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J Gen Intern Med. May 2010; 25(5): 441–447.
Published online Feb 24, 2010. doi:  10.1007/s11606-010-1256-6
PMCID: PMC2855002

Results of the Medications At Transitions and Clinical Handoffs (MATCH) Study: An Analysis of Medication Reconciliation Errors and Risk Factors at Hospital Admission

Abstract

Background

This study was designed to determine risk factors and potential harm associated with medication errors at hospital admission.

Methods

Study pharmacist and hospital-physician medication histories were compared with medication orders to identify unexplained history and order discrepancies in 651 adult medicine service inpatients with 5,701 prescription medications. Discrepancies resulting in order changes were considered errors. Logistic regression was used to analyze the association of patient demographic and clinical characteristics including patients’ number of pre-admission prescription medications, pharmacies, prescribing physicians and medication changes; and presentation of medication bottles or lists. These factors were tested after controlling for patient demographics, admitting service and severity of illness.

Results

Over one-third of study patients (35.9%) experienced 309 order errors; 85% of patients had errors originate in medication histories, and almost half were omissions. Cardiovascular agents were commonly in error (29.1%). If undetected, 52.4% of order errors were rated as potentially requiring increased monitoring or intervention to preclude harm; 11.7% were rated as potentially harmful. In logistic regression analysis, patient’s age ≥65 [odds ratio (OR), 2.17; 95% confidence interval (CI), 1.09–4.30] and number of prescription medications (OR, 1.21; 95% CI, 1.14–1.29) were significantly associated with errors potentially requiring monitoring or causing harm. Presenting a medication list (OR, 0.35; 95% CI, 0.19–0.63) or bottles (OR, 0.55; 95% CI, 0.27–1.10) at admission was beneficial.

Conclusion

Over one-third of the patients in our study had a medication error at admission, and of these patients, 85% had errors originate in their medication histories. Attempts to improve the accuracy of medication histories should focus on older patients with a large number of medications. Primary care physicians and other clinicians should help patients utilize and maintain complete, accurate and understandable medication lists.

KEY WORDS: medication reconciliation, medication errors, medication history taking

Obtaining medication histories among hospitalized patients is an error-prone process.111 Factors affecting the quality and completeness of medication histories at the time of hospital admission include language and cultural barriers, which can be compounded by multiple prescribing physicians or use of multiple pharmacies due to economic, insurance and/or convenience factors.

Older patients taking a large number of medications may not recall indications or doses. Look-alike/sound-alike medications increase the risk of inaccurate histories, especially if patients are unclear about the rationale for use.12 Patients or their surrogates with low health literacy may be poor historians or may withhold medication compliance information.13,14 Clinician time constraints and interview skills may also affect the quality of medication histories. Even medication lists in electronic medical records (EMR) can lag behind prescription changes and be incomplete.11

This prospective study was designed to identify and analyze the frequency and types of admission medication errors in our hospital’s medicine service. Ratings for each error’s potential for patient harm during hospitalization are presented. Finally, the complex association of medication errors with individual patient risk factors was analyzed.

METHODS

Sample Selection

This study was conducted at Northwestern Memorial Hospital in Chicago, Illinois, and approved by the Institutional Review Board of Northwestern University. The study was designed to obtain in-depth, pharmacist interviews within 24–48 h of hospital admission with at least 400 adult medicine service patients. Our sample size was derived from preliminary power calculations indicating that a two-group chi-square test with p < 0.05 two-sided significance level will have 88% power to detect the difference between a group of patients with a risk factor proportion of 0.20 and another group of patients with a risk factor proportion of 0.35 (odds ratio of 2.15) when the sample sizes are 134 and 267, respectively (a total sample size of 400).

Over 14 months in 2006–2007, study pharmacists obtained a list of patients admitted the previous day. Patients with limited English proficiency (LEP), reporting their understanding of English as “fair,” “poor” or “not at all” during hospital registration (less than 5% of medicine service admissions), were prioritized and interviewed using a language line phone service. All other eligible, sampled inpatients were approached sequentially, based on daily generated random numbers, by one of two study pharmacists during their available (Monday through Friday) research time. Any patient who was too ill or unwilling to participate and for whom the family/caregiver was unavailable, who was unavailable to be interviewed despite two attempts due to tests or procedures, transferred to another service or already discharged was excluded.

Medication History Interview

Prior to interviewing the patient, the study pharmacist reviewed the patient’s EMR and recorded the physician-obtained medication history, admission medication orders and the patient’s demographic information. A comprehensive interview with the patient and/or their caregiver was then conducted by the study pharmacist to obtain the patient’s current medication regimen. The study pharmacist inquired about all prescriptions, investigational therapies, over-the-counter medications, vitamins, herbals and any other products used to supplement the patient’s health. Other sources of information included the patient’s prescription bottle labels, self-prepared medication lists and/or consultation with community pharmacies. If the patient was previously hospitalized or cared for by a hospital or university-affiliated outpatient physician utilizing the EMR system within their clinic, available discharge summaries and outpatient medication lists were also reviewed.

