Although persistent pulmonary hypertension of the newborn (PPHN) and infantile hypertrophic pyloric stenosis (HPS) are both well-known diseases that occur in early infancy, PPHN complicated by HPS is rare. As nitric oxide (NO) is an important mediator of biological functions, on both the vascular endothelium and smooth muscle cells, the decreased production of NO might play a role in the pathogenesis of both PPHN and HPS. We present the case of a neonate who developed HPS following PPHN, including a detailed review on research published to date, and we discuss the pathogenesis of PPHN and HPS.
Case presentation
A female neonate born at 38 weeks of gestation, weighing 3140 g, developed PPHN due to meconium aspiration syndrome. Intensive treatment with high frequency oscillations and inhaled NO were initiated, and sildenafil and bosentan were added. She gradually recovered. At 15 days of age, the patient developed recurrent vomiting after feeding and the diagnosis of HPS was made. Intravenous atropine therapy was started at 20 days of age, but the efficacy was clinically unsatisfactory. The coadministration with transdermal nitroglycerin improved the symptoms, and oral feeding was successfully re-introduced.
Conclusions
Our patient recovered from both PPHN and HPS using NO-related medications. A decrease in NO synthesis is likely to be a common pathway for PPHN and HPS.
Abkürzungen
CDH
Congenital diaphragmatic hernia
eNOS
Endothelial nitric oxide synthetases
HPS
Hypertrophic pyloric stenosis
nNOS
Neuronal nitric oxide synthetases
NO
Nitric oxide
NOS
Nitric oxide synthetases
PH
Pulmonary hypertension
PPHN
Persistent pulmonary hypertension of the newborn
Background
Persistent pulmonary hypertension of the newborn (PPHN) is a life-threatening syndrome of failed circulatory adaptation at birth with persistently increased pulmonary vascular resistance [1]. Inhaled nitric oxide (NO), which improves oxygenation through selective pulmonary vasodilation without causing systemic hypotension, is the mainstay of PPHN treatment. On the other hand, hypertrophic pyloric stenosis (HPS) is a common surgical cause of vomiting during early infancy [2]. This condition is characterized by an abnormal thickening of the pyloric sphincter muscle layer, creating an obstruction of the gastric outlet. Although the exact etiology and pathogenesis of HPS are unknown, one hypothesis is impaired function of acetylcholine and muscarinic receptors [3], and medical treatment with atropine, a cholinergic blocking agent with antimuscarinic activity, is an available alternative to pyloromyotomy [4‐6]. Moreover, the increased sphincter tone is believed to be related to a decrease in NO production [7]. Recently in Japan, the efficacy of transdermal nitroglycerin, a NO donor, as a non-surgical treatment option was reported [8]. Although PPHN and HPS are well-known diseases, their co-occurrence is rare. In this report, we describe a neonate with PPHN who subsequently developed HPS and discuss the relationship between these two diseases.
Case presentation
The patient was a female neonate born at 38 weeks of gestation, weighing 3140 g. She was delivered to a 34-year-old primigravida uncomplicated mother by emergency cesarean section due to fetal distress following idiopathic oligohydramnios which occurred during the third trimester. At birth, the infant was non-vigorous due to meconium aspiration and required resuscitation using endotracheal intubation and tracheal suctioning. The Apgar scores were 5 and 7 at 1 and 5 min, respectively. She required mechanical ventilation after transfer to the neonatal intensive care unit due to the development of respiratory insufficiency. A chest X-ray revealed bilateral diffused, grossly patchy opacities, which is a typical finding in meconium aspiration syndrome. Moreover, a > 10% difference between pre- and post-ductal saturation of peripheral oxygen, measured by pulse oximetry, persisted despite increased oxygen supplementation and ventilatory support. An echocardiogram revealed a structurally normal heart with marked tricuspid regurgitation, right-to-left shunting through the ductus arteriosus, and suprasystemic pulmonary pressures. Based on the clinical presentation and findings on imaging, a diagnosis of PPHN was made and intensive treatment with high frequency oscillations and inhaled NO were initiated. Subsequently, sildenafil, a specific phosphodiesterase type 5 inhibitor that enhances NO-mediated vasodilation, and bosentan, an endothelin receptor-inhibitor that increases internal activity of endogenous NO, were added to treatment. The symptoms gradually improved, and the infant was subsequently weaned from inhaled NO and ventilatory support, with extubation performed at 11 days of age.
