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      Trends in Suspected Opioid Overdoses from Emergency Departments in 11 States and DC

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          Objective This presentation will provide insight into how the extensive spread of illicitly-manufactured fentanyl impacted opioid overdose rates throughout the Midwest and neighboring states. Introduction Recent reporting using data from CDC’s National Syndromic Surveillance Program indicates that rates of emergency department (ED) visits involving suspected opioid overdoses increased by 70% in the Midwest from the third quarter (Q3) 2016 (July–September) to the Q3 2017. Large increases in the use and distribution of illicitly-manufactured fentanyl (IMF) and fentanyl analogs, are a key factor driving increased opioid overdose rates in the Midwest and east of the Mississippi River. Fentanyl is a synthetic opioid 50–100 times more potent than morphine. A better understanding of the distribution of changes in opioid overdose rate from Q3 2016 to Q3 2017 within states needed to inform response and prevention efforts. Methods The CDC’s Enhanced State Opioid Overdose Surveillance Program currently funds 32 states and Washington DC to increase timeliness of opioid overdose reporting and detect rapid changes in trends. Data from nine states (IL, MD, MO, NC, OH, PA, VA, WI, WV) were analyzed. Midwest states sharing subregional data with CDC were selected to better understand geographic and temporal patterns driving previously reported increases in ED visits involving suspected opioid overdoses from Q3 2016 through Q3 2017. Bordering states (MD, NC, PA, VA, WV) sharing subregional data with CDC were also included to determine trends in states contiguous to the Midwest. State subregions were defined using publicly available state government sources in consultation with state public health departments and were mainly divided by public health districts. . Fifty of 56 possible state subregions across 9 states met two inclusion criteria: 1) reported 25 opioid overdose ED visits per quarter and 2) did not report a change of 50% between any two quarters. Opioid overdoses were defined according to jurisdictional and national definitions that included searches of chief complaint text (e.g., searching for words “opioid” and “overdose”) and ICD-10-CM diagnostic/billing codes. State subregional rates were defined as number of opioid overdoses divided by the total number of ED visits in the state subregion, multiplied by 10,000. Quarterly and yearly percent change in opioid overdose ED visits from Q3 2016 to Q3 2017 were described with a focus on high burden subregions reporting large yearly increases of 25% from Q3 2016 to Q3 2017. We categorized a subregion as having an opioid overdose outbreak when at least one quarterly rate increase in opioid overdoses of 50% occurred. Results Over 7 million ED visits were reported each quarter. Average subregional opioid overdose rates increased at a consistent quarterly rate of between 16% - 19% during Q3 2016 to Q2 2017. From Q2 2017 to Q3 2017, opioid overdose rates only increased 1%. Overall, subregions reported a mean yearly increase in opioid overdose rates of 51% from Q3 2016 to Q3 2017. This yearly increase in opioid overdose from Q3 2016 to Q3 2017 was unequally distributed across subregions with 9 (18%) of subregions reporting an increase in opioid overdose rates of 100%, 13 (26%) reporting an increase of 50% - <100%, 7 (14%) reporting an increase of 25% - <50%, 13 (26%) reporting an increases of 0% to <25%, and 8 (16%) reporting a decrease. Analyses of the 29 high burden subregions found that 16 (55%) reported at least one opioid overdose outbreak compared to 3 of 21 other subregions (14%) (Table 1). The 16 high burden subregions that reported any outbreak had a mean yearly increase in opioid overdose rates from Q3 2016 to Q3 2017 of 107%, range 33% to 266%. Eight of these 16 high