. 2017 Dec 28;9(2):123–155. doi: 10.1177/2042098617748868

Table 2.

Summary of study characteristics and results by primary intervention theme.

Study (country)	Study setting	Intervention type	Intervention detail	Comparator	Main type of error collected	Detail of medication error	Main finding
Technology
Abboud et al.⁴¹ (US)	N/P	CPOE + CDS	Integration of reminder for aminoglycoside monitoring into CPOE system	Pre–post	Monitoring	Failure to appropriately monitor aminoglycoside	No change in appropriate monitoring [31/177 (17.5%) versus 31/159 (19.5%)]
Balaguer Santamaria et al.²⁴ (Spain)	N	Calculator	Development of Neodosis, an electronic spreadsheet to assist in calculating medication doses and standardize dilutions of commonly used drugs	Calculations performed without use of calculator	Prescribing	Errors in calculation of dose	Use of electronic calculator resulted in significant reduction in number of staff making errors [19/27 (70.3%) versus 4/27 (14.8%); p < 0.001]
Boling et al.⁴⁰ (US)	N/P	CPOE + CDS	CPOE with dose range checking system	Pre–post	Prescribing	Dosing errors involving opioids, benzodiazepines, and potassium, requiring administration of antidote	Reduction in opioid prescribing errors [8/13,997 (0.06%) versus 1/7256 (0.01); p = 0.17], while there were no errors involving benzodiazepines or potassium in the pre- or postperiod
Brown et al.³⁰ (US)	N	Computer programme	Computerized worksheet for parenteral nutrition orders	Pre–post	Prescribing	Any prescribing errors associated with TPN orders	Reduction in errors from 44/303 (14.5%) to 12/177 (6.8%); p = 0.016
Cordero et al.³⁸ (US)	N	CPOE + CDS	CPOE with NICU-specific physician order sets	Pre–post	Prescribing and administration	Caffeine loading dose administration > 3 h after being prescribed and gentamicin prescribed dose > 10% deviation from recommended dose	Significant improvement in administration of caffeine within 3 h of prescription (12% versus 63%; p < 0.05), and reduction in gentamicin dosing errors from 16/136 (11.7%) to 0/117 (0%); p < 0.05
Farrar et al.³⁷ (US)	N/P	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Prescribing	Any prescribing error	Reduction in errors from 46/103 (44.7%) orders to 7/114 (6.1%) orders (p < 0.001)
Ferranti et al.⁴⁷ (US)	N/P	CPOE + CDS	CPOE incorporating advanced dosing model	Pre–post	Any type	Any errors resulting in patient harm (e.g. transient adverse effects which required corrective therapy or increased length of stay)	Reduction in errors in NICU from 75/567 (13.2%) to 23/272 (8.5%); p = 0.006
Garner et al.³⁵ (US)	N	CDS	Interactive computerized order set with decision support for antibiotic orders	Pre–post	Prescribing	Any errors in antibiotic prescribing	Overall error rate decreased from 1.7 per medication order to 0.8 per medication order (p < 0.001)
Hardmeier et al.³³ (US)	N	Barcoding	Implementation of barcode medication administration system	None	Administration	Any nursing-related administration errors	Total of 7/300 (2.3%) nursing-related administration errors reported during study period
Hennings et al.²⁰ (US)	N/P	IV administration technology	Automated infusion devices with programmed alerts	None	Administration	Alerts requiring reprogramming events 2.5 times above or below the predefined limits for high-risk medications	Total of 36/5268 infusions (0.7%) required reprogramming; reprogramming much more common in the paediatric compared with adult ICU (RR 1.68 95% CI 1.18–2.38)
Hilmas et al.²⁷ (US)	N/P	Computer programme	Computer-based order forms for parenteral nutrition ordering	Pre–post	Prescribing	Any TPN prescribing errors	Reduction in errors from 38/152 (25%) orders to 7/442 (1.6%) orders (p < 0.01)
Holdsworth et al.⁴³ (US)	N/P	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Any type	Any error which may result in ADE (dispensing error, overdose, underdose, wrong dose	Reduction in any errors (RR 0.34; 95% CI 0.24–0.49) and serious or life-threatening errors (RR 0.23; 95% CI 0.07–0.80)
Jozefczyk et al.⁵⁹ (US)	N	CPOE	CPOE system implementation	Pre–post	Prescribing	Any prescribing errors	Number of orders without any prescribing errors increased from 209/500 (41.9%) to 480/500 (96%) medication orders (p = 0.001)
Kadmon et al.⁴⁶ (Israel)	N/P	CPOE + CDS	Multistep process of introduction of CPOE, followed by introduction of CPOE + CDS	Pre–post	Prescribing	Any prescribing error	Compared with errors occurring in baseline period [103/1250 (8.2%) orders], there were significant reductions in errors occurring following the introduction of CPOE [97/1250 (7.8%) orders (p = 0.66)], CPOE and CDS [55/1250 (4.4%) orders (p < 0.001)], and further modification to CPOE and CDS system [18/1250 (1.4%) orders (<0.001)]
