Running Head: EBT TASK 2 1 Research Integration EBT Task 2 Western Governor’s University EBT TASK 2 2 Review and Classification of Evidence Source Type Appropriate Type of (American Academy of Pediatrics; American Academy of Family Physicians, 2004) or inappropriate Filtered Appropriate: This article establishes diagnosis and …show more content…
(Kelley, Friedman, & Johnson, 2007) Filtered Appropriate: This article (chapter N/A EBT TASK 2 3 of a textbook) provides generalized information and descriptions the mechanisms of AOM, along with a host of information about other conditions that are not pertinent to this inquiry. It does appear to provide supporting research to aid in diagnosis and treatment of AOM and
The recommendation about excluding the sentence “In 2007, Philipsen et al. [4] reviewed the world literature and, based on 1082 cases, described the profile of AOT, including epidemiological aspects as well as its clinical behavior” from the manuscript (1st paragraph of the introduction, lines 49-54) was accepted by the authors and the sentence was excluded.
A recent publication in the Journal of Pediatrics (Sara L. Toomey, Alon Peltz, and colleagues,
The American Academy of Pediatrics published a systematic review with recommendations for treatment. This is high quality evidence so we
This article was published by Science Based Medicine; the website does not list any accreditations. However, all editors and contributors have minimum of a MD. The website provides easily obtainable contact information for the website but no information for the author.
Correspondence concerning this article should be addressed to Keri Sexton, Department of Medical Specialties, Stevens-Henager College, 1444 South Entertainment Avenue, Boise, Idaho, 83709. Contact: keri.sexton208@gmail.com
The initial CPG discussing AOM was published in 2004 by the AAP and AAFP. The research for the 2004 guideline was funded and conducted by the Agency for Healthcare Research and Quality (AHRQ). In 2008, AHRQ and the Southern California Evidence Based Practice Center began a review of literature pertaining to AOM published subsequent to the original AHRQ report. The review was completed in 2010, and comprises a large portion of the data used for the AAP 2013 guideline revision (CITE GUIDELINE)
McCance, K. L. & Huether, S. E. (Eds.). (2014). Pathophysiology: The Biologic Basis of Disease in Adults and Children (7th ed.). St. Louis, MO: Mosby Elsevier.
METHODS: Review of literature of various journal articles considering: pathophysiology, risk factors, incidence and novel diagnostic and treatment modalities.
Since this is such a common condition and may affect quality of life, it is important to become educated about its causes, diagnosis, and treatment. By the end of this article, you will be able to answer the following important questions:
The condition is most frequency seen in African-American children. There appears to be a higher prevalence in males compared to females.
As a whole, the article was detailed, descriptive, and organized. This case was published more than five years ago but there are no related studies that have been conducted more recently. This article is still relevant to the field today because it gives insight to a rare condition that may affect others around the
Co-instructor for DPT 776: Complex Conditions V. The topics in this course focus on Neurological Disorders in Pediatrics.
Patients with either condition experience somewhat similar symptoms. Both OM and IOE are characterized by severe pain, decreased hearing, and a discharge of pus. This pus is white, yellow, or reddish brown because of blood, and it can be oily. In addition, the pus appears as a dry crusted material on the patient's pillow. In OM, dizziness is experienced if the ear drum bursts from pressure. Patients with OM also suffer from a fever, which is slightly equals 37.5 C, and a redness of the ear drum. A rare complication of OM is mastoiditis, or infection of the the mastoid bone, which is located behind the ear drum, and may affect the brain and nearby nerves. If the patient with OM experiences other unusual symptoms, he sees his doctor. In contrast,
A subset of children with OI may have an underlying disorder (autoimmune condition, mitochondrial insufficiency, diabetes mellitus etc.) and thus diagnosis can be elusive and expensive.6 Syncope is obvious and readily recognized to the extent that patients are frequently evaluated in an emergency room and office setting. Clinical characteristics are described in children with syncope but literature is limited in describing those many patients who present with symptoms other than syncope.7,8 We studied the epidemiological and clinical characteristics of children and adolescents with OI who had autonomic dysfunction based on head up tilt table test (HUTT).
Nuffield Department of Clinical Medicine, University of Oxford, John Radcliffe Hospital, OX3 9DU, Oxford, UK