… support technologies can help avoid these errors. … van Balveren JA, Verboeket-van de Venne WPHG, Erdem-Eraslan L, et al; Dutch Society for …

This review article describes drug–laboratory test interactions, in which medications can affect test results and impede diagnosis. Although the quality of studies varies, researchers identified a potential benefit of clinical decision support to inform ordering clinicians about these potential interactions.

Prior research has shown that providers frequently override drug interaction alerts, sometimes as a result of alert fatigue. In this study, researchers observed providers as they completed medication orders, addressing both high- and low-severity drug interaction alerts using five distinct electronic health records in two countries. The authors found that providers engaged in complex clinical reasoning prior to declining an alert, balancing various aspects of patient care including safety- and patient-specific factors.

Clinical decision support alerts can help identify potential drug–drug interactions, but they can also contribute to alert fatigue. This commentary provides recommendations to inform the design of decision support to address drug–drug interactions. The authors suggest that improvement strategies focus on standardizing terminology and visual cues.

Implementation of health information technology (IT) has presented several unanticipated patient safety issues, particularly related to computerized provider order entry. Health IT vendors generally have a "hold harmless" clause that removes their liability for patient harm due to health IT failures. This review explores patient safety initiatives for health IT systems across six countries, including the United States. Significant gaps in health IT safety initiatives were identified, including inadequate regulatory oversight in the US for these medical devices. The authors conclude that greater standardization and oversight is required to ensure safety for all types of health IT systems. An AHRQ WebM&M interview with Dr. David Bates discusses the benefits and potential risks of health IT.

Clinical decision support system medication alerts have the potential to decrease adverse drug events, but physicians ignore many of these repeated warnings. Alert fatigue is particularly common in drug–drug interaction (DDI) alerts, with prior studies reporting override rates of up to 90%. In this study, an expert panel created a list of 33 class-based, low-priority DDIs that do not warrant interruptive alerts. The goal was to devise a standardized list to help reduce alert fatigue across electronic health records. The authors recommend developing a consortium to maintain this list over time. Dr. David Blumenthal discusses DDI alert fatigue and other issues related to medical information technology in an AHRQ WebM&M interview.

This commentary discusses reliability theory in patient safety and describes an assessment framework to help measure the reliability of processes and practices in hospitals.

This qualitative study identified workarounds and unintended consequences associated with implementation of a computerized provider order entry system.

This study highlights contributing factors that lead to physician overrides of drug safety alerts, including incorrect rules and reasoning applied to justify such actions.

Alerts within a computerized provider order entry system were not able to prevent medication errors resulting from drug–drug interactions. The authors hypothesize that the inadequacy of the alerts themselves was responsible for this failure, with problems including an excessive number of false-positive alerts and unclear instructions for preventing drug interactions.

This qualitative study examines the factors that led to failed implementation of a computerized provider order entry system.

This review highlights the mixed impact of CPOE systems on clinical workflow, including the noted impact on efficiency and limitations caused by poor user–system interactions.

This review of computerized provider order entry (CPOE) usage in seven countries (the United States, Australia, and five Western European countries) found that CPOE has not been widely implemented and remains poorly integrated with other types of health information technology.

This study found that implementation of a computerized physician order entry system appeared to impair some aspects of nurse–physician communication.

This study found that provider satisfaction with computerized provider order entry systems is influenced as much by the work structures and processes before and after implementation as by the technology itself.

This study examined nearly 2000 drug–drug interaction (DDI) alerts that were overridden by providers and noted differential triggers based on clinician knowledge or specialty. The authors conclude that simply turning off DDI alerts is limited by these differential triggers and inconsistent drug monitoring, which may raise safety concerns that are prevented by the alerts themselves.

The authors analyze the success of the Open Care Information System, a communication protocol for exchanging medication data, within the context of the stakeholders involved.

The authors review the literature on physician response to electronic medication safety alerts and interpret the results through Reason's model of accident causation. They also suggest potential improvements to the alerting process.

The authors report on the development of a set of performance indicators for all hospitals in the Netherlands.