Is late treatment with acetaminophen safe and effective in avoiding surgical ligation among extremely preterm neonates with persistent patent ductus arteriosus?

OBJECTIVE: Evaluate the association of late treatment with acetaminophen vs. immediate surgical ligation with death or neurodevelopmental impairment (NDI) among extremely low gestational age neonates (ELGANs) with persistent patent ductus arteriosus (pPDA). STUDY
DESIGN: Retrospective comparative epoch study of ELGANs with pPDA being considered for surgical ligation. ELGANs in epoch 1 (2009-2012) were referred for ligation, while infants in epoch 2 (2012-2015) were treated with oral acetaminophen and referred for ligation in the absence of improvement. The primary outcome was a composite of death/NDI at 18-24 months.
RESULTS: Ninety-two ELGANs with median[IQR] GA 25.2 weeks [24.4, 26.3] had pPDA (43 in epoch 1, 49 in -epoch 2) with acetaminophen-exposed neonates receiving 7 days [7, 7] of treatment. ELGANs in epoch 2 had reduced ligation (aOR 0.30; 95%CI: [0.11, 0.87]), but there was no difference in death/NDI (aOR 1.03; 95%CI: [0.30, 3.56]).
CONCLUSIONS: Late treatment with acetaminophen to avoid surgery for pPDA is associated with reduced ligation but no difference in death/NDI, supporting the safety and effectiveness of this approach.

Introduction

The management of patent ductus arteriosus (PDA), which occurs in up to 60% of infants born extremely preterm [1], is an area of significant controversy. Persistent PDA after treatment with cyclooxygenase inhibitors (COXI) has been associated with increased mortality and neonatal morbidity [2]. However, methods of definitive ductal closure, such as surgical ligation, have been associated with adverse outcomes, including neurodevelopmental impairment (NDI) in early childhood [3-5], culminating in a trend of clinicians avoiding surgical PDA treatment over the past decade [6-9]. Late treatment with acetaminophen is an effective alternative to facilitate closure of persistent PDA [10] and avoid surgical ligation among extremely preterm neonates [11]. With no demonstrated early adverse effects or neonatal outcomes associated with acetaminophen treatment, neonatologists are now commonly prescribing acetaminophen for PDA, with over 25% of extremely preterm infants with PDA receiving treatment with acetaminophen [12].

There remains, however, significant uncertainty regarding the long-term safety of administering acetaminophen for PDA treatment, including among ELGANs being considered for surgical ligation, among whom over half are subsequently diagnosed with neurodevelopmental impairment in early childhood [13, 14]. Foetal exposure to acetaminophen has been associated with increased language delay, attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) [15-18]. While the administration of short courses of acetaminophen for analgesia [19], PDA prophylaxis [20] or very early PDA treatment [21] among neonates has not been associated with NDI, no studies have evaluated the association of later or prolonged courses of acetaminophen treatment for symptomatic PDA with neurodevelopmental outcomes. Developmental evaluation in early childhood has been recommended for preterm neonates treated with acetaminophen for PDA in light of concerns regarding the risk of NDI following postnatal exposure [22].

The objective of this study was to evaluate the association of late acetaminophen treatment (with surgical ligation ‘back-up’) vs. immediate ligation for persistent large PDA with death or neurodevelopmental impairment in early childhood.

Methods

We conducted a retrospective comparative epoch cohort study of extremely low gestational age neonates (ELGANs, born at gestational age [GA] ≤28 weeks) with persistent large PDA being considered for surgical ligation after failure of COXI and/or conservative therapy. The neonatal intensive care unit at Sunnybrook Health Sciences Centre in Toronto, Canada is a tertiary perinatal centre that admits approximately 200 ELGANs annually. The standard of care in our unit is to treat extremely low birthweight infants (<1000 g) with prophylactic indomethacin (0.1 mg/kg intravenous [IV] daily for 3 days), beginning within the first 6 h after birth. However, in 2010–2011, a prolonged shortage of indomethacin resulted in its administration being temporarily restricted to infants born at GA ≤ 25 weeks. Beyond the transitional period, PDA treatment was considered for neonates who developed a clinically symptomatic PDA (e.g. increasing ventilator support, cardiac murmur and/or wide pulse pressure) and sonographic evaluation was performed by a neonatologist with expertise in targeted neonatal echocardiography. Up to two courses of COXI therapy (indomethacin [0.2 mg/kg intravenously every 12 h for three doses] or ibuprofen [10 mg/kg intravenously/enterally once, followed by 5 mg/kg intravenously/enterally daily for two doses]) were administered to facilitate ductal closure among infants with clinically and echocardiographically significant PDA. The echocardiography criteria for large PDA included ductal diameter ≥2.0 mm and an unrestrictive systemic-to-pulmonary shunt [23], accompanied by echocardiography signs of left heart volume loading and pulmonary overcirculation (e.g. left atrium to aortic root ratio ≥1.5, left ventricular dilatation, increased left ventricular output [>300 ml/kg/min]) and/or diastolic flow reversal in the abdominal aorta. Echocardiography was performed using a Vivid E9 ultrasound machine (GE Healthcare, Chicago, USA) and a 12 MHz phased array multi-frequency probe.

