1. By Dr.Asmaa Al sanjary

2.  Preterm delivery is defined by a birth occurring before 37 completed weeks of gestation.  Prematurity is multifactorial and its incidence has increased during the last decade in most occidental countries, probably due to increased risk factors responsible for elective prematurity.  The mechanisms for preterm labour are still unclear. It could be associated either with a premature activation of the physiological contracting process or with a pathological factor responsible for uterine contractions, leading to preterm delivery.

3.  Tocolytic drugs have been available for several decades but their actions are directed toward the effects and not the causes of preterm labour.  Tocolysis aims not only to inhibit uterine contractions but also to allow a safe transfer of the pregnant patient to a tertiary care centre,It gives the opportunity to administrate corticosteroids for preventing neonatal risks associated with prematurity  Their efficacy depend on an early and accurate diagnosis of the condition; the fetal fibronectin, and cervical length ultrasonography.

5. Drugs safety and side effect profile is a major concern not only for the pregnant women but also for the fetus. administration route and the optimal range of gestational age for these treatments

6. Are utilized as a tocolytic since the 1970s. Ritodrine was the first tocolytic approved by the FDA in 1980; it was voluntarily removed from the market in 1993 due to concerns of serious adverse effects. Due to recent warnings from the FDA concerning the lack of safety with the prolonged use of terbutaline, its use as a preventative agent or use beyond 48 to 72 hours is no longer recommended. In addition, oral terbutaline is not recommended as its effectiveness has not been established

7. Common adverse effects, when beta-agonists are compared to no treatment or placebo, include palpitation(68% with beta-agonists vs. 5% with controls), Tremor (39% vs. 4%), nausea (20% vs. 12%), headache (23%vs. 6%) and chest pain (10% vs. 1%). Rare, but serious and potentially life threatening adverse effects have been reported following beta-agonists use and a few maternal deaths associated with the use of these drugs were reported.

8. Pulmonary edema is a well-documented Complication, usually associated with aggressive Intravenous hydration. A systematic review reported one case of pulmonary edema among 850 women (1/425 with beta-agonists vs. 0/427 with placebo).

9. In conclusion, despite their efficiency, β 2 agonists’ safety profile is a real concern responsible for therapy discontinuation and choosing alternative tocolytic drugs.

10. (magnesium sulphate, Other tocolytic drugs (magnesium sulphate, indomethacin and atosiban) indomethacin and atosiban),has fewer types of adverse effects reported and these occurred Less frequently.

11.  These agents are in competition with the myometrial and decidual oxytocin receptors. The only drug used in clinical practice is atosiban. It blocks in a reversive manner the intracytoplasmic calcium release associated with contractions and downregulates prostaglandin synthesis.

12.  Atosiban is widely used in clinical practice because of its low side effects profile and seems to be an adequate therapeutic choice for Effective tocolysis with a low maternal and fetal adverse effects profile.

13. Atosiban represents an advance in currently available tocolytics, and should be considered a first-line tocolytic for the management of SPTL. Atosiban is licensed in Europe for treatment of SPTL. The recommended dosage and administration schedule for atosiban is a three-step procedure. Duration of treatment should not exceed 48 h and the total dose given during a full course should preferably not exceed 330 mg of atosiban. In the early gestational age with or without PPROM, the use of atosiban can be prolonged for a further few days without any significant side effects.

14. For atosiban, the only documented adverse effect is nausea (11% with atosiban vs.5% with placebo) but this is only of short duration and only in association within about a minute during which the bolus dose is administered.

15.  As magnesium is a calcium antagonist, it decreases calcium intracellular concentration  no benefit of Magnesium sulphate administration over placebo use in preterm labour.  As the drug is crossing the placenta, there were concerns about fetal safety.  An increased risk of perinatal death and neonatal neurological and metabolic adverse effects at high dosage.  Higher risk of death but a non-significant reduction in cerebral palsy at 18-months (corrected age) in infants exposed to magnesium sulfate.

16. It can also affect maternal neuromuscular system. Over a serum concentration of 9 mg/dL, there is a high toxicity risk resulting in disappearance of reflexes and respiratory depression and at 18mg/dl there is risk of cardiac arrest. Despite questionable safety and efficacy, still be used by obstetrician as their primary tocolytic therapy.

