mcpbeat

Cohort Compare

nvidia/cohort-compare

Analyze a cohort of patients from FHIR endpoints to find care gaps and patterns. Use when asked to compare patients, find quality gaps, or analyze a population.

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Install

one command, takes just this skill from the repository
npx skills add https://github.com/NVIDIA/dgx-spark-playbooks --skill cohort-compare

The instruction itself

4 sections, as written by the author

Analyze a patient cohort: $ARGUMENTS

Use your fhir-basics skill to query FHIR endpoints. Use your clinical-knowledge skill to identify care gaps and apply correct thresholds. Use your analysis-methods skill to write correct Python analysis code.

Execution Rules

  • Do NOT explore the workspace or list files. Begin the analysis immediately.
  • Write ONE Python script that does everything: FHIR queries, analysis, chart, and summary.
  • Write the script correctly the first time. Do NOT write a draft and then edit it.
  • Run it with python (NOT python3).
  • All HTTP calls must use subprocess.run(["curl", "-sf", "--max-time", "30", url], capture_output=True, text=True) -- the requests library does NOT work through the sandbox proxy. See the fhir-basics skill for the fhir_get helper pattern.
  • Save the script to /tmp/<name>.py, run it once, interpret the output.

Steps

  • Identify the cohort -- Query GET /Condition?code={snomed_code}&_count=200 and follow pagination links to get all matching Condition resources. Extract unique patient IDs from entry[].resource.subject.reference. Report the cohort size.
  • Pull clinical data in BATCHED queries (do NOT loop per-patient):
  • Lab values: Use get_latest_labs_batch(loinc_code, patient_ids) to fetch ALL observations for the LOINC code in one call and filter client-side. This queries GET /Observation?code={loinc_code}&_count=500&_sort=-date without a patient filter, then builds a dict keyed by patient ID. Handle both valueQuantity (numeric) and valueString (text) formats. For blood pressure, query the BP panel code 85354-9 in batch and parse components.
  • Medications: Use get_all_medications_batch(patient_ids) to fetch GET /MedicationRequest?status=active&_count=500 in one call, then filter to cohort patients client-side.
  • NEVER write a for pid in patient_ids: loop that makes FHIR HTTP calls inside the loop. The sandbox proxy adds 1-3s latency per call. With 24 patients x 4 LOINC codes = 96 calls = 5+ minutes. Batching brings this to 4-6 total calls = 30 seconds.
  • Build a pandas DataFrame with one row per patient:
  • patient_id (string)
  • {lab_name} (float or None)
  • lab_date (string)
  • on_target_med (boolean -- True if the patient is on the specified medication class)
  • medications (comma-separated string of all active med names)
  • med_count (int)
  • Data quality check:
  • Report how many patients have the lab recorded vs. missing
  • If > 30% missing, flag as a data quality issue but continue analysis
  • If < 5 patients have data, warn that the sample is too small for meaningful statistics
  • Identify care gap patients: Apply the threshold and medication check:
  • Gap = lab value exceeds threshold AND patient is NOT on the specified medication class
  • Report: total with condition, total with lab data, total above threshold, total in care gap
  • Compute gap rate as percentage of patients with lab data (not total cohort)
  • Generate visualization:
  • Histogram of the lab value distribution with threshold line
  • Use NVIDIA dark theme: plt.style.use('dark_background'), primary color #76B900, background #1a1a1a
  • Annotate with sample size (N = ...) and gap count
  • Save as PNG with dpi=150
  • Write a plain-English summary including:
  • Cohort size and data completeness
  • Distribution statistics (mean, median, range)
  • Gap patient count and percentage with absolute numbers
  • Comparison to relevant CMS quality measure if applicable
  • Any notable patterns (e.g., "All gap patients had no medications recorded at all")
  • Disclaimer: "This analysis is for research and operational purposes. Clinical decisions should be made by qualified clinicians."

Example: Diabetes Gap Analysis (CMS122)

Condition: Type 2 Diabetes (SNOMED 44054006)

Lab: HbA1c (LOINC 4548-4)

Threshold: > 9.0%

Gap medication: insulin or GLP-1 agonist

Quality measure: CMS122v12 (poor glycemic control)

INSULIN_AND_GLP1 = ["insulin", "liraglutide", "semaglutide", "dulaglutide",
                     "exenatide", "tirzepatide", "victoza", "ozempic",
                     "trulicity", "byetta", "mounjaro", "rybelsus"]

def is_on_insulin_or_glp1(med_list):
    med_lower = [m.lower() for m in med_list]
    return any(drug in med_text for drug in INSULIN_AND_GLP1 for med_text in med_lower)

Example: Hypertension Gap Analysis (CMS165)

Condition: Essential Hypertension (SNOMED 38341003)

Lab: Systolic BP (LOINC 8480-6) -- use component Observation pattern

Threshold: >= 140 mmHg

Gap medication: any antihypertensive

Quality measure: CMS165v12 (controlling high blood pressure)

Note: Use get_latest_bp() from the analysis-methods skill to handle both BP panel (85354-9) and standalone systolic Observations.

ANTIHYPERTENSIVES = ["lisinopril", "enalapril", "ramipril", "benazepril",
    "losartan", "valsartan", "irbesartan", "olmesartan", "telmisartan",
    "amlodipine", "nifedipine", "diltiazem",
    "metoprolol", "atenolol", "carvedilol", "bisoprolol",
    "hydrochlorothiazide", "hctz", "chlorthalidone",
    "furosemide", "spironolactone"]

def is_on_antihypertensive(med_list):
    med_lower = [m.lower() for m in med_list]
    return any(drug in med_text for drug in ANTIHYPERTENSIVES for med_text in med_lower)

How to use it

Copy the folder

Take nvidia/cohort-compare from the repository into ~/.claude/skills for personal use, or into .claude/skills inside a project.

Check the name does not clash

The agent identifies a skill by the name field in its header. Two skills with the same name cannot sit side by side — one of them will be ignored.