Literature DB >> 14608435

A Survey of Team Physicians on the Participation Status of Hemophilic Athletes in National Collegiate Athletic Association Division I Athletics.

Kelly A. Fiala1, Sandra J. Hoffmann, Donna M. Ritenour.   

Abstract

OBJECTIVE: To determine if team physicians would allow individuals with hemophilia A to participate in National Collegiate Athletic Association Division I athletics and what factors influence their decisions. An additional purpose was to determine if individuals with hemophilia A are presently participating in Division I athletics. DESIGN AND
SETTING: The data were collected with a mail survey designed by the researchers.
SUBJECTS: 66 Division I team physicians. MEASUREMENTS: The questions in the survey were considered important in understanding the history of team physicians with hemophilic athletes, the self-established standard that team physicians would follow in the future with regard to athletic participation by hemophilic players, and the team physicians' reasoning for their standards.
RESULTS: Of the 231 surveys sent, 72 were returned and 66 were analyzed. Sixteen hemophilic players were reported to have participated in Division I athletics. Several team physicians allowed hemophilic athletes to participate under many circumstances. As the severity of hemophilia A and risk of injury due to sport type (noncontact, contact, or collision) increased, the number of team physicians allowing participation decreased. Also, it was reported that hemophilic athletes were currently participating in sports.
CONCLUSIONS: Athletes with hemophilia are currently participating in Division I athletics, but they have special needs regarding their conditions. Prevention and management plans have been devised to expedite the care of these athletes.

Entities:  

Year:  2003        PMID: 14608435      PMCID: PMC233179     

Source DB:  PubMed          Journal:  J Athl Train        ISSN: 1062-6050            Impact factor:   2.860


  7 in total

Review 1.  Hereditary plasma clotting factor disorders and their management.

Authors:  C K Kasper
Journal:  Haemophilia       Date:  2000-07       Impact factor: 4.287

2.  Adverse events during use of intranasal desmopressin acetate for haemophilia A and von Willebrand disease: a case report and review of 40 patients.

Authors:  A L Dunn; J R Powers; M J Ribeiro; F R Rickles; T C Abshire
Journal:  Haemophilia       Date:  2000-01       Impact factor: 4.287

3.  Participation in sports by Dutch persons with haemophilia.

Authors:  L Heijnen; E P Mauser-Bunschoten; G Roosendaal
Journal:  Haemophilia       Date:  2000-09       Impact factor: 4.287

4.  Traumatic Hemarthrosis of the Knee Secondary to Hemophilia A in a Collegiate Soccer Player: A Case Report.

Authors:  Kelly A Fiala; Sandra J Hoffmann; Donna M Ritenour
Journal:  J Athl Train       Date:  2002-09       Impact factor: 2.860

Review 5.  Treatment of inherited coagulation disorders.

Authors:  A J Cohen; C M Kessler
Journal:  Am J Med       Date:  1995-12       Impact factor: 4.965

Review 6.  Musculoskeletal disorders in the haemophilias.

Authors:  J R York
Journal:  Baillieres Clin Rheumatol       Date:  1991-08

7.  Nasal spray desmopressin (DDAVP) for mild hemophilia A and von Willebrand disease.

Authors:  E H Rose; L M Aledort
Journal:  Ann Intern Med       Date:  1991-04-01       Impact factor: 25.391

  7 in total
  1 in total

1.  Hemophilia in Sports: A Case Report and Prophylactic Protocol.

Authors:  Mark Maffet; Jimmy Roton
Journal:  J Athl Train       Date:  2016-11-18       Impact factor: 2.860

  1 in total

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