burden subregions either reported two opioid overdose outbreaks or an opioid overdose outbreak and a quarterly increase of between 25% - <50%. All states had at least one subregion report an opioid overdose outbreak between Q3 2016 to Q2 2017. Also, within OH, PA, WI, and WV, half or more of their subregions reported an outbreak between Q3 2016 and Q3 2017 (Table 1). Fifteen of the 22 (68%) quarterly opioid overdose outbreaks occurred either during Q4 2016 or Q1 2017 (Table 1). Across all outbreaks, state subregions reported a mean quarterly increase of 83% with a range from 50 - 156%. Table 1 Number and percent of opioid overdose outbreaks by quarter, high burden subregions, and state: 9 states July 2016 to September 2017 Conclusions Opioid overdose outbreaks in a subset of 16 high burden subregions across all 9 states were a key factor driving increases in the states’ opioid overdose rates. Half of these 16 subregions experienced a single opioid overdose outbreak while the other half experienced two or more sharp increases. The majority of opioid overdose outbreaks occurred during October 2016 to March 2017 were concentrated in Ohio, a state reporting extremely large increase in IMF supply and overdose deaths involving fentanyl, and states contiguous with Ohio. Although most subregions reported outbreaks at the beginning of the study period, higher opioid overdose rates persisted in the vast majority of subregions reporting opioid overdose outbreaks. This outbreak pattern is consistent with previous findings showing large increases in the supply of IMF and fentanyl analogs, including carfentanil, in Midwestern states during 2016 and in early 2017. Although opioid overdose outbreaks were concentrated in subregions in OH, PA, and WV, all 9 states included in the analysis were impacted by at least one outbreak during the study period. Findings highlight the need for targeting of hotspots within states and implementation of public health interventions to reduce harm and surge resources during an outbreak. These short-term efforts, however, must be complemented by a sustained response to reduce increased drug overdose rates that persist after an initial outbreak. A key limitation of this study was that it only included data from a single year and as a result may underestimate the length and severity of outbreaks. As changes in the illicit opioid market continue, surveillance of local outbreaks must be supplemented by broader surveillance designed to detect both localized introduction of new novel psychoactive substances as well as large scale changes in the illicit opioid market.

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          Deaths Involving Fentanyl, Fentanyl Analogs, and U-47700 — 10 States, July–December 2016

          Preliminary estimates of U.S. drug overdose deaths exceeded 60,000 in 2016 and were partially driven by a fivefold increase in overdose deaths involving synthetic opioids (excluding methadone), from 3,105 in 2013 to approximately 20,000 in 2016 ( 1 , 2 ). Illicitly manufactured fentanyl, a synthetic opioid 50–100 times more potent than morphine, is primarily responsible for this rapid increase ( 3 , 4 ). In addition, fentanyl analogs such as acetylfentanyl, furanylfentanyl, and carfentanil are being detected increasingly in overdose deaths ( 5 , 6 ) and the illicit opioid drug supply ( 7 ). Carfentanil is estimated to be 10,000 times more potent than morphine ( 8 ). Estimates of the potency of acetylfentanyl and furanylfentanyl vary but suggest that they are less potent than fentanyl ( 9 ). Estimates of relative potency have some uncertainty because illicit fentanyl analog potency has not been evaluated in humans. This report describes opioid overdose deaths during July–December 2016 that tested positive for fentanyl, fentanyl analogs, or U-47700, an illicit synthetic opioid, in 10 states participating in CDC’s Enhanced State Opioid Overdose Surveillance (ESOOS) program.