In May 2013, the Rhode Island State Health Laboratories noticed an unusual pattern
of toxicology results among 10 overdose deaths of suspected illicit drug users that
had occurred during March 7–April 11, 2013. An enzyme-linked immunosorbent assay (ELISA)
for fentanyl in blood was positive for fentanyl in all 10 cases, but confirmatory
gas chromatography/mass spectrometry (GC/MS) did not detect fentanyl. The mass spectrum
was instead consistent with acetyl fentanyl, a fentanyl analog. Acetyl fentanyl, a
synthetic opioid, has not been documented in illicit drug use or overdose deaths,
and is not available as a prescription drug anywhere. Animal studies suggest that
acetyl fentanyl is up to five times more potent than heroin as an analgesic (1).
During May 14–21, 2013, CDC and Rhode Island public health officials conducted a field
investigation to determine whether this cluster of 10 deaths represented an increase
in the typical number of overdose deaths and what role might have been played by acetyl
fentanyl. Data on illicit drug (cocaine, heroin, synthetic cathinones [bath salts],
gamma-hydroxybutyric acid, and methamphetamine) overdose deaths during March 1, 2012–March
31, 2013 were abstracted from the Rhode Island Office of State Medical Examiners database
and examined using Poisson regression. Data also were abstracted from autopsy reports,
toxicology results, and medical records relating to the 10 deaths that were preliminarily
positive for acetyl fentanyl. The state health laboratories performed all toxicology
testing for acetyl fentanyl.
Investigators found that the number of illicit drug overdose deaths in Rhode Island
was significantly higher in March 2013 (21, including 10 attributed to acetyl fentanyl),
compared with the monthly average during March 2012–February 2013 (8.9, p<0.001).
During the field investigation, two additional acetyl fentanyl overdose deaths were
confirmed (dates of death: March 20 and May 16, 2013), bringing the total number of
acetyl fentanyl deaths to 12. Among the 12 acetyl fentanyl decedents, ages ranged
from 19 to 57 years, and eight were male. All but one of the deaths occurred in northern
Rhode Island: six occurred in the same small city and none in the capital city, Providence.
Evidence suggested that acetyl fentanyl was administered intravenously in at least
four (33%) of the deaths. The route of acetyl fentanyl administration was undetermined
for the remaining eight decedents.
The GC/MS toxicology results for 10 of the 12 decedents showed, in addition to acetyl
fentanyl, various mixtures of other drugs, including cocaine (58%), other opioids
(33%), ethanol (25%), and benzodiazepines (17%). None of the decedents tested positive
for fentanyl by GC/MS. Toxicology results for one decedent showed only acetyl fentanyl.
Since completion of the field investigation, two persons using acetyl fentanyl together
died on May 26, 2013, increasing the number of acetyl fentanyl deaths to 14.
Acetyl fentanyl overdose deaths have recently been confirmed in Pennsylvania (2).
If states observe clusters or increases in illicit opioid-related overdoses above
expected levels, acetyl fentanyl could be involved and confirmatory testing will be
needed. CDC encourages public health officials and laboratories, when feasible, to
use an ELISA test to screen specimens from suspected illicit, nonpharmaceutical opioid
overdose deaths. If an ELISA test is positive for fentanyl, CDC recommends laboratories
conduct confirmatory testing by GC/MS; if no fentanyl is detected by GC/MS, then fentanyl
analogs should be suspected, and subsequent testing should be considered.
Naloxone is an opioid antagonist that can reverse potentially fatal opioid-induced
respiratory depression and is used as part of the initial treatment of suspected opioid
overdose. Because of the increased potency of acetyl fentanyl, larger doses of naloxone
might be needed to achieve reversal (3); health-care providers who administer naloxone
in emergencies might consider increasing the amount they keep on hand. In addition,
expansion of community-based programs that provide opioid-overdose prevention services,
including distribution of and training in the use of naloxone, might be an effective
strategy to help reduce opioid-related overdose deaths (4).