González-Pérez Antonio, Sáez María E, Johansson Saga, Nagy Péter, García Rodríguez Luis A
The Spanish Centre for Pharmacoepidemiologic Research (CEIFE), Madrid, Spain; Andalusian Bioinformatics Research Centre (CAEBi), Seville, Spain.
AstraZeneca R&D, Mölndal, Sweden.
PLoS One. 2014 Jul 8;9(7):e101768. doi: 10.1371/journal.pone.0101768. eCollection 2014.
Few epidemiologic studies have investigated predictors of uncomplicated peptic ulcer disease (PUD) separately from predictors of complicated PUD.
To analyze risk factors associated with uncomplicated PUD and medication use after diagnosis.
Patients diagnosed with uncomplicated PUD (n = 3,914) were identified from The Health Improvement Network database among individuals aged 40-84 years during 1997-2005, with no previous history of PUD. Prescription records for the year after the date of diagnosis were reviewed and a nested case-control analysis was performed to calculate the odds ratios for the association of potential risk factors with PUD.
Medications associated with developing uncomplicated PUD included current use of acetylsalicylic acid (ASA), nonsteroidal anti-inflammatory drugs (NSAIDs), paracetamol, selective serotonin reuptake inhibitors, antidepressants, antihypertensives or acid suppressants. Uncomplicated PUD was significantly associated with being a current or former smoker and having had a score of at least 3 on the Townsend deprivation index. Approximately 50% of patients who were users of ASA (19% of patients) or chronic users of NSAIDs (7% of patients) at diagnosis did not receive another prescription of the medication in the 60 days after diagnosis, and 30% were not represcribed therapy within a year. Among patients who were current users of ASA or chronic NSAIDs at the time of the PUD diagnosis and received a subsequent prescription for their ASA or NSAID during the following year, the vast majority (80-90%) also received a proton pump inhibitor coprescription.
Our results indicate that several risk factors for upper gastrointestinal bleeding are also predictors of uncomplicated PUD, and that some patients do not restart therapy with ASA or NSAIDs after a diagnosis of uncomplicated PUD. Further investigation is needed regarding the consequences for these patients in terms of increased cardiovascular burden due to discontinuation of antiplatelet therapy.
很少有流行病学研究将单纯性消化性溃疡疾病(PUD)的预测因素与复杂性PUD的预测因素分开进行调查。
分析与单纯性PUD相关的危险因素以及诊断后的用药情况。
从健康改善网络数据库中识别出1997年至2005年期间年龄在40至84岁、既往无PUD病史且被诊断为单纯性PUD的患者(n = 3914)。回顾诊断日期后一年的处方记录,并进行巢式病例对照分析,以计算潜在危险因素与PUD关联的比值比。
与发生单纯性PUD相关的药物包括当前使用的乙酰水杨酸(ASA)、非甾体抗炎药(NSAIDs)、对乙酰氨基酚、选择性5-羟色胺再摄取抑制剂、抗抑郁药、抗高血压药或抑酸剂。单纯性PUD与当前或既往吸烟者以及汤森德贫困指数得分至少为3显著相关。诊断时使用ASA的患者(占患者的19%)或长期使用NSAIDs的患者(占患者的7%)中,约50%在诊断后的60天内未收到该药物的另一张处方,30%在一年内未再次开具治疗处方。在PUD诊断时当前使用ASA或长期使用NSAIDs且在次年接受了ASA或NSAIDs后续处方的患者中,绝大多数(80% - 90%)还同时接受了质子泵抑制剂的联合处方。
我们的结果表明,上消化道出血的几个危险因素也是单纯性PUD的预测因素,并且一些患者在被诊断为单纯性PUD后未重新开始使用ASA或NSAIDs进行治疗。需要进一步调查这些患者因停用抗血小板治疗而增加心血管负担的后果。