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Notes from the Field: Emergency Department Visits and Hospitalizations for Buprenorphine Ingestion by Children — United States, 2010–2011

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Notes from the Field: Emergency Department Visits and Hospitalizations for Buprenorphine Ingestion by Children — United States, 2010–2011

HHS, CDC and MMWR Logos
MMWR Weekly
Volume 62, No. 3
January 25, 2013

Notes from the Field: Emergency Department Visits and Hospitalizations for Buprenorphine Ingestion by Children — United States, 2010–2011


Weekly

January 25, 2013 / 62(03);56-56

Buprenorphine (Subutex) and buprenorphine/naloxone (Suboxone) received Food and Drug Administration approval in 2002 for the treatment of opioid dependence. Introduction of these drugs expanded the availability of opioid-dependence treatment options to reduce the morbidity and mortality associated with opioid abuse, and buprenorphine has become an increasingly prescribed component of office-based treatment. However, unsupervised ingestion of buprenorphine-containing products by children is a growing concern (1).
During 2010–2011, the National Electronic Injury Surveillance System — Cooperative Adverse Drug Event Surveillance project (2) identified 68 cases involving buprenorphine product ingestions (out of 226 cases of opioid product ingestions) by children aged <6 class="callout-pink" span="">years.*
Based on these cases, CDC estimates that, during 2010–2011, an average of 1,499 (95% confidence interval [CI] = 905–2,092) children aged <6 1="" 2004.="" 2="" 58.4="" aged="" all="" and="" as="" because="" boys="" buprenorphine-product="" buprenorphine="" cases="" children="" class="callout-pink" contrast="" departments="" depression="" each="" ed="" emergency="" evaluated="" exposures="" for="" half-life="" in="" ingestion-related="" ingestions="" involved="" is="" long="" medications="" most="" naloxone.="" nearly="" of="" other="" pediatric="" reported="" required="" respiratory="" risk="" s="" span="" the="" to="" typical="" u.s.="" unsupervised="" visits="" were="" year="" years="" zero="">hospitalization. Buprenorphine products were involved in disproportionate numbers of unsupervised ingestions by children aged <6 20.1="" 29.8="" 38.9="" 59.5="" and="" buprenorphine="" class="callout-pink" compared="" drugs.="" ed="" emergent="" for="" hospitalizations="" in="" involved="" of="" opioid="" other="" prescription="" product="" products="" span="" visits="" were="" with="" years="">ingestions.
§ Ingestion of buprenorphine/naloxone caused 9.5% of emergent hospitalizations for drug ingestion by children aged <6 0.16="" 2.2="" 2009="" a="" all="" amounted="" and="" any="" buprenorphine="" even="" greater="" i="" in="" medication="" of="" only="" opioid="" other="" prescriptions="" products="" proportion="" retail="" single="" than="" though="" to="" years="">3). Ingestions of buprenorphine-containing products by children are serious and have increased rapidly nationally. Fatalities have been reported in children after unsupervised ingestions of single doses (4). Innovative injury prevention approaches beyond current child-resistant bottles and safety warnings might be required to safeguard children while preserving availability of medications such as this important addiction treatment option for adults. Providers should remind patients to keep buprenorphine-containing products in child-resistant packaging, stored up, away, and out of the sight of children. Patients should post the Poison Help telephone number (1-800-222-1222) in their homes, and telephone 911 in the event of emergencies.

Reported by

Maribeth Lovegrove, MPH, Lee M. Hampton, MD, Daniel S. Budnitz, MD, Div of Healthcare Quality Promotion, National Center for Emerging Zoonotic and Infectious Diseases; Andrew I. Geller, MD, EIS Officer, CDC. Corresponding contributor: Andrew I. Geller, wia0@cdc.gov, 404-639-4050.

References

  1. CDC. Buprenorphine prescribing practices and exposures reported to a poison center—Utah, 2002–2011. MMWR 2012;61:997–1001.
  2. Jhung MA, Budnitz DS, Mendelsohn AB, Weidenbach KN, Nelson TD, Pollock DA. Evaluation and overview of the National Electronic Injury Surveillance System-Cooperative Adverse Drug Event Surveillance project (NEISS-CADES). Med Care 2007;45(10 Suppl 2):S96–102.
  3. Food and Drug Administration. Total number of prescriptions dispensed for long-acting/extended-release and immediate-release opioids from U.S. outpatient retail pharmacies, years 2000–2009. In: briefing information for the July 22–23, 2010, Joint Meeting of the Anesthetic and Life Support Drugs Advisory Committee and Drug Safety and Risk Management Advisory Committee. Silver Spring, MD: US Department of Health and Human Services, Food and Drug Administration; 2010.
  4. Kim HK, Smiddy M, Hoffman RS, Nelson LS. Buprenorphine may not be as safe as you think: a pediatric fatality from unintentional exposure. Pediatrics 2012;130:e1700–3.

* A case was defined as an emergency department (ED) visit at one of the participating NEISS-CADES hospitals during 2010–2011 for assessment and treatment for a buprenorphine product ingestion by a child aged <6 accessed="" adult="" child="" her="" his="" ingestion="" medication="" on="" or="" oversight="" own="" p="" permission="" the="" unsupervised="" where="" without="" years="">
Hospitalizations included ED visits that resulted in admission to a hospital or transfer to another hospital.
§ Excluding opioid-containing antitussive formulations.

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