Kazemi et al.⁴⁸ (Iran)	N	CPOE + CDS	Multistep process of introduction of CPOE, followed by introduction of CPOE + CDS	Pre–post	Prescribing	Dosing errors related to antibiotic and anticonvulsant orders	Compared with errors occurring in baseline period [876/1668 (52%) orders], a similar number occurred following the introduction of CPOE alone [749/1489 (50%) orders], with a reduction following introduction of CPOE and CDS [442/1331 (33%) orders (p_trend <0.001)]
Kelly et al.²³ (US)	N/P	Computer programme	Electronic infusion calculator	Conventional calculator	Administration	Incorrect infusion rate calculation	Significant improvement in calculation accuracy from 61.9 ± 8.15% to 100 ± 0% (p < 0.001)
Larsen et al.¹⁹ (US)	N/P	IV administration technology	Automated infusion devices with standard infusion concentrations	Pre–post	Administration	Any administration errors involving one of the standardized medications	Absolute risk reduction of 2.3 errors per 1000 medication doses (95% CI 1.1–3.4)
Lehmann et al.²⁶ (US)	N	Computer programme	Online parenteral nutrition calculator	Pre–post	Prescribing	Any TPN prescribing errors	Reduction in errors from 60/557 (10.7%) orders to 20/471 (4.2%) orders (p < 0.001)
Lehmann et al.²⁸ (US)	N	Computer programme	Online parenteral nutrition calculator	Pre–post	Prescribing	Any prescribing errors associated with TPN orders	Reduction in errors from 60/557 (10.7%) orders to 8/656 (1.2%) orders (p < 0.001)
Lehmann et al.⁴² (US)	N/P	CPOE + CDS	Web-based calculator for IV continuous infusions	Pre–post	Prescribing	Any prescribing errors involving medication infusions	Reduction in errors from 35/129 (27%) orders to 8/142 (6%) orders (p < 0.001)
Maat et al.⁴⁹ (Netherlands)	N	CPOE + CDS	Computerizing prescribing and calculating system on hypo/hyper-glycaemia	Pre–post	Prescribing	Calculation error of glucose intake	No difference in incidence of hypoglycaemia [4.0/100 hospital days (95% CI 3.2–4.8) to 3.1/100 hospital days (2.7–3.5), p = 0.88)] or hyperglycaemia [6.0/100 hospital days (95% CI 4.3–7.7) to 5.0/100 hospital days (3.7–6.3), p = 0.75]
MacKay et al.⁵⁰ (US)	N/P	CPOE + CDS	Electronic ordering and compounding system for parenteral nutrition	Pre–post	Any type	Any errors involved in prescribing, transcribing, preparation, and administration of TPN	Reduction from 15.6/1000 orders to 2.7/1000 orders (p < 0.001)
Manrique-Rodriguez et al.²¹ (Spain)	N/P	IV administration technology	Automated infusion devices with programmed alerts	None	Administration	Compliance with drug library	After 9 months of implementation, overall compliance with the drug library was 85%, with 94% of nursing staff recommending the introduction of this technology in other units
Manrique-Rodriguez et al.²² (Spain)	N/P	IV administration technology	Automated infusion devices with programmed alerts	None	Administration	Compliance with drug library, and smart-pump programming errors	Overall user compliance 78%, leading to interception of 92 errors (from 486,875 programming events; 0.02%) of which 42% of intercepted errors were considered to be catastrophic
Menke et al.²⁵ (US)	N/P	Computer programme	Computerized clinical documentation system	Pre–post	Administration	Medication administration delay (difference between scheduled administration times versus actual administration time)	Increase in medication administration delay from 8.5 ± 27.9 min to 16.9 ± 34.9 min (p < 0.01)
Morriss Jr et al.³¹ (US)	N	Barcoding	Barcode medication administration system	Pre–post	Administration	Any nursing-related administration errors	Reduction in likelihood of preventable ADE (HR 0.53; 95% CI 0.29–0.91)
Morriss Jr et al.³² (US)	N	Barcoding	Barcode medication administration system	Pre–post	Administration	Any nursing-related administration errors	Reduction in likelihood of preventable ADE (HR 0.48; 95% CI 0.23–0.98)
Myers et al.³⁶ (US)	N	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Any type	Any error leading to adverse drug reaction report	Reduction in errors from 3.2 to 0.6 per 1000 patient days
Peverini et al.³⁴ (US)	N	CDS	Graphic user interface for parenteral nutrition decision support	Pre–post	Prescribing	Any TPN prescribing errors	Reduction in errors from 62/266 (23.3%) orders to 0/290 (0%) orders (p < 0.001)
Potts et al.³⁹ (US)	N/P	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Prescribing	Any prescribing errors	Reduction in errors from 2662/6803 (39.1%) orders to 110/7025 (1.6%) orders (p < 0.001)
