Abstract:Clinical data on the transfer of triptans into human breast milk remain scarce. In a lactation study including 19 breastfeeding women with migraine, we examined the excretion of six different triptans into milk. Following intake of a single dose, each participant collected seven breast milk samples at predefined intervals up to 24 hours after dose. Triptan concentrations in milk were measured using liquid chromatography‐tandem mass spectrometry (LC‐MS/MS). Infant drug exposure was estimated by calculating the … Show more
“…Low levels of sumatriptan are present in breastmilk, but because of poor bioavailability, the amount of sumatriptan transferred to fetal circulation is very small. In a study comparing concentrations in breast milk among six different triptans, both eletriptan and sumatriptan were shown to have very low fetal exposure: mean (range) relative infant dose of 0.6% (0.3–0.8%) and 0.7% (0.2–1.8%), respectively, compared with the two triptans with the greatest exposure, zolmitriptan, 2.1% (0.7–5.3%) and naratriptan, 5.0% (one participant) (148).…”
Section: Clinical Overviewmentioning
confidence: 96%
“…ACOG suggests triptans may be used by lactating patients but advises a shared decision-making model regarding the need to avoid breastfeeding for a specified timeframe after its use (27–29, 36, 115, 148).…”
PURPOSE:To provide updated evidence-based recommendations for the evaluation and treatment of primary and secondary headaches in pregnancy and postpartum.TARGET POPULATION:Pregnant and postpartum patients with a history of or experiencing primary or new secondary headaches.METHODS:This guideline was developed using an a priori protocol in conjunction with a writing team consisting of two specialists in obstetrics and gynecology appointed by the ACOG Committee on Clinical Practice Guidelines–Obstetrics and one external subject matter expert. ACOG medical librarians completed a comprehensive literature search for primary literature within Cochrane Library, Cochrane Collaboration Registry of Controlled Trials, EMBASE, PubMed, and MEDLINE. Studies that moved forward to the full-text screening stage were assessed by two authors from the writing team based on standardized inclusion and exclusion criteria. Included studies underwent quality assessment, and a modified GRADE (Grading of Recommendations Assessment, Development, and Evaluation) evidence-to-decision framework was applied to interpret and translate the evidence into recommendation statements.RECOMMENDATIONS:This Clinical Practice Guideline includes recommendations on interventions to prevent primary headache in individuals who are pregnant or attempting to become pregnant, postpartum, or breastfeeding; evaluation for symptomatic patients presenting with primary and secondary headaches during pregnancy; and treatment options for primary and secondary headaches during pregnancy and lactation. Recommendations are classified by strength and evidence quality. Ungraded Good Practice Points are included to provide guidance when a formal recommendation could not be made because of inadequate or nonexistent evidence.
“…Low levels of sumatriptan are present in breastmilk, but because of poor bioavailability, the amount of sumatriptan transferred to fetal circulation is very small. In a study comparing concentrations in breast milk among six different triptans, both eletriptan and sumatriptan were shown to have very low fetal exposure: mean (range) relative infant dose of 0.6% (0.3–0.8%) and 0.7% (0.2–1.8%), respectively, compared with the two triptans with the greatest exposure, zolmitriptan, 2.1% (0.7–5.3%) and naratriptan, 5.0% (one participant) (148).…”
Section: Clinical Overviewmentioning
confidence: 96%
“…ACOG suggests triptans may be used by lactating patients but advises a shared decision-making model regarding the need to avoid breastfeeding for a specified timeframe after its use (27–29, 36, 115, 148).…”
PURPOSE:To provide updated evidence-based recommendations for the evaluation and treatment of primary and secondary headaches in pregnancy and postpartum.TARGET POPULATION:Pregnant and postpartum patients with a history of or experiencing primary or new secondary headaches.METHODS:This guideline was developed using an a priori protocol in conjunction with a writing team consisting of two specialists in obstetrics and gynecology appointed by the ACOG Committee on Clinical Practice Guidelines–Obstetrics and one external subject matter expert. ACOG medical librarians completed a comprehensive literature search for primary literature within Cochrane Library, Cochrane Collaboration Registry of Controlled Trials, EMBASE, PubMed, and MEDLINE. Studies that moved forward to the full-text screening stage were assessed by two authors from the writing team based on standardized inclusion and exclusion criteria. Included studies underwent quality assessment, and a modified GRADE (Grading of Recommendations Assessment, Development, and Evaluation) evidence-to-decision framework was applied to interpret and translate the evidence into recommendation statements.RECOMMENDATIONS:This Clinical Practice Guideline includes recommendations on interventions to prevent primary headache in individuals who are pregnant or attempting to become pregnant, postpartum, or breastfeeding; evaluation for symptomatic patients presenting with primary and secondary headaches during pregnancy; and treatment options for primary and secondary headaches during pregnancy and lactation. Recommendations are classified by strength and evidence quality. Ungraded Good Practice Points are included to provide guidance when a formal recommendation could not be made because of inadequate or nonexistent evidence.
“…Second-line treatments include other NSAIDs and triptans (with eletriptan being preferred if effective due to its likely lower excretion in breast milk). 51 The safety of gepants and lasmiditan in the setting of lactation is currently unknown, although the excretion of rimegepant into breastmilk is low. 52 These treatments should be avoided until more information is available.…”
Section: Always Avoid Avoidmentioning
confidence: 99%
“…Acute treatments with the best evidence for safe use in lactation are acetaminophen and ibuprofen. Second-line treatments include other NSAIDs and triptans (with eletriptan being preferred if effective due to its likely lower excretion in breast milk) 51 . The safety of gepants and lasmiditan in the setting of lactation is currently unknown, although the excretion of rimegepant into breastmilk is low 52 .…”
Section: Acute Treatment During Pregnancy and Lactationmentioning
Objective
Most patients with migraine require acute treatment for at least some attacks. This article reviews the approach to the acute treatment of migraine, migraine-specific and nonspecific treatment options, rescue treatment and options for management in the emergency department and inpatient settings, and treatment during pregnancy and lactation.
Latest Developments
Triptans, ergot derivatives, and nonsteroidal anti-inflammatory drugs have historically been the main acute treatments for migraine. The development of new classes of acute treatment, including the small-molecule calcitonin gene-related peptide receptor antagonists (gepants) and a 5-HT1F receptor agonist (lasmiditan), expands available options. These new treatments have not been associated with vasospasm or increased cardiovascular risk, therefore allowing migraine-specific acute treatment for the more than 20% of adults with migraine who are at increased risk of cardiovascular events. Neuromodulation offers a nonpharmacologic option for acute treatment, with the strongest evidence for remote electrical neuromodulation.
Essential Points
The number of available migraine treatments continues to expand, although triptans are still the mainstay of migraine-specific acute treatment. There is no one-size-fits-all acute treatment and multiple treatment trials are sometimes necessary to determine the optimal regimen for patients. Switching within and between classes, using the maximum allowed dose, using combination therapy, and counseling patients to treat early are all strategies that may improve patient response to acute treatment.
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