Conjugated Estrogens for the Management of Bleeding Associated with Renal Failure
Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have...
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Published in | The New England journal of medicine Vol. 315; no. 12; pp. 731 - 735 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Boston, MA
Massachusetts Medical Society
18.09.1986
|
Subjects | |
Online Access | Get full text |
ISSN | 0028-4793 1533-4406 |
DOI | 10.1056/NEJM198609183151204 |
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Abstract | Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis.
Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens.
We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified. (N Engl J Med 1986; 315:731–5.)
BLEEDING is a common complication of chronic renal failure.
1
,
2
How to manage bleeding in patients with uremia has been the subject of extensive research in recent years.
3
4
5
Janson et al.
6
showed that cryoprecipitate enriched with factor VIII and von Willebrand factor was effective in shortening the skin bleeding time, the best laboratory index of clinical bleeding,
7
in uremic patients with this complication. Cryoprecipitate also allowed surgical procedures to be performed without excessive bleeding. The main problems with cryoprecipitate appear to be the heterogeneity of various preparations and the risk of the transmission of AIDS, hepatitis, or other blood-borne diseases. The . . . |
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AbstractList | Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis. Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens. We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified.Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis. Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens. We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified. Abstract Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis. Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens. We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified. (N Engl J Med 1986; 315:731-5.) Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis. Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens. We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified. Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence clinical bleeding, but the former carries the risk of transmitting blood-borne infectious diseases, and both cryoprecipitate and desmopressin have a short duration of action. Preliminary evidence has suggested that estrogens may be useful, and we therefore performed a randomized, double-blind, crossover trial comparing the effect of conjugated estrogens with that of placebo on hemorrhagic tendencies and the bleeding time in six patients with uremia who were on maintenance hemodialysis. Five daily infusions of placebo or conjugated estrogens were administered at the beginning of one-month trial periods. Estrogen shortened the bleeding time in all six patients. The effect was detectable six hours after the first infusion, reached its maximum in all patients between days 5 and 7, and lasted for 14 days. By day 16 after the last infusion, the bleeding time had returned to base line in four of the six patients. No side effects were noted during or after estrogen infusion. Estrogens did not influence the circulating level of von Willebrand factor or change its multimeric structure. Moreover, the defective platelet aggregation and thromboxane formation observed in the patients were not corrected by estrogens. We conclude that conjugated estrogens are an adequate alternative to cryoprecipitate or desmopressin for the treatment of bleeding associated with renal failure, especially when a longer duration of action is needed and immediate onset of the effect is not essential. The mechanism of action of estrogens remains to be clarified. (N Engl J Med 1986; 315:731–5.) BLEEDING is a common complication of chronic renal failure. 1 , 2 How to manage bleeding in patients with uremia has been the subject of extensive research in recent years. 3 4 5 Janson et al. 6 showed that cryoprecipitate enriched with factor VIII and von Willebrand factor was effective in shortening the skin bleeding time, the best laboratory index of clinical bleeding, 7 in uremic patients with this complication. Cryoprecipitate also allowed surgical procedures to be performed without excessive bleeding. The main problems with cryoprecipitate appear to be the heterogeneity of various preparations and the risk of the transmission of AIDS, hepatitis, or other blood-borne diseases. The . . . |
Author | Viganò, Gianluigi Mecca, Giuliano Remuzzi, Giuseppe Mingardi, Giulio Lombardi, Rossana Livio, Manuela Mannucci, Pier Mannuccio |
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Issue | 12 |
Keywords | Human Chemotherapy Urinary system disease Intravenous administration Steroid hormone Renal failure Estrogen Coagulation factor Hemorrhage |
Language | English |
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PublicationDate | 1986-09-18 |
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PublicationDecade | 1980 |