* Fentanyl analogs are similar in chemical structure to fentanyl but not routinely detected because specialized toxicology testing is required. Fentanyl was detected in at least half of opioid overdose deaths in seven of 10 states, and 57% of fentanyl-involved deaths also tested positive for other illicit drugs, such as heroin. Fentanyl analogs were present in >10% of opioid overdose deaths in four states, with carfentanil, furanylfentanyl, and acetylfentanyl identified most frequently. Expanded surveillance for opioid overdoses, including testing for fentanyl and fentanyl analogs, assists in tracking the rapidly changing illicit opioid market and informing innovative interventions designed to reduce opioid overdose deaths. The 10 states † reporting data abstracted information from preliminary death certificates and medical examiner/coroner reports on unintentional and undetermined opioid overdose deaths using standard definitions for variables. Data were entered into the State Unintentional Drug Overdose Reporting System (SUDORS), the component of ESOOS designed for tracking fatal opioid overdoses. § For each death, available data on demographic characteristics, circumstances of the overdose collected from death scene investigations (e.g., evidence of illicit drug use), and results of forensic toxicology testing were entered into SUDORS. Opioid overdose deaths occurring during July–December 2016 with positive test results for fentanyl, fentanyl analogs, and U-47700 in 10 states are described, and key demographic and overdose circumstance factors are stratified by substance. Full toxicology findings of decedents were reviewed, including the presence of heroin, cocaine, and methamphetamine. Because heroin involvement in overdose deaths is difficult to distinguish from prescription morphine, deaths in which heroin was confirmed by toxicologic findings were combined with deaths in which heroin was suspected because morphine was detected and death scene evidence suggested heroin use. ¶ The use of medical examiner/coroner reports, previously unavailable across states, provides unique insights into specific substances and circumstances associated with overdoses, which can inform interventions. Fentanyl was detected in 56.3% of 5,152 opioid overdose deaths in the 10 states during July–December 2016 (Figure). Among these 2,903 fentanyl-positive deaths, fentanyl was determined to be a cause of death by the medical examiner or coroner in nearly all (97.1%) of the deaths. Northeastern states (Maine, Massachusetts, New Hampshire, and Rhode Island) and Missouri** reported the highest percentages of opioid overdose deaths involving fentanyl (approximately 60%–90%), followed by Midwestern and Southern states (Ohio, West Virginia, and Wisconsin), where approximately 30%–55% of decedents tested positive for fentanyl. New Mexico and Oklahoma reported the lowest percentage of fentanyl-involved deaths (approximately 15%–25%). In contrast, states detecting any fentanyl analogs in >10% of opioid overdose deaths were spread across the Northeast (Maine, 28.6%, New Hampshire, 12.2%), Midwest (Ohio, 26.0%), and South (West Virginia, 20.1%) (Figure) (Table 1). FIGURE Percentage of opioid overdose deaths testing positive for fentanyl and fentanyl analogs, by state — 10 states, July–December 2016 The figure above is a bar chart showing the percentage of opioid overdose deaths testing positive for fentanyl and fentanyl analogs in 10 states, during July–December 2016. TABLE 1 Number and percentage of opioid overdose decedents testing positive for fentanyl analogs and U-47700 — 10 states, July–December 2016 State Total opioid overdose deaths Any fentanyl analog present* No. (%) Fentanyl analogs U-47700 synthetic opioid No. (%) Carfentanil No. (%) Furanylfentanyl No. (%) Acetylfentanyl No. (%) Other† No. (%) Total§ 5,152 720 (14.0) 389 (7.6) 182 (3.5) 147 (2.9) 74 (1.4) 40 (0.8) Maine 154 44 (28.6) 0 25 (16.2) 17 (11.0) 5 (3.3) — Massachusetts 1,071 17 (1.6) 0 10 (0.9) —¶ — — New Hampshire 131 16 (12.2) 0 — 13 (9.9) 0 — New Mexico 166 11 (6.6) 0 — 7 (4.2) 0 — Ohio 2,043 531 (26.0) 354 (17.3) 85 (4.2) 91 (4.5) 40 (2.0) 15 (0.7) West Virginia 393 79 (20.1) 35 (8.9) 44 (11.2) 6 (1.5) 23 (5.9) 7 (1.8) Wisconsin 413 14 (3.4) 0 6 (1.5) 5 (1.2) — 5 (1.2) Other three states** 781 8 (1.0) 0 — — — — * Individual fentanyl analog deaths might sum to a number greater than the number of deaths with any fentanyl analog present because more than one fentanyl analog could be present in an opioid overdose death. † Includes 3-methylfentanyl, acrylfentanyl, butyrylfentanyl, para-fluorofentanyl (or 4-fluorofentanyl), para-fluorobutyrylfentanyl (or 4-fluorobutyrylfentanyl), and para-fluoroisobutyrylfentanyl (or 4-fluoroisobutyrylfentanyl). § Data from 10 states included in the total numbers; individual states presented if five or more deaths tested positive for any fentanyl analog. ¶ Five or more deaths tested positive for acetylfentanyl in Massachusetts, but the number was suppressed to prevent calculation of number for other states, which was less than five. ** Missouri (22 counties), Oklahoma, and Rhode Island. Fentanyl analogs were present in 720 (14.0%) opioid overdose deaths, with the most common being carfentanil (389 deaths, 7.6%), furanylfentanyl (182, 3.5%), and acetylfentanyl (147, 2.9%) (Table 1). Fentanyl analogs contributed to death in 535 of the 573 (93.4%) decedents. Cause of death was not available for fentanyl analogs in 147 deaths. †† Five or more deaths involving carfentanil occurred in two states (Ohio and West Virginia), furanylfentanyl in five states (Maine, Massachusetts, Ohio, West Virginia, and Wisconsin), and acetylfentanyl in seven states (Maine, Massachusetts, New Hampshire, New Mexico, Ohio, West Virginia, and Wisconsin). U-47700 was present in 0.8% of deaths and found in five or more deaths only in Ohio, West Virginia, and Wisconsin (Table 1). Demographic characteristics of decedents were similar among overdose deaths involving fentanyl analogs and fentanyl (Table 2). Most were male (71.7% fentanyl and 72.2% fentanyl analogs), non-Hispanic white (81.3% fentanyl and 83.6% fentanyl analogs), and aged 25–44 years (58.4% fentanyl and 60.0% fentanyl analogs) (Table 2). TABLE 2 Demographic characteristics and overdose circumstance factors for decedents in opioid overdose deaths involving fentanyl, fentanyl analogs, and U-47700, by substance — 10 states, July–December 2016 Characteristic Fentanyl (N = 2,903) Any fentanyl analog* (N = 720) Fentanyl analogs U-47700 synthetic opioid (N = 40) Carfentanil (N = 389) Furanylfentanyl (N = 182) Acetylfentanyl (N = 147) Other†(N = 74) No. (%) No. (%) No. (%) No. (%) No. (%) No. (%) No. (%) Age group (yrs) § 15–24 276 (9.5) 63 (8.8) 31 (8.0) —¶ 15 (10.2) — — 25–34 926 (31.9) 220 (30.6) 124 (31.9) 50 (27.5) 46 (31.3) 27 (36.5) 19 (47.5) 35–44 768 (26.5) 212 (29.4) 103 (26.5) 61 (33.5) 48 (32.7) 22 (29.7) 6 (15.0) 45–54 540 (18.6) 133 (18.5) 73 (18.8) 32 (17.6) 26 (17.7) 9 (12.2) 6 (15.0) 55–64 343 (11.8) 77 (10.7) 50 (12.9) 18 (9.9) — 8 (10.8) — ≥65 47 (1.6) 15 (2.1) 8 (2.1) — — — 0 Median age (IQR) in yrs 37 (29–48) 38 (30–48) 39 (30–49) 38 (31–47) 36 (30–45) 36 (29–46) 32 (27–43) Sex Male 2,080 (71.7) 520 (72.2) 276 (71.0) 134 (73.6) 111 (75.5) 49 (66.2) 32 (80.0) Female 820 (28.2) 200 (27.8) 113 (29.0) 48 (26.4) 36 (24.5) 25 (33.8) 8 (20.0) Race and Hispanic origin White, non-Hispanic 2,360 (81.3) 602 (83.6) 340 (87.4) 148 (81.3) 120 (81.6) 62 (83.8) 36 (90.0) Black, non-Hispanic 274 (9.4) 75 (10.4) 42 (10.8) 17 (9.3) 9 (6.1) 9 (12.2) — Other, non-Hispanic 37 (1.3) 9 (1.3) — — — — — Hispanic 189 (6.5) 20 (2.8) — — — — 0 Other fentanyl(s) present Fentanyl or other fentanyl analog n/a 330 (45.8) 120 (30.9) 93 (51.1) 143 (97.3) 46 (62.2) 24 (60.0) Fentanyl n/a 299 (41.5) 105 (27.0) 62 (34.1) 139 (94.6) 31 (41.9) 16 (40.0) 1 fentanyl analog present** 263 (9.1) 653 (90.7) 352 (90.5) 129 (70.9) 129 (87.8) 43 (58.1) 12 (30.0) ≥2 