Anzeige
Oral feeds with breast milk were started at 12 days of age. However, 3 days later, the infant developed non-bilious vomiting after feeding, which increased in frequency in the following days. The daily clinical examination was unremarkable and no mass was palpable in the abdomen. Plain abdominal X-ray at 17 and 19 days of age showed a dilated stomach. A contrast study was not performed. At 20 days of age, abdominal ultrasonography (US) revealed a hypertrophic pylorus, with a 5–6-mm mural thickening over a length of 18 mm, confirming the diagnosis of HPS. At this time, the plasma arginine level was 53.3 μmol/L (reference range: 53.6–133.6 μmol/L). The parents selected conservative treatment for their child, and atropine therapy was started. Atropine was administered intravenously at a dose of 0.1 mg/kg/day, which was divided equally by the number of oral feedings. Frequency of vomiting did not decrease in 3 days, and the dose was increased to 0.13 mg/kg/day. Subsequently, the frequency of vomiting decreased, but significant gastric residuals continued for more than 7 days after the start of atropine therapy. Hypertrophic pyloric muscle remained unchanged on repeated US. We considered the efficacy of the treatment was clinically unsatisfactory referring to previous studies [6, 9]. Then, transdermal nitroglycerin (5 mg/day) was added to the treatment at 29 days of age. Thereafter, the infant tolerated full enteral feeds, with no further vomiting, and oral feeding was successfully re-introduced. At 34 days of age, atropine was changed to oral administration at a dose of 0.2 mg/kg/day. Transdermal nitroglycerin was ceased over a day after that (the total dosing period was 7 days). Subsequently, the infant remained well and was discharged home at 43 days of age.
Discussion
PPHN occurs in 2 per 1000 live births [1], with the incidence of HPS estimated at 1–8 in 1000 live births [2]. However, to the best of our knowledge, there are only five previously reported cases in the literature on the occurrence of both conditions in a patient [10‐12]. The characteristics of those cases of HPS and PPHN or PH are summarized in Table 1 [10‐13]. Brouwers et al. considered that if there was no common pathophysiologic pathway between HPS and PPHN, the combination of both conditions would occur in approximately 1 per 100,000 live births, and they proposed a deficiency in NO as a common pathway [10].
Table 1
Cases of hypertrophic pyloric stenosis following persistent pulmonary hypertension of the newborn or pulmonary hypertension
PPHN persistent pulmonary hypertension of the newborn, PH pulmonary hypertension, HPS hypertrophic pyloric stenosis, MAS meconium aspiration syndrome, CDH congenital diaphragmatic hernia, CHD congenital heart disease, ECMO extracorporeal membrane oxygenation, NO nitric oxide
a treatment associated with nitric oxide
NO has many physiological and pathological functions, and is endogenously synthesized from L-arginine by the family of NO synthetases (NOS) [14]. NOS is one of the most regulated enzymes in biology; in mammals, three isoforms have been identified, with two being constitutive (neuronal NOS [nNOS] and endothelial NOS [eNOS]) and the third being inducible NOS (Table 2) [14, 15]. NO is a potent vasodilator that is involved in the normal transition from fetal to neonatal circulation. In PPHN, an impairment in endothelial NO production was previously reported [1]. Hypoxia causing PPHN may reduce NO production through an uncoupling of NOS in pulmonary arterial endothelial cells [16]. On the other hand, NO has been demonstrated as a major inhibitory non-adrenergic and non-cholinergic neurotransmitter in the gastrointestinal tract, causing relaxation of the smooth muscle of the myenteric plexus upon its release [17]. There is evidence suggesting that impairment in NO synthesis contributes to HPS. Mice with reduced NOS activity developed grossly enlarged stomachs, with hypertrophy of the circular muscle wall [18]. In humans, decreases in serum NO and tissue expression of nNOS were observed in patients with HPS [7]. Therefore, NO deficiency may play a role in the pathogenesis of both PPHN and HPS. However, previous case reports have not demonstrated a substantial relationship between these two disorders and NO [10, 11]. In the case