| name | tooluniverse-clinical-risk-scoring |
| description | Compute and interpret validated bedside clinical risk scores and pretest probabilities for an INDIVIDUAL patient — pick the right score for the scenario, gather inputs, run the deterministic calculator tool, and read the result against an interpretation table. Covers CHA2DS2-VASc (AF stroke risk), HAS-BLED (bleeding on anticoagulation), CURB-65 (pneumonia severity / admit decision), qSOFA (sepsis screen), Child-Pugh + MELD-Na (cirrhosis severity / transplant priority), Wells DVT and Wells PE (VTE pretest probability), ASCVD (10-year cardiovascular risk / statin decision), and eGFR CKD-EPI (kidney function / drug dosing). Use when asked things like "stroke risk for this AF patient", "should this patient be anticoagulated", "pneumonia severity — admit or not?", "sepsis screen this patient", "DVT/PE pretest probability", "10-year cardiovascular risk", "cirrhosis severity / MELD score", or "eGFR / kidney function". Pairs CHA2DS2-VASc with HAS-BLED to weigh anticoagulation. NOT for polygenic/genetic risk (use tooluniverse-polygenic-risk-score), NOT for population-level epidemiology/incidence (use tooluniverse-epidemiological-analysis), and NOT for diagnostic test sensitivity/specificity/likelihood-ratio math (use tooluniverse-diagnostic-test-evaluation). |
| disable-model-invocation | true |
Clinical Risk Scoring
Turn a clinical scenario into the right validated risk score, compute it with a deterministic calculator tool, and interpret the number into a clinical action. All 10 backing tools are pure-compute (no network, no API key) and return {status, data:{score, interpretation, components, ...}}.
This skill is decision-support only — see LIMITATIONS. It does not replace clinical judgment.
Step 1 — Map the scenario to the score(s)
| Clinical scenario | Score(s) | Tool(s) |
|---|
| Atrial fibrillation — stroke risk / anticoagulate? | CHA2DS2-VASc and HAS-BLED (pair) | ClinicalCalc_CHA2DS2_VASc + ClinicalCalc_HAS_BLED |
| Community-acquired pneumonia — severity / admit? | CURB-65 | ClinicalCalc_CURB_65 |
| Suspected sepsis (infection + ? deterioration) | qSOFA | ClinicalCalc_qSOFA |
| Cirrhosis / chronic liver disease severity | Child-Pugh and MELD-Na (pair) | ClinicalCalc_Child_Pugh + ClinicalCalc_MELD_Na |
| Suspected DVT — pretest probability | Wells DVT | ClinicalCalc_Wells_DVT |
| Suspected PE — pretest probability | Wells PE | ClinicalCalc_Wells_PE |
| Primary CVD prevention — 10-yr risk / statin? | ASCVD | ClinicalCalc_ASCVD_risk |
| Kidney function / renal drug dosing / CKD stage | eGFR CKD-EPI | ClinicalCalc_eGFR_CKD_EPI |
When the scenario names a pair, always run both — one alone is misleading (e.g. stroke risk without bleeding risk, or Child-Pugh without MELD-Na).
Step 2 — Gather the required inputs
Required vs optional inputs per tool (omitted booleans default to false/absent; omitted scalars are rejected when required):
| Tool | Required | Key optional booleans/values |
|---|
ClinicalCalc_CHA2DS2_VASc | age | chf, hypertension, diabetes, stroke_history(2pt), vascular_disease, female |
ClinicalCalc_HAS_BLED | age | hypertension, renal_disease, liver_disease, stroke_history, bleeding_history, labile_inr, drugs, alcohol |
ClinicalCalc_CURB_65 | age | confusion, elevated_urea(BUN>19), high_resp_rate(>=30), low_bp |
ClinicalCalc_qSOFA | (none) | high_resp_rate(>=22), altered_mentation, low_sbp(<=100) |
ClinicalCalc_Child_Pugh | bilirubin, albumin, inr | ascites(none/mild/moderate), encephalopathy(none/grade1-2/grade3-4) |
ClinicalCalc_MELD_Na | creatinine, bilirubin, inr, sodium | dialysis (forces creatinine to 4.0) |
ClinicalCalc_Wells_DVT | (none) | active_cancer, immobilization, recent_surgery, localized_tenderness, leg_swollen, calf_swelling, pitting_edema, collateral_veins, previous_dvt, alternative_diagnosis(-2) |
ClinicalCalc_Wells_PE | (none) | clinical_dvt(3), pe_most_likely(3), tachycardia(1.5), immobilization(1.5), previous_vte(1.5), hemoptysis(1), malignancy(1) |
ClinicalCalc_ASCVD_risk | age(40-79), total_cholesterol, hdl_cholesterol, systolic_bp | bp_treated, smoker, diabetes, female, race("white"/"black") |
ClinicalCalc_eGFR_CKD_EPI | creatinine, age | female |
If a required value is missing, ask the user for it — do not guess. State explicitly which booleans you assumed false.