fentanyl analogs present 36 (1.2) 67 (9.3) 37 (9.5) 53 (29.1) 18 (12.2) 31 (41.9) 6 (15.0) 4-ANPP †† 60 (2.1) 82 (11.4) — 77 (42.3) — 13 (17.6) 8 (20.0) Other illicit drugs present Any illicit drugs 1,656 (57.0) 369 (51.3) 190 (48.8) 91 (50.0) 91 (61.9) 42 (56.8) 15 (37.5) Suspected/Confirmed heroin§§ 1,132 (39.0) 250 (34.7) 123 (31.6) 60 (33.0) 75 (51.0) 26 (35.1) 11 (27.5) Cocaine 1,011 (34.8) 202 (28.1) 99 (25.4) 52 (28.6) 43 (29.3) 26 (35.1) 7 (17.5) Methamphetamine 167 (5.8) 64 (8.9) 43 (11.1) 12 (6.6) 10 (6.8) — — Evidence of injection 1,358 (46.8) 303 (42.1) 151 (38.8) 76 (41.8) 81 (55.1) 35 (47.3) 19 (47.5) No evidence of injection but evidence of other route ¶¶ 532 (18.3) 138 (19.2) 85 (21.9) 33 (18.1) 19 (12.9) 10 (13.5) 11 (27.5) Evidence of snorting 279 (52.4) 95 (68.8) 57 (67.1) 21 (63.6) 15 (78.9) 9 (90.0) 8 (72.7) Evidence of ingestion 203 (38.2) 41 (29.7) 27 (31.8) 8 (24.2) 7 (36.8) — — Evidence of smoking 95 (17.9) 25 (18.1) 16 (18.8) 7 (21.2) — — — Evidence of transdermal 35 (6.6) — — 0 — 0 0 Evidence of sublingual 6 (1.1) — — 0 0 0 0 No evidence of route 1,013 (34.9) 279 (38.8) 153 (39.3) 73 (40.1) 47 (32.0) 29 (39.2) 10 (25.0) Abbreviation: n/a = not applicable. * Individual fentanyl analog deaths might sum to a number greater than the number of deaths with any fentanyl analog present because more than one fentanyl analog could be present in an opioid overdose death. † Includes 3-methylfentanyl, acrylfentanyl, butyrylfentanyl, para-fluorofentanyl (or 4-fluorofentanyl), para-fluorobutyrylfentanyl (or 4-fluorobutyrylfentanyl), and para-fluoroisobutyrylfentanyl (or 4-fluoroisobutyrylfentanyl). § Fewer than five persons aged ≤14 years died of an overdose that tested positive for a fentanyl analog. ¶ Data suppressed because fewer than five deaths, or suppressed to prohibit calculation of other suppressed cell. ** For fentanyl analogs, indicates no other analog present. †† Despropionylfentanyl is a fentanyl compound that can serve as a marker for illicitly manufactured fentanyl and fentanyl analogs because it is both a precursor and a metabolite of these illicit products (but not pharmaceutical fentanyl), while having low metabolic activity that does not contribute to overdose toxicity. Despropionylfentanyl is also known as 4-anilino-N-phenethylpiperidine, or 4-ANPP. §§ Includes decedents testing positive for heroin metabolite 6-acetylmorphine, plus decedents testing positive for morphine where there was a history of heroin use, death scene evidence of illicit drug use, or evidence of injection, and no scene evidence of prescription drug use or other evidence of prescription morphine. ¶¶ Percentage of deaths with evidence of routes of administration other than injection calculated out of the number of deaths in this row. Other illicit drugs co-occurred in 57.0% and 51.3% of deaths involving fentanyl and fentanyl analogs, respectively, with cocaine and confirmed or suspected heroin detected in a substantial percentage of deaths (Table 2). Nearly half (45.8%) of deaths involving fentanyl analogs tested positive for two or more analogs or fentanyl, or both. Specifically, 30.9%, 51.1%, and 97.3% of deaths involving carfentanil, furanylfentanyl, and acetylfentanyl, respectively, tested positive for fentanyl or additional fentanyl analogs. Forensic investigations found evidence of injection drug use in 46.8% and 42.1% of overdose deaths involving fentanyl and fentanyl analogs, respectively. Approximately one in five deaths involving fentanyl and fentanyl analogs had no evidence of injection drug use but did have evidence of other routes of administration. Among these deaths, snorting (52.4% fentanyl and 68.8% fentanyl analogs) and ingestion (38.2% fentanyl and 29.7% fentanyl analogs) were most common. Although rare, transdermal administration was found among deaths involving fentanyl (1.2%), likely indicating pharmaceutical fentanyl (Table 2). More than one third of deaths had no evidence of route of