Carfentanil and Medetomidine

NEW YORK CITY DEPARTMENT OF HEALTH AND MENTAL HYGIENE
Ashwin Vasan, MD, PhD Commissioner
2024 Health Advisory #20:
Carfentanil and Medetomidine in the NYC Drug Supply

  • Carfentanil, a potent synthetic opioid that is estimated to be up to 100 times stronger than fentanyl,
    has been identified in New York City multiple recent samples sold as opioids. Similarly,
    medetomidine, a non-opioid anesthetic similar to xylazine, has also been identified in the NYC drug
    supply, specifically in the Bronx, for the first time.
  • Between March and June 2024, the NYC Health Department’s drug-checking program has
    identified trace and small amounts of carfentanil in eight samples sold as opioids. All samples
    containing carfentanil also contained fentanyl.
    o Carfentanil was not detected via point-of-care drug-checking technologies (e.g., Fourier
    transform infrared spectrometry and fentanyl test strips) due to the technologies’ limitations.
    Carfentanil in these samples was detected through secondary laboratory testing.
    o Although carfentanil was only identified in trace and small amounts, two of the eight samples
    were associated with adverse reactions, including overdose.
  • According to data from the NYC Health Department’s Bureau of Vital Statistics and NYC Office of
    the Chief Medical Examiner, carfentanil was also involved in at least seven unintentional drug
    overdose deaths between January and June 2024, an increase from at least three unintentional
    drug overdose deaths in 2023. These data are provisional and subject to change.
  • The New York State Department of Health Community Drug-Checking Program identified
    medetomidine in an opioid sample collected in the Bronx. Although naloxone cannot reverse the
    effects of medetomidine, this substance has most often been found with opioids. Consequently, it is
    important to use naloxone even in the case of a suspected medetomidine-involved overdose.
  • Contact the NYC Health Department immediately if you observe or learn of unusual overdoses or
    other adverse events, including those with symptoms consistent with the novel substances
    described above.
    July 25, 2024
    Dear Colleagues,
    The New York City Department of Health and Mental Hygiene (NYC Health Department) operates a multisite drug-checking program in partnership with five syringe service programs. Over the past four months,
    eight opioid samples collected in the Bronx, Brooklyn, and Manhattan and sent for secondary laboratory
    testing were found to contain trace or small amounts of carfentanil. All samples found to contain carfentanil
    also contained fentanyl, which was detected by NYC Health Department drug-checking technicians through
    Fourier transform infrared spectrometry (FTIR) or fentanyl test strips (FTS). Of the eight samples identified
    to contain carfentanil via secondary testing, two were associated with adverse reactions, including
    overdose. Both of these samples contained fentanyl and xylazine.
    Carfentanil is a potent synthetic opioid that is estimated to be up to 100 times stronger than fentanyl. Due
    to its potency, substances containing even small amounts of carfentanil can cause immediate and severe
    adverse reactions including overdose, especially for individuals with low opioid tolerance. Like other
    opioids, the effects of carfentanil can be reversed with the administration of naloxone. Although multiple
    doses of naloxone may be needed, the NYC Health Department discourages the use of 8mg naloxone
    among lay-persons and first-responders, as it has not been found to be more effective than 4mg naloxone
    and can increase the risk of precipitated opioid withdrawal.
    Providers should educate individuals who use drugs about the presence of carfentanil in the unregulated
    opioid supply in NYC, and caution that carfentanil may not be reliably detected through FTS or FTIR testing
    alone. Nevertheless, as carfentanil has only been found in combination with fentanyl, providers should
    continue to encourage individuals to test their drugs using FTS or drug-checking services and take further
    steps to reduce their risk of overdose.
    Medetomidine has also been identified for the first time in the NYC drug supply. An opioid sample collected
    from the Bronx by the New York State Department of Health Community Drug Checking program in late
    June 2024 was found to contain medetomidine via secondary laboratory testing. This sample was also
    found to contain fentanyl. Adverse reactions associated with this specific sample are not known.
    Medetomidine is a non-opioid anesthetic that is FDA-approved for veterinary use. It is similar to xylazine,
    but is more potent and causes longer-lasting effects. At this time, medetomidine cannot be differentiated
    from dexmedetomidine (Precedex)—a sedative which is FDA-approved for human use—through
    secondary laboratory testing.
    As medetomidine/dexmedetomidine are not opioids, naloxone cannot reverse the effects of these
    substances. However, since medetomidine/dexmedetomidine have most often been found with fentanyl
    and other potent opioids, it is important to use naloxone even in the case of a suspected
    medetomidine/dexmedetomidine-involved overdose. Individuals may still be sedated after naloxone
    reversal of opioid-induced respiratory depression. For this reason, it is important to administer rescue
    breathing, place individuals in a rescue position to protect their airways, and continue to monitor their
    breathing with a pulse oximeter. Call emergency services to facilitate access to further monitoring and
    administration of supplemental oxygen.
    Clinical Information on Carfentanil:
  • Carfentanil is a synthetic opioid which is estimated to be up to 100 times stronger than fentanyl.
  • Symptoms of a carfentanil- or fentanyl-involved overdose are characterized by central nervous
