Explain the purpose
Connect documentation to handoff, continuity of care, accountability, quality review, and useful EMS data.
EMS documentation · 45–55 minutes
Learn what belongs in a strong patient care report, how to protect patient information, and how common narrative formats organize the same facts. Then practice with EMSCodeSim’s current templates and fictional-case AI grader.
Use fictional scenarios in this class and linked tools. Do not enter, paste, or upload a real patient report or patient-identifying information. The Narrative Coach may save drafts in this browser; the AI Writing Lab sends submitted text to an AI service for feedback. Use your agency-approved ePCR and field documentation process for actual calls.
Your course checklist
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By the end, you can
Connect documentation to handoff, continuity of care, accountability, quality review, and useful EMS data.
Distinguish what the patient said, what others reported, what you observed, what you assessed, and what you did.
Compare chronological, CHART, SOAP, and DCHART while following your agency’s approved style.
Keep real patient information inside systems and workflows your agency has approved.
The standard
A strong PCR lets another clinician or reviewer understand what happened, what the crew found, what care was provided, and how the encounter ended. Write in a logical order, use specific observations, and make each statement traceable to a source.
Patient reports: “Patient states pain began while walking.”
Witness reports: “Bystander reports the patient fell from standing.”
Crew observes: “Patient found seated on the floor, speaking in full sentences.”
Crew assesses: “Left wrist swollen; distal pulse present.”
Crew performs: “Wrist supported with a splint.”
Patient response: “Patient reports pain decreased from 6/10 to 4/10 after splinting.”
Compare the writing
“Elderly patient fell. No injuries. Vitals normal. Treated and transported.”
“Patient states she slipped while stepping out of the shower and denies loss of consciousness. Crew found the patient seated on the bathroom floor. Patient reports left wrist pain rated 6/10. At 0718, BP was 148/86, pulse 88, respirations 18, and SpO₂ 97% on room air. The wrist was supported with a splint. At 0730, patient reported pain of 4/10. Patient was transported to the receiving facility and care was transferred to the receiving nurse.”
Avoid common problems
Choose a format
These formats organize a narrative; they do not replace your agency’s requirements. Acronym definitions and local expectations can differ. Keep the same facts and timeline whichever format you use.
| Style | Typical organization | Advantages | Tradeoffs |
|---|---|---|---|
| Chronological | Dispatch and arrival → history → assessment → care and reassessment → disposition and handoff. | Easy to follow event sequence and see changes over time. | Can become long or repetitive unless the writer stays focused. |
| CHART | Chief complaint → History → Assessment → Rx/treatment → Transport. | Familiar sections help organize a complete call. | May feel like separate boxes; timing and transitions can get lost. |
| SOAP | Subjective → Objective → Assessment → Plan. | Separates reported information from observed findings and organizes impression and plan. | Can obscure the operational timeline; “Assessment” should not become an unsupported diagnosis. |
| DCHART | Dispatch → Chief complaint → History → Assessment → Rx/treatment → Transport. | Calls attention to dispatch and transport as part of the encounter. | Can feel checklist-driven; local expansions and required details may vary. |
Protocol-informed documentation
The Denver Metro EMS Medical Directors’ protocols are organized by protocol number and condition/procedure. Their introduction says protocols support decision-making, may not cover every scenario, and may require clinically justified variance. When writing a report, review the current protocol(s) that apply to the encounter and your agency’s implementation, ePCR fields, and documentation policy.
For any weight-based medication, document the patient’s dosing weight and units, and identify whether it was measured, estimated, or obtained from an approved length-based system. If the dose uses kilograms and the weight was obtained in pounds, record the conversion method and the kilogram value used.
Show the calculation so another reviewer can follow it: weight (kg) × ordered dose (mg/kg) = calculated dose (mg). Document any maximum-dose adjustment and the actual dose given in mg. If converting to a volume, show dose (mg) ÷ concentration (mg/mL) = volume (mL). Include route, time, and patient response in the appropriate medication fields and narrative as required by your ePCR and local policy. If a weight cannot be obtained, follow the current protocol and document the approved estimate or dosing system used—never invent a weight.
Denver Metro Protocol 9000 recommends a standardized age-, weight-, or length-based system for every pediatric patient. Use your agency’s current approved method and cross-check the calculation before administration.
When your agency requires or the narrative benefits from it, name the protocol actually used and include its number (and version/date if needed to distinguish it). Use the local protocol title and number exactly as published—for example, “Denver Metro Protocol 3060, Chest Pain,” only when that protocol was in effect for your agency and applied to the call.
If more than one protocol guided care, identify the applicable protocols without implying steps you did not perform. Do not add a protocol number as a substitute for documenting the assessment, treatment, response, consultation, or clinical reasoning.
Example framework: “Care provided under [agency protocol title/number and version, if required]. [Relevant assessment and timeline]. [Interventions and response]. [Consultation or variance and rationale, if applicable].” Replace every bracket with verified facts; follow your ePCR structure.
Denver Metro reference: Denver Metro EMS Medical Directors — current protocols and revision materials (the site identifies its July 2026 protocols as current). See General Guidelines 0010, 0020, 0031, 0032, 0120, and the protocol specific to the call. Agencies may have locally approved changes or different versions; verify what applies to your service.