administration. Discussion This analysis of opioid overdose deaths in 10 states participating in the ESOOS program found that illicitly manufactured fentanyl is a key factor driving opioid overdose deaths and that fentanyl analogs are increasingly contributing to a complex illicit opioid market with significant public health implications. Previous reports have indicated that use of illicitly manufactured fentanyl mixed with heroin, with and without users’ knowledge, is driving many fentanyl overdoses, particularly east of the Mississippi River ( 3 , 4 ). Consistent with these findings, at least half of opioid overdose deaths in six of the seven participating states east of the Mississippi tested positive for fentanyl. Over half the overdose deaths involving fentanyl and fentanyl analogs tested positive for confirmed or suspected heroin (the most commonly detected illicit substance), cocaine, or methamphetamine. This supports findings from other reports indicating that fentanyl and fentanyl analogs are commonly used with or mixed with heroin or cocaine ( 3 , 4 ). Nearly half of overdose deaths involving fentanyl and fentanyl analogs, however, did not test positive for other illicit opioids, suggesting that fentanyl and fentanyl analogs might be emerging as unique illicit products. Fentanyl and fentanyl analogs are highly potent and fast-acting synthetic compounds that can trigger rapid progression to loss of consciousness and death and thus might require immediate treatment and high doses of naloxone ( 5 ). Because of the potency of fentanyl and fentanyl analogs and the rapid onset of action, these drugs were determined by medical examiners and coroners to play a causal role in almost all fatal opioid overdoses in which they were detected. Injection, the most commonly reported route of administration in fatal overdoses, exacerbates these risks because of rapid absorption and high bioavailability. The high potency of fentanyl and fentanyl analogs, however, can result in overdose even when administered via other routes. Nearly one in five deaths involving fentanyl and fentanyl analogs had evidence of snorting, ingestion, or smoking, with no evidence of injection. Multiple overdose outbreaks and law enforcement drug product submissions across the country have reported counterfeit prescription pills laced with fentanyl and fentanyl analogs ( 10 ). With few exceptions, fentanyl analogs are illicitly manufactured, because they do not have a legitimate medical use in humans. §§ The detection of fentanyl analogs in >10% of opioid overdoses in four states raises the concern that fentanyl analogs have become a part of illicit opioid markets in multiple states. The fentanyl analogs most commonly detected were carfentanil, furanylfentanyl, and acetylfentanyl. Carfentanil, which is intended for sedation of large animals, is much more potent than fentanyl, whereas furanylfentanyl and acetylfentanyl are less potent ( 9 ). Carfentanil contributed to approximately 350 overdose deaths in Ohio, but was detected in only one other state (West Virginia). Because of its extreme potency, even limited circulation of carfentanil could markedly increase the number of fatal overdoses. Recent data suggest that carfentanil deaths are occurring in multiple other states, including Kentucky, which reported 10 overdose deaths involving carfentanil in the second half of 2016 (Kentucky Department of Public Health, unpublished data, 2017) and New Hampshire, which reported 10 deaths in 2017. ¶¶ Forty-six percent of SUDORS opioid overdose deaths involving fentanyl analogs tested positive for fentanyl or an additional fentanyl analog, ranging from 31% for carfentanil to 97% for acetylfentanyl. The increased mixing or co-use of fentanyl, heroin, cocaine, and varying fentanyl analogs might contribute to increased risk for overdose because persons misusing opioids and other drugs are exposed to drug products with substantially varied potency. The findings in