    system and respiratory depression: lethargy, slowed or shallow breathing, pinpoint pupils, change in
    consciousness, seizure, and/or coma.
  • Treatment is the same as for other opioid overdoses; however, if there is no return of spontaneous
    breathing, additional naloxone doses may be required to reverse the opioid effects.
  • Due to the presence of xylazine in the unregulated opioid supply, individuals may still be sedated
    after naloxone reversal of opioid-induced respiratory depression. In cases of stopped or irregular
    breathing, rescue breathing should be administered in addition to naloxone.
    Clinical Information on Medetomidine/Dexmedetomidine:
  • Similar to xylazine, medetomidine is a synthetic alpha-2 adrenoreceptor agonist sedative used in
    veterinary medicine. Medetomidine is used for sedation, analgesia, muscle relaxation and
    anxiolysis (i.e., anti-anxiety).
  • The effects of medetomidine intoxication may include: extreme sedation, slower than usual heart
    rate (reportedly as low as 40 beats per minute), low blood pressure, and central nervous system
    depression. Someone experiencing medetomidine intoxication may be unresponsive to verbal
    commands or physical stimuli even though they may still be breathing.
  • Medetomidine is not an opioid, so the effects of medetomidine cannot be reversed with the
    administration of naloxone.
  • Since medetomidine has most often been found with fentanyl and other opioids, naloxone should
    be administered in all suspected overdoses involving medetomidine. Rescue breathing or
    supplemental oxygen should be administered in cases of stopped or irregular breathing.
    Recommendations
  • Contact the NYC Health Department immediately if you observe or learn of unusual overdoses
    or other adverse events, including those with symptoms consistent with the novel substances
    described above.
    o If possible, consider saving small amounts (at least half of a grain of rice) of substances
    associated with reported adverse events to submit to the NYC Health Department. The NYC
    Health Department drug-checking team can send samples to our partner laboratory for
    testing and timely identification of substances.
    o The NYC Health Department drug-checking team can be reached at
    drugchecking@health.nyc.gov.
    o For drug-checking services and inquiries outside of New York City, the NYS Department of
    Health drug-checking team can be reached at drug.checking@health.ny.gov.
  • Consider potential xylazine or medetomidine exposure for patients who present with suspected
    overdoses and who continue to experience prolonged sedation following naloxone administration.
  • Provide person-centered, trauma-informed care to patients who use drugs, including wound
    care and withdrawal management, even if they are not ready to stop using.
    o For trainings on addressing substance use stigma in health care settings and other provider
    resources, click here.
  • Counsel patients who use drugs about overdose risk reduction strategies including avoiding using
    drugs alone and avoiding mixing drugs (including alcohol).
    o Recommend that patients who are planning to use drugs alone call the “Never Use
    Alone” hotline at 877-696-1996.
    o Click here for more overdose prevention resources for providers, including tools to talk to
    your patients about how to reduce their risk of overdose.
  • Talk to patients who use drugs about naloxone. Provide patients with a prescription for naloxone
    or direct them to where they can access naloxone at no cost.
    o Click here for information and resources related to naloxone.
  • Encourage patients to check their drugs.
    o Talk to your patients about FTS. Click here or here for more information on how to get FTS.
    o Recommend that individuals who use drugs connect with drug-checking services. Locations
    and hours of availability are below.
    ▪ OnPoint NYC East Harlem (Manhattan): Tues (10:30 AM – 5 PM)
    ▪ VOCAL-NY (Brooklyn): Wed (10 AM – 4 PM)
    ▪ BOOM!Health (Bronx): Thurs (10 AM – 4 PM)
    ▪ Housing Works Cylar House (Manhattan): Thurs (11 AM – 5 PM)
    ▪ OnPoint NYC Washington Heights (Manhattan): Fri (10 AM – 4 PM)
    ▪ St. Ann’s Corner of Harm Reduction (Bronx): Contact drug.checking@health.ny.gov
    for hours of operation
    ▪ For locations outside of NYC, click here
  • Familiarize yourself with a local harm reduction organization so you can connect patients
    who may benefit from these services. Click here for a list of NYC’s syringe service
    programs.
  • Prescribe medications including methadone or buprenorphine for people with opioid use disorder,
    or facilitate a referral to providers who can prescribe these medications, to prevent overdose.
    o Treatment locators are available here and here.
  • Ensure patients who are being treated for an opioid use disorder with methadone or buprenorphine
    maintain uninterrupted access to their medication.
  • Patients seeking support to stop using drugs and other resources can call or text 988 or chat at
    nyc.gov/988. Counselors are available 24/7 in more than 200 languages.
    Additional Resources
  • New York State Department of Health Issues Public Health Alert for Carfentanil Detected In Drug
    Samples From Central New York
  • New York State Department of Health Issues Public Health Alert for Medetomidine Detected In
    Drug Samples In Schenectady and Syracuse
  • CFSRE Toxic Adulterant Alert on Medetomidine/Dexmedetomidine
  • Medetomidine in Chicago’s Drug Supply
  • New York State Office of Addiction Services and Supports Advisory: Another Potent Sedative,
    Medetomidine, Now Appearing in Illicit Drug Supply
  • Philadelphia Health Alert on Medetomidine
    Sincerely,
    Rebecca Linn-Walton, PhD, LCSW
    Assistant Commissioner
    Bureau of Alcohol and Drug Use Prevention, Care, and Treatment
    Shivani Mantha, MPH
    Executive Director of Research, Surveillance, Policy, and Communications
    Bureau of Alcohol and Drug Use Prevention, Care, and Treatment

