Clustering patterns in polysubstance mortality in the United States in 2017: a multiple correspondence analysis of death certificate data

Ann Epidemiol. 2023 Jan:77:119-126. doi: 10.1016/j.annepidem.2022.03.011. Epub 2022 Apr 2.

Abstract

Purpose: The main goal of this analysis was to identify mortality patterns apparent when many drug classes are analyzed together.

Methods: The Drug Involved Mortality database is a registry of drug terms mentioned on death certificates of all drug-related deaths in the United States. Means of total number of drugs involved and percentages of specific drug combinations were calculated. Dimensionality reduction using multiple correspondence analysis and hierarchical clustering identified clusters of drugs listed on death certificates.

Results: An average of 2.4 specific drugs were listed on death certificates in 2017. For 9 of the top 10 drugs involved, over 80% of deaths involved at least one other drug. As expected, opioid drugs and psychostimulants clustered together, but other psychoactive substances (non-opioid analgesics, sedatives, antidepressants, antipsychotics) clustered together into multi-class groups. Other drugs (e.g., acetaminophen, oxymorphone) were frequently involved in polysubstance death, but did not cluster with any other specific drug. Deaths involving illicit drugs listed fewer drugs than deaths involving prescription drugs.

Conclusions: While individual drug substances might contribute to many deaths (e.g., fentanyl), polysubstance mortality is more common than single substance mortality. Multidimensional analyses integrating all drugs involved are useful to identify uncommon patterns of overdose and changing trends.

Keywords: Clustering; Drug overdose; Mortality; Multiple correspondence analysis; Polysubstance.

MeSH terms

  • Analgesics, Opioid
  • Cluster Analysis
  • Death Certificates*
  • Drug Overdose*
  • Fentanyl
  • Humans
  • United States / epidemiology

Substances

  • Analgesics, Opioid
  • Fentanyl