Russell et al.¹⁸ (US)	N/P	CPOE + computer programmes	CPOE with bidirectional interface between pharmacy and CPOE systems for infusion-pump orders	Pre–post	Prescribing and administration	Any error related to prescribing or administration of infusions	Reduction in errors with IV fluids from 97/231 to 46/152 orders (p = 0.01), with smaller reduction in errors with medication (72/296 to 54/303 orders; p = 0.05)
Skouroliakou et al.²⁹ (Greece)	N	Computer programme	Computer-assisted parenteral nutrition ordering programme	Pre–post	Prescribing	Any prescribing errors associated with TPN orders	Reduction in errors from 28/941 (3%) orders to 0/941 (0%) orders (p < 0.001)
Taylor et al.⁵² (US)	N	CPOE	CPOE system implementation	Pre–post	Administration	Any administration errors	Reduction in errors from 50/253 (20%) administration episodes to 31/268 (12%) administration episodes (RR 0.53 95% CI 0.33–0.84)
Trotter and Maier⁵³ (Germany)	N/P	CPOE	CPOE system implementation	Pre–post	Prescribing	Any prescribing errors involving parenteral nutrition or IV medications	Reduction in errors from 484/4118 (12%) orders to 3/5480 (0.1%) orders (p < 0.001)
Upperman et al.⁵¹ (US)	N/P	CPOE	CPOE system implementation	Pre–post	Any type	Any error leading to possible or actual ADE	No reduction in total errors from 0.3 ± 0.04/1000 doses to 0.37 ± 0.04/1000 doses (p = 0.3), but reduction in harmful ADEs from 0.05 ± 0.017/1000 doses to 0.03 ± 0.003 doses (p = 0.05)
Vardi et al.⁴⁴ (Israel)	N/P	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Prescribing	Any prescribing errors related to resuscitation medication orders	Reduction in errors from 3/13,124 (0.02%) orders to 0/46,970 (0%) orders
Walsh et al.⁴⁵ (US)	N/P	CPOE + CDS	CPOE system with CDS implementation	Pre–post	Any type	Any error leading to potential or actual patient harm	No difference in serious medication errors from 31.7/1000 patient-days to 33.0/1000 patient-days (IRR 1.04; 95% CI 0.70–1.54) with slight reduction in errors causing patient harm from 7.9/1000 patient-days to 6.5/1000 patient-days (IRR 0.83; 95% CI 0.37–1.87)
Warrick et al.⁵⁴ (UK)	N/P	CPOE	CPOE system implementation	Pre–post	Prescribing and administration	Any prescribing and administration errors	Reduction in prescribing errors from 14/159 (9%) orders to 12/257 (5%) orders (p = 0.09) and administration errors from 43/528 (8%) to 4/278 (1%) orders (p < 0.05)
Organizational
Aguado-Lorenzo et al.⁷⁰ (US)	N	Medication distribution and supply	Preparation of ready-to-use morphine infusion from pharmacy	Morphine infusions prepared on ward by nurses	Administration	Deviation (>7.5%) from labelled concentration	Number of infusions outside of acceptable concentration limits lower among those prepared by pharmacy compared with those prepared on the ward by nurses [19/99 (19.2%) versus 9/115 (7.8%); p = 0.015]
Allegeart et al.⁶⁸ (US)	N	Medication distribution and supply	Use of paediatric amikacin vials (50 mg/ml)	Preparation of doses from adult-strength vials (250 mg/ml)	Administration	Inability to achieve target plasma concentrations/pharmacokinetic parameters	Achievement of target concentrations higher with use of paediatric vial compared with adult-strength vial [40/56 (72%) versus 44/75 (58%); p = 0.132]
Broussard et al.⁵⁹ (US)	N/P	GPPs	Implementation of preformatted order sheets with dosing instructions and sedation monitoring form	Pre–post	Prescribing	Any prescribing errors (e.g. wrong dose, units) relating to sedatives	Reduction in medication-ordering errors, including using units/kg (p < 0.05), ordering of the appropriate reversal agent (p = 0.02), and correct medication dosage (p < 0.001)
Conroy⁶⁹ (US)	N/P	Medication distribution and supply	Use of medications licensed for use in paediatrics	Unlicensed/off-label medication use	Any type	All medication errors identified by clinical staff	Unlicensed/off-label medication use in neonates associated with more medication errors (OR 5.81; 2.32–14.55)
Hilmas et al.⁶² (US)	N	GPPs	Parenteral nutrition prescribing process	None	Prescribing	Any prescribing and transcribing errors related to parenteral nutrition orders	Prescribing process demonstrated 50–60% compliance with recommended standards, while pharmacist interventions were made for 5% of orders
Kazemi et al.⁷¹ (Iran)	N	Nurse prescribing	Transcription of order by nurse into electronic prescribing programme	Physician order directly into electronic prescribing programme	Prescribing	Any errors related to use of antibiotics or anticonvulsants	Involvement of nurses in prescribing resulted in reduction in medication errors (RR 0.50; 0.50–0.71)
O’Brodovich and Rappaport⁶⁶ (Canada)	N/P	Medication distribution and supply	Unit dose drug distribution system	Pre–post	Administration	Any administration errors	Observed medication incident rates decreased from 10.3% to 2.9% (p < 0.05) and the nurses’ time spent on medication-related activities decreased from 23.7% to 21.6%
