Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)
Because of the very short half-life of factor VII, prophylaxis in factor VII deficiency is considered a difficult endeavor. The clinical efficacy and safety of prophylactic regimens, and indications for their use, were evaluated in factor VII-deficient patients in the Seven Treatment Evaluation Regi...
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th-cmuir.6653943832-480432018-04-25T08:47:01Z Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) Mariasanta Napolitano Muriel Giansily-Blaizot Alberto Dolce Jean F. Schved Guenter Auerswald Jørgen Ingerslev Jens Bjerre Carmen Altisent Pimlak Charoenkwan Lisa Michaels Ampaiwan Chuansumrit Giovanni Di Minno Ümran Caliskan Guglielmo Mariani Because of the very short half-life of factor VII, prophylaxis in factor VII deficiency is considered a difficult endeavor. The clinical efficacy and safety of prophylactic regimens, and indications for their use, were evaluated in factor VII-deficient patients in the Seven Treatment Evaluation Registry. Prophylaxis data (38 courses) were analyzed from 34 patients with severe factor VII deficiency ( < 1-45 years of age, 21 female). Severest phenotypes (central nervous system, gastrointestinal, joint bleeding episodes) were highly prevalent. Twenty-one patients received recombinant activated factor VII (24 courses), four received plasma-derived factor VII, and ten received freshfrozen plasma. Prophylactic schedules clustered into "frequent" courses (three times weekly, n=23) and "infrequent" courses (≤2 times weekly, n=15). Excluding courses for menorrhagia, "frequent" and "infrequent" courses produced 18/23 (78%) and 5/12 (41%) "excellent" outcomes, respectively; relative risk, 1.88; 95% confidence interval, 0.93-3.79; P=0.079. Long-term prophylaxis lasted from 1 to > 10 years. No thrombosis or new inhibitors occurred. In conclusion, a subset of patients with factor VII deficiency needed prophylaxis because of severe bleeding. Recombinant activated factor VII schedules based on "frequent" administrations (three times weekly) and a 90 μg/kg total weekly dose were effective. These data provide a rationale for long-term, safe prophylaxis in factor VII deficiency (clinicaltrials.gov: NCT01269138). © 2013 Ferrata Storti Foundation. 2018-04-25T08:47:01Z 2018-04-25T08:47:01Z 2013-04-01 Journal 15928721 03906078 2-s2.0-84875640037 10.3324/haematol.2012.074039 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875640037&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48043 |
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Because of the very short half-life of factor VII, prophylaxis in factor VII deficiency is considered a difficult endeavor. The clinical efficacy and safety of prophylactic regimens, and indications for their use, were evaluated in factor VII-deficient patients in the Seven Treatment Evaluation Registry. Prophylaxis data (38 courses) were analyzed from 34 patients with severe factor VII deficiency ( < 1-45 years of age, 21 female). Severest phenotypes (central nervous system, gastrointestinal, joint bleeding episodes) were highly prevalent. Twenty-one patients received recombinant activated factor VII (24 courses), four received plasma-derived factor VII, and ten received freshfrozen plasma. Prophylactic schedules clustered into "frequent" courses (three times weekly, n=23) and "infrequent" courses (≤2 times weekly, n=15). Excluding courses for menorrhagia, "frequent" and "infrequent" courses produced 18/23 (78%) and 5/12 (41%) "excellent" outcomes, respectively; relative risk, 1.88; 95% confidence interval, 0.93-3.79; P=0.079. Long-term prophylaxis lasted from 1 to > 10 years. No thrombosis or new inhibitors occurred. In conclusion, a subset of patients with factor VII deficiency needed prophylaxis because of severe bleeding. Recombinant activated factor VII schedules based on "frequent" administrations (three times weekly) and a 90 μg/kg total weekly dose were effective. These data provide a rationale for long-term, safe prophylaxis in factor VII deficiency (clinicaltrials.gov: NCT01269138). © 2013 Ferrata Storti Foundation. |
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Mariasanta Napolitano Muriel Giansily-Blaizot Alberto Dolce Jean F. Schved Guenter Auerswald Jørgen Ingerslev Jens Bjerre Carmen Altisent Pimlak Charoenkwan Lisa Michaels Ampaiwan Chuansumrit Giovanni Di Minno Ümran Caliskan Guglielmo Mariani |
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Mariasanta Napolitano Muriel Giansily-Blaizot Alberto Dolce Jean F. Schved Guenter Auerswald Jørgen Ingerslev Jens Bjerre Carmen Altisent Pimlak Charoenkwan Lisa Michaels Ampaiwan Chuansumrit Giovanni Di Minno Ümran Caliskan Guglielmo Mariani Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
author_facet |
Mariasanta Napolitano Muriel Giansily-Blaizot Alberto Dolce Jean F. Schved Guenter Auerswald Jørgen Ingerslev Jens Bjerre Carmen Altisent Pimlak Charoenkwan Lisa Michaels Ampaiwan Chuansumrit Giovanni Di Minno Ümran Caliskan Guglielmo Mariani |
author_sort |
Mariasanta Napolitano |
title |
Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
title_short |
Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
title_full |
Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
title_fullStr |
Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
title_full_unstemmed |
Prophylaxis in congenital factor VII deficiency: Indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER) |
title_sort |
prophylaxis in congenital factor vii deficiency: indications, efficacy and safety. results from the seven treatment evaluation registry (ster) |
publishDate |
2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875640037&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/48043 |
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