Reconciliation of Medication Histories and Admission Medication Orders

Study pharmacist-obtained medication histories were compared with hospital physician-obtained medication histories and admission medication orders. Progress notes and changes made to patients’ medication orders since admission were reviewed to identify intentional discrepancies (e.g., formulary substitutions or modifications to pre-admission medications in response to a patient’s clinical status). The prescribing physician was then contacted regarding remaining unexplained discrepancies. Clarifications of unexplained discrepancies resulting in order changes were considered medication errors. This restrictive error definition should be more clinically meaningful as changes would be deemed appropriate to incorporate into patients’ treatment plans.

All medication results reported are for prescription medications only. Over-the-counter medications and herbals were excluded from analysis, although aspirin taken for cardiovascular purposes was classified as a “prescription” medication for analysis, similar to other published studies.2

Classification of Medication Errors and Potential Harm Assessment

Medication errors were classified by drug class and type of error: omission of a pre-admission prescription medication, incorrect addition of a medication not part of the patient’s pre-admission regimen (commission), different dose, different route and different frequency or different medication (within the same drug class). Each medication error was rated for its potential to cause harm during hospitalization if the error had not been identified and corrected. The National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) Index for Categorizing Medication Errors was adapted and utilized for rating potential harm.15,16 This nationally recognized NCC MERP harm level taxonomy was chosen because it is widely utilized by hospitals participating in the largest adverse drug event reporting system developed by the United States Pharmacopeia (USP).17 NCC MERP criteria were collapsed to group errors into three categories: (1) no potential harm (NCC MERP category C); (2) monitoring or intervention potentially required to preclude harm (NCC MERP category D); (3) potential harm (NCC MERP categories E and above).5

Ratings of potential rather than actual harm are based on face validity only. The two study pharmacists collaboratively rated each medication error for potential harm followed by blinded, independent review by one of two board-certified internists. Pharmacist-physician harm ratings were then analyzed to determine inter-rater reliability of harm ratings across the three categories. There was a high overall initial agreement rate between pharmacist and physician ratings (Cohen’s kappa = 0.84). Remaining disagreements were independently re-rated by the second board-certified physician to obtain the final harm rating.

Risk Factor Interview

Following the medication interview, the study pharmacist continued with further interview questions to identify risk factors including the number of prescribing physicians involved in the patient’s pre-hospitalization care, number of pharmacies utilized to fill prescriptions and recent changes (additions, deletions or modifications) within the last month to their medications. Study pharmacists also inquired whether patients’ medication bottles and/or medication lists were presented to the health care team upon hospitalization. Study patients lacking at least one prescription medication prior to hospitalization or patients admitted from a nursing home or rehabilitation facility where medications were managed by health care professionals were not evaluated.

Patient Medication Error Risk Factors

For all study patients, demographic factors analyzed for their association with medication errors included patients’ age, sex, race and ethnicity, and LEP, if applicable. Measures of potential clinical and severity of illness factors included the number of home medications, Medicare Diagnosis-Related Group (DRG) case mix index weight, length of stay and whether the patient was transferred to the intensive care unit during hospitalization. Finally, we controlled for whether the admission was to a hospitalist or teaching (resident care) service.

Statistical Analysis

For study patients with complete risk factor interviews, chi-square tests were used to determine the significance of categorical variables and t-tests for continuous variables. Multiple logistic regression analyses were estimated for the combined likelihood of errors rated as either potentially requiring additional monitoring or intervention to preclude harm, or errors rated as potentially harmful. Controlling for the same clinical and demographic variables described above, regression models tested the significance of patients’ multiple pharmacy use, whether multiple physicians were involved in the patient’s pre-hospitalization care, history of recent medication or dosage changes, and whether the patient presented a medication list or bottles on admission. SPSS software version 16 (SPSS Inc., Chicago, IL) was used for all statistical analyses. A p value  0.05 was considered statistically significant.

RESULTS

Comparison of Patients with and without Medication Order Errors

Study pharmacists performed medication history interviews and reconciliation on 651 patients. Figure 1 describes the medication reconciliation process. The mean time per patient for completion of pharmacists’ chart reviews, patient/caregiver interviews, reconciliation and interventions was 21.2 min (SD = 13.2). After clarification with hospital physicians, 309 out of 449 prescription medications flagged as unexplained discrepancies resulted in physician order changes; these were classified as medication order errors. These errors affected 234 (35.9%) study patients; 85% of these patients had medication errors originate in their medication histories and carry through to their inpatient orders. While 90 patients (14%) had a single medication order error, 47 (7%) had two errors, 21 (3%) had three and 13 (2%) had four or more errors. Additionally, 792 unexplained prescription medication history discrepancies were clarified and classified as history errors; documentation was subsequently corrected in patients’ medical records (Figure 1). These historical medications were intentionally not ordered primarily due to patients’ clinical status. However, correction of medication history documentation was important to prevent errors and potential harm when historical medications were reviewed at discharge.

