Document Detail


Orofacial pain in patients with sickle cell disease.
MedLine Citation:
PMID:  2206667     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The potential danger of low oxygen tension to patients with sickle cell disease is widely known. However, less well known is the phenomenon of patients with sickle cell disease presenting with toothache in the absence of any dental pathology. This study investigated the experience of orofacial pain in three matched groups, comprising patients with sickle cell disease, sickle cell trait and patients with no known blood dyscrasia. There were no differences in pain experience between those groups with sickle cell trait and no known blood dyscrasia. The sickle cell disease patients experienced significantly more orofacial pain in the same 12-month period than the other groups. The pain was also more frequent and of longer duration. In two-thirds of those sickle cell disease patients who experienced toothache, no dental pathology was found, in direct contrast to patients with trait or no known blood dyscrasia. Sickling of blood cells within the dental pulp in a sickle cell crisis may result in pain within teeth. These patients may then present as experiencing toothache in the absence of any dental pathology. General dental practitioners should be aware of this phenomenon when providing care for these susceptible patients.
Authors:
C O'Rourke; C Mitropoulos
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  British dental journal     Volume:  169     ISSN:  0007-0610     ISO Abbreviation:  Br Dent J     Publication Date:  1990 Sep 
Date Detail:
Created Date:  1990-11-08     Completed Date:  1990-11-08     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  7513219     Medline TA:  Br Dent J     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  130-2     Citation Subset:  D; IM    
Affiliation:
Dental Department, Central Manchester Health Authority, Moss Side Health Centre.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Anemia, Sickle Cell / complications*
Child
Child, Preschool
Female
Hemoglobin SC Disease / complications*
Humans
Male
Questionnaires
Retrospective Studies
Sickle Cell Trait / complications*
Toothache / etiology*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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