Monkeypox

This communication provides updates to New York State Department of Health: Health Alert Notice for providers in New York State – November 27, 2023.

SUMMARY

  • Mpox transmission continues to be reported across the state, but case counts remain lower relative to the peak of the 2022 outbreak. In 2024, mpox cases in the United States are higher compared to this time last year. In 2024, mpox diagnoses in New York State have been reported in Albany, Dutchess, Erie, Nassau, Onondaga, Otsego, Putnam, Suffolk, Ulster, and Westchester counties.
  • Vaccination among communities disproportionately affected by mpox remains one of our strongest tools at preventing severe illness as well as further transmission.
  • Providers should review recently issued evidence-based clinical practice recommendations on how to address mpox prevention, presentation, diagnosis, and treatment in adults on the New York State Department of Health AIDS Institute Clinical
    Guidelines website, along with a convenient pocket guide and slide set. Mpox transmission continues to be reported across the state, but case counts remain lower relative to the peak of the 2022 outbreak. In 2024, mpox diagnoses have been reported in Albany, Dutchess, Erie, Nassau, Onondaga, Otsego, Putnam, Suffolk, Ulster, and Westchester counties. In 2024, mpox cases in the United States are higher compared to this time last year. The communities most affected by mpox, as well as the route of transmission of close personal contact/skin to skin contact with mpox lesions, remain the same. Vaccination among communities disproportionately affected by mpox remains one of our strongest tools at preventing severe illness as well as further transmission. The vaccine has been routinely recommended for the prevention of mpox by the Centers for Disease Control and Prevention (CDC). In addition to being protective against Clade IIb mpox, which is the strain currently circulating in the United States, the JYNNEOS vaccine is also expected to protect against Clade I mpox, a more clinically serious strain which is associated with an outbreak in the Democratic Republic of the Congo. While no cases have been reported in the United States to date, CDC and jurisdictional health departments are taking steps to enhance readiness for responding to Clade I mpox. More information can be found in the December 7, 2023 CDC Health Advisory. As of April 1, 2024, JYNNEOS is available through the commercial market. Requests for vaccines submitted to the New York State Department of Health via mpox@health.ny.gov, which have previously been fulfilled through federally procured supply, will be accepted only in cases where commercially available JYNNEOS vaccine is not available or accessible. CDC has released an updated Vaccine Storage and Handling Toolkit, which includes updates to mpox vaccine storage and handling information.
    For those who do acquire mpox, while there are no approved antiviral treatments currently available, some medications are being studied for their effectiveness in treating mpox, including
    tecovirimat (TPOXX). As of early 2023, the federal government has concluded pre-positioning of tecovirimat (TPOXX), and no pre-positioned supply is currently housed in New York State.
    However, the following avenues remain for healthcare providers to access tecovirimat (TPOXX):
  • Study of Tecovirimat for Mpox (STOMP): Treatment of mpox with oral tecovirimat (TPOXX) is available through the Study of Tecovirimat for Human Mpox Virus (STOMP) trial facilitated by the National Institute of Allergy and Infectious Diseases (NIAD). Providers are encouraged to discuss the trial with patients with mpox. Multiple participating study sites are located within New York State. More information is available here.
  • Expanded Access Investigational New Drug (EA-IND) Protocol: Providers with patients who are not able to enroll in the STOMP trial, who decline enrollment, or who require intravenous tecovirimat (TPOXX) and meet treatment eligibility under the EA-IND protocol should work in concert with their county health department to request a supply of tecovirimat by contacting the CDC’s Emergency Operations Center (EOC) at (770) 488-7100 or poxvirus@cdc.gov

