ETRO Working Party on Factor XIII questionnaire on congenital factor XIII deficiency in Europe: status and perspectives. Study Group
Autor: | Rainer Seitz, Uri Seligsohn, F Duckert, László Muszbek, F. Rodeghiero, S. Lopaciuk |
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Rok vydání: | 1996 |
Předmět: |
Adult
Male Pediatrics medicine.medical_specialty Abortion Habitual Genotype Hemorrhage Umbilical cord Severity of Illness Index Hemorrhagic disorder Congenital deficiency Pregnancy Surveys and Questionnaires Coagulopathy Medicine Humans Factor XIII deficiency Wound Healing Factor XIII business.industry Pregnancy Complications Hematologic Infant Newborn Hematology medicine.disease Factor XIII Deficiency Europe Mild symptoms medicine.anatomical_structure Phenotype Female Cardiology and Cardiovascular Medicine business medicine.drug |
Zdroj: | Seminars in thrombosis and hemostasis. 22(5) |
ISSN: | 0094-6176 |
Popis: | A questionnaire was sent out in 1993 to more than 350 European institutions caring for patients with hemorrhagic disorders with the request to provide data of patients with congenital factor XIII deficiency, to pursue the following aims: (1) establish a registry of congenital factor XIII deficiency patients, (2) promote exchange between clinicians and basic researchers, (3) improve diagnostic and therapeutic approaches, and (4) stimulate research on gene defects and their impact on factor XIII function. So far, 72 patient questionnaires from 60 families have been collected. Their bleeding pattern is typical, with frequent involvement of the umbilical cord and the central nervous system. Forty-nine patients receive regular factor XIII replacement, but obviously some patients with mild symptoms do not require prophylactic substitution, despite low factor XIII levels. On the other hand, 18 patients had factor XIII activities of > or = 5% of normal, but only 3 of those patients were reported to have no bleeding symptoms. Furthermore, 17 symptomatic, apparently heterozygous relatives in eight families were observed. Seven out of 30 females aged over 18 years had experienced spontaneous abortions; wound healing problems were seen in 26 patients. Currently, a second questionnaire is being distributed to obtain more detailed information on bleeding and other symptoms, diagnostic approaches, and exclusion of concurrent other bleeding diatheses. Future activities will be validation and standardization of assays, and study of gene defects and their impact on the structure of factor XIII and symptoms of patients. We intend to expand the survey to countries outside Europe. |
Databáze: | OpenAIRE |
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