Fig. 1
Medication reconciliation process (n = 651 patients).

Patient demographic and clinical characteristics are presented in Table 1. The only patient factors with significant univariate association with the frequency of medication errors were older patient age, female sex and a greater number of prescription medications on admission.

Table 1
Patient Demographics and Clinical Characteristics by Prescription Medication Order Errors (n = 651 patients)

Error Types, Drug Classes and Potential Harm Ratings

The most frequent type of error was an omission (48.9%) followed by different dose (30.4%) and then by different frequency (11.0%); 7% involved errors in both dose and frequency. The five most common medication classes involved in errors were cardiovascular agents, antidepressants, gastrointestinal agents, neurological agents and anti-diabetics. Classes with the largest proportion of errors included ophthalmic/otic agents, genitourinary agents, neurological agents, antivirals and antidepressants.

Among the 309 prescription medication order errors, 4 (1.3%) were rated as involving potentially longer hospitalization, 32 (10.4%) rated as potentially causing temporary harm, and 162 (52.4%) rated as potentially requiring increased monitoring or intervention to preclude harm. Remaining errors were classified as not likely to have been harmful. Table 2 provides examples of medication errors with potential harm ratings.

Table 2
Examples of Potential Harm Ratingsa for Prescription Medication Order Errors

Logistic Regression Results for Risk Factors

Among the 651 study patients, a further risk factor interview was completed with 428 (65.7%) patients. Excluded patients included 98 patients who lacked a prescription medication prior to admission, 24 patients whose pre-hospital prescription medications were controlled by health professionals, and 101 patients where the risk factor interview could not be completed because of severity of illness or inability to answer all questions. There were no significant differences in study demographic or clinical severity measures between excluded patients and the subset of 428 patients with completed risk factor interviews.

Table 3 presents multiple logistic regression results for the association of each risk factor with the likelihood of a patient having a medication error rated as either potentially requiring monitoring or intervention (n = 162) or potentially causing harm (n = 36). These regression results differed little from models solely based on estimating the likelihood of the smaller (n = 36) number of potentially harmful errors. Advanced age (≥65 years old) (OR = 2.17; 95% CI, 1.09–4.30) and increased number of prescription medications (OR = 1.21; 95% CI, 1.14–1.29) were the only risk factors independently associated with an increased risk for these errors. Presenting a medication list (OR = 0.35; 95% CI, 0.19–0.63) upon admission was a significant protective factor for avoiding errors. Although presenting medication bottles was also beneficial, it was not quite statistically significant (OR = 0.55; 95% CI, 0.27–1.10).

Table 3
Multiple Logistic Regression Results: Risk Factors for Patients with Prescription Medication Order Errors Rated as Potentially Requiring Monitoring or Intervention or Potentially Causing Harm (N = 428)

DISCUSSION

Study Implications for Improving Medication Safety at Hospital Admission

To our knowledge, this is the largest study analyzing admission medication reconciliation risk factors for a hospitalized general medicine population. There are limited data available identifying patient or medication risk factors associated with medication errors.18 The Joint Commission National Patient Safety Goal on medication reconciliation put a spotlight on medication discrepancies and gaps in communication and handoffs.19 Admission medication errors are not surprising given patients’ large number of medicines, complexity of medication regimens, look-alike/sound-alike medication name confusion and increased number of drug formulations. In our study, medication classes such as cardiovascular agents, antidiabetics, antidepressants, and anticonvulsants with various formulations such as regular and extended release, with similar strengths and directions, frequently resulted in error. With the complexity of medication regimens for common co-morbidities such as heart disease, diabetes and depression, medications to treat glaucoma, allergies or dermatological issues were often missed.

Although the number of unexplained prescription medication discrepancies requiring clarification (n = 1,093, Fig. 1) was large in this study population, the actual number of potentially harmful errors (n = 36) or errors potentially requiring increased monitoring or intervention to preclude harm (n = 162) was relatively small. Potential harm was driven by type of medication class and type of error; drug omissions, incorrect medications prescribed or dosing discrepancies in cardiovascular medications, anti-diabetics, anticonvulsants or anticoagulants were found to be most likely to result in patient harm.