Olsen et al.⁶⁵ (Denmark)	N/P	Medication distribution and supply	Implementation of a satellite pharmacy incorporating unit dose drug distribution	Pre–post	Administration	Any administration errors	Introduction of satellite pharmacy led to overall increase in errors from 389/856 (45%) to 280/540 (52%; p = 0.020), but a reduction in serious errors from 66/856 (7.7%) to 0/544 (0%; p < 0.05)
Palmero et al.⁶⁴ (Switzerland)	N	GPPs	Implementation of preformatted order sheets	Pre–post	Prescribing	Any error related to prescribing identified by pharmacist review of all medication orders	Significant reduction in prescribing errors [146/505 (28.9%) versus 71/525 (13.5); p < 0.05]
Roman⁵⁷ (US)	N/P	GPPs	Standardized infusion concentrations (SC)	None	Administration	Any administration-related errors	In the 2 years since the implementation of SC, only five medication errors involving medication administration were identified
Ross et al.⁵⁶ (UK)	N/P	GPPs	Introduction of pharmacy dispensing double-check; education of nursing staff regarding IV administration; nonpunitive error reporting policy	Pre–post	Any type	Any reported medication errors	Introduction of double checking policy with pharmacy dispensing led to reduction in medication errors from 9.8 per year to 6 per year. Introduction of increased education of nursing staff regarding IV administration led to reduction in medication errors from 37 per year to 32 per year. Change in error reporting form to make it less punitive increased the error reporting rate from 33 per year to 38 per year
Sturgess et al.⁶⁰ (UK)	N/P	GPPs	Implementation of zero-tolerance prescribing policy incorporating a dedicated prescribing area and daily feedback of prescribing errors	Pre–post	Prescribing	Any error related to prescribing (e.g. wrong drug, dose, frequency)	Reduction in prescribing errors from 969/1111 patient days (87%) to 796/1781 patient days (45%) (p < 0.001)
Thomas et al.⁶¹ (UK)	N	GPPs	Introduction of standardized gentamicin pathway for prescribing and monitoring	Pre–post	Administration	Errors related to gentamicin administration and monitoring (e.g. not given within 60 min of scheduled dose, inappropriate action take after level results)	Introduction led to significant improvement in number of doses given within 60 min of scheduled dosing time (82% versus 73%; p = 0.02), documentation of gentamicin level (78% versus 62%; p = 0.04), appropriate action taking according to level result (77% versus 61%; p = 0.04), and documentation of length of gentamicin therapy (61% versus 42%; p = 0.045)
Valizadeh et al.⁶³ (Iran)	N	GPPs	Preparation of oral solutions using tablets	Target oral solution strength	Administration	Accuracy of prepared dose concentration for spironolactone and captopril prepared oral solutions	Significant differences and variability in prepared oral solution strength compared with the prescribed dose. The difference was statistically significant for captopril (0.35 ± 0.41 mg; p < 0.001), but not spironolactone (0.23 ± 1.58 mg; p = 0.26)
Watanachai et al.⁶⁷ (Thailand)	N	Medication distribution and supply	Use of needle nonremovable syringes for preparation of medication dilutions	Use of needle removable syringes	Administration	Inaccuracy in preparation of insulin infusion compared with prescribed dose	Compared with target concentration of 300 µU/ml, preparation of infusion using needle nonremovable syringes was most accurate (335 ± 28 µU/ml) compared with the use of needle removable syringes [Terumo(R) 540 ± 54 µU/ml; Nipro(R) 617 ± 45 µU/ml)
White et al.⁵⁸ (US)	N/P	GPPs	Introduction of mandatory medication request form for potassium chloride	Pre–post	Prescribing	Post-infusion elevation of serum potassium > 4.35 mmol/l	Significant reduction in errors from 103/1341 (7.7%) to 0/150 (0%); p < 0.001
Personnel
Alemanni et al.⁷⁷ (Canada)	N/P	Education	Education to nursing staff regarding medication process including drug verification, preparation, and administration	Pre–post	Administration	Any nursing errors in medication preparation and administration process	Increase in overall compliance with all steps of the medication administration process from 23/142 (16%) administration episodes to 39/140 (28%) administration episodes (p = 0.021)
Campino et al.⁷⁴ (Spain)	N	Education	Comprehensive preventive educational strategy delivered by pharmacist on medication errors	Pre–post	Prescribing	Any prescribing errors	Reduction in errors from 868/4182 (21%) orders to 47/1512 (3%) orders (p < 0.001)
