| Tocolytic | |
|---|---|
| Specialty | OB/GYN |
Tocolytics (also called anti-contraction medications or labor suppressants) are medications used to suppress premature labor (from Greek τόκος tókos, "childbirth", and λύσις lúsis, "loosening"). Preterm birth accounts for 70% of neonatal deaths.[1] Therefore, tocolytic therapy is provided when delivery would result in premature birth, postponing delivery long enough for the administration of glucocorticoids, which accelerate fetal lung maturity but may require one to two days to take effect.
Commonly used tocolytic medications include β2 agonists, calcium channel blockers, NSAIDs, and magnesium sulfate. These can assist in delaying preterm delivery by suppressing uterine muscle contractions and their use is intended to reduce fetal morbidity and mortality associated with preterm birth.[2] The suppression of contractions is often only partial and tocolytics can only be relied on to delay birth for a matter of days. Depending on the tocolytic used, the pregnant woman or fetus may require monitoring (e.g., blood pressure monitoring when nifedipine is used as it reduces blood pressure; cardiotocography to assess fetal well-being). In any case, the risk of preterm labor alone justifies hospitalization.
Tocolytics are used in preterm labor, which refers to when a baby is born too early before 37 weeks of pregnancy. As preterm birth represents one of the leading causes of neonatal morbidity and mortality, the goal is to prevent neonatal morbidity and mortality through delaying delivery and increasing gestational age by gaining more time for other management strategies like corticosteroids therapy that may help with fetus lung maturity.[3][4] Tocolytics are considered for women with confirmed preterm labor between 24 and 34 weeks of gestation age and used in conjunction with other therapies that may include corticosteroids administration, fetus neuroprotection, and safe transfer to facilities.[5]
There is no clear first-line tocolytic agent.[6][7] Current evidence suggests that first line treatment with β2 agonists, calcium channel blockers, or NSAIDs to prolong pregnancy for up to 48 hours is the best course of action to allow time for glucocorticoid administration.[1]
Various types of agents are used, with varying success rates and side effects. Some medications are not specifically approved by the U.S. Food and Drug Administration (FDA) for use in stopping uterine contractions in preterm labor, instead being used off-label.[citation needed]
According to a 2022 Cochrane review, the most effective tocolytics for delaying preterm birth by 48 hours, and 7 days were the nitric oxide donors, calcium channel blockers, oxytocin receptor antagonists and combinations of tocolytics.[8]
| Drug | Mechanism of action | Description | Possible contraindications |
Maternal side effects | Fetal and neonatal side effects |
|---|---|---|---|---|---|
| Terbutaline (Brethine) | β2 agonist | Off-label use, FDA has advised that injectable terbutaline should only be used in urgent situations, and that the oral form of the drug should never be used[9] | Cardiac tachyarrhythmias, poorly controlled diabetes mellitus, hyperthyroidism, prolonged tocolysis(>48 to 72 hours)[1] | Tachycardia, palpitations, hypotension, dyspnea, chest pain, hypokalemia, hyperglycemia, lipolysis, pulmonary edema, myocardial ischemia[10] | Fetal tachycardia, hyperinsulinemia, hypoglycemia, myocardial and septal hypertrophy, myocardial ischemia[11] |
| Ritodrine (Yutopar) | β2 agonist | No longer FDA approved[12] | Poorly controlled thyroid disease, hypertension, and diabetes[13] | Metabolic hyperglycemia, hyperinsulinemia, hypokalemia, antidiuresis, altered thyroid function, physiologic tremor, palpitations, nervousness, nausea or vomiting, fever, hallucinations[14] | Neonatal tachycardia, hypoglycemia, hypocalcemia, hyperbilirubinemia, hypotension, intraventricular hemorrhage[14] |
| Fenoterol | β2 agonist | Not approved for tocolysis by FDA | Diabetes, tachyarrhythmia, hypertrophic obstructive cardiomyopathy, hypersensitivity to fenoterol[15] | Palpitations, tachycardia, and chest pain[16] | Tachycardia,[17] impaired carbohydrate tolerance, hyperinsulinaemia[18] |
| Salbutamol (INN) or albuterol (USAN) | β2 agonist | Shown to be less effective than nifedipine for tocolysis regarding neonatal outcome[19] | Diabetes, ischemic cardiopathy, cardiac arrhythmia, placenta praevia, hyperthyroidism, hypersensitivity to salbutamol (albuterol) [20][21] | Headache, palpitations, tachycardia, tremor, sweating, and shortness of breath[22] | Fetal tachycardia, hypoglycemia, hyperinsulinaemia[22] |
| Hexoprenaline (Gynipral) | β2 agonist | Not FDA approved | Hyperthyroidism, cardiovascular diseases, glaucoma, placental abruption, vaginal bleeding, inflammatory diseases of internal genitalia, 1st trimester of pregnancy, breastfeeding[23][24] | Vertigo, anxiety, tremor, hyperhidrosis, tachycardia, hypotension, hyperglycemia, edema | Hypoglycemia, bronchospasm, anaphylactic shock[24] |