described by Brouwers et al., recovery from PPHN and HPS was obtained with treatments not associated with NO. Similarly, Malwade et al. did not provide a NO-related treatment for PPHN. In contrast, the present case of PPHN and HPS was successfully treated using inhaled NO, sildenafil, bosentan, and transdermal nitroglycerin. Regarding the HPS, transdermal nitroglycerin alone was not effective; coadministration with intravenous atropine was effective. Carr et al. demonstrated in their animal study that the inhibition of myopia by atropine is dependent on production of NO [19]. This suggests that the effect of atropine for HPS might also be mediated by NO and might support the efficacy of our treatment. Therefore, the approaches provided in our case all contributed to increasing NO in the affected organs. Regarding the mechanism of NO synthesis, eNOS, associated with PPHN, and nNOS, associated with HPS, do not have an association that can be explained by a single gene abnormality because these NOSs are encoded by different genes (Table 2) [14]. As NOS requires L-arginine for the production of NO regardless of the type, an impairment in arginine metabolism is likely to play an important role in NOS dysfunction. Therefore, the association between PPHN and HPS may be explained by a decrease in plasma concentration of arginine, leading to a deficiency in NO synthesis in the affected organ systems (Fig. 1). A previous study demonstrated that infants with PPHN had a low plasma concentration of arginine [20]. In HPS, Glass et al. reported an increase in plasma arginine levels in patients with HPS after surgery [21], but, to the best of our knowledge, there is no evidence of a decreased level of plasma arginine. In our patient, the plasma level of arginine at the time of diagnosis of HPS was borderline low, and we measured the arginine level only once for HPS, without measurement for PPHN. Further research is required to evaluate arginine metabolism in patients with either PPHN or HPS.
Table 2
Characteristics of different forms of nitric oxide synthase [14, 15]
Type
Gene(s)
Location
Function
Neuronal NOS
(nNOS)
NOS 1
Chromosome 12
(12q24.22)
Nervous tissue
Skeletal muscle type II
Cell communication:
Neurotransmission
Skeletal muscle contraction
Sexual function
Body fluid homeostasis
Inducible NOS
(iNOS)
NOS 2
Chromosome 17
(17q11.2)
Immune system
Cardiovascular system
Immune defense against pathogens:
Inflammation
Infection
Malignant diseases
Blood pressure regulation
Endothelial NOS
(eNOS)
NOS 3
Chromosome 7
(7q36.1)
Endothelium
Cardiovascular homeostasis:
Vasodilation
Inhibition of platelet aggregation
and adhesion
Inhibition of vascular inflammation
NOS nitric oxide synthase
×
Conclusions
The present patient recovered from both PPHN and HPS using NO-related medications. A decrease in NO synthesis is likely to be a common pathway for PPHN and HPS. If an infant recovering from PPHN develops recurrent vomiting, physicians should consider HPS as a complication.
Anzeige
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
Ethics approval and consent to participate
Our ethics committee waived the requirement of ethics approval because all medical and laboratory procedures are routinely carried out and do not affect decisions concerning treatment.
Consent for publication
Written informed consent was obtained from the patient’s parents for publication of this case report.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Wenn Kinder an Werktagen zum Arzt gehen, werden neu auftretender Typ-1-Diabetes und diabetische Ketoazidosen häufiger erkannt als bei Arztbesuchen an Wochenenden oder Feiertagen.
Augentropfen mit niedrig dosiertem Atropin können helfen, das Fortschreiten einer Kurzsichtigkeit bei Kindern zumindest zu verlangsamen, wie die Ergebnisse einer aktuellen Studie mit verschiedenen Dosierungen zeigen.
Seit 2021 ist die Untersuchung auf spinale Muskelatrophie Teil des Neugeborenen-Screenings in Deutschland. Eine Studie liefert weitere Evidenz für den Nutzen der Maßnahme.
Im Choosing-Wisely-Programm, das für die deutsche Initiative „Klug entscheiden“ Pate gestanden hat, sind erstmals Empfehlungen zum Umgang mit Notfällen von Kindern erschienen. Fünf Dinge gilt es demnach zu vermeiden.
Update Pädiatrie
Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.