Chedoe et al.⁸² (Netherlands)	N	Education	1 h theoretical teaching session to nurses, individual practical teaching session of commonly used medications; guided pharmacy tour	Pre–post	Administration	Any preparation and administration errors	Reduction in errors from 151/311 (49%) administration episodes to 87/284 (31%) administration episodes (p < 0.001)
Eisenhut et al.⁸⁰ (UK)	N/P	Education	Personalized assessment and feedback for medical trainees	Pre–post	Prescribing	Any prescribing errors	Reduction in total errors from 188/421 patients to 120/588 patients (p < 0.05) and reduction in major errors from 36/421 patients to 35/588 patients (p < 0.001)
Gordon et al.⁸¹ (UK)	N/P	Education	E-learning resources for paediatric prescribing for trainee doctors	No access to e-learning resource	Prescribing	Total score on prescribing assessment	Intervention associated with higher mean score on prescribing assessment at 4 weeks (79 ± 12.1 versus 63 ± 13.5) and 12 weeks (79 ± 10.1 versus 69 ± 12.4; p < 0.001) postintervention
Leonard et al.⁷³ (US)	N/P	Education	Educational website with competency examination; distribution of a personal digital assistant-based standardized dosing reference; zero-tolerance policy for incomplete/incorrect orders; prescriber performance feedback; publicizing of error/data	Pre–post	Prescribing	Any prescribing errors	Absolute risk reduction in errors of 38/100 orders written (p < 0.001)
Ligi et al.⁷⁸ (France)	N	Education	Continuous incident reporting and subsequent educational interventions to combat identified errors	Pre–post	Any type	Any error leading to patient harm	Reduction in incidence of severe errors from 7.6 to 4.8 per 1000 patient-days (p = 0.005), as well as reduction in 10-fold dosing errors from 2.3/100 admissions to 0.6/100 admissions (p = 0.022)
Munoz Labian et al.⁷² (Spain)	N	Education	Education programme regarding common medication errors occurring within the neonatal unit	Pre–post	Prescribing	Any prescribing errors	Reduction in illegible orders from 22% to 8% (p = 0.005), missing route of administration from 28% to 5% (p < 0.001) and missing dose calculation from 54% to 22% (p < 0.001); no change in dosing errors from 4% to 4%
Niemann et al.⁸⁴ (US)	N/P	Education	Multifaceted intervention including: provision of information on common medication preparation errors; training course on error prevention and drug handling; and provision of a comprehensive reference book	Pre–post	Administration	Any preparation error	Overall frequency of errors decreased from 527/581 (91%) administration episodes to 116/441 (26%) administration episodes (p < 0.001)
Raja Lope et al.⁷⁵ (Malaysia)	N	Education	Education programme regarding medication administration process for nursing staff	Pre–post	Administration	Noncompliance to 10 standard medication administration steps	Reduction in medication administration errors from 59/188 (31%) to 26/169 (15%) administration episodes (p < 0.001)
Sagy⁷⁶ (US)	N/P	Education	Education programme on medication prescribing for residents and nursing staff	Pre–post	Prescribing	Any prescribing error	Reduction in errors from 533/256 orders (2.1/order) to 38/140 orders (0.3/order); p < 0.05
Sullivan et al.⁷⁹ (US)	N/P	Education	Interactive online nursing educational module on reducing insulin administration errors	Pre–post	Administration	Administration errors involving insulin (e.g. wrong dose, incorrect documentation, inadequate monitoring following dose)	Reduction in errors from 131/882 (15%) episodes to 19/119 (2%) episodes (p < 0.001)
Sullivan et al.⁸³ (US)	N	Education	Personalized performance feedback of prescribing errors	Pre–post	Prescribing	Any prescribing error involving opioids and antibiotics	Reduction in opioid related errors by 83%, with increase in number of days between opioid prescribing errors from 3.94 days to 22.63 days; no change in number of days between antibiotic prescribing errors (averaged 2.14 days)
Pharmacy
Condren et al.⁸⁶ (US)	N/P	Pharmacy service	Paediatric clinical pharmacy service	None	Any type	All actual or potential medication errors requiring pharmacist intervention	4605 interventions performed for 3978 patients with 223 adverse drug events or medications errors prevented or detected during the study period
Folli et al.⁹² (US)	N/P	Pharmacy service	Dispensary-based pharmacy service	None	Prescribing	Errors in medication order (e.g. wrong drug, dose, frequency, route, illegible order, drug–drug interaction, drug–disease interaction)	Overall error rates for the two hospitals were 1.35 and 1.77 per 100 patient-days, and 4.9 and 4.5 per 1000 medication orders, respectively
