Abstract:Background
Recent studies show a rapid growth among pregnant women using high potency opioids for common pain management during their pregnancy. No study has examined the duration of treatment among strong opioid users and weak opioid users during pregnancy. We aimed to investigate the prevalence of prescribed opioid use during pregnancy, in Quebec; and to compare the duration of opioid treatment between strong opioid users and weak opioid users.
Methods
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“…The prevalence of opioid use during pregnancy is relatively similar across trimesters, suggesting that the timing and duration of exposure may have differential effects on the offspring ( Zhao et al, 2021 ). One caveat of studying prenatal opioid exposure in rodents is that the third trimester in humans corresponds to the first two weeks of postnatal life in rats ( Zeiss, 2021 ).…”
Opioid misuse among pregnant women is rapidly increasing in the United States. The number of maternal opioid-related diagnoses increased by 131% in the last 10 years, resulting in an increased number of infants exposed to opioids
in utero
and a subsequent increase in infants developing neonatal abstinence syndrome (NAS). The most prescribed treatment to combat maternal opioid use disorder is buprenorphine, a partial μ-opioid receptor agonist and κ-opioid receptor antagonist. Buprenorphine treatment effectively reduces NAS but has been associated with disrupted cortical development and neurodevelopmental consequences in childhood. Less is known about the long-term neurodevelopmental consequences following buprenorphine exposure
in utero
. Previous research has shown that gestational buprenorphine exposure can induce anxiety-like and depressive-like phenotypes in adult rats, suggesting that exposure to buprenorphine
in utero
may render individuals more susceptible to psychiatric illness in adulthood. A common pathology observed across multiple psychiatric illnesses is dopamine system dysfunction. Here, we administered the highly-abused opioid, oxycodone (10 mg/kg, i.p.) or a therapeutic used to treat opioid use disorder, buprenorphine (1 mg/kg, i.p) to pregnant Sprague Dawley rats from gestational day 11 through 21, then examined neurophysiological alterations in the mesolimbic dopamine system and dopamine-dependent behaviors in adult offspring. We found that gestational exposure to buprenorphine or oxycodone increases dopamine neuron activity in adulthood. Moreover, prenatal buprenorphine exposure disrupts the afferent regulation of dopamine neuron activity in the ventral tegmental area (VTA). Taken together, we posit that gestational buprenorphine or oxycodone exposure can have profound effects on the mesolimbic dopamine system in adulthood.
“…The prevalence of opioid use during pregnancy is relatively similar across trimesters, suggesting that the timing and duration of exposure may have differential effects on the offspring ( Zhao et al, 2021 ). One caveat of studying prenatal opioid exposure in rodents is that the third trimester in humans corresponds to the first two weeks of postnatal life in rats ( Zeiss, 2021 ).…”
Opioid misuse among pregnant women is rapidly increasing in the United States. The number of maternal opioid-related diagnoses increased by 131% in the last 10 years, resulting in an increased number of infants exposed to opioids
in utero
and a subsequent increase in infants developing neonatal abstinence syndrome (NAS). The most prescribed treatment to combat maternal opioid use disorder is buprenorphine, a partial μ-opioid receptor agonist and κ-opioid receptor antagonist. Buprenorphine treatment effectively reduces NAS but has been associated with disrupted cortical development and neurodevelopmental consequences in childhood. Less is known about the long-term neurodevelopmental consequences following buprenorphine exposure
in utero
. Previous research has shown that gestational buprenorphine exposure can induce anxiety-like and depressive-like phenotypes in adult rats, suggesting that exposure to buprenorphine
in utero
may render individuals more susceptible to psychiatric illness in adulthood. A common pathology observed across multiple psychiatric illnesses is dopamine system dysfunction. Here, we administered the highly-abused opioid, oxycodone (10 mg/kg, i.p.) or a therapeutic used to treat opioid use disorder, buprenorphine (1 mg/kg, i.p) to pregnant Sprague Dawley rats from gestational day 11 through 21, then examined neurophysiological alterations in the mesolimbic dopamine system and dopamine-dependent behaviors in adult offspring. We found that gestational exposure to buprenorphine or oxycodone increases dopamine neuron activity in adulthood. Moreover, prenatal buprenorphine exposure disrupts the afferent regulation of dopamine neuron activity in the ventral tegmental area (VTA). Taken together, we posit that gestational buprenorphine or oxycodone exposure can have profound effects on the mesolimbic dopamine system in adulthood.
“…The review involved a meticulous examination of articles accessible through PubMed, published between January 2009 and December 2021, and conducted using the following keywords: 'pregnant,' 'addicted,' 'opioids,' 'NAS,' and 'withdrawal syndrome in obstetrics.' 1,2,4 The search encompassed relevant research from international sources as well as the Polish literature, considering articles available in Polish and English. 1,3 To ensure the inclusion of highquality research, particular attention was paid to the impact factor of the journals in which the articles were published.…”
Section: Methodsmentioning
confidence: 99%
“…Among pregnancies ending in delivery (249,234), 5.4% were exposed to opioids; the incidence of this phenomenon increased by 40.3% from 3.9% in 1998 to 5.5% in 2015, a significant increase was recorded in the 2nd and 3rd trimester of pregnancy. 4 A disturbing phenomenon was the rapid increase in the percentage of newborns with withdrawal syndrome. 2,3,5 As many as 2 out of 3 infants born with NAS were at risk of these complications because the mother used strong opioids during pregnancy.…”
Section: Addiction and Drug Abuse Trendsmentioning
IntroductionStimulant use during pregnancy is a growing concern, particularly in the USA and Europe. This article explores anesthesia challenges in pregnant patients with substance abuse, optimizing analgesic treatment, and addressing newborns of addicted mothers. Understanding substance use differences is crucial for managing complications and providing long-term care.AimInvestigate anesthesia management, analgesic optimization, and care for newborns of drug-addicted pregnant patients.Material and methodsA comprehensive literature review included articles from PubMed (from January 2009 to December 2021) and relevant Polish, English, and German literature.Results and discussionOpioid use by pregnant women, especially in North America, raises concerns for maternal and child health. The incidence of newborns with withdrawal syndrome is rapidly increasing. Anesthesia challenges arise in managing pregnant patients with addiction, including analgesia optimization and reducing neonatal abstinence syndrome risk. Individualized approaches like regional anesthesia minimize systemic opioids and neonatal withdrawal symptoms. Medication-assisted therapy, e.g., buprenorphine and methadone, reduces illicit opioid use and improves outcomes for mother and baby. Collaborative care among providers is essential.ConclusionsManaging drug-addicted pregnant women requires a multidisciplinary approach. Anesthesia providers play a crucial role in ensuring safety and pain control.
“…The Pregnancy Risk Assessment Monitoring System (PRAMS) estimated that 6.6% of pregnant women reported using prescription opioids [ 8 ]. The Quebec Pregnancy Cohort study from 1998 to 2015 showed that 4.7% of pregnant women were exposed to opioids [ 9 ]. Limited data are available on the prevalence of substance use among pregnant women in Iran.…”
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