Our error findings during medication history taking and performing reconciliation are similar to other studies. In a smaller sample of 180 general medicine inpatients by Pippen and colleagues,18 186 (72%) of unintended, potentially harmful discrepancies were more often medication history-taking errors rather than reconciliation errors. A systematic review by Tam and coworkers4 of medication history errors upon hospitalization revealed up to 54% of patients experienced at least one medication history discrepancy. For this review, an “error” was defined as “discrepancy between physician-acquired medication history and comprehensive medication history.”4 In our study, only unexplained discrepancies clarified with hospital physicians resulting in order changes were considered medication errors. Our restrictive error definition may have accounted for a lower number of errors in patients (e.g., 35.9% of study patients) compared to prior studies.

Medication History Taking: a System Defect?

Our study and others35,7,18 found the majority of unexplained inpatient medication errors originated in obtaining patients’ medication histories, a process relying heavily on clinicians’ interview skills, patients’ ability to participate, and access and accuracy of patients’ outpatient medication lists or community pharmacy dispensing records. Pharmacists’ ability to obtain more complete and accurate medication histories has been previously demonstrated.5,18,20 Incorporating teaching on medication history taking and reconciliation in medical school curriculums may increase students’ knowledge and comfort in these areas.21 As physicians, nurses and pharmacists play key roles in medication management including ordering, monitoring and educating patients during hospitalization and at discharge, a multidisciplinary team approach to medication reconciliation becomes even more important, especially with errors often originating in medication histories.

Patient and System Risk Factors

A prior study of patient risk factors for actual adverse drug events (ADEs) in hospitalized patients found no independent predictors of preventable ADEs, leading authors to suggest improving medication systems rather than focusing on individual patient risks.22 This observation is consistent with our study, where the only statistically significant risk factors contributing to medication errors potentially causing harm were advanced age and a large number of medications. Although information technology can facilitate medication reconciliation,23,24 a well-designed process for medication history verification with patients by clinicians must still be in place to determine what patients are actually taking and uncover medication-related issues.

To our knowledge, this is also the first study to demonstrate presenting a medication list is a significant protective factor for avoiding medication errors if lists and prescription bottles are appropriately utilized and validated by clinicians. Although the prescribing inpatient physician and study pharmacist both utilized the same patient’s self-prepared medication list or pharmacy bottles, unexplained discrepancies still occurred. After pharmacist consultation with physicians, these discrepancies were attributed to physicians copying lists or prescription labels verbatim without systematically reviewing each medication. This systematic review is an important step as labels on prescription bottles may not accurately reflect patients’ current regimens and newly prescribed medications or recent changes may not be incorporated into patients’ self-prepared medication lists. These findings provide support for primary care physicians to involve patients/caregivers in the medication reconciliation process and empower patients to maintain, review and update their medication list at each health care encounter. These recommendations are summarized in the MATCH Medication Reconciliation Toolkit available at http://www.nmh.org/nm/for+physicians+match.

Study Limitations

This study has important limitations. It was conducted at a single academic hospital among a medicine service population. Because we were unable to interview patients who were too ill or unwilling to participate and had no caregivers present, we may have underestimated the number of medication errors. Our harm assessment is based on rating ‘potential’ harm determined by expert review of the medical record. The actual harm of errors intercepted by study pharmacists is unknown. If a patient had two blood pressure medications unintentionally omitted or dosed in error, we rated harm on each medication separately rather than taking all discrepant medications into account and assigning one potential harm rating per patient. Since we did not analyze cumulative effects of multiple medication errors for a single patient, and used only the highest harm level to analyze patient-level risk factors, ratings may underestimate preventable harm. Also, a shift to greater harm may occur if unidentified and unresolved medication history or order discrepancies introduced upon hospitalization continue post-discharge,2,2528 highlighting the importance of thorough discharge planning and reliable, comprehensive continuity of care processes.

Conclusion

Despite these limitations, our findings suggest early identification and correction of admission medication errors may mitigate or prevent harm. Our findings suggest the importance of accurate, complete admission medication histories, especially in older patients with a large number of medications. When feasible, hospital pharmacists can also be invaluable in obtaining complex medication histories and collaborating with physicians, nurses and other health care providers on medication reconciliation. Finally, this study underscores the value of primary care physicians and other clinicians encouraging patients to maintain complete, accurate medication lists that can be used by multiple providers, especially during transitions and handoffs of care.

Acknowledgments

This study was supported, in part, by a grant from the Agency for Healthcare Research and Quality (AHRQ) number 5 U18 HS015886. The opinions expressed in this document are those of the authors and do not reflect the official position of AHRQ or the US Department of Health and Human Services. The funding source had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript.

Portions of this work were presented at the 9th Annual National Patient Safety Foundation (NPSF) Patient Safety Congress May, 2007, and at the AHRQ 2007 Annual Conference.

Conflict of Interest

None Disclosed

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