this report are subject to at least five limitations. First, results are limited to 10 states and therefore might not be generalizable. Second, the presence of fentanyl analogs is underestimated because commonly used toxicologic testing does not include fentanyl analogs, some fentanyl analogs are difficult to detect ( 9 ), and specialized testing for fentanyl analogs varied across states and over time. Third, the route of fentanyl and fentanyl analog administration must be interpreted cautiously because the data do not link specific drugs to routes of administration and thus the precise route of administration of fentanyl or fentanyl analogs cannot be determined in overdose deaths involving multiple substances (e.g., heroin and cocaine) and routes (e.g., injection and snorting). Fourth, the combination of deaths with toxicologic confirmation of heroin with those with detection of morphine and death scene evidence suggesting heroin use might have resulted in misclassification of some deaths. Finally, fentanyl source could not be definitively determined; however, only a small percentage of fentanyl deaths had evidence consistent with prescription fentanyl (e.g., transdermal use versus injection). Illicitly manufactured fentanyl is now a major driver of opioid overdose deaths in multiple states, with a variety of fentanyl analogs increasingly involved, if not solely implicated, in these deaths. This finding raises concern that in the near future, fentanyl analog overdose deaths might mirror the rapidly rising trajectory of fentanyl overdose deaths that began in 2013 and become a major factor in opioid overdose deaths. In response to this concern, CDC expanded ESOOS to 32 states and the District of Columbia in 2017 and added funding for all 33 recipients to improve forensic toxicologic testing of opioid overdose deaths to include capacity to test for a wider range of fentanyl analogs.*** Increased implementation of evidence-based efforts targeting persons at high risk for illicit opioid use, including increased access to medication-assisted treatment, increased availability of naloxone in sufficient doses, and other innovative intervention programs targeting this group, is needed to address a large and growing percentage of opioid overdose deaths involving fentanyl and fentanyl analogs. Summary What is already known about this topic? Sharp increases in opioid overdose deaths since 2013 are partly explained by the introduction of illicitly manufactured fentanyl into the heroin market. Outbreaks related to fentanyl analogs also have occurred. One fentanyl analog, carfentanil, is estimated to be 10,000 times more potent than morphine. Fentanyl analogs are not routinely detected because specialized toxicology testing is required. What is added by this report? This is the first report using toxicologic and death scene evidence across multiple states to characterize opioid overdose deaths. Fentanyl was involved in >50% of opioid overdose deaths, and >50% of deaths testing positive for fentanyl and fentanyl analogs also tested positive for other illicit drugs. Approximately 700 deaths tested positive for fentanyl analogs, with the most common being carfentanil, furanylfentanyl, and acetylfentanyl. What are the implications for public health practice? Increasing mixing or co-use of fentanyl, heroin, cocaine, and fentanyl analogs might contribute to increased overdose risk, because users are exposed to drug products that vary substantially in potency and that include some extremely potent products. Surveillance for opioid overdoses needs to expand to track the rapidly changing illicit opioid market. In fall 2017, CDC funded 33 jurisdictions to expand forensic toxicology testing. Increased implementation of evidence-based efforts targeting persons at high risk for using illicit opioids, including increased access to medication-assisted treatment and increased availability of naloxone, and innovative interventions are needed.