Gibson et al.⁹¹ (UK)	N/P	Pharmacy service	Dispensary-based pharmacy service	Pre–post	Prescribing	Errors in medication order (e.g. wrong drug, dose, frequency, route, illegible order, drug–drug interaction, drug–disease interaction)	No significant reduction in prescribing errors (53/439 (12%) versus 46/441 (10%); p = 0.577)
Kaushal et al.⁸⁷ (US)	N/P	Pharmacy service	Ward-based paediatric clinical pharmacy service	Pre–post	Any type	Any actual or potential medication errors relating to prescribing, transcribing, dispensing, administering, or monitoring	Reduction in medication errors from 29/1000 patient-days to 6/1000 patient-days (p < 0.01)
Khan et al.⁹⁰ (India)	N	Pharmacy service	Ward-based paediatric clinical pharmacy service	None	Any type	All actual or potential medication errors requiring pharmacist intervention	Medication errors identified in 80 of 150 patients; total of 87 interventions made, with 60 accepted by clinician
Krupicka et al.⁸⁵ (US)	N/P	Pharmacy service	Ward-based paediatric clinical pharmacy service	None	Any type	All actual or potential medication errors requiring pharmacist intervention	A total of 172 recommendations made for 77 of 215 patients, equivalent to 35 recommendations per 100 patient-days
Takata et al.⁹³ (US)	N/P	Pharmacy service	Dispensary-based pharmacy service	None	Prescribing	Errors in medication order (e.g. wrong drug, dose, frequency, route, illegible order, drug–drug interaction, drug–disease interaction)	A total of 2.67 (95% CI 2.4–3.0) interventions per 1000 patient-days and 0.82 (0.73–0.91) interventions per 1000 medication orders; 12% (8.8–15.9%) of interventions occurred in NICU
Tripathi et al.⁸⁹ (US)	N/P	Pharmacy service	Ward-based paediatric clinical pharmacy service	None	Any type	All actual or potential medication errors requiring pharmacist intervention	Total of 27,773 interventions related to 10,963 admissions, with 22,765 (80%) interventions resulting in change in therapy or monitoring
Zhang et al.⁸⁸ (China)	N/P	Pharmacy service	Ward-based paediatric clinical pharmacy service	None	Any type	All actual or potential medication errors requiring pharmacist intervention	Interventions resulted from a total of 31 medication errors identified from 683 prescriptions (4.5%)
Hazard and risk analysis
Apkon et al.⁹⁵ (US)	N/P	Quality improvement tools	Redesign of medication infusion ordering; preparation; and administration process	Pre–post	Prescribing and administration	Failure mode effects analysis (FMEA) for severity (S), likelihood of error occurrence (O), likelihood that failures will escape detection (D) before causing harm RPN (risk priority number = S × O × D) assigned	According to FMEA analysis, changes in process led to significant reduction in criticality index associated with the following processes: prescribing the correct rate (136 to 26), calculating the correct amount of medication to prepare infusion (234 to 49), preparation of infusion (314–88), programming of infusion pump (269 to 99)
Bonnabry et al.⁹⁶ (Switzerland)	N/P	Quality improvement tools	Use of failure modes; effects, and criticality analysis (FMECA) to improve TPN production process	Pre–post	Prescribing and manufacturing	Any errors related to parenteral nutrition from prescribing to manufacture	Significant 59% reduction in criticality index for TPN production process from 3415 to 1397
Frey et al.⁹⁴ (Switzerland)	N/P	Safe learning systems	Use of critical incident reporting to implement changes to prevent medication errors	None	Any type	Any real or potential harm resulting from errors in the medication management process	A total of 284 critical incident reports were made over a 12-month process, with suggestions to prevent such future incidents provided in 62% of reports; overall, 46 critical incident reports were followed by system changes
Li et al.⁹⁸ (US)	N	Error detection tool	Automated detection of adverse events and medical errors	Voluntary incident reporting	Prescribing and administration	Errors related to narcotic dosing and administration	18 errors identified through automated detection, only one of which was identified through voluntary incident reporting or use of a trigger tool with PPV of 39–100%
Li et al.⁹⁹ (US)	N	Error detection tool	Automated detection of medication administration errors	Voluntary incident reporting	Administration	Errors related to administration of incorrect dose compared with prescription	Similar specificity (98.2% versus 100%), but much greater sensitivity (82.1% versus 5.5%) and precision (70.2% versus 50.0%) than incident reporting for error recognition
Suresh et al.¹⁰ (US)	N	Quality improvement tools	Numerous safety projects including education/training; use of FMEA; improving preparation and administration, etc.	None	Any type	Any real or potential harm resulting from errors in the medication management process	Multisite sharing of critical incident reports useful in identifying common medication errors occurring in the NICU setting
