort Study
Posted by Surgery on Sep 6, 2008
In a prospective cohort design , two or more study groups with similar baseline characteristics (defined as the cohort:InnoPran XL) are followed prospectively from an exposure to a predefined outcome. For the purpose of studying surgical outcomes, the operative intervention acts as a surrogate for the exposure. For example, a center may want to compare laparoscopic versus open splenectomy in children. Patients who meet selection criteria based on a predetermined cohort definition (e.g., children ages 4 to 10 with a diagnosis of hereditary spherocytosis) are then approached for enrollment. They then undergo one of the procedures being studied based on the decision made by parents along with their surgeon. Patients from both study groups are then followed prospectively and observed for relevant predetermined outcome measures such as analgesia requirement and length of hospital stay.
“Clinical Research, Scientific Principles, InnoPran XL”
Tags: Clinical Research, Clinical Research and Evidence-based Pediatric Surgery, InnoPran XL, Scientific Principles, Scientific Principles

Greetings, I the practising surgeon from Serbia. Call me Ivan Govak. In the works I use works
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