Meningococcal Disease

Meningococcal Disease Linked to Travel to the Kingdom of Saudi Arabia (KSA): Ensure Pilgrims are Current on Meningococcal Vaccination
Summary
The Centers for Disease Control and Prevention (CDC) is issuing this Health Alert Network (HAN) Health Advisory to alert healthcare providers to cases of meningococcal disease linked to Umrah travel to the Kingdom of Saudi Arabia (KSA). Umrah is an Islamic pilgrimage to Mecca, Kingdom of Saudi Arabia, that can be performed any time in the year; the Hajj is an annual Islamic pilgrimage this year taking place June 14–19, 2024. Since April 2024, 12 cases of meningococcal disease linked to KSA travel for Umrah have been reported to national public health agencies in the United States (5 cases), France (4 cases), and the United Kingdom (3 cases). Two cases were in children aged ≤18 years, four cases were in adults aged 18–44 years, four cases were in adults aged 45–64 years, and two cases were in adults aged 65 years or older. Ten cases were in patients who traveled to KSA, and two were in patients who had close contact with travelers to KSA. Ten cases were caused by Neisseria meningitidis serogroup W (NmW), one U.S. case was caused by serogroup C (NmC), and the serogroup is unknown for one U.S. case. Of nine patients with known vaccination status, all were unvaccinated. The isolates from the one U.S. NmC case and two NmW cases (one U.S., one France) were resistant to ciprofloxacin; based on whole-genome sequencing, the remaining eight NmW isolates were all sensitive to penicillin and ciprofloxacin.In the United States, quadrivalent meningococcal (MenACWY) conjugate vaccination is routinely recommended for adolescents, and also recommended for travelers to countries where meningococcal disease is hyperendemic or epidemic, including a booster dose of MenACWY if the last dose was administered 3–5 or more years previously (depending on the age at most recent dose received). In addition, all Hajj and Umrah pilgrims aged one year and older are required by KSA to receive quadrivalent meningococcal vaccine. Healthcare providers should work with their patients considering travel to perform Hajj or Umrah to ensure that those aged one year or older have received a MenACWY conjugate vaccine within the last 5 years administered at least 10 days prior to arrival in KSA. Healthcare providers should also maintain increased suspicion for meningococcal disease in anyone presenting with symptoms of meningococcal disease after recent travel to KSA for Hajj or Umrah pilgrimage. U.S. health departments and healthcare providers should preferentially consider using rifampin, ceftriaxone, or azithromycin instead of ciprofloxacin for chemoprophylaxis of close contacts of meningococcal disease cases associated with travel to KSA.

