Pippins Jennifer R, Gandhi Tejal K, Hamann Claus, Ndumele Chima D, Labonville Stephanie A, Diedrichsen Ellen K, Carty Marcy G, Karson Andrew S, Bhan Ishir, Coley Christopher M, Liang Catherine L, Turchin Alexander, McCarthy Patricia C, Schnipper Jeffrey L
Division of General Medicine, Brigham and Women's Hospital, Boston, MA 02120-1613, USA.
J Gen Intern Med. 2008 Sep;23(9):1414-22. doi: 10.1007/s11606-008-0687-9. Epub 2008 Jun 19.
Failure to reconcile medications across transitions in care is an important source of potential harm to patients. Little is known about the predictors of unintentional medication discrepancies and how, when, and where they occur.
To determine the reasons, timing, and predictors of potentially harmful medication discrepancies.
Prospective observational study.
Admitted general medical patients.
Study pharmacists took gold-standard medication histories and compared them with medical teams' medication histories, admission and discharge orders. Blinded teams of physicians adjudicated all unexplained discrepancies using a modification of an existing typology. The main outcome was the number of potentially harmful unintentional medication discrepancies per patient (potential adverse drug events or PADEs).
Among 180 patients, 2066 medication discrepancies were identified, and 257 (12%) were unintentional and had potential for harm (1.4 per patient). Of these, 186 (72%) were due to errors taking the preadmission medication history, while 68 (26%) were due to errors reconciling the medication history with discharge orders. Most PADEs occurred at discharge (75%). In multivariable analyses, low patient understanding of preadmission medications, number of medication changes from preadmission to discharge, and medication history taken by an intern were associated with PADEs.
Unintentional medication discrepancies are common and more often due to errors taking an accurate medication history than errors reconciling this history with patient orders. Focusing on accurate medication histories, on potential medication errors at discharge, and on identifying high-risk patients for more intensive interventions may improve medication safety during and after hospitalization.
在医疗护理转接过程中未能对药物治疗进行核对是对患者造成潜在伤害的一个重要原因。对于无意的用药差异的预测因素以及这些差异在何时、何地发生知之甚少。
确定潜在有害用药差异的原因、时间和预测因素。
前瞻性观察研究。
入住普通内科的患者。
研究药师获取了金标准用药史,并将其与医疗团队的用药史、入院和出院医嘱进行比较。由不知情的医生团队使用对现有分类法的修改版本对所有无法解释的差异进行判定。主要结局是每位患者潜在有害的无意用药差异数量(潜在药物不良事件或PADEs)。
在180名患者中,共识别出2066处用药差异,其中257处(12%)是无意的且有潜在危害(每位患者1.4处)。其中,186处(72%)是由于入院前用药史采集错误,而68处(26%)是由于用药史与出院医嘱核对错误。大多数PADEs发生在出院时(75%)。在多变量分析中,患者对入院前用药的理解程度低、从入院前到出院的用药变化数量以及由实习医生采集用药史与PADEs相关。
无意的用药差异很常见,更多是由于准确用药史采集错误而非用药史与患者医嘱核对错误所致。关注准确的用药史、出院时潜在的用药错误以及识别需要更强化干预的高危患者,可能会改善住院期间及出院后的用药安全。