Key result
Acquired thrombocytopenia during ACS is linked to ~2.6-fold higher in-hospital mortality.
Why the study?
The incidence, severity, and prognostic significance of acquired thrombocytopenia during ACS in community practice have not been well defined.
Does the development of acquired thrombocytopenia during NSTE-ACS hospitalization increase the risk of in-hospital mortality and bleeding?
Observational (n=36,182)
Yes
Does the development of acquired thrombocytopenia during NSTE-ACS hospitalization increase the risk of in-hospital mortality and bleeding?
Even mild acquired thrombocytopenia or a ≥50% relative drop in platelet count during NSTE-ACS hospitalization is strongly associated with increased in-hospital mortality and bleeding risks.
Answers are grounded in this paper and cite their sources.
Acquired thrombocytopenia signals elevated in-hospital mortality and bleeding risk in NSTE-ACS; extends prior trial associations to community practice but leaves causal inference and interventions open.
Background— Prior studies examining thrombocytopenia among patients with acute coronary syndromes (ACS) evaluated highly selected patients in a clinical trial setting using varying definitions of thrombocytopenia. The incidence, severity, and prognostic significance of acquired thrombocytopenia during ACS in community practice have not been well defined. Methods and Results— We examined 36 182 patients with non–ST-segment elevation ACS enrolled at 379 US hospitals participating in the Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes With Early Implementation of the American College of Cardiology/American Heart Association Guidelines (CRUSADE) quality improvement initiative between June 2004 and December 2006. Patients with baseline platelet counts <150×10 9 /L were excluded. Overall, 4697 patients (13%) developed new thrombocytopenia, defined as nadir platelet count <150×10 9 /L (referenced lower limit of normal), during their ACS hospitalization. Risks of in-hospital mortality and bleeding correlated directly with severity of thrombocytopenia; even mild thrombocytopenia (nadir 100 to 149×10 9 /L) was associated with increased risks of mortality (adjusted odds ratio [OR], 2.01; 95% CI, 1.69 to 2.38) and bleeding (adjusted OR, 3.76; 95% CI, 3.43 to 4.12). Each 10% drop in platelet count was associated with increased mortality and bleeding risks (adjusted ORs, 1.39 [95% CI, 1.33 to 1.46] and 1.89 [95% CI, 1.83 to 1.95], respectively). A ≥50% drop in platelet count was associated with higher risk of adverse outcomes regardless of the nadir count. A novel combined definition of acquired thrombocytopenia—nadir <150×10 9 /L or platelet count drop ≥50%—identifies a population of ACS patients at higher risk of mortality and major bleeding (adjusted ORs, 2.58 [95% CI, 2.23 to 2.98] and 4.32 [95% CI, 3.97 to 4.70], respectively). Conclusions— Thrombocytopenia, a common complication of ACS, is associated with increased mortality and bleeding risks. Even mild thrombocytopenia or a platelet count drop ≥50% in the setting of normal nadir values is clinically significant. Application of a combined definition for thrombocytopenia using both absolute and relative thresholds permits increased sensitivity for patients at high risk of adverse outcomes.
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Wang et al. (2009) conducted an observational in Non-ST-segment elevation acute coronary syndrome (n=36,182). Acquired thrombocytopenia (combined definition: nadir <150×10^9/L or platelet drop ≥50%) vs. No acquired thrombocytopenia was evaluated on In-hospital mortality (OR 2.58, 95% CI 2.23 to 2.98). Acquired thrombocytopenia (nadir <150×10^9/L or drop ≥50%) during ACS was associated with significantly increased risks of in-hospital mortality (OR 2.58; 95% CI 2.23-2.98) and major bleeding.
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