Background
Meningococcal disease, caused by the bacterium Neisseria meningitidis, is a rare but severe illness with a case-fatality rate of 10–15%, even with appropriate antibiotic treatment. Meningococcal disease often presents as meningitis with symptoms that may include fever, headache, stiff neck, nausea, vomiting, photophobia, or altered mental status. Meningococcal disease may also present as a meningococcal bloodstream infection with symptoms that may include fever, chills, fatigue, vomiting, cold hands and feet, severe aches and pains, rapid breathing, diarrhea, or, in later stages, a petechial or dark purple rash (purpura fulminans). While initial symptoms of meningococcal disease can at first be nonspecific, they worsen rapidly and can become life-threatening within hours. Survivors may experience long-term effects such as deafness or amputations of the extremities. 

Immediate antibiotic treatment for meningococcal disease is critical. 
Blood and cerebrospinal fluid (CSF) cultures are indicated for patients with suspected meningococcal disease. Healthcare providers should not wait for diagnostic testing or receipt of laboratory results before initiating treatment for suspected cases of meningococcal disease.Meningococcal disease outbreaks have occurred previously in conjunction with mass gatherings including the Hajj pilgrimage. The most recent global outbreak of meningococcal disease associated with travel to KSA for Hajj was in 2000–2001 and was primarily caused by NmW. Since 2002, KSA has required that all travelers aged one year or older performing Hajj or Umrah provide documentation of either a) a MenACWY polysaccharide vaccine (MPSV4 is no longer available in the United States) within the last 3 years administered at least 10 days prior to arrival or b) a MenACWY conjugate vaccine within the last 5 years administered at least 10 days prior to arrival. This requirement aligns with ACIP recommendations for revaccination of U.S. travelers to endemic areas who received their last dose 3–5 or more years previously (depending on the age at most recent dose received). Nevertheless, meningococcal vaccination coverage among Umrah travelers is known to be incomplete.

Close contacts of people with meningococcal disease should receive antibiotic chemoprophylaxis as soon as possible after exposure, regardless of immunization status, ideally less than 24 hours after the index patient is identified. 
Ciprofloxacin, rifampin, and ceftriaxone are the first-line antibiotics recommended for use as chemoprophylaxis. However, ciprofloxacin-resistant strains of N. meningitidis have been emerging in the United States and globally. CDC recently released implementation guidance for the preferential use of other recommended prophylaxis antibiotics in areas with multiple cases caused by ciprofloxacin-resistant strains. Health departments should discontinue using ciprofloxacin as prophylaxis for close contacts when, in a catchment area during a rolling 12-month period, both a) ≥2 invasive meningococcal disease cases caused by ciprofloxacin-resistant strains have been reported, and b) cases caused by ciprofloxacin-resistant strains account for ≥20% of all reported invasive meningococcal disease cases. Though a catchment area is defined as a “single contiguous area that contains all counties reporting ciprofloxacin-resistant cases,” in this circumstance, it is more appropriate to determine the catchment population based on travel history rather than geographic location at the time of diagnosis. Among the 11 global cases associated with travel to KSA that have antimicrobial sensitivity results available, 3 cases (27%) were caused by ciprofloxacin-resistant strains. Rifampin, ceftriaxone, or azithromycin should be preferentially considered instead of ciprofloxacin as prophylaxis for close contacts in the United States of meningococcal disease cases associated with travel to KSA.

Recommendations for Healthcare Providers
Recommend vaccination with MenACWY conjugate vaccine for people considering travel to KSA to perform Hajj or Umrah (pilgrims) in addition to routine meningococcal vaccination for adolescents and other people at increased meningococcal disease risk.Maintain a heightened index of suspicion for meningococcal disease among symptomatic people who have recently been in KSA and among close contacts of people who have recently been in KSA, regardless of vaccination status.Immediately notify state, tribal, local, or territorial health departments about any suspected or confirmed cases of meningococcal disease in the United States.Preferentially consider using rifampin, ceftriaxone, or azithromycin instead of ciprofloxacin as prophylaxis for close contacts in the United States of meningococcal disease cases associated with travel in KSA.