Step 3 — Compute
tu run ClinicalCalc_CHA2DS2_VASc '{"age":76,"female":true,"hypertension":true,"diabetes":true}'
Every tool returns data.score plus a human-readable data.interpretation and a data.components breakdown (per-factor points). MELD/eGFR/ASCVD also return unit; Child-Pugh returns child_pugh_class; Wells PE returns three_tier and two_tier. Echo the components so the user can audit which factors drove the score.
Step 4 — Interpret (per-score tables)
CHA2DS2-VASc (stroke risk in AF, 0–9)
| Score | Stroke risk | Action |
|---|
| 0 (men) / 1 (women, sex point only) | Low | No anticoagulation |
| 1 (men) | Intermediate | Consider anticoagulation |
| >=2 (men) / >=3 (women) | Elevated | Oral anticoagulation recommended |
HAS-BLED (major bleeding on anticoagulation, 0–9)
| Score | Bleeding risk | Action |
|---|
| 0–2 | Low–moderate | Anticoagulation reasonable |
| >=3 | High | Caution; correct reversible factors (BP, labile INR, antiplatelet/NSAID, alcohol), closer follow-up — NOT an automatic contraindication |
How to weigh CHA2DS2-VASc + HAS-BLED together
A high HAS-BLED does not by itself withhold anticoagulation. If CHA2DS2-VASc meets the threshold, the stroke benefit usually outweighs bleeding risk; HAS-BLED instead flags modifiable risk factors to fix and patients needing closer monitoring. Only a very high, non-modifiable bleeding risk shifts the decision against anticoagulation.
CURB-65 (CAP severity, 0–5)
| Score | 30-day mortality | Disposition |
|---|
| 0–1 | Low (~1.5–3%) | Outpatient |
| 2 | Intermediate (~9%) | Short-stay / inpatient admission |
| 3–5 | High (~15–40%) | Inpatient; assess for ICU at 4–5 |
qSOFA (sepsis screen, 0–3)
| Score | Meaning |
|---|
| 0–1 | Lower risk — does not rule out sepsis; reassess |
| >=2 | Higher risk of poor outcome — escalate, full sepsis workup, consider full SOFA / lactate |
| qSOFA is a screen, not a diagnosis; a low score never excludes sepsis. | |
Child-Pugh (cirrhosis severity, class A/B/C)
| Class | Score | 1-yr survival (approx) | Meaning |
|---|
| A | 5–6 | ~100% | Well-compensated |
| B | 7–9 | ~80% | Significant functional compromise |
| C | 10–15 | ~45% | Decompensated; high surgical/anesthetic risk |
MELD-Na (90-day mortality / transplant priority, 6–40)
| MELD-Na | 90-day mortality (approx) | Transplant relevance |
|---|
| <=9 | ~2% | Low priority |
| 10–19 | ~6% | |
| 20–29 | ~20% | Rising allocation priority |
| 30–39 | ~50% | High priority |
| >=40 | >50% | Highest priority |
| Pair with Child-Pugh: Child-Pugh class anchors chronic severity / surgical risk; MELD-Na drives short-term mortality and transplant listing. | | |
Wells DVT (pretest probability)
| Score | Probability | Workup |
|---|
| <2 (esp. <=0) | DVT unlikely | D-dimer; if negative, DVT excluded |
| >=2 | DVT likely | Proceed to compression ultrasound |
Wells PE (pretest probability)
| Two-tier | Three-tier | Workup |
|---|
| PE unlikely (<=4) | low (0–1) / moderate (2–6) | D-dimer; if negative, PE excluded (consider PERC if very low) |
| PE likely (>4) | high (>6) | CT pulmonary angiography (D-dimer not sufficient to exclude) |
ASCVD 10-year risk (%)
| Risk % | Category | Statin guidance (with shared decision-making) |
|---|
| <5% | Low | Lifestyle |
| 5–7.4% | Borderline | Consider if risk-enhancers present |
| 7.5–19.9% | Intermediate | Moderate-intensity statin reasonable |
