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老年双联抗血小板治疗患者上消化道出血的危险因素分析 被引量:8

Risk factors analysis of upper gastrointestinal bleeding in elderly patients with aspirin and clopidogrel co-therapy
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摘要 目的 探讨双联抗血小板治疗的老年冠心病患者上消化道出血的发生情况及可能的预防措施.方法 收集长期就诊及随诊的758例经双联抗血小板治疗老年冠心病患者的临床资料,包括既往病史、入选时的一般状况、临床用药情况、生化指标及临床转归,观察终点包括发生上消化道出血、死亡、停止应用双联抗血小板药物10 d以上,随诊时间6个月.结果 共有48例患者发生上消化道出血,发生率6.3%(48/758).联合应用质子泵抑制剂(PPI)、H2受体拮抗剂(H2RA)、L谷氨酰胺呱仑酸钠颗粒(麦滋林)+PPI、麦滋林+H2RA及单纯应用双联抗血小板药物患者上消化道出血发生率分别为3.7%(4/108)、5.0%(12/240)、1.4%(1/70)、2.9%(3/102)、11.8%(28/238),5种治疗方法上消化道出血发生率比较差异有统计学意义(x2=18.63,P=0.001).结论 双联抗血小板药物随访6个月上消化道出血的发生率较高,联合应用麦滋林类胃黏膜保护剂与PPI可最大限度地减少上消化道出血的发生. Objective To explore the current occurrence of upper gastrointestinal bleeding (UGIB)in elderly patients and its possible risk factors and treatment program. Methods The clinical data of 758 elderly coronary heart disease patients with aspirin and clopidogrel co-therapy were collected, including past medical history,common condition,clinical medication,biochemical indicator and clinical turnover. The follow-up ended on the dates of a first occurrence of UGIB and death or after stopping co-therapy above 10 days. The follow-up time was 6 months. Results UGIB occurred in 48 patients,the occurrence rate was 6.3% (48/758). The occurrence rate of UGIB in proton pump inhibitor (PPI), H2-receptor antagonist (H2RA), gastric mucosa protective agents plus PPI, gastric mucosa protective agents plus H2RA and control was 3.7% (4/108),5.0% (12/240),1.4% (1/70),2.9% (3/102),11.8% (28/238). There were statistic differences in different methods (x2 = 18.63,P = 0.001). Conclusions The occurrence rate of UGIB combined with aspirin and clopidogrel co-therapy in elderly is high. Co-prescription with PPI and gastric mucosa protective agents is associated with a lower risk.
出处 《中国医师进修杂志》 2011年第10期34-36,共3页 Chinese Journal of Postgraduates of Medicine
关键词 阿司匹林 老年人 硫酸氢氯吡格雷 上消化道出血 Aspirin Aged Clopidogrel Upper gastrointestinal bleeding
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  • 1Pham SV, Pham PC, Pham PM, et al. Antithrombotic strategies inpatients undergoing percutaneous coronary intervention for acute coronary syndrome.Drug Des Devel Ther, 2010,4:203-220.
  • 2Eikelboom JW, Mehta SR, Anand SS, et al. Adverse impact of bleeding on prognosis in patients with acute coronary syndromes. Circulation, 2006, 114(8) : 774-782.
  • 3Lanas A, Fuentes J, Benito R, et al. Helicobacter pylori increases the risk of upper gastrointestinal bleeding in patients taking low-dose aspirin. Aliment Pharmacol Ther, 2002,16( 4 ) : 779-786.
  • 4Juurlink DN, Comes T, Ko DT,et al. A population-based study of the drug interaction between proton pump inhibitors and clopidogrel. CMAJ, 2009, 180(7) :713-718.
  • 5Holmes DR Jr, Kereiakes DJ, Laskey WK, et al. Thrombosis and drug-eluting stents: an objective appraisal. J Am Coil Cardiol, 2007,50(2) : 109-118.
  • 6Grines CL, Bonow RO, Casey DE Jr, et al. Prevention of premature discontinuation of dual antiplatelet therapy in patients with coronary artery stents: a science advisory from the American Heart Association, American College of Cardiology, Society for Cardiovascular Angiography and Interventions, American College of Surgeons, and American Dental Association, with representation from the American College of Physicians. Circulation,2007,115 (6):813-818.
  • 7Manoukian SV. The relationship between bleeding and adverse outcomes in ACS and PCI: pharmacologic and nonpharmacologic modification of risk. J Invasive Cardiol, 2010, 22(3 ): 132-141.

同被引文献63

  • 1Guo JJ, Xu E, Lin QY, et al. Effect of cilostazol on cerebral ar- teries in secondary prevention of ischemic stroke. Neurosci Bull, 2009,25 ( 6 ) :383-390.
  • 2Bazan NG, Eady TN, Khoutorova L, et al. Novel aspirin-triggered neuroprotectin D1 attenuates cerebral ischemic injury after experi- mental stroke. Exp Neurol, 2012, 236( 1 ) :122-130.
  • 3Huang ES, Strate LL, Ho WW, et al. Long-term use of aspirin and the risk of gastrointestinal bleeding. Am J Med, 2011, 124 (5) : 426-433.
  • 4Kerr DM, Fulton RL, Lees KR, et al. Seven-day NIHSS is a sen- sitive outcome measure for exploratory clinical trials in acute stroke: evidence from the Virtual International Stroke Trials Ar- chive. Stroke, 2012, 43(5) : 1401-1403.
  • 5Alli O, Smith C, Hoffman M, et al. Incidence, predictors, and outcomes of gastrointestinal bleeding in patients on dual antiplatelet therapy with aspirin and clopidogrel. J Clin Gastroenterol, 2011, 45(5) : 410-414.
  • 6Connolly S, Pogue J, Hart R, et al. Clopidogrel plus aspirin versus oral anticoagulation for atrial fibrillation in the Atrial fibrillation Clopidogrel Trial with Irbesartan for prevention of Vascular Events (ACTIVE W): a randomised controlled trial. Lancet,2006,367 (9526) : 1903-1912.
  • 7Paraskevas KI, Mikhailidis DP, Veith FJ. Letter by Paraskevas et al regarding article, "Guidelines for the prevention of stroke in patients with stroke or transient ischemic attack: a guideline for healthcare professionals from the American Heart Association/American Stroke Association". Stroke, 2011,42 (6) : 387.
  • 8Dippel DW, van Kooten F, Leebeek FW, et al. What is the lowest dose of aspirin for maximum suppression of in vivo thromboxane production after a transient ischemic attack or ischemic stroke? Cerebrovasc Dis, 2004,17(4) :296-302.
  • 9Gum PA, Kottke-Marchant K, Welsh PA, et al. A prospective, blinded determination of the natural history of aspirin resistance among stable patients with cardiovascular disease. J Am Coil Cardiol, 2003,41 ( 6 ) : 961-965.
  • 10Tantry US, Bliden KP, Gurbel PA. Overestimation of platelet aspirin resistance detection by thrombelastograph platelet mapping and validation by conventional aggregometry using arachidonic acid stimulation. J Am Coll CardiO1, 2005,46(9) : 1705-1709.

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