- Case report
- Open Access
- Open Peer Review
Early-onset fetal growth restriction treated with the long-acting phosphodiesterase-5 inhibitor tadalafil: a case report
© The Author(s). 2016
- Received: 14 March 2016
- Accepted: 12 October 2016
- Published: 8 November 2016
Severe early-onset fetal growth restriction occurs in 0.4 % of all pregnancies, and the prognoses of these patients are dismal. Severely growth-restricted fetuses (far below 500 g) are thought to be nonviable. Since there have not been effective treatments for such fetal patients, obstetricians have simply tried to identify the optimal timing for their delivery. There are a few reports suggesting that the phosphodiesterase type 5 inhibitor sildenafil has some limited beneficial effects on fetal growth, but there are no such reports on tadalafil, another derivative phosphodiesterase type 5 inhibitor which has a much longer half-life than sildenafil. Here we present a case in which the administration of tadalafil to the mother revived the arrested growth and severe oligohydramnios of the very prematurely growth-restricted fetus.
We describe a case of early-onset fetal growth restriction with oligohydramnios in a 41-year-old primigravida Japanese woman who was treated with tadalafil (20-mg tablet daily) from 22 weeks’ gestational age. Ten days after the initiation of the tadalafil therapy, the amniotic fluid level rose and the weight of the fetus began to increase. A 1024-g baby boy was delivered by cesarean at 32 weeks’ gestation. The z-score for fetal head circumference had increased from −2.2 to −1.2, whereas the z-score of the femur legth was decreased to −4.3, indicating that tadalafil preferentially increased the blood flow to important organs.
We achieved two positive results by administering tadalafil to the mother carrying a severely growth-restricted fetus with oligohydramnios. First, the z-scores of head circumference and abdominal circumference had at first declined but started to rise after the tadalafil administration. Second, the amniotic fluid, which was emptied before the tadalafil treatment, recovered to normal range with this treatment. Tadalafil administration to mothers could be a promising therapy to reverse severe fetal growth restriction and oligohydramnios.
- Fetal growth restriction
- Phosphodiesterase-5 inhibitor
The management of fetal growth restriction is based on the prolongation of gestation long enough for fetal organs to mature while simultaneously preventing irreversible deterioration of the fetus’ well-being. This policy is used because there has been no treatment to reverse fetal growth in utero until now. The administration of aspirin or oxygen to the mother and in-patient bed rest for the mother were all found to have no beneficial effects on fetal growth in randomized control studies [1–3]. Several promising therapies are currently under development to reverse fetal growth restriction . One of these therapies is sildenafil, a phosphodiesterase (PDE) 5 inhibitor that is used to treat both pulmonary hypertension and erectile dysfunction. In an open-label pilot study, treatment with the PDE5 inhibitor sildenafil seemed to be effective in increasing fetal abdominal circumference (AC) of patients with early-onset fetal growth restriction .
The PDE5 inhibitor tadalafil was developed as a medication that was longer acting than sildenafil (the biological half-life of tadalafil is 14 to 15 hours versus sildenafil’s 3 hours) for the treatment of pulmonary hypertension, erectile dysfunction, and prostatic hypertrophy. We used tadalafil successfully in the following single case of early-onset severe fetal growth restriction.
At a 19-weeks gestational checkup of a post-in vitro fertilization pre-embryo transfer (IVF-ET) pregnancy of a 41-year-old primigravida Japanese woman, the result of a fetal chromosomal test was normal, and normal amniotic fluid was observed. At 22 weeks and 4 days, severe oligohydramnios was observed (the amniotic fluid index decreased to nearly 0) with the fetal bladder emptied. The estimated fetal weight was 309 g: −2.6 standard deviation (SD). As judged by the biparietal diameter (BPD), the growth of the fetus had been arrested by nearly 4 weeks.
The weight of the fetus increased by approximately 50 to 100 g per week. The amniotic fluid maximum vertical distance increased from 0.9 cm to 4.4 cm at 27 weeks’ gestational age, then decreased to <2 cm at 32 week’s gestation. At this time, fetal heart rate monitoring showed many variable decelerations, and the fetus was in the breech position. We informed our patient about this situation, and after careful consideration she and her husband chose to continue to the delivery. At 32 weeks 2 days, we performed a cesarean because the weight of the fetus had reached >1000 g, which is generally thought to guarantee intact survival . At the moment of the cesarean delivery, the umbilical artery pulsatility index (PI) was 0.97, the middle cerebral artery PI was 1.48, and the ductus venosus wave was negative. A 1024-g baby boy was delivered without acidemia, with Apgar scores of 5 and 7 at 1 minute and 5 minutes after birth. The baby boy is now on an uneventful course at 3-months old.