Takata et al.⁹³ (US)	N/P	Error detection tool	Use of electronic trigger tool	Voluntary incident reporting	Any type	Any injury, large or small, caused by the use (including nonuse) of a medication	Use of trigger tool identified more ADEs than voluntary incident reports (22.3/1000 versus 1.7/1000; p < 0.001), with a positive predictive value of 4.7% (3.7–5.8%)
Arenas Villafranca et al.⁹⁷ (Spain)	N	Quality improvement tools	Use of failure modes; effects; analysis and development of checklist to improve TPN production process	Pre–post	Prescribing and manufacturing	Any errors related to parenteral nutrition from prescribing to manufacture	Use of FMEA identified a total of 82 possible failures; the development of a checklist to address potential failures reduced mean criticality index from 137 to 48 for each item
Multifactorial
Abstoss et al.¹¹¹ (US)	N/P	GPPs; education; technology	Seven overlapping interventions including: poster tracking of errors; performance metric display in staff lounge; multiple didactic curricula; unit-wide emails summarizing medication errors; CPOE; introduction of unit-based pharmacy technicians; and patient safety report form streamlining	Pre–post	Any type	Any real or potential harm resulting from errors in the medication management process	Reported error rate increased from 3.16/10,000 to 3.95/10,000 dispensed doses (p = 0.09); errors causing harm reduced from 0.56/10,000 to 0.16/10,000 doses dispensed (p < 0.001)
Alagha et al.¹¹⁵ (Egypt)	N/P	GPPs; education; pharmacy	New structured medication order chart; physician education; provision of dosing guide; and physician performance feedback	Pre–post	Prescribing	Any prescribing error	Reduction in errors from 1107/1417 to 391/1097 (78.1% versus 35.6%; p < 0.001)
Booth et al.¹⁰⁴ (UK)	N/P	GPPs; education	Application of prescribing guidelines with a zero-tolerance policy; providing feedback and education	Pre–post	Prescribing	Any prescribing errors	Reduction from 892/1000 to 447/1000 errors per occupied bed days (p < 0.001)
Bullock et al.¹⁰⁰ (US)	N/P	GPPs; education	Development ; dissemination and implementation of standardized IV infusion concentration list; intensive education and one-on-one coaching and mentoring	Pre–post	Administration	Any preparation or administration errors involving parenteral medications	Reduction in percentage of IV infusion orders that did not have standardized IV concentration used from 31/120 (26%) to 17/128 (13%), as well as reduction in associated medication errors related to improper dose from 26/50 (52%) to 7/28 (25%) and reduction in medication errors related to improper concentration from 6/26 (23%) to 0/7 (0%)
Burmester et al.¹⁰² (US)	N/P	GPPs; education	Post-cardiac surgery admission prescription forms; systematic physician education; publicizing error rates	Pre–post	Prescribing	Any prescribing error	Reduction in errors from 613/3648 to 366/8929 (16.8% versus 4.1%; p < 0.001)
Campino et al.¹⁰⁶ (Spain)	N	GPPs; education	Protocol standardization and educational programme consisting of theoretical and practical teaching session	Pre–post	Administration	Calculation errors (i.e. dose drawn up versus prescribed dose), or accuracy errors (i.e. theoretical concentration versus actual concentration) in preparing IV medications	Reduction in calculation errors from 6/444 to 0/291 (1.35% versus 0%; p = 0.086) and accuracy errors from 243/444 to 61/291 (54.7% versus 23%; p < 0.001)
Cimino et al.¹¹² (US)	N/P	GPPs; education; pharmacy	Various interventions delivered across different sites including: preprinted order sheets; provision of real-time feedback to prescribers on medication errors; improving availability of dosing guides; increase in pharmacist staffing; publicizing medication errors	Pre–post	Prescribing	Any prescribing error	Reduction in errors from 3259/12,026 to 217/9187 (27.9% versus 23.7%; p < 0.001) and reduction in harmful errors from 16/12,026 to 3/9187 (0.13% versus 0.03%)
Costello et al.¹¹³ (US)	N/P	GPPs; education; pharmacy	Multiple interventions introduced over two phases including: introduction of a clinical pharmacist; paediatrics clinical pharmacist-led medication safety team; new incident reporting form and educational forums	Pre–post	Any type	Any errors	Significant increase in number of errors reported, while errors identified as being severe reduced from 46% to 8% and then 0% over each phase