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PublicationYear | 1986 |
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References | Tanaka (r023) 1985; 28 Watson (r009) 1982; 32 Deykin (r004) 1983; 24 Steiner (r007) 1979; 7 Mannucci (r015) 1985; 66 Elam (r025) 1980; 20 Shapiro (r010) 1984; 4 Macconi (r018) 1985; 52 Patrono (r019) 1980; 17 Fernandez (r022) 1985; 59 Caldwell (r013) 1984; 28 Remuzzi (r020) 1983; 71 Larsson (r002) 1971; 15 Remuzzi (r017) 1979; 16 Livio (r005) 1985; 5 Rabiner (r001) 1972; 1 Smith (r024) 1981; 29 Janson (r006) 1980; 303 Liu (r012) 1984; 2 Hellem (r016) 1970; 7 Ylikorkala (r026) 1982; 142 Canavese (r029) 1985; 1 r027 Sakariassen (r011) 1979; 279 Remuzzi (r028) 1977; 2 Livio (r021) 1982; 2 Rabiner (r003) 1972; 201 Mannucci (r008) 1983; 308 Kumar (r014) 1978; 70 |
References_xml | – volume: 24 start-page: 698 year: 1983 ident: r004 publication-title: Kidney Int doi: 10.1038/ki.1983.214 – volume: 28 start-page: 357 year: 1985 ident: r023 publication-title: Kidney Int – volume: 20 start-page: 1039 year: 1980 ident: r025 publication-title: Prostaglandins doi: 10.1016/0090-6980(80)90058-1 – volume: 29 start-page: 133 year: 1981 ident: r024 publication-title: Nephron doi: 10.1159/000182330 – volume: 15 start-page: 1 year: 1971 ident: r002 publication-title: Scand J Haematol [Suppl] – volume: 2 start-page: 887 year: 1984 ident: r012 publication-title: Lancet doi: 10.1016/S0140-6736(84)90652-4 – volume: 279 start-page: 636 year: 1979 ident: r011 publication-title: Nature doi: 10.1038/279636a0 – volume: 52 start-page: 159 year: 1985 ident: r018 publication-title: Lab Invest – volume: 142 start-page: 573 year: 1982 ident: r026 publication-title: Am J Obstet Gynecol doi: 10.1016/0002-9378(82)90764-5 – volume: 4 start-page: 260 year: 1984 ident: r010 publication-title: Am J Nephrol doi: 10.1159/000166822 – volume: 2 start-page: 1013 year: 1982 ident: r021 publication-title: Lancet doi: 10.1016/S0140-6736(82)90050-2 – volume: 5 start-page: 82 year: 1985 ident: r005 publication-title: Semin Nephrol – volume: 2 start-page: 1195 year: 1977 ident: r028 publication-title: Lancet doi: 10.1016/S0140-6736(77)90437-8 – volume: 303 start-page: 1318 year: 1980 ident: r006 publication-title: N Engl J Med doi: 10.1056/NEJM198012043032302 – volume: 71 start-page: 762 year: 1983 ident: r020 publication-title: J Clin Invest doi: 10.1172/JCI110824 – volume: 66 start-page: 796 year: 1985 ident: r015 publication-title: Blood doi: 10.1182/blood.V66.4.796.796 – volume: 70 start-page: 642 year: 1978 ident: r014 publication-title: Am J Clin Pathol doi: 10.1093/ajcp/70.4.642 – ident: r027 – volume: 7 start-page: 374 year: 1970 ident: r016 publication-title: Scand J Haematol doi: 10.1111/j.1600-0609.1970.tb01917.x – volume: 59 start-page: 139 year: 1985 ident: r022 publication-title: Br J Haematol doi: 10.1111/j.1365-2141.1985.tb02974.x – volume: 1 start-page: 867 year: 1985 ident: r029 publication-title: Lancet doi: 10.1016/S0140-6736(85)92225-1 – volume: 17 start-page: 317 year: 1980 ident: r019 publication-title: Thromb Res doi: 10.1016/0049-3848(80)90066-3 – volume: 32 start-page: 49 year: 1982 ident: r009 publication-title: Nephron doi: 10.1159/000182801 – volume: 16 start-page: 345 year: 1979 ident: r017 publication-title: Thromb Res doi: 10.1016/0049-3848(79)90082-3 – volume: 7 start-page: 107 year: 1979 ident: r007 publication-title: Am J Hematol doi: 10.1002/ajh.2830070203 – volume: 308 start-page: 8 year: 1983 ident: r008 publication-title: N Engl J Med doi: 10.1056/NEJM198301063080102 – volume: 28 start-page: 53 year: 1984 ident: r013 publication-title: Clin Obstet Gynecol doi: 10.1097/00003081-198528010-00008 – volume: 201 start-page: 234 year: 1972 ident: r003 publication-title: Ann NY Acad Sci doi: 10.1111/j.1749-6632.1972.tb16301.x – volume: 1 start-page: 233 year: 1972 ident: r001 publication-title: Prog Hemost Thromb |
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Snippet | Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably influence... Abstract Bleeding is a major complication of uremia. Both cryoprecipitate and desmopressin effectively shorten the prolonged bleeding time and favorably... |
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SubjectTerms | Adult Biological and medical sciences Bleeding Bleeding Time Blood platelets Clinical trials Clinical Trials as Topic Desmopressin Disease Double-Blind Method Double-blind studies Estrogens Estrogens, Conjugated (USP) - therapeutic use Factor VIII - analysis Female Health risk assessment Hemodialysis Hemorrhage Hemorrhage - blood Hemorrhage - drug therapy Hemorrhage - etiology Humans Infectious diseases Kidney Failure, Chronic - blood Kidney Failure, Chronic - complications Kidneys Laboratories Male Medical sciences Middle Aged Nephrology Patients Pharmacology. Drug treatments Platelet aggregation Random Allocation Renal failure Transplants & implants Uremia Uremia - blood Uremia - complications Urinary system Von Willebrand factor von Willebrand Factor - analysis Womens health |
Title | Conjugated Estrogens for the Management of Bleeding Associated with Renal Failure |
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