Key result
Elevated monocyte distribution width linked to ~11.6-fold higher odds of post-PCI infection in AMI.
Why the study?
Infection rates in AMI patients undergoing primary PCI range from 2.4% to 16.6%. This study evaluated the association of increased monocyte distribution width (MDW) with infection occurrence and assessed MDW-based models for predicting infection risk and prolonged hospital length of stay.
Does a monocyte distribution width (MDW)-based predictive model improve the detection of newly acquired infection and prolonged length of stay compared to the C-ACS score and stress hyperglycemia ratio in patients with acute myocardial infarction undergoing primary PCI?
Cohort (n=252)
Open-label
No
Does a monocyte distribution width (MDW)-based predictive model improve the detection of newly acquired infection and prolonged length of stay compared to the C-ACS score and stress hyperglycemia ratio in patients with acute myocardial infarction undergoing primary PCI?
Incorporating monocyte distribution width (MDW) with age, qSOFA, and CRP at emergency department presentation accurately predicts post-PCI infection and prolonged hospitalization in acute myocardial infarction patients, outperforming standard C-ACS and stress hyperglycemia ratio scores.
Answers are grounded in this paper and cite their sources.
MDW may aid post-PCI infection risk stratification in AMI; hypothesis-generating and should not yet change practice.
BACKGROUND: Monocyte distribution width (MDW) may serve as an infection marker in acute myocardial infarction (AMI) patients undergoing primary percutaneous coronary intervention (PCI), where infection rates range from 2.4% to 16.6%. We evaluated the association of increased MDW levels with infection occurrence and to assess MDW-based models for predicting infection risk and prolonged hospital length of stay (LOS) ≥ 7 days. METHODS AND RESULTS: This retrospective cohort study included AMI patients undergoing PCI at a Taiwanese tertiary teaching hospital from January 1, 2020, to September 30, 2021. Logistic regression models incorporating MDW, Quick Sequential Organ Failure Assessment (qSOFA) score, age, and C-reactive protein (CRP) levels were compared to the Canada Acute Coronary Syndrome (C-ACS) score and stress hyperglycemia ratio (SHR). Among 252 patients, 12.7% developed infections, a rate that falls within the expected range. Infections were more frequent among patients with LOS ≥ 7 days (42.9% vs. 1.1%). A three-parameter model (qSOFA score ≥2, age ≥ 65, and MDW ≥ 20) demonstrated good performance for new infection (AUC: 0.834) and LOS ≥ 7 days (AUC: 0.714). Adding CRP ≥ 2 mg/dL improved predictions for infection (AUC: 0.909) and LOS ≥ 7 days (AUC: 0.798), outperforming the C-ACS score (AUC: 0.807) and SHR (AUC: 0.784). CONCLUSION: MDW emerges as a promising biomarker for assessing the risks of infection and prolonged hospital LOS in patients with AMI. Its early use may facilitate timely clinical interventions, including earlier initiation of antibiotic therapy.
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Lin et al. (2025) conducted a cohort in Acute myocardial infarction (STEMI and NSTEMI) undergoing primary percutaneous coronary intervention (n=252). Monocyte distribution width (MDW) ≥ 20 vs. Monocyte distribution width (MDW) < 20 was evaluated on Newly acquired infection during hospitalization (OR 11.57, 95% CI 5.07-26.42, p=<0.0001). Monocyte distribution width ≥ 20 strongly predicted newly acquired post-PCI infection in acute myocardial infarction patients (OR 11.57, 95% CI 5.07–26.42, P<0.0001), achieving an AUC of 0.909 in a 4-parameter model.
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