17.  There is no evidence any more to recommend this drug as a first-line tocolytic agent.

18.  Prostaglandin-synthase or cyclooxygenase (COX) isoforms COX-1 and -2 are essential enzymes for converting arachidonic acid to prostaglandins.  Indomethacin, a nonspecific COX inhibitor, has been reported in studies and in a recent meta- analysis to be an efficient tocolytic drug compared to placebo, significantly delaying preterm delivery.  It can be administrated rectally or orally.

19.  Its use should be restricted in duration as the drug use for 2 days will not cause oligohydraminos. It should be limited to pregnancies below 32 weeks because of fetal ductus arteriosus closure risk and decreased urine production responsible for oligohydramnios. These treatments also have maternal side effects including gastric ulcer or asthma recurrence.  COX-2 inhibitors such as nimesulide or rofecoxib have been studied in animal but not yet in humans and are not actually recommended for preventing preterm labour in clinical practice. In conclusion, indomethacin is an efficient tocolytic drug with no serious adverse drug reaction and is indicated for short-term effect during the second trimester of pregnancy.

20.  Calcium-Channel Blockers :These agents are interfering with the calcium ions transfer through the myometrial cell membrane. They decrease intracellular free calcium concentration and induce myometrial relaxation.  Nifedipine is the most commonly used single drug for preterm labour inhibition. nifedipine compared with β adrenergic receptor agonists has higher efficiency and a lower side effects.

21. Nifidipine is used at a daily dose of 30–60 mg daily. An initial loading dose of 20 mg orally is given orally, followed by 10–20 mg every 6–8 hours. The sublingual form is not recommended for treatment of preterm labor because it acts more treatment of preterm labor because it acts more rapidly than the oral form and can cause acute hypotension.

22. Nifidipine is commonly used in clinical practice as they has being generally well-tolerated as a single agent therapy. Use with magnesium sulfate should be avoided as it has resulted in harmful consequences including cardiovascular collapse.

23. nifedipine is aN efficient tocolytic agent, with an easy oral route of administration, few side effects, and a low neonatal complications rate. However, it should be used with caution in patients with compromised cardiovascular condition as they may be at risk of pulmonary oedema and cardiac failure

24.  NO is a powerful vasodilator synthesized during an amino acid oxidation process catalysed by NO synthase. It is present in myometrial cells and increases cGMP content by interaction with guanylyl cyclase. Transdermal nitroglycerin administration has been used in preterm labour only in small series, It has better tocolytic effect than placebo on delaying delivery for two days(similar to ritodrine). Major side effects are maternal headache and sever hypotension. There is risk of tocolysis failure

25.  there is no large randomized studies available,  NO is not used in clinical routine.  Its use still exparmental.

26.  Some drugs are used as first-line single therapy such as β adrenergic receptor agonists and atosiban in Europe.while in America Atosiban is not licensed for use as it’s believed not reduce the incidence of preterm birth or improve neonatal outcomes when compared to placebo,with increase in fetal/infant death seen in those exposed to atosiban.

27.  severe cases, combined therapy could be offered but should be restricted because of adverse effects addition and no improvement in perinatal outcome.  The combination of magnesium sulphate and nifedipine should be avoided because of reported cases of symptomatic hypocalcemia, Neuromuscular blockade, and cardiac toxicity, including maternal death.

28. calcium channel blockers, particularly nifedipine, are used as a reasonable choice for initial tocolysis due to the low incidence of adverse effects, oral route of administration, efficacy in improving neonatal outcomes, and potential for use at any gestational age. Indomethacin is an available alternative for pregnancies of less than 32 weeks gestation as Premature closure of the ductus arteriosus has been shown to occur more often in those >32 weeks, it should be avoided in patients at increased risk of bleeding and those with renal or hepatic insufficiency, gastrointestinal disease, or asthma.

29.  Specific conditions are subject to discussion: in multiple pregnancies, expanded blood volume and anaemia may predispose to pulmonary oedema when tocolytic agents such as β adrenergic receptor agonists,magnesium sulphate, and calcium channel blockers are prescribed. In these pregnancies, atosiban, with its low side effects incidence, seems to be the safest choice.

30.  Last generation of oxytocin receptor antagonists such as barusiban could be more efficient and have less affinity for the vasopressin receptors.  Specific COX-2 inhibitors or “coxibs,” prostaglandin receptors antagonists could be promising tocolytic alternatives