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  4. /San Francisco Syncope Rule

San Francisco Syncope Rule

Calculator

Results

Enter values to see results

CHESS Criteria Met

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Risk Assessment

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Results

Enter values to see results

CHESS Criteria Met

—

Risk Assessment

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The San Francisco Syncope Rule (SFSR) is a clinical decision tool developed to identify emergency department patients presenting with syncope who are at risk for serious outcomes within 30 days. Published by Quinn et al. in 2004, the SFSR was designed to safely identify low-risk patients who could be discharged without extensive workup while flagging those requiring further evaluation.

Syncope accounts for approximately 1-3% of all emergency department visits. While most episodes are benign (vasovagal, orthostatic), approximately 10% of patients will experience a serious outcome within 30 days, including death, myocardial infarction, arrhythmia, pulmonary embolism, stroke, subarachnoid hemorrhage, significant hemorrhage, or need for a procedure.

The SFSR uses the mnemonic CHESS: Congestive heart failure history, Hematocrit less than 30%, abnormal ECG (new changes or non-sinus rhythm), complaint of Shortness of breath, and Systolic blood pressure less than 90 mmHg at triage. If none of these criteria are present, the patient is classified as low risk.

CHF captures patients with cardiac dysfunction at elevated risk for arrhythmias. Hematocrit below 30% identifies significant anemia possibly from occult hemorrhage. Abnormal ECG findings may indicate cardiac pathology. Shortness of breath suggests pulmonary pathology or cardiac decompensation. Hypotension indicates hemodynamic instability requiring investigation.

The original validation reported 96% sensitivity and 62% specificity for serious 30-day outcomes. Subsequent external validations show sensitivity ranging from 74-98%. Despite variations, the SFSR remains valuable when combined with clinical judgment.

The rule is designed as a screening tool to identify patients who can safely be discharged, not as a standalone diagnostic instrument. Patients meeting no CHESS criteria have approximately a 2% serious event rate, supporting discharge with appropriate follow-up. Any positive criterion warrants further evaluation.

It is important to note that the SFSR was validated for true syncope (transient loss of consciousness with spontaneous recovery), not for near-syncope or presyncope. Patients with ongoing symptoms, trauma from the syncopal episode, or clear neurological deficits require evaluation regardless of CHESS criteria.

This calculator evaluates all five CHESS criteria and provides a binary risk classification with the number of positive criteria to guide clinical decision-making in the evaluation of syncope patients.

How It Works

Evaluate five CHESS criteria: CHF history, Hematocrit <30%, ECG abnormalities, Shortness of breath, Systolic BP <90. All negative = low risk. Any positive = high risk requiring further workup.

Understanding Your Results

0/5 criteria: Low risk (~2% serious outcome rate); consider discharge with follow-up. 1+/5 criteria: High risk; cardiac monitoring, echocardiography, and potential admission recommended.

Worked Examples

Low-Risk Patient

Inputs

chf0
hct0
ecg0
sob0
sbplow0

Results

count0
riskLow risk - consider discharge (2% serious event rate)

No CHESS criteria met; safe for discharge consideration.

High-Risk Patient

Inputs

chf1
hct0
ecg1
sob0
sbplow0

Results

count2
riskHigh risk - further workup recommended

CHF + abnormal ECG: suggests cardiac etiology requiring admission.

Frequently Asked Questions

A clinical decision tool using five CHESS criteria to identify syncope patients at risk for serious 30-day outcomes.

CHF, Hematocrit <30%, ECG abnormal, Shortness of breath, Systolic BP <90 mmHg.

Death, MI, arrhythmia, PE, stroke, SAH, hemorrhage, or need for procedure within 30 days.

Original study: 96% sensitivity. External validations: 74-98% depending on population.

Patients with no CHESS criteria have ~2% event rate, supporting discharge with follow-up.

Any new changes, non-sinus rhythm, or findings suggesting acute cardiac pathology.

Validated for true syncope only. Near-syncope applicability is less established.

Yes, any single positive CHESS criterion classifies as high risk.

1-3% of ED visits, with ~10% having a serious outcome within 30 days.

Quinn et al., University of California San Francisco, published 2004.

Sources & Methodology

Quinn JV, et al. Ann Emerg Med. 2004;43(2):224-232. Quinn JV, et al. Prospective validation. Ann Emerg Med. 2006;47(5):448-454.
R

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