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            Notes from the Field: Overdose Deaths with Carfentanil and Other Fentanyl Analogs Detected — 10 States, July 2016–June 2017

            Fentanyl and fentanyl analogs are increasingly involved in opioid overdose deaths, and new fentanyl analogs continue to be identified ( 1 ). Carfentanil, the most potent fentanyl analog detected in the United States, is intended for sedation of large animals and is estimated to have 10,000 times the potency of morphine ( 2 ). It has recently been reported in an alarming number of deaths in some states. Ohio reported nearly 400 carfentanil-involved deaths during July–December 2016, and Florida reported >500 such deaths for all of 2016 ( 3 , 4 ). CDC funds 32 states and the District of Columbia (DC) to abstract detailed data on opioid overdose deaths from death certificates and medical examiner and coroner reports through the State Unintentional Drug Overdose Reporting System (SUDORS). Twelve states began reporting in August 2017, and 20 states and DC will begin reporting in August 2018.* CDC analyzed trends in overdose deaths testing positive for carfentanil and other fentanyl analogs during July 2016–June 2017 in 10 SUDORS states (Kentucky, Maine, Massachusetts, New Hampshire, New Mexico, Ohio, Oklahoma, Rhode Island, West Virginia, and Wisconsin). † States abstract data on all substances (both opioids and nonopioids) that contributed to death, as well as all substances for which the decedent tested positive. § During July 2016–June 2017, among 11,045 opioid overdose deaths, 2,275 (20.6%) decedents tested positive for any fentanyl analog, and 1,236 (11.2%) tested positive for carfentanil. Fourteen different fentanyl analogs were detected. ¶ Among overdose deaths with fentanyl analogs detected, the analogs were determined by medical examiners or coroners to have contributed to the death in >95% of deaths. During the first half of 2017, the number of deaths with any fentanyl analog detected (1,511) nearly doubled, compared with the number during the second half of 2016 (764); deaths with carfentanil detected increased 94%, from 421 to 815. The proportions of deaths with any fentanyl analog or with carfentanil detected nearly doubled during this period. Ohio reported the largest numbers and most substantial increases in deaths with any fentanyl analog detected, including carfentanil (Figure). The number of carfentanil deaths in Ohio initially peaked in September 2016 (86 deaths), decreased during October 2016–February 2017, and peaked again in April 2017 (218 deaths). Changes in the number of deaths with any fentanyl analog detected mirrored changes in deaths with carfentanil detected, except during October 2016–February 2017, when deaths with carfentanil decreased. During this period, the number of deaths with any fentanyl analog detected instead increased, mainly driven by acrylfentanyl (202 deaths) and furanylfentanyl (192 deaths). The number of deaths with carfentanil present in other states followed a similar pattern, with peaks occurring slightly after those in Ohio. During the first half of 2017, seven states reported detecting carfentanil in overdose deaths, compared with three during the second half of 2016; the number of counties in which overdose deaths with carfentanil present occurred increased from 54 to 77. FIGURE Number of overdose deaths with carfentanil and any fentanyl analog detected* — Ohio and nine other SUDORS states, † July 2016–June 2017 Abbreviation: SUDORS = State Unintentional Drug Overdose Reporting System. * “Any fentanyl analog” includes carfentanil, so the categories are not mutually exclusive. † Kentucky, Maine, Massachusetts, New Hampshire, New Mexico, Oklahoma, Rhode Island, West Virginia, and Wisconsin. The figure above is a bar chart showing the number of overdose deaths with carfentanil and any fentanyl analog detected in Ohio and nine other SUDORS states during July 2016–June 2017. In 2015, CDC issued a nationwide public health advisory about increases in fentanyl-related overdose deaths in multiple states ( 5 ), and in 2016 issued an update to that advisory to warn about increasing availability of fentanyl and fentanyl-related substances being pressed into counterfeit pills, and the potential for broad distribution across the United States ( 6 ). In response to findings in SUDORS data, on July 11, 2018, CDC issued a second update highlighting the emerging prevalence of fentanyl analogs contributing to opioid overdose deaths ( 7 ). Growing outbreaks associated with fentanyl analogs are occurring at a time when sharp increases in fentanyl overdose deaths are already straining the capacity of medical examiner and coroner offices and public health departments. The increasing array of fentanyl analogs highlights the need to build forensic toxicological testing capabilities to identify and report emerging threats and to enhance capacity to rapidly respond to evolving drug trends. The highly potent nature of many analogs, particularly carfentanil, might warrant multiple administrations of the effective opioid overdose reversal medication naloxone.
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              Author and article information

              Journal
              Online J Public Health Inform
              Online J Public Health Inform
              OJPHI
              Online Journal of Public Health Informatics
              University of Illinois at Chicago Library
              1947-2579
              30 May 2019
              2019
              : 11
              : 1
              : e446
              Affiliations
              [1]Centers for Disease Control and Prevention (CDC) , Atlanta, Georgia, United States
              Article
              ojphi-11-e446
              10.5210/ojphi.v11i1.9935
              6606259
              1a595002-d957-4b16-b91b-d65b83ae26f5
              ISDS Annual Conference Proceedings 2019

              This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License.

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