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Controlled trial of dipyridamole in cerebral vascular disease.双嘧达莫治疗脑血管疾病的对照试验。
Br Med J. 1969 Mar 8;1(5644):614-5. doi: 10.1136/bmj.1.5644.614.
2
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4
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5
Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial.动脉源性脑缺血后阿司匹林联合双嘧达莫与单用阿司匹林的疗效比较(ESPRIT):随机对照试验
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Lancet Neurol. 2010 Feb;9(2):159-66. doi: 10.1016/S1474-4422(09)70361-8. Epub 2010 Jan 7.
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Antiplatelet regimens after ischemic stroke or transient ischemic attack: a systematic review and updated network meta-analysis.缺血性中风或短暂性脑缺血发作后的抗血小板治疗方案:一项系统评价与更新的网状Meta分析
Ann Transl Med. 2022 Mar;10(5):245. doi: 10.21037/atm-21-3748.
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Antithrombotic Therapy for Secondary Prevention in Patients with Non-Cardioembolic Stroke or Transient Ischemic Attack: A Systematic Review.非心源性卒中或短暂性脑缺血发作患者二级预防的抗栓治疗:一项系统评价
Life (Basel). 2021 May 15;11(5):447. doi: 10.3390/life11050447.
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Comparative Efficacy and Safety of Nine Anti-Platelet Therapies for Patients with Ischemic Stroke or Transient Ischemic Attack: a Mixed Treatment Comparisons.九种抗血小板疗法对缺血性中风或短暂性脑缺血发作患者的疗效和安全性比较:混合治疗比较
Mol Neurobiol. 2017 Mar;54(2):1456-1466. doi: 10.1007/s12035-016-9739-z. Epub 2016 Feb 5.
4
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Calif Med. 1971 Sep;115(3):51.
5
THE PATHOGENESIS OF PULMONARY ARTERIOSCLEROSIS: PROPHYLAXIS WITH DRUGS WHICH AFFECT PLATELET AGGREGATION.肺动脉硬化的发病机制:使用影响血小板聚集的药物进行预防。
Cardiovasc Dis. 1974;1(2):137-152.
6
Clinical pharmacokinetics of antiplatelet agents used in the secondary prevention of stroke.用于卒中二级预防的抗血小板药物的临床药代动力学
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Rapid development of tolerance to dipyridamole-associated headaches.对双嘧达莫相关头痛的耐受性迅速发展。
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8
Do we still need dipyridamole?我们仍然需要双嘧达莫吗?
Br J Clin Pharmacol. 1998 Apr;45(4):323-8. doi: 10.1046/j.1365-2125.1998.t01-1-00677.x.
9
North of England evidence based guideline development project: guideline on the use of aspirin as secondary prophylaxis for vascular disease in primary care. North of England Aspirin Guideline Development Group.英格兰北部循证指南制定项目:初级保健中阿司匹林用于血管疾病二级预防的指南。英格兰北部阿司匹林指南制定小组。
BMJ. 1998 Apr 25;316(7140):1303-9. doi: 10.1136/bmj.316.7140.1303.
10
Current management of ischaemic stroke.缺血性中风的当前管理
J Neurol Neurosurg Psychiatry. 1993 Jan;56(1):6-16. doi: 10.1136/jnnp.56.1.6.

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LONG TERM DIPYRIDAMOLE THERAPY OF ANGINA PECTORIS.
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PERSANTIN-- A DOUBLE BLIND STUDY.潘生丁——一项双盲研究。
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EXPERIMENTAL STUDIES ON THE EFFECTS OF PERSANTIN WITH NORMAL AND GO-DOGS.潘生丁对正常和患犬影响的实验研究
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AUGMENTATION OF INTERCORONARY ANASTOMOSIS BY LONG-TERM ADMINISTRATION OF A VASODILATOR DRUG, DIPYRIDAMOLE (PERSANTIN).通过长期服用血管扩张剂双嘧达莫(潘生丁)增强冠状动脉间吻合术
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Evaluation of dipyridamole (Persantin).双嘧达莫(潘生丁)的评估。
Am Heart J. 1963 Mar;65:423-4. doi: 10.1016/0002-8703(63)90018-8.
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The effect of persantin on intercoronary collateral circulation and survival during gradual experimental coronary occlusion. A preliminary report.潘生丁对实验性冠状动脉逐渐闭塞期间冠状动脉侧支循环及存活的影响。初步报告。
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Experimental and clinical observations on 2,6-bis-(diethanolamino)-4,8-dipiperidino-pyrimido-(5,4-d) pyrimidine (Persantin).
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[Function and energy metabolism of the exhausted heart muscle under the effects of 2,6-bis-(diethanolamino)-4,8-dipiperidino-pyrimido-(5,4-d)-pyrimidine].
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Controlled double-blind trial of "persantin" in treatment of angina pectoris.“潘生丁”治疗心绞痛的对照双盲试验。
Br Med J. 1960 Sep 17;2(5202):835. doi: 10.1136/bmj.2.5202.835.

双嘧达莫治疗脑血管疾病的对照试验。

Controlled trial of dipyridamole in cerebral vascular disease.

作者信息

Acheson J, Danta G, Hutchinson E C

出版信息

Br Med J. 1969 Mar 8;1(5644):614-5. doi: 10.1136/bmj.1.5644.614.

DOI:10.1136/bmj.1.5644.614
PMID:4885615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1982429/
Abstract

A controlled double-blind study of the effect of dipyridamole was performed in 169 patients with established cerebral vascular disease. A dose of 400 mg. was used initially, given daily for an average of 14 months; the dose was then increased to 800 mg. daily for a further average period of 11 months. When the incidence of cerebral ischaemic episodes during treatment was compared in the drug-treated and placebo-treated groups no significant difference was found.

摘要

对169例已确诊的脑血管疾病患者进行了一项关于双嘧达莫疗效的对照双盲研究。初始剂量为400毫克,每日服用,平均服用14个月;然后剂量增加至每日800毫克,再平均服用11个月。比较药物治疗组和安慰剂治疗组在治疗期间脑缺血发作的发生率,未发现显著差异。