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泌乳抑制剂对凝血机制的影响。

Effect of lactation suppressants on the coagulation mechanism.

作者信息

Wodzicki A M, Coopland A T

出版信息

Can Med Assoc J. 1974 Apr 20;110(8):905-9.

PMID:4824964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1947398/
Abstract

The effect on the coagulation mechanism of lactation suppressants was determined by comparing observations on a group of untreated women and two other groups, one receiving Vallestril (methallenestrill 20 mg) and the other Ortho-Novum 5 (5 mg norethindrone and 0.075 mg mestranol). Blood was drawn on the first, fourth and tenth days post partum. Patients given Ortho-Novum 5 showed a continued significant elevation of levels of factors VIII and IX for the duration of the study, and the partial thromboplastin time reflected this increase on days 4 and 10. Vallestril appeared to have the same effect on factors VIII and IX, although to a lesser, nonsignificant degree. In addition, the day 10 levels of fibrinogen and factors VII and X, as well as platelet adhesiveness, of the untreated group were lower than those of the groups undergoing treatment, although the medication had been discontinued five days previously. However, this difference was not statistically significant.In view of the growing evidence of the increased incidence of thromboembolic disease during the puerperium, it is perhaps unwise to give drugs that cause changes in the plasma coagulation system, such as those we have described, to patients who are already in a hypercoagulable state.

摘要

通过比较一组未治疗的妇女以及另外两组妇女(一组服用瓦莱斯特里尔(炔雌醇甲醚20毫克),另一组服用炔诺酮5号(5毫克炔诺酮和0.075毫克炔雌醇甲醚))的观察结果,确定了哺乳期抑制药物对凝血机制的影响。在产后第1天、第4天和第10天采集血液。服用炔诺酮5号的患者在研究期间因子VIII和IX水平持续显著升高,部分凝血活酶时间在第4天和第10天反映出这种升高。瓦莱斯特里尔对因子VIII和IX似乎有相同的作用,尽管程度较小且不显著。此外,未治疗组第10天的纤维蛋白原、因子VII和X水平以及血小板黏附性均低于接受治疗的组,尽管药物在五天前已停用。然而,这种差异无统计学意义。鉴于越来越多的证据表明产褥期血栓栓塞性疾病的发病率增加,对于已经处于高凝状态的患者,给予会引起血浆凝血系统变化的药物(如我们所描述的那些药物)可能是不明智的。

相似文献

1
Effect of lactation suppressants on the coagulation mechanism.泌乳抑制剂对凝血机制的影响。
Can Med Assoc J. 1974 Apr 20;110(8):905-9.
2
A study of the effect of an oral contraceptive on blood coagulation factors, platelets and fibrinolytic activity.一项关于口服避孕药对血液凝固因子、血小板及纤溶活性影响的研究。
Contraception. 1974 Apr;9(4):379-92. doi: 10.1016/0010-7824(74)90081-x.
3
Effects of green pit viper (Trimeresurus erythrurus and Trimeresurus popeorum) venoms on blood coagulation, platelets and the fibrinolytic enzyme systems: studies in vivo and in vitro.竹叶青蛇(红口竹叶青蛇和坡普氏竹叶青蛇)毒液对血液凝固、血小板及纤维蛋白溶解酶系统的影响:体内和体外研究
Am J Clin Pathol. 1973 Nov;60(5):654-62. doi: 10.1093/ajcp/60.5.654.
4
Effects of progestogen oral contraception with norethisterone on blood clotting and platelets.炔诺酮口服孕激素避孕药对血液凝固和血小板的影响。
Br Med J. 1972 Nov 18;4(5837):391-3. doi: 10.1136/bmj.4.5837.391.
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Studies on coagulation and fibrinolysis in blood from puerperal women with and without oestrogen treatment.对接受和未接受雌激素治疗的产后妇女血液中的凝血和纤溶研究。
Br J Obstet Gynaecol. 1975 Feb;82(2):151-7. doi: 10.1111/j.1471-0528.1975.tb02214.x.
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Obstet Gynecol. 1972 May;39(5):775-8.
7
Progestational agents and blood coagulation. V. Changes induced by sequential oral contraceptive therapy.孕激素与血液凝固。五、序贯口服避孕药疗法引起的变化。
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[The effect of plasma fraction I-O, ACC 76, PAMBA and haemarctin on the blood coagulation system of premature newborn infants].[血浆I-O组分、ACC 76、止血芳酸和马猬蛋白对早产新生儿凝血系统的影响]
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本文引用的文献

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CORONARY THROMBOSIS: ITS MECHANISM AND POSSIBLE PREVENTION BY LINOLENIC ACID.
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THE ESTIMATION OF FIBRINOGEN. A REVISION.纤维蛋白原的测定。修订版。
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The levels of the plasma coagulation factors after trauma and childbirth.创伤和分娩后血浆凝血因子的水平。
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The maintenance of a sustained thrombolytic state in man. I. Induction and effects.人体持续溶栓状态的维持。I. 诱导与效果。
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Coagulation and fibrinolytic studies during pregnancy.孕期的凝血与纤溶研究。
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Thrombophlebitis in pregnancy.妊娠期血栓性静脉炎
Am J Obstet Gynecol. 1967 Apr 1;97(7):901-5. doi: 10.1016/0002-9378(67)90514-5.
9
Increased factor IX levels in puerperium during administration of diethylstilboestrol.在服用己烯雌酚期间产褥期因子IX水平升高。
Br Med J. 1968 Mar 30;1(5595):801-3. doi: 10.1136/bmj.1.5595.801.
10
Improved coagulation screening by an activated recalcification test.
J Clin Pathol. 1967 May;20(3):244-8. doi: 10.1136/jcp.20.3.244.