Medical Termination of Pregnancy

Chapter 216


Medical Termination of Pregnancy



A perfect pregnancy termination drug could be given at any stage of estrus or pregnancy, would be 100% effective, would cause no vaginal discharge, would have no side effects, would not impair future fertility, would be readily available, and would be inexpensive. Unfortunately such a drug does not exist. In cases in which the patient is not a valuable breeding animal, the client should be counseled that the best option is to terminate the pregnancy and to prevent future pregnancies surgical sterilization is recommended. Drugs available for pregnancy termination are discussed under the general categories of those used after pregnancy is confirmed and those used before pregnancy is confirmed. A comprehensive list of drugs to terminate pregnancy commonly available in the United States is discussed.



Drugs Used After Confirmed Pregnancy


If the bitch mated or is thought to have mated, a pregnancy diagnosis should be performed before proceeding to terminate the pregnancy. Even though conception rates in controlled breeding situations resulted in a pregnancy rate of about 90% when only a single mating was allowed on any day of estrus (up to the last 2 days of estrus) (Holst and Phemister, 1974), only 38% of bitches presented for mismate actually may be pregnant (Feldman et al, 1993). A pregnancy examination should be performed at least 30 to 40 days after the last possible breeding to minimize false-negative diagnoses caused by errors in calculating the gestation duration from a mating that occurred early in estrus. Therapy is instituted only if a bitch is pregnant. Drugs that terminate pregnancy can cause premature luteal demise by acting as a direct luteolytic, inhibiting prolactin secretion, or blocking the progesterone receptors or unknown mechanisms.



Prostaglandins




Protocols


Prostaglandin F (PGF) induces lysis of the corpora lutea. In dogs, the natural PGF (Lutalyse) given at a dosage of 0.1 to 0.25 mg/kg q8-12h SC is effective at terminating pregnancy after pregnancy confirmation. One protocol reported to have few side effects is administration of PGF at 0.1 mg/kg q8h SC for 2 days and then 0.2 mg/kg q8h SC until abortion is complete (Feldman et al, 1993). Abortion usually is complete within 9 days, but some dams still have live fetuses after 9 days. It is extremely important to continue the treatments until abortion is complete. In queens, natural PGF is most effective after 40 days of gestation. Beginning at 45 days of gestation, PGF (0.2 mg/kg q12h SC first day, 0.5 mg/kg q12h SC for up to 5 days) caused abortion in 75% of queens.


Synthetic PGF analogs are more potent and have fewer side effects than natural PGF. Cloprostenol (Estrumate) at a dosage of 1 to 2.5 µg/kg q24h SC for 4 to 5 days was 100% effective at inducing abortion (Verstegen, 2000). Once-per-day treatments with synthetic PGF analogs provide an advantage over the three-times-per-day treatments required with natural PGF. Hospitalization or frequency of injections adds greatly to client cost when using PGF as an abortifacient.


To shorten the treatment period required to induce abortion with PGF, PGF (0.1 mg/kg q8h SC for 2 days and then 0.2 mg/kg q8h SC to effect) can be combined with PGE1 (misoprostol, Cytotec) at a dosage of 1 to 3 µg/kg q24h deposited into the cranial vaginal vault. The mean time to complete abortion using this combination was 2 days shorter compared with PGF alone (5 days vs. 7 days, respectively) (Davidson et al, 1997). Similar results have been reported using PGE1 with the synthetic PGF, alfaprostenol (Agaoglu et al, 2011).



Adverse Effects


Adverse effects of natural PGF are more common in dogs than cats and include vomiting, diarrhea, and possibly circulatory collapse. The adverse effects usually subside within 20 minutes, but the bitch should be monitored carefully during this time. To minimize caloric loss, bitches should be fed at least 1 hour after treatment. Minimal to no adverse effects are observed when using PGF analogs at a 1 µg/kg q24h SC dosage.


