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Published on: July 21, 2023
Microvascular Disease and Perioperative Outcomes of Non-Cardiac Surgery
Nathaniel R Smilowitz1, Gabriel Redel-Traub2, Jeffery S Berger3
1Leon H. Charney Division of Cardiology, Department of Medicine, New York University School of Medicine, New York, New York; Division of Cardiology, Department of Medicine, Veterans Affairs New York Harbor Health Care System, New York, New York.
Abstract:
Contemporary approaches to cardiovascular risk stratification before noncardiac surgery focus on macrovascular atherosclerotic disease and risk factors. We sought to determine the prevalence of microvascular disease (MVD) and its associated perioperative outcomes. Adults ≥18 years old undergoing noncardiac surgery between 2004 and 2014 were identified using the Nationwide Inpatient Sample (NIS). Prevalent MVD (retinopathy, neuropathy, and nephropathy) was identified by ICD-9 diagnosis codes. The primary outcomes were all-cause in-hospital mortality and the composite of major adverse cardiac events (MACE; death, myocardial infarction, and ischemic stroke). Multivariable logistic regression models were used to estimate associations between MVD and outcomes after adjusting for demographics and clinical covariates. Among 81,297,003 hospitalizations for noncardiac surgery, 4,236,932 (5.0%) had a diagnosis of MVD. Patients with MVD were older and more likely to have traditional cardiovascular risk factors. In-hospital perioperative MACE (4.1% vs. 1.9%; adjusted odds ratio [aOR] 1.15, 95% confidence interval [CI] 1.13 to 1.17) and mortality (2.0% vs. 1.1%; aOR 1.15, 95% CI 1.12 to 1.17) were greater in hospitalizations with MVD compared with those without. Microvascular disease was associated with postoperative outcomes in when stratified by age, sex, and coronary artery disease (CAD). Compared with surgical hospitalizations without CAD or MVD, MVD alone (aOR 1.12; 95% CI 1.11 to 1.14), CAD alone (aOR 1.44; 95% CI 1.42 to 1.46), and MVD with CAD (aOR 2.01; 95% CI 1.96 to 2.06) were associated with perioperative MACE. In conclusion, microvascular disease was present in 1 in 20 hospitalizations for noncardiac surgery, and was associated with perioperative mortality and MACE independent of macrovascular disease and traditional risk factors.
Insights
Microvascular disease (MVD) affects 5% of patients undergoing noncardiac surgery and increases perioperative mortality and major adverse cardiac events (MACE). MVD poses a significant risk independent of traditional cardiovascular factors.
Area of Science:
- Cardiology
- Vascular Medicine
- Perioperative Medicine
Background:
- Current cardiovascular risk stratification for noncardiac surgery primarily targets macrovascular atherosclerotic disease.
- The prevalence and impact of microvascular disease (MVD) on perioperative outcomes remain less understood.
Purpose of the Study:
- To determine the prevalence of MVD (retinopathy, neuropathy, nephropathy) in patients undergoing noncardiac surgery.
- To investigate the association between MVD and in-hospital mortality and major adverse cardiac events (MACE).
Main Methods:
- Retrospective analysis of adults undergoing noncardiac surgery from the Nationwide Inpatient Sample (NIS) (2004-2014).
- Identification of prevalent MVD using ICD-9 diagnosis codes.
- Multivariable logistic regression to assess the association of MVD with mortality and MACE, adjusting for covariates.
Main Results:
- Among over 81 million hospitalizations, 5.0% had a diagnosis of MVD.
- Patients with MVD had higher rates of in-hospital MACE (4.1% vs. 1.9%) and mortality (2.0% vs. 1.1%) compared to those without MVD.
- MVD was independently associated with increased perioperative MACE and mortality, even when stratified by age, sex, and coronary artery disease (CAD).
Conclusions:
- Microvascular disease is prevalent in patients undergoing noncardiac surgery and is a significant independent risk factor for adverse perioperative outcomes.
- The findings highlight the importance of considering MVD in cardiovascular risk assessment before noncardiac surgery.
- MVD, alone or in combination with CAD, substantially increases the risk of perioperative MACE.
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