Writing Medication Protocols for the Emergency Department
Emergency department medication protocols should be developed using a standardized, system-level approach that prioritizes medication safety through explicit labeling requirements, standardized drug concentrations, pharmacy-prepared high-risk medications, and protocol-driven verification processes at every step from storage to administration. 1
Core Protocol Development Framework
Medication Storage and Organization
- Standardize all medication storage locations across the ED, with identical drug tray configurations in every treatment area to minimize confusion during high-stress situations 1
- Label all tray divisions clearly and position medications to minimize look-alike/sound-alike errors 1
- Remove concentrated or high-risk medications from standard carts; store these in separate, clearly marked locations with alert labels 1
- Eliminate unusual or rarely-used drugs from routine storage areas; maintain these in a single designated location managed by pharmacy 1
- Use single-use vials preferentially; if multi-dose vials are required, implement mandatory discard protocols at case completion 1
High-Risk Medication Management
- Prohibit concentrated drugs on standard medication carts; pharmacy must provide all diluted, ready-to-administer high-risk medications including insulin and heparin 1
- Restrict epinephrine to standard concentrations only (1 mg/1 mL for cardiac arrest, 1 mg/10 mL for anaphylaxis); remove large-volume preparations from general access 1
- Require two-person verification for all weight-based dosing and high-risk medication administration 1
- Implement barcode scanning systems with audible and visual alerts for medication verification whenever possible 1
Medication Administration Protocols
Labeling Requirements (Non-Negotiable)
- Every medication must be labeled with drug name, concentration, and preparation date before leaving the pharmacy or preparation area 1
- Use preprinted, color-coded labels conforming to ISO standards rather than handwritten labels 1
- Discard any unlabeled syringe immediately without exception—no attempts to identify contents 1
- Label all infusion lines and ports with drug name and route-specific identifiers (yellow for epidural, red for arterial) 1
Verification and Administration Steps
- Read and verify every vial, ampoule, and syringe label before drawing up and again immediately before administration 1
- Use smart pumps with standardized drug libraries and guardrails for all continuous infusions; ensure pumps are identical across all ED treatment areas 1
- Implement speak-back verification for all verbal medication orders; announce medication name and dose when administered and document immediately 1
- Perform "clean sweep" protocols at patient discharge or transfer: discard all syringes, containers, and multi-dose vials unless actively connected to the patient 1
Specific Drug Class Protocols
Opioid Prescribing Protocols
- Prescribe short-acting opioids only for acute pain management in ED discharge patients; long-acting or extended-release formulations are contraindicated for acute pain 1
- Utilize state prescription drug monitoring programs before prescribing opioids to identify patients at high risk for diversion or doctor shopping 1
- Limit initial prescriptions to 3-5 days for acute pain conditions; avoid routine opioid prescriptions for chronic pain exacerbations 1
- Never co-prescribe opioids with multiple sedative-hypnotics or muscle relaxants due to additive CNS depression and increased mortality risk 1, 2
Muscle Relaxant Protocols
- Prescribe muscle relaxants for maximum 2 weeks only; all clinical trials demonstrating efficacy were 2 weeks or less in duration 2
- Avoid co-prescribing multiple muscle relaxants or combining with sedative-hypnotics; specifically, cyclobenzaprine and methocarbamol should not be combined with other sedating medications 2
- In patients over 65 years, avoid muscle relaxants entirely when possible due to increased anticholinergic effects, sedation, and fall risk 2
- If switching muscle relaxants is necessary, replace rather than add; consider tizanidine as the alternative with strongest evidence base 2
Antiepileptic Drug Protocols
- Administer additional antiepileptic medication to all patients with refractory status epilepticus who fail initial benzodiazepine treatment 1
- Use intravenous phenytoin, fosphenytoin, or valproate as second-line agents for status epilepticus; levetiracetam, propofol, or barbiturates are acceptable alternatives 1
- When discontinuing levetiracetam, taper by 500 mg increments every 1-2 weeks to minimize seizure recurrence risk 3
- Monitor closely for breakthrough seizures at each dose reduction during antiepileptic drug tapers 3
Quality Assurance and Safety Culture
Reporting and Analysis Systems
- Establish non-punitive incident reporting systems for medication errors with mandatory analysis and intervention protocols 1
- Conduct regular medication safety reviews involving ED physicians, nurses, and pharmacists to identify system vulnerabilities 1
- Implement written policies for medication safety with mandatory education for all new staff before independent practice 1
Pharmacy Integration
- Assign dedicated pharmacists to support the ED with 24/7 availability for medication questions 1
- Pharmacy must prepare all compounded or diluted high-risk drugs; minimize provider-prepared medications 1
- Pharmacy manages complete medication flow from ordering through delivery, stocking, and disposal of unused medications 1
- Alert ED staff to any changes in supplied medications (new labels, concentrations, or formulations) with prominent warning labels during transition periods 1
Common Pitfalls to Avoid
- Do not rely on memory or assumptions about medication concentrations; verify every label even for familiar drugs 1
- Avoid abbreviations and trailing zeros in all medication documentation (write "5 mg" not "5.0 mg") 1
- Never pass multiple medications to the sterile field simultaneously; verify each medication aloud with two persons before transfer 1
- Do not assume younger patients are low-risk for opioid complications; ED opioid prescribing ranks third among all specialties for patients aged 10-29 years 1
- Recognize that lack of high-quality evidence does not justify inaction; implement system-level safeguards based on expert consensus when randomized trials are unavailable 1