Title |
Woman presenting with chronic iron deficiency anemia associated with hereditary hemorrhagic telangiectasia: a case report
|
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Published in |
Drug, Healthcare and Patient Safety, November 2013
|
DOI | 10.2147/dhps.s38962 |
Pubmed ID | |
Authors |
Paul Stross |
Abstract |
Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder associated with frequent nose bleeds that can be troublesome and difficult to contain. A further manifestation is telangiectasia, which may develop in the upper and lower gastrointestinal tract. The associated blood loss can be chronic, resulting in iron deficiency anemia which, when severe, has historically been treated by blood transfusions. Further pulmonary, neurologic, and hepatic complications may appear in later life, and are well documented. Administering blood transfusions requires provision, storage, and serological testing to select suitable units. Recognition of the inherent potential risks of donated blood, the expense, and the concerns regarding blood supply, has resulted in a national policy for conservation and appropriate use of blood. For an individual patient, there may be development of alloantibodies which complicates future cross-matching for transfusions. |
X Demographics
Geographical breakdown
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Unknown | 2 | 100% |
Demographic breakdown
Type | Count | As % |
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Practitioners (doctors, other healthcare professionals) | 2 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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Portugal | 1 | 4% |
Unknown | 26 | 96% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Master | 7 | 26% |
Student > Bachelor | 4 | 15% |
Librarian | 2 | 7% |
Unspecified | 2 | 7% |
Other | 1 | 4% |
Other | 4 | 15% |
Unknown | 7 | 26% |
Readers by discipline | Count | As % |
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Medicine and Dentistry | 11 | 41% |
Unspecified | 2 | 7% |
Pharmacology, Toxicology and Pharmaceutical Science | 1 | 4% |
Biochemistry, Genetics and Molecular Biology | 1 | 4% |
Nursing and Health Professions | 1 | 4% |
Other | 3 | 11% |
Unknown | 8 | 30% |