| Nifedipine (Procardia, Adalat) | Ca2+ channel blocker | Is one of the most commonly used tocolytic agents.[25] | Hypotension, preload-dependent cardiac disease.[26] It should not be used concomitantly with magnesium sulfate[27] | Flushing, headache, dizziness, nausea, transient hypotension. Administration of calcium channel blockers should be used with care in patients with renal disease and hypotension. Concomitant use of calcium channel blockers and magnesium sulfate may result in cardiovascular collapse[28] | Calcium channel blockers have the fewest neonatal adverse effects[5] |
| Atosiban | Oxytocin receptor antagonist | Safer than both nifedipine and beta agonists; As effective as nifedipine and more effective than beta agonists.[29] Fewer side effects than β2 agonists.[30] Although not FDA approved in the US, atosiban was developed specifically to delay preterm labor.[31] | No current contraindications | No maternal adverse effects[32] | No adverse effects to the baseline fetal heart rate. No significant difference in neonatal side effect compared to other treatments[32] |
| Indomethacin | NSAID | Shown to effectively delay premature birth, studies show that it is safer and more effective for pregnant women that are <= 32 weeks of gestation [33] | Late pregnancy (ductus arteriosus), significant renal or hepatic impairment[34] | Nausea, heartburn[35] | Constriction of ductus arteriosus, pulmonary hypertension, reversible decrease in renal function with oligohydramnios, intraventricular hemorrhage, hyperbilirubinemia, necrotizing enterocolitis[36] |
| Sulindac | NSAID | Studies show that it has similar efficacy to that of indomethacin and has a milder effect on the fetal ductus arteriousus [37] | Coagulation disorders or thrombocytopenia, NSAID-sensitive asthma, other sensitivity to NSAID[38] | GI complications such as nausea, vomiting and stomach pain due to COX inhibition[39] | NSAIDs have been shown to be associated with constriction of the ductus arteriousus and oligohydramnios[34] |
| Magnesium sulfate[40] | Myosin light chain inhibitor | Probably effective in delaying preterm birth by 48 hours.[8] It is used for its neuro-protective effects since it is shown to decrease the risk of cerebral palsy in infants.[41] | Absolute contraindication: myasthenia gravis.[42] Use as a tocolytic agent may result in death of the fetus or infant.[40] | Flushing, lethargy, headache, muscle weakness, diplopia, dry mouth, pulmonary edema, cardiac arrest[42] | Lethargy, hypotonia, respiratory depression, demineralization with prolonged use[42] |
| Ethanol | GABAA receptor PAM | Shown to be ineffective: no better than placebo.[22]Source revision needed Was a frequently used tocolytic in the mid-20th century, but later double-blind studies[43] found it was not effective. | Pregnancy: no amount of ethanol is safe to the fetus[44] | Intoxication, withdrawal[22] | Fetal alcohol syndrome: ethanol is a teratogen and can harm fetus[44] |
Calcium-channel blockers (such as nifedipine) and oxytocin antagonists (such as atosiban) may delay delivery by 2 to 7 days, depending on how quickly the medication is administered.[45] NSAIDs (such as indomethacin) and calcium channel blockers (such as nifedipine) are the most likely to delay delivery for 48 hours, with the least amount of maternal and neonatal side effects.[46] Otherwise, tocolysis is rarely successful beyond 24 to 48 hours because current medications do not alter the fundamentals of labor activation.[47] However, postponing premature delivery by 48 hours appears sufficient to allow pregnant women to be transferred to a center specialized for management of preterm deliveries, and thus administer corticosteroids for the possibility to reduce neonatal organ immaturity.[46]
The efficacy of β-adrenergic agonists, atosiban, and indomethacin is a decreased odds ratio (OR) of delivery within 24 hours of 0.54 (95% confidence interval (CI): 0.32-0.91) and 0.47 within 48 hours (OR 0.47, 95% CI: 0.30-0.75).[6]
Antibiotics were thought to delay delivery, but no studies have shown any evidence that using antibiotics during preterm labor effectively delays delivery or reduces neonatal morbidity.[41] Antibiotics are used in people with premature rupture of membranes, but this is not characterized as tocolysis.[48]
In addition to drug-specific contraindications,[41] several general factors may contraindicate delaying childbirth with the use of tocolytic medications.
Most tocolytics are currently being used off-label. The future direction of the development of tocolytics agents should be directed toward better efficacy in intentionally prolonging pregnancy. This will potentially result in less maternal, fetal, and neonatal adverse effects when delaying preterm childbirth. A few tocolytic alternatives worth pursuing include Barusiban, a last generation of oxytocin receptor antagonists, as well as COX-2 inhibitors.[50] More studies on the use of multiple tocolytics must be directed to research overall health outcomes rather than solely pregnancy prolongation.[51]