A pathological examination of the placenta revealed excessive torsion of the cord, chorangiosis, and infarction, which suggested that placental hypoperfusion may have contributed to the growth of the fetus. There was no funisitis or chorioamnionitis.
This is the first report of tadalafil being used for the treatment of early-onset fetal growth restriction, to the best of our knowledge. Twenty mg per day of tadalafil — which is the same dosage as that used for the treatment of pulmonary hypertension — not only restarted the growth of the fetus but also improved the condition of the fetus, increasing fetal urine and amniotic fluid levels.
Tadalafil was developed in 2009 as a new PDE-5 inhibitor with a longer biological half-life than sildenafil, and it has recently become more widely used for the treatment of pulmonary hypertension, erectile dysfunction, and prostate hypertrophy. Tadalafil has an advantage in that it can be taken even on a full stomach, unlike sildenafil. To-date, case reports [7, 8] and a small pilot trial study  demonstrated that sildenafil had a beneficial effect on early-onset fetal growth restriction. von Dadelszen et al.  reported that their group (n = 10) of cases of fetal growth restriction treated with sildenafil showed significantly increased ACs compared with a group of retrospectively gathered cases of fetal growth restriction (n = 17). Theoretically, tadalafil seems to be a better choice than sildenafil because it can achieve a steadier blood concentration and effects.
The rationale for the use of tadalafil therapy in the present case – the reason why the fetus would have died without life-saving intervention – is twofold. First, early-onset fetal growth restriction that shows umbilical venous fluctuation and reverse ductus venosus flow, which were observed in this case, is the strongest predictive factor for intrauterine fetal death . Second, almost one-half of the reported cases of early-onset fetal growth restriction were complicated with severe oligohydramnios and destined to die . We believe that in the present case the tadalafil therapy contributed to the improved intrauterine environment and to the extension of the pregnancy to 32 week’s gestation, and finally to the uncomplicated post-delivery course.
It is interesting to note the different rates of the growth curves of the HC, AC, and FL z-scores in our patient (Fig. 2). The HC z-score increased significantly after the initiation of tadalafil therapy and finally became within normal range, whereas the FL z-score progressively worsened to −4.3. The AC z-score remained between −1.8 and −2.5. These findings indicate that tadalafil preferentially dilates the fetal arteries and distributes blood flow to more important organs such as the brain. In contrast, tadalafil might have increased the placental circulation through the internal iliac arteries at the expense of the blood flow of the external iliac arteries to inferior extremities.
The umbilical artery PI decreased after the initiation of tadalafil treatment in the present case, as Dastjerdi et al. reported for sildenafil , whereas the middle cerebral artery PI temporarily decreased for 1 week after the initiation of tadalafil treatment in our patient, unlike the Dastjerdi report. This result indicates that tadalafil was transferred through the placenta and dilated the cerebral arteries as well as placental arteries, even as its brain-sparing effect had already been exerted.
Another interesting finding in the present case was that the reverse flow of the ductus venosus appeared intermittently after the normalization that was induced by tadalafil therapy. This indicates that tadalafil dilated not only arteries but also veins of the placenta, which led to an increase in the venous flow to the heart, manifested as a reverse return of the ductus venosus.
A limitation of this case report is that it involves only one case, and thus no conclusions can be made regarding the best timing for tadalafil treatment or its potential maternal and fetal adverse effects (including long-term effects), or the evolution of Doppler parameters.
Tadalafil administration to mothers could be a promising therapy to reverse severe fetal growth restriction and oligohydramnios. However, the present case highlights the need for further research about this use of tadalafil, with animal models and clinical studies.
The authors have not received any funding for the present study.
Availability of data and materials
MS, KO, and TI equally contributed to writing the manuscript. KO and TI contributed to the conception and design of the work. MK, MN, HT, NM, and YK contributed to the collection and interpretation of the data. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Ethics approval and consent to participate
Mie University Hospital Institutional Ethics Committee approved the treatment of our patient. Ethical approval number was 135-392.
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