Meulendijks Lieke G, Adomako Emmanuel A, Appiah Emmanuel B, Kramers Cornelis
Department of Pharmacology-Toxicology, Radboud University Nijmegen Medical Center, Nijmegen, the Netherlands.
Department of Medicine, Agogo Presbyterian Hospital, Agogo Asante-Akyem, Ghana.
Ghana Med J. 2016 Mar;50(1):22-30. doi: 10.4314/gmj.v50i1.4.
Preventable adverse events of medication are an important cause of hospital admissions in the developed world, in which non-steroidal anti-inflammatory drugs (NSAIDs) and renin-angiotensin system (RAS-) inhibitors are frequently involved. NSAIDs and RAS-inhibitors are also often used in Ghana. The purpose of this study is to assess whether biochemical monitoring in patients on RAS-inhibitors, and co-administration of gastro protective agents (GPAs) in patients on NSAIDs, is done properly in Ghana.
Two retrospective cross-sectional studies were carried out at the Agogo Presbyterian Hospital, Ghana, in 2013. In 114 out-and inpatients who are on NSAIDs, the risk for gastrointestinal side effects and the frequency of co-administration of GPAs were determined. In 301 outpatients who are on RAS-inhibitors, the risk for renal dysfunction and the frequency of biochemical monitoring were determined. Fisher's exact test was used to determine the statistical strength.
Co-administration of GPAs was done in 1.8% of patients on NSAIDs. Serum creatinine and potassium monitoring within one month after initiation of treatment with RAS-inhibitors were performed in 6.3% and 3.7%, respectively. Risk factors were neither associated with prescription of a GPA in patients on NSAIDs (p=0.134), nor in performing biochemical monitoring in patients on RAS-inhibitors (p=0.219 for creatinine, p=0.062 for potassium).
Biochemical monitoring in patients on RAS-inhibitors and use of GPAs in patients on NSAIDs is poorly performed at the Agogo Presbyterian Hospital in Ghana. Improving the already existing Ghanaian guidelines, especially those for RAS-inhibitors, and encouraging their widespread use among prescribers should be pursued.
在发达国家,可预防的药物不良事件是住院的一个重要原因,其中非甾体抗炎药(NSAIDs)和肾素 - 血管紧张素系统(RAS)抑制剂经常涉及。NSAIDs和RAS抑制剂在加纳也经常使用。本研究的目的是评估在加纳,对使用RAS抑制剂的患者进行生化监测,以及对使用NSAIDs的患者联合使用胃保护剂(GPA)的情况是否得当。
2013年在加纳的阿戈戈长老会医院进行了两项回顾性横断面研究。在114名使用NSAIDs的门诊和住院患者中,确定了胃肠道副作用的风险以及GPA联合使用的频率。在301名使用RAS抑制剂的门诊患者中,确定了肾功能不全的风险以及生化监测的频率。采用Fisher精确检验来确定统计学强度。
使用NSAIDs的患者中,1.8%联合使用了GPA。在开始使用RAS抑制剂治疗后一个月内,分别有6.3%和3.7%的患者进行了血清肌酐和钾的监测。风险因素与使用NSAIDs的患者使用GPA的处方无关(p = 0.134),也与使用RAS抑制剂的患者进行生化监测无关(肌酐p = 0.219,钾p = 0.062)。
在加纳的阿戈戈长老会医院,对使用RAS抑制剂的患者进行生化监测以及对使用NSAIDs的患者使用GPA的情况较差。应努力改进现有的加纳指南,特别是关于RAS抑制剂的指南,并鼓励开处方者广泛使用这些指南。