| >=20% | High | High-intensity statin |
eGFR CKD-EPI (mL/min/1.73m^2) → CKD stage
| eGFR | Stage | Note |
|---|
| >=90 | G1 | Normal (CKD only if other markers of damage) |
| 60–89 | G2 | Mildly decreased |
| 45–59 | G3a | Mild–moderate |
| 30–44 | G3b | Moderate–severe |
| 15–29 | G4 | Severe — nephrology referral |
| <15 | G5 | Kidney failure |
| Use eGFR for renal drug dosing and CKD staging; a single value is an estimate — confirm with a repeat/eGFR trend for staging. | | |
Worked example A — Atrial fibrillation, weigh anticoagulation (paired)
76-year-old woman with AF, hypertension, type 2 diabetes; on an NSAID; no prior stroke/bleed, BP controlled, stable INR.
tu run ClinicalCalc_CHA2DS2_VASc '{"age":76,"female":true,"hypertension":true,"diabetes":true}'
tu run ClinicalCalc_HAS_BLED '{"age":76,"hypertension":true,"drugs":true}'
Interpretation. CHA2DS2-VASc 5 (>=3 for a woman) → anticoagulation recommended. HAS-BLED 3 is high but driven by modifiable factors: stop the NSAID and control BP and 2 of the 3 points disappear, lowering bleeding risk. The high HAS-BLED does not cancel anticoagulation — it directs you to fix reversible risks and monitor more closely.
Worked example B — Cirrhosis severity and transplant priority (paired)
Cirrhotic patient: bilirubin 3.5 mg/dL, albumin 2.5 g/dL, INR 2.4, moderate ascites, grade 1–2 encephalopathy; creatinine 2.0, sodium 128, not on dialysis.
tu run ClinicalCalc_Child_Pugh '{"bilirubin":3.5,"albumin":2.5,"inr":2.4,"ascites":"moderate","encephalopathy":"grade1-2"}'
tu run ClinicalCalc_MELD_Na '{"creatinine":2.0,"bilirubin":5.0,"inr":2.0,"sodium":128,"dialysis":false}'
Interpretation. Child-Pugh class C (14) = decompensated cirrhosis, very high surgical/anesthetic risk — avoid elective surgery. MELD-Na 31 implies roughly a third-or-higher 90-day mortality and a high transplant-allocation priority. Together they justify urgent hepatology / transplant evaluation. (Note MELD uses bilirubin 5.0 and INR 2.0 from this patient's labs; lower bounds of 1.0 are applied internally.)
Completeness checklist
LIMITATIONS
- Decision-support only. These scores inform, but do not replace, clinical judgment and the full clinical picture. Do not present output as a treatment directive.
- Validated populations. Each score was derived/validated in specific cohorts and may not transfer to children, pregnancy, valvular AF (CHA2DS2-VASc is for non-valvular AF), or other excluded groups.
- ASCVD Pooled Cohort Equations are validated only for ages 40–79 and the White / African-American coefficient sets; they can mis-estimate for other ancestries and are for primary prevention (no prior ASCVD event).
- eGFR CKD-EPI assumes stable kidney function (steady-state creatinine); it is unreliable in acute kidney injury, extremes of muscle mass, or amputees, and a single value does not stage CKD on its own.
- qSOFA / CURB-65 / Wells are screening / pretest-probability tools — a reassuring score does not exclude the diagnosis; combine with clinical gestalt and confirmatory testing.
- MELD-Na / Child-Pugh apply to chronic liver disease; they do not capture acute liver failure or hepatocellular-carcinoma exception points.
- Inputs are taken at face value — garbage in, garbage out. Verify lab units (mg/dL vs mmol/L, BUN vs urea) before entry.
- Not a substitute for institutional protocols, guideline updates, or specialist consultation.