Infants with persistent large PDA after unsuccessful pharmacological and/or conservative therapy and concomitant respiratory insufficiency (dependence on mechanical ventilation and/or high non-invasive mean airway pressure [MAP ≥ 8 cm H2O] or fraction of inspired oxygen ≥ 0.3) and/or end-organ hypoperfusion (e.g. renal insufficiency, inability to tolerate increases in enteral feeding volume) were considered candidates for surgical ligation [24, 25]. Infants were transported to our local quaternary centre for the procedure, which included a left lateral thoracotomy, and an intra- or extra-pleural approach using a clip or ligature at the discretion of the attending surgeon.

In July 2012, oral acetaminophen was introduced as a late therapy after failure or contraindication of COXI treatment among preterm infants with persistent large PDA being considered for surgical ligation. Acetaminophen treatment was administered with the goal of promoting sufficient ductal restriction to effect improvement in clinical stability and echocardiography indices of ductal shunting and avoid ligation.

To evaluate the association of late oral acetaminophen therapy vs. immediate surgical ligation with neonatal outcomes, we compared successive three-year cohorts of extremely preterm neonates who were considered candidates for PDA ligation. In the first epoch (July 1, 2009 to June 30, 2012), infants were referred for PDA surgery directly after failure of COXI therapy [immediate surgical ligation epoch]. In the second epoch (July 1, 2012 to June 30, 2015), neonates with persistent large PDA were treated with a 7 day course of acetaminophen administered orally at a dose of 15 mg/kg every 6 h [acetaminophen epoch] [26]. Infants underwent echocardiography within 3 days of completing acetaminophen treatment and those with persistent clinical and echocardiography signs of large PDA after completion of the treatment course were referred for surgical ligation. Percutaneous transcatheter device closure for PDA among extremely preterm neonates was not available at our centre during either epoch.

Outcomes and assessment

Surviving infants underwent neurodevelopmental assessment at 18–24 months corrected age, which consisted of a clinical examination, visual and hearing assessment, and cognitive, language and motor evaluation using the Bayley Scales of Infant Development, Third Edition (BSID III). Clinical examinations and standardised motor assessments identified the presence of cerebral palsy, which was classified according to the Gross Motor Functional Classification System [27]. Standardised screening for autism spectrum disorder was performed and at-risk children were assessed using the Autism Diagnostic Observational Schedule.

We previously reported that late treatment with acetaminophen in this cohort was associated with reduced surgical ligation, but an increase in chronic lung disease [11]. In this follow-up study, we sought to evaluate the association of late acetaminophen treatment vs. immediate surgical ligation on clinical outcomes at 18–24 months corrected GA. The primary outcome was death or neurodevelopmental impairment. Neurodevelopmental impairment was defined as a composite of neuromotor, neurocognitive and/or neurosensory impairment. (Supplementary Table 1) Secondary outcomes (all estimated at 18–24 months corrected age) included death or severe NDI, mortality alone, NDI alone (any and severe), autism spectrum disorder, and PDA ligation.

Data sources and collection

Eligible infants were identified using local, comprehensive clinical and echocardiography databases and those with chromosomal abnormalities or congenital heart disease (other than secundum atrial septal defect or muscular ventricular septal defect) were excluded. Data on important antenatal and perinatal characteristics was abstracted from patient charts. To guide the appropriate collection of postnatal confounders, a date of study ‘enrolment’ was determined for each infant. Infants in both epochs were considered ‘enroled’ on the earliest date that they were considered a candidate for surgical ligation. The enrolment date for infants in the immediate surgical ligation epoch was the date of referral for PDA surgery. Infants in the acetaminophen epoch were considered enroled on the date of initiation of the course of acetaminophen. Detailed collection of postnatal, pre-enrolment characteristics was performed to enable adjustment for indices of illness severity and morbidities of prematurity that arose or were acquired prior to enrolment.

Statistical analysis

Descriptive statistics were used to summarise antenatal, perinatal and pre-enrolment characteristics for infants in the two epochs. Mean (standard deviation [SD]) and median (interquartile range [IQR]) were used to characterise normally distributed and skewed data, respectively. The characteristics of the infants in each epoch were compared using the Student’s t test or Wilcoxon rank-sum test for continuous variables and the chi-square test or Fisher’s exact test for categorical variables, as appropriate. Multivariable logistic regression analysis was used to estimate the association between epoch and all outcomes, adjusting for perinatal and postnatal, pre-enrolment confounders. Covariates were included in the final model if associated with the primary outcome on univariate analysis (p < 0.20). (Supplementary Table 2) Goodness of fit was assessed using the Hosmer-Lemeshow statistic and all models were evaluated for collinearity and overspecification. Statistical analyses were performed using SAS version 9.4 (Cary, North Carolina). All statistical tests were two-sided with significance evaluated at the 5% level. This study was approved by the local hospital Research Ethics Board and was performed in accordance with the Declaration of Helsinki. Informed consent from the parents of study participants was waived due to the retrospective nature of the study.