Drugs used to decrease the adverse effects of natural PGF include a combination of atropine sulfate (0.025 mg/kg), prifinium bromide (0.1 ml/kg), and metopimazine (0.5 mg/kg) SC 15 minutes before PGF administration. Lower doses of natural PGF also decrease adverse effects. Complete pregnancy termination 5 days after starting treatment with minimal adverse effects (tachypnea lasting less than 15 minutes) was reported after administration of natural PGF at a dose of 0.012 mg/kg q6h SC at 30 days of gestation (Len et al, 2011). Clients must be able to administer safely multiple injections to their animals, or the animals must be hospitalized. The safety and efficacy of this protocol makes it the author’s primary choice as an abortifacient in the bitch.



Prolactin Inhibitors


Dopaminergic drugs are prolactin inhibitors. Commercially available prolactin inhibitors include bromocriptine, cabergoline, and metergoline. Bromocriptine (Parlodel) administered at a dosage of 62.5 µg/kg q12h PO to dogs at 43 to 45 days after ovulation resulted in only 50% of bitches aborting; side effects included emesis and loose stools (Wichtel et al, 1990). Because the dosage is so low and the tablets contain so much active drug the bromocriptine tablets can be crushed and dissolved in water to ease dosing. Cabergoline at a dose of 1.65 µg/kg q24h SC for 5 to 6 days at 25 to 40 days after the first mating resulted in abortion for 100% of bitches greater than 40 days of gestation but only for 25% and 67% at 25 days and 30 days of gestation, respectively. Side effects were minimal, and bitches that aborted became pregnant after treatment. In the United States, cabergoline is available in a 0.5-mg tablet. When given at a dose of 160 µg PO to a 32-kg German shepherd dog after 40 days of gestation, it resulted in abortion after 7 days with no side effects (Arbeiter and Flatscher, 1996). Although cabergoline is not expensive for each dose, it may be difficult to administer because of the amount of drug per tablet (0.5 mg) is considerably higher than the dose for a 10-kg dog (0.05 mg). Metergoline (0.6 mg/kg q12h PO starting after the onset of cytologic diestrus and continued to effect) induced abortion in 89% of bitches with no side effects (Nöthling et al, 2003). Cabergoline (5 to 15 µg/kg q24h PO) administered to feral cats 36 to 40 days of pregnancy for 4 to 9 days caused abortion in 100% of queens (Jochle and Jochle 1993).




Prolactin Inhibitors in Combination with Prostaglandin F Analogs


Combining prolactin inhibitors with PGF increases the efficacy of pregnancy termination and reduces the side effects of treatment. Cloprostenol (1 or 2.5 µg/kg q24h SC once) in combination with cabergoline (1.65 µg/kg q24h SC for 5 days) from midgestation induced abortion with no adverse side effects (Onclin et al, 1995). After an average of 9 days, cabergoline (5 µg/kg q24h PO) 1 hour after cloprostenol (1 µg/kg q48h SC) caused fetal death with no side effects when started at 25 days of gestation peak (Onclin and Verstegen, 1996). Treatment with cabergoline (5 µg/kg q24h PO) for 10 days combined with either one dose (2.5 µg/kg SC) or two doses (1 µg/kg SC repeated 4 days later) of cloprostenol at the start of the treatment was successful at inducing pregnancy termination. Similarly, bromocriptine (30 µg/kg q8h PO) for 10 days with either one dose (2.5 µg/kg SC) or two doses (1 µg/kg SC repeated 4 days later) of cloprostenol at the start of the treatment was successful at inducing pregnancy termination (Onclin and Verstegen, 1999). All bitches in the aforementioned study became pregnant during the subsequent estrous cycle, which occurred sooner than normally anticipated. As with PGF alone, using PGE1 with the cabergoline combined with a synthetic PGF decreased the time to abortion compared with those not receiving PGE1. Oral cabergoline (5 µg/kg q24h PO) combined with cloprostenol (5 µg/kg q48h SC) starting at the thirtieth day after coitus caused abortion in 100% of queens after an average of 9 days of treatments.

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Jul 18, 2016 | Posted by in PHARMACOLOGY, TOXICOLOGY & THERAPEUTICS | Comments Off on Medical Termination of Pregnancy

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