Showing posts with label clonidine. Show all posts
Showing posts with label clonidine. Show all posts

Wednesday, October 16, 2024

Clonidine May Be Effective Non-Opioid Treatment
for Neonatal Opioid Withdrawal Syndrome

Clonidine, a non-opioid approved for the treatment of hypertension, may be an effective alternative to morphine for neonatal opioid withdrawal syndrome (NOWS), according to a report in Pediatrics.

Babies who are exposed to opioids in the womb can develop significant withdrawal symptoms after birth. “Despite the detrimental effects of in utero opioid exposure, the opiate morphine remains a common first-line drug for NOWS treatment, resulting in additional weeks to months of exposing the developing brain to opioids,” wrote Henrietta Bada, M.D., M.P.H., of the University of Kentucky, and colleagues.

Between December 2017 and February 2022, Bada and colleagues randomized 120 infants with NOWS to receive either oral clonidine at 1 µg/kg/dose or morphine at 60 µg/kg/dose, every three hours. Infants with no improvement had their doses increased by 25% every 12 to 24 hours, up to a maximum of 2 μg/kg/dose for clonidine and 120 µg/kg/dose for morphine. Those without improvement by the maximum dose received an adjunct medication such as phenobarbital. Once withdrawal symptoms stabilized, medication doses were weaned by 10% every 24 hours.

All infants also had non-pharmacological interventions including swaddling, low noise and lighting environment, infant massage, and maternal rooming with the infant.

Primary outcomes were length of treatment and neurobehavioral performance as measured by the Neonatal Intensive Care Unit Network Neurobehavioral Scale (NNNS).

Neither length of treatment nor length of hospital stay differed significantly between the two groups. Clonidine treatment lasted between 15 to 19 days while morphine treatment lasted 13 to 17 days; length of stay was between 20 to 24 days for clonidine and 17 to 20 days for morphine. However, 45% of clonidine-treated infants needed adjunct medication compared with just 10% in the morphine group, a concerning finding that the authors said may be related to the dosing schedule for clonidine.

Clonidine-treated infants performed as well on the NNNS as morphine-treated infants. At the initial testing—conducted as soon as withdrawal symptoms stabilized—clonidine-treated babies scored worse on arousal, hypertonicity, and stress abstinence, but at their following treatment, they showed significant improvement with less handling required, reduced excitability and stress abstinence, and improved arousal and regulation.

“We were able to successfully provide an opioid-sparing, medication-assisted treatment regimen to a cohort of infants with significant NOWS,” Bada and colleagues wrote. “Future studies are needed to investigate the optimal dose and frequency of clonidine administration for improved efficacy and the decreased need for adjunctive therapy in NOWS.”

For related information, see the Psychiatric News article “Neonatal Abstinence Syndrome Linked to Unemployment, Mental Health Shortages.”

(Image: Getty Images/iStock/Orbon Alija)




Don't miss out! To learn about newly posted articles in Psychiatric News, please sign up here.




Wednesday, March 18, 2015

Clonidine Lengthens Abstinence Time in Opioid Treatment


Adding clonidine to buprenorphine treatment increased the duration of abstinence for opioid-dependent patients, according to a study published online today in the American Journal of Psychiatry by William Kowalczyk, Ph.D., a postdoctoral fellow in the Clinical Pharmacology and Therapeutics Branch of the National Institute on Drug Addiction, and colleagues.

The 118 participants began the trial on buprenorphine. Once abstinent from opioids for two weeks, they were randomized to either clonidine or placebo. Clonidine is already used in opioid withdrawal and does not have special prescribing requirements like buprenorphine or methadone.

Overall, clonidine lengthened the time to opioid lapse (defined as a positive or missing urine test), but not significantly. However, after controlling the results for cocaine use, the researchers found that taking clonidine “significantly increased the time to initial opioid lapse.” Time to relapse (two or more lapses) was not extended significantly, possibly because of the priming effect of the drug use in the first lapse.

As part of the trial protocol, participants received small electronic devices that prompted them four times a day to record stress, mood, craving, and any drug-related cues around them.

This “ecological momentary assessment” demonstrated that clonidine “partly decoupled daily-life stress, but not daily-life drug-cue exposure, from increases in drug craving,” said Kowalczyk. “Participants in the clonidine group were less likely than those in the placebo group to report heroin craving at moderately high levels of stress.”

Use of the ecological momentary assessment also added to evidence supporting animal models of stress and drug use and may help individualize treatment by identifying patients who lapse because of stress rather than drug cues or priming doses.

For more in Psychiatric News about pharmacotherapies for drug addiction, see “Psychiatrists Describe Trends in Medications to Treat Addiction.”

--aml  (Image: Evdokimov Maxim/Shutterstock.com)

The content of Psychiatric News does not necessarily reflect the views of APA or the editors. Unless so stated, neither Psychiatric News nor APA guarantees, warrants, or endorses information or advertising in this newspaper. Clinical opinions are not peer reviewed and thus should be independently verified.