Special situations
Use the same rules—source, objective detail, sequence, and accuracy—when a patient refuses, an assessment is limited, or the encounter ends without transport. Follow your service’s approved workflow and local requirements.
Make clear what the patient declined (assessment, treatment, or transport); document capacity, the care offered, risks explained and understood, the patient’s decision and stated reason, alternatives discussed, and the final disposition. Follow your current local refusal protocol and agency form.
Identify the authorization path: document the base-contact physician’s name and direction when consultation is required, or identify the applicable standing-order protocol and confirm the criteria were met when that pathway is authorized for your agency by its Medical Director. Never imply that a physician was contacted when one was not.
Obtain the patient or authorized representative’s signature and a witness signature on the agency refusal form. For this class, include a witness signature whenever a witness is available; record the witness’s name and role. If the patient or witness declines or no witness is available, document that fact and follow agency procedure.
Denver Metro Protocol 0032 calls for the authorizing Base Contact physician’s name unless the standing-order pathway applies, and a signed refusal form if possible. Its documentation list does not specify a witness signature, so verify the witness requirement in your agency’s policy and form.
State which information or measurement could not be obtained, what was attempted, and the documented reason or patient response. Distinguish “not assessed,” “unable to obtain,” and “patient declined” when your ePCR allows it. None of those means “normal.”
For canceled calls, no-contact encounters, or a patient whose condition changes, document what actually happened and follow your agency’s disposition fields. For changes, place the relevant findings, times, actions, and response in sequence.
Corrections and late entries
Follow agency policy for late entries. Make clear that it is a later entry, who made it, when it was entered, what event/time it relates to, and why it was added when those details are required. Keep the added information factual and verifiable.
Read the NEMSIS PCR Data QuickGuide on amendments and retaining reports →
Privacy and field boundaries
Patient information handled by EMS organizations must be protected under applicable privacy and security requirements. HIPAA compliance depends on the organization’s policies, systems, vendors, access controls, and workflows; using a template or removing a name alone does not make a tool appropriate for real patient information.
Use fictional scenarios. Never paste a real PCR, names, dates of birth, addresses, phone numbers, incident numbers, exact locations, images, or details that could identify a patient.
Document in the agency-approved ePCR and follow agency policy. Do not use EMSCodeSim’s public practice tools to create, store, or submit real patient reports.
The AI Writing Lab sends submitted narrative text to an AI service for educational grading. Feedback can be imperfect and is not clinical or protocol review. Keep submissions fictional.
Official references: NEMSIS PCR Data QuickGuide · HHS HIPAA Security Rule summary · HHS minimum necessary guidance · CMS ambulance documentation guidance
After reviewing the report-writing, protocol, refusal, correction, and privacy sections above, mark this step complete to unlock the guided narrative.
Practice and revise
Choose a fictional call in the PCR Narrative Coach. Complete relevant sections, select chronological, SOAP, CHART, or DCHART, then check every generated sentence against the facts you entered. Remove anything unsupported.
Open the PCR Narrative Coach →Select a fictional scenario in the AI Narrative Writing Lab and write your own report. The grader supports chronological, CHART, and SOAP. The Coach also offers DCHART for template practice.
Open the AI Narrative Writing Lab →Review rubric scores, missing facts, unsupported statements, contradictions, and sentence-level feedback. Compare comments with the scenario facts, revise, and resubmit. Treat the score as coaching, not an official evaluation.
Write the same fictional call in another supported format. Check whether a reader can follow the source of each fact, timeline, care, response, and disposition.
Choose a fictional case in the AI Narrative Writing Lab. Before asking for a grade, write a complete narrative in a supported format and use the checklist below. Then compare your self-review with the AI feedback and revise only facts supported by the case.
If the grader suggests adding a fact that is not in the scenario, leave it out. Ask an instructor to review questions the AI feedback does not resolve.
The grader compares writing with the fictional scenario. It does not verify a real encounter, determine protocol compliance, or replace instructor or agency review.
Knowledge check
Answer: Attribute it: “Patient denies dizziness.” Do not add “steady gait” unless it was observed or assessed.
Answer: “Normal” is vague and cannot be checked. Record the measurements, relevant times, and changes instead of relying on a summary label.
Answer: Use a fictional scenario without patient-identifying details. Removing only a name does not necessarily make a real report appropriate to share.
Answer: None. Choose a format accepted by your agency and ensure facts are complete, objective, correctly attributed, and consistent.
Written test and completion record
After completing the guided narrative and one AI-graded narrative, answer all 10 content questions. You need at least 8 correct (80%) to pass. If you do not pass, review the material and try again. When every step is complete, select Finish class. The roster stores your name, passing test score, first AI narrative score, and completion time. It does not store your email or narrative text. Never use real patient information.
Department administrator: view or print the class roster →
Complete the AI-graded narrative before taking this test. You may submit extra narratives for practice; only the first required AI grade is recorded.
Open AI narrative grading →Ready to practice?
Start with a fictional case and focus on one improvement at a time.