Davey et al.¹⁰³ (UK)	N/P	GPPs; education	Junior doctor prescribing tutorial and introduction of a bedside prescribing guideline	Pre–post	Prescribing	Dose >10% deviation from guideline or good prescribing practices not followed	Prescribing tutorial associated with reduction in errors from 76/249 to 44/266 (30.5% versus 16.5%; p = 0.023) but no further reduction with subsequent implementation of bedside guideline [59/320 (18.4%) to 56/330 (17.0%) p = 0.73]
Di Pentima et al.¹⁰⁹ (US)	N/P	GPPs; education; technology	Development of antimicrobial stewardship programme on vancomycin utilizing CPOE + CDS together with provision of individualized real-time feedback	Pre–post	Prescribing	Incorrect vancomycin order according to clinical indications, microbiology data or dosing guidelines	Reduction in errors from 1.8/1000 patient days to 1.4/1000 patient days (p < 0.05)
Hilmas et al.¹¹⁰ (US)	N/P	GPPs; education; technology	Development of standardized approach to deliver continuous infusions; CPOE + CDS with standardized concentrations; smart-pump infusions and intensive educational sessions	Pre–post	Prescribing and administration	Incorrect continuous infusion syringe concentration, incomplete and illegible orders; incorrect administration rate and dose	Reduction in errors from 98/200 to 0/200 (49% versus 0%)
Irwin et al.¹⁰⁷ (Canada)	N/P	GPPs; education; technology	Standardizing infusion concentrations; CDS to assist with drug concentration and infusion rate; competency evaluation of staff with provision of educational programme	Pre–post	Any type	Any errors reported through incident monitoring programme involving parental medications	No change in errors from 2.4/year to 2.0/year
Martinez-Anton et al.¹⁰⁵ (Spain)	N/P	GPPs; education	Standardizing of dosing guidelines; pocket tables with dosing guidelines; updated protocols; education programme on correct prescribing	Pre–post	Prescribing and administration	Any medication error related to prescribing or administration (e.g. wrong medication, frequency, route, dose)	Reduction in errors from 761/2228 to 388/1791 (34.2% versus 21.7%; p < 0.001)
Otero et al.¹¹⁴ (Argentina)	N/P	GPPs; education; pharmacy	Positive safety culture with nonpunitive management of medication errors; active interaction with pharmacists during ward rounds; provision of education regarding medication prescribing and administration	Pre–post	Prescribing and administration	Any medication error related to prescribing or administration (e.g. wrong medication, frequency, route, dose)	Reduction in errors related to prescribing, from 102/590 to 105/1144 (17% versus 9%; p < 0.05) and administration from 150/1174 to 99/1588 (13% versus 6%; p < 0.05)
Pallás et al.¹⁰⁸ (Spain)	N	GPPs; education; technology	Education regarding good prescribing practice; implementation of a pocket personal computer-based automatic calculation system	Pre–post	Prescribing	Any medication error related to prescribing (e.g. wrong medication, frequency, route, dose)	Reduction in errors from 2498/6320 to 171/1435 (39.5% versus 11.9%; p < 0.001)
Simpson et al.¹¹⁷ (UK)	N	Education; pharmacy	Pharmacist-led education programme; daily pharmacist review of medication orders; competency assessment of all neonatal unit staff; and greater publicizing of medication errors	Pre–post	Prescribing and administration	Any medication error related to prescribing or administration (e.g. wrong medication, frequency, route, dose)	Reduction in errors from 24.1/1000 to 5.1/1000 patient-days (p = 0.037)
Wang et al.¹¹⁶ (US)	N/P	Pharmacy; technology	Utilization of clinical pharmacists to review and intercept any adverse drug events and CPOE	None	Any type	Any error within the medication process	Total of 865 errors identified, of which 178 considered potentially harmful; clinical pharmacists intercepted 96/178 (54%) errors, while the addition of a CPOE had the potential to intercept 130/178 (73%) errors
Yamanaka et al.¹⁰¹ (Brazil)	N/P	GPPs; education	Redevelopment of the nursing administration process; provision of nursing education regarding medication errors; provision of dosing guidelines	Pre–post	Prescribing and administration	Any medication error related to prescribing or administration (e.g. wrong medication, frequency, route, dose)	Reduction in errors from 1717/8152 to 1498/8550 (29% versus 22%; p < 0.001)

ADE, adverse drug event; CDS, clinical decision support; CI, confidence interval; CPOE, computerized physician order entry; GPPs, guidelines, policies, and procedures; HR, hazard ratio; ICU, intensive care unit; IRR, incident rate ratio; IV, intravenous; N, neonatal only; NICU, neonatal intensive care unit; N/P, neonatal and paediatric; OR, odds ratio; PICU, paediatric intensive care unit; PPV, positive predictive value; RR, relative risk; TPN, total parenteral nutrition.