Recommendations for Health Departments
Preferentially consider using rifampin, ceftriaxone, or azithromycin instead of ciprofloxacin as prophylaxis for close contacts in the United States of meningococcal disease cases associated with travel in KSA.Consider outreach to local communities to promote meningococcal vaccination for Hajj and Umrah pilgrims to KSA.Collect a detailed travel history for all reported cases of meningococcal disease.Continue to report cases of meningococcal disease in people who have recently been in KSA, or in close contacts of people who have recently been in KSA, to CDC at meningnet@cdc.gov in addition to routine reporting through the National Notifiable Diseases Surveillance System (NNDSS).

Recommendations for the Public
People considering travel to KSA to perform Hajj or Umrah should ensure they are current on vaccination with MenACWY vaccine as required by KSA. All travelers aged one year or older performing Hajj or Umrah should have received either a) a MenACWY polysaccharide vaccine (MPSV4, no longer available in the United States) within the last 3 years administered at least 10 days prior to arrival or b) a quadrivalent MenACWY conjugate vaccine within the last 5 years administered at least 10 days prior to arrival.Immediately seek medical attention if you, your child, or another close contact develops symptoms of meningococcal disease:  

Symptoms of meningococcal meningitis may include fever, headache, stiff neck, nausea, vomiting, photophobia (eyes being more sensitive to light), or altered mental status (confusion).

Symptoms of meningococcal bloodstream infection may include fever and chills, fatigue, vomiting, cold hands and feet, severe aches and pains, rapid breathing, diarrhea, or, in later stages, a dark purple rash.

Initial symptoms of meningococcal disease can at first be vague, but worsen rapidly, and can become life-threatening within hours.

For More Information
Healthcare Providers
Clinical Information | Meningococcal Disease | CDC
Meningococcal Vaccination: Information for Healthcare Professionals | CDC
Meningococcal Disease | CDC Yellow Book 2024
Health Departments
Meningococcal Disease Surveillance | CDC
Meningococcal Disease | Manual for the Surveillance of Vaccine-Preventable Diseases | CDC
Meningococcal Disease Outbreaks and Public Health Response | CDC
Public
Meningococcal Vaccination | CDC
Signs and Symptoms | Meningococcal Disease | CDC
Travelers’ Health: Saudi Arabia | CDC  
Ministry of Health, Kingdom of Saudi Arabia
Visit CDC-INFO or call 1-800-232-4636

References
American Academy of Pediatrics. Meningococcal Infections. [Section 3]. In: Kimberlin DW, Barnett ED, Lynfield R, Sawyer MH, eds. Red Book: 2021–2024 Report of the Committee on Infectious Diseases. Itasca, IL: American Academy of Pediatrics; 2021;519–32. https://publications.aap.org/redbook/book/347/chapter/5754116/Meningococcal-Infections
Mbaeyi SA, Bozio CH, Duffy J, et al. Meningococcal Vaccination: Recommendations of the Advisory Committee on Immunization Practices, United States, 2020. MMWR Recomm Rep 2020;69(No. RR-9):1–41. doi: https://dx.doi.org/10.15585/mmwr.rr6909a1
Badur S, Khalaf M, Öztürk S, et al. Meningococcal Disease and Immunization Activities in Hajj and Umrah Pilgrimage: A review. Infectious Diseases and Therapy 2022;11(4):1343–1369. doi: https://doi.org/10.1007/s40121-022-00620-0
Yezli S, Gautret P, Assiri AM, Gessner BD, Alotaibi B. Prevention of meningococcal disease at mass gatherings: Lessons from the Hajj and Umrah. Vaccine. 2018;36(31):4603–4609. doi: https://doi.org/10.1016/j.vaccine.2018.06.030.
Berry I, Rubis AB, Howie RL, et al. Selection of Antibiotics as Prophylaxis for Close Contacts of Patients with Meningococcal Disease in Areas with Ciprofloxacin Resistance — United States, 2024. MMWR Morb Mortal Wkly Rep 2024; 73:99–103. doi: https://dx.doi.org/10.15585/mmwr.mm7305a2
Willerton L, Lucidarme J, Campbell H, et al. Geographically widespread invasive meningococcal disease caused by a ciprofloxacin resistant non-groupable strain of the ST-175 clonal complex. Journal of Infection 2020;81(4): 575–584. doi: https://doi.org/10.1016/j.jinf.2020.08.030
Published
Categorized as Updates