30 closest matches · ranked by relevance
Medication Management
Primary: Observed Dosing Accuracy — 3.3; 1.0 percent difference — p=<0.001
Pain · Fever
Primary: Number of Participants Reporting Safe Dosing at 48-72 Hours — 28; 25 Participants
Adverse Drug Events
Primary: Mean Severity-weighted Admission Medication History (AMH) Error Score — 23; 4.1; 4.1 Mean Severity-weighted AMH Error Score
Cardiopulmonary Arrest · Resuscitation · Pediatrics
Primary: Medication Dosage Errors — 5.7; 62.8 percentage of medication errors
Kidney Failure, Acute
Primary: Adverse Drug Events or Potential Adverse Drug Events — 99; 104 Patient-Medication Pairs
Adverse Drug Events
Primary: Health Services Utilization 3 Months Following Hospital Discharge — 3.33; 3.40 Health Services Utilizations — p=.87
Acute Coronary Syndrome · Heart Failure
Primary: Number of Serious Medication Errors as Determined by Interview and Medical Chart Review — 0.95; 0.87 serious medication errors
Medication Reconciliation
Primary: Number of Participants With Changes/Updates in Medication List — 101; 43 Participants — p=<0.0001
Medication Adherence · Mobile Application
Primary: Usability of the SAM App — 1.14; 1.32; 1.35; 1.81 score on a scale
Machine Intelligence in the Pharmacy
Primary: Reaction Time — 3668; 4727; 4510 millisecond (ms)
Drug Toxicity
Primary: Transition Drug Risk — 6.4; 5.8 units: risk-weighted discrepancies — p=0.175
Medical Errors · Medical Order Entry Systems
Primary: Wrong-patient Order Sessions, Defined as Order Sessions That Include at Least One Wrong-Patient Retract-and-Reorder (RAR) Event, As-randomized Analysis — 3015; 3058…
Polypharmacy
Primary: Number of Participants With Changes in Signs and Symptoms Related to Adverse Effects of Prescribed Medicines. Clinical Gains and Benefits to Residents — 17 Participants
Diabetes Mellitus, Type 2 · Hypertension · Hyperlipidemia
Primary: Primary Effectiveness Outcome - LDL — 57.9; 54.8 percentage of time spent at goal
Asthma · Chronic Obstructive Pulmonary Disease
Primary: Inhaler Use Correctness — 3.52 correct steps
Interdisciplinary Communication · Management, Medication Therapy
Primary: Incident Rate for Communication Events — 47.6; 34.74; 34.07 mean events per observation — p=0.01
Medical Errors · Electronic Medical Records
Primary: Number of Order Sessions With at Least One Retract-and-Reorder (RAR) Event as Identified by the Wrong-Patient Retract-and-Reorder (RAR) Measure. — 5587; 5836; 5598; 6279…
Alzheimer Disease
Primary: Time to Dispensing of Inappropriate Medication Prescription — 76.7; 77.9; 77.5 Percentage of Cumulative Incidence — p=0.76
High-risk Medications
Primary: Medication Knowledge (0-100) — 71.2; 71.9; 73.2; 74.9 score on a scale
Transplant
Primary: Any Hospitalization or Any Emergency Room Visits — 497; 574; 380; 391 Participants — p=<.001
Family Reported Errors and Adverse Events
Primary: Family Safety Reporting Rates — 61; 60 Participants
Medication Adherence
Primary: Medication Adherence — 94.8; 82.8 percentage of doses taken
Infectious Disease
Primary: Percentage of Participants First Achieving Therapeutic Levels at 36 Hours — 20; 18 percentage of participants
Aging · Benzodiazepine Sedative Adverse Reaction · Anticholinergic Adverse Reaction
Primary: Change in Inappropriate Prescribing — 106; 145; 122 Participants — p=0.002
Medication Adherence
Primary: Medication Specific Knowledge — 63.82; 62.80 score (0-100)
Behavior
Primary: Number of Prescribing Errors by Study Arm — 8; 34; 8; 31 Medication orders
Medication Adherence
Primary: Medication Adherence — 88.1; 96.6; 94.4 percentage of doses taken (pill count)
Asthma
Primary: Percentage of Participants Making at Least One Critical Error After the First Assessment of Metered Dose Inhaler (MDI) Technique on Day 14 — 14 Percentage of Participants
Children Requiring Sedation to Facilitate Laceration Repair
Primary: Median Time (Minutes) After Administration of Intranasal Midazolam Until Patient Achieves Minimal Sedation — 4.7; 4.3; 5.2 minutes
Acute Stress Ulcer and Acute Gastric Mucosal Lesions
Primary: Number of Participants Reporting One or More Adverse Drug Reactions — 0 participants