Effect of danazol on coagulation parameters and bleeding in hemophilia
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Oral danazol administration to hemophiliacs significantly shortened APTT but did not consistently increase factor activity, while simultaneously increasing bleeding episodes and fibrinolytic activity.
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Abstract
Danazol was given orally at a dose of 600 mg/day to six hemophiliacs for eight to 14 weeks. All patients showed a significant decrease in activated partial thromboplastin time (APTT) beginning with the first measurement (two weeks) and persisting until use of the drug was discontinued. However, a corresponding increase in the deficient factor activity could not be consistently demonstrated. Despite the shortened APTT, bleeding episodes continued in the severe hemophiliacs and the patient with Christmas disease. In four patients, bleeding appeared to increase in severity or change in pattern, and in two cases the bleeding manifestations did not respond to usual factor infusions but responded to discontinuation of the drug therapy and further factor replacement. Euglobulin lysis times were measured in five patients (one hemophiliac and four with nonhemophilic conditions) who were receiving danazol. The lysis times were markedly shortened. Increased fibrinolytic activity may be responsible for the increased bleeding manifestations in danazol-treated hemophiliacs. (JAMA1985;253:1154-1156)
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Cited by (3)
- Efficacy of danazol in pure red cell aplasia 1986
- Danazol: <i>in vitro</i> effects on human hemopoiesis and <i>in vivo</i> activity in hypoplastic and myelodysplastic disorders 1991
- Danazol fails to increase factor VIII or IX levels in a double‐blind crossover study of patients with haemophilia A and B 1986
Cited by (3)
- Danazol: <i>in vitro</i> effects on human hemopoiesis and <i>in vivo</i> activity in hypoplastic and myelodysplastic disorders 1991
- Danazol fails to increase factor VIII or IX levels in a double‐blind crossover study of patients with haemophilia A and B 1986
- Efficacy of danazol in pure red cell aplasia 1986
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