Results

From July 1, 2009 to June 30, 2015, 92 of 1034 infants born at ≤28 weeks gestation had persistent large PDA and were considered candidates for surgical ligation after failure or contraindication to COXI and/or conservative therapy (43 of 467 [9.2%] of infants in the immediate surgical ligation epoch and 49 of 567 [8.6%] in the acetaminophen epoch) [Fig. 1]. The final analysis included 82 infants (38 in epoch 1 and 44 in epoch 2) for whom complete outcome information (death or neurodevelopmental impairment) was known, as five infants in each epoch were lost to neurodevelopmental follow-up. There were few significant differences between the acetaminophen and immediate surgical ligation groups in their antenatal and perinatal characteristics, except for known secular trends in clinical management (antenatal magnesium sulphate for foetal neuroprotection [50% vs. 21%, p < 0.01] and exclusively non-invasive delivery room respiratory support [23% vs. 5%, p = 0.02]). (Table 1)

Fig. 1

Flow chart of infants included in the study.

Forty-three of 468 extremely low gestational age neonates (ELGANs) in epoch 1 and 49 of 567 ELGANs in epoch 2 had persistent PDA and were candidates for surgical ligation. The primary outcome of death or neurodevelopmental impairment at 18-24 months was known for 38 (88%) and 45 (92%) of ELGANs in epochs 1 and 2, respectively.

Table 1

Antenatal and perinatal characteristics of preterm infants being considered for surgical ligation.

	Immediate surgical ligation epoch (n = 38)	Acetaminophen epoch (n = 44)	p value
Antenatal and perinatal characteristics
Gestational age at birth (weeks)	25.1 (24.6, 26.0)	25.3 (24.3, 26.3)	0.88
Birthweight (g)	707 (640, 805)	730 (636, 890)	0.57
Small for gestational age (<10th percentile), n (%)	4 (11%)	5 (11%)	0.90
Female sex, n (%)	20 (53%)	24 (55%)	0.86
Outborn, n (%)	10 (26%)	6 (14%)	0.15
Multiple gestation, n (%)	9 (24%)	17 (39%)	0.15
Antenatal corticosteroids, n (%)	34 (89%)	39 (89%)	1.00
Magnesium sulfate for foetal neuroprotection, n (%)	8 (21%)	22 (50%)	<0.01
Caesarean delivery, n (%)	26 (68%)	28 (64%)	0.65
Five-minute Apgar score	7 (6, 8)	7 (5, 7)	0.27
Delivery room resuscitation			0.02
Mask CPAP only, n (%)	2 (5%)	10 (23%)
Endotracheal intubation, n (%)	36 (95%)	34 (77%)
Intubation in first 24 h after birth, n (%)	37 (97%)	41 (93%)	0.38
Prophylactic indomethacin, n (%)	14 (37%)	35 (80%)	<0.01
Score for Neonatal Acute Physiology II	14 (14, 27)	19 (9, 25)	0.95

Data shown for infants for whom complete outcome information was available (death or neurodevelopmental impairment). Five infants in each group were lost to neurodevelopmental follow-up.

Continuous data presented as mean (SD) or median (IQR).

COXI cyclooxygenase inhibitors, CPAP continuous positive airway pressure, PDA patent ductus arteriosus.

Infants in the acetaminophen group started COXI treatment later (10 vs. 6 days after birth, p < 0.01), had a lower percentage of days of invasive mechanical ventilation at enrolment (93% vs. 100%, p < 0.01), and there were no differences in the age of PDA diagnosis, total dose of COXI treatment, or any other clinical characteristic. (Table 2) Infants treated with acetaminophen (40 of 49 infants in the acetaminophen epoch) received a median of 7 days of therapy (IQR: 7, 7) beginning at 26.5 days after birth (IQR: 21, 30.5; range 12–45). No infant in epoch 1 received acetaminophen treatment for PDA.

Table 2

Clinical and echocardiography characteristics at enrolment and neonatal outcomes.

	Immediate surgical ligation epoch (n = 38)	Acetaminophen epoch (n = 44)	p value
Clinical characteristics
Enrolment (day of life)	26 (19, 30)	27 (21, 31.5)	0.44
Enrolment weight (g)	970 (846, 1052)	1004 (822, 1180)	0.40
PDA initial diagnosis (day of life)	4 (4, 6)	5 (3, 7)	0.94
Any COXI treatment (including prophylactic indomethacin), n (%)	36 (95%)	41 (93%)	1.00
First COXI treatment for symptomatic PDA (day of life)	6 (5, 10)	10 (7, 16)	<0.01
Total COXI dose (including prophylactic indomethacin) (mg/kg)a	1.2 (1.2, 1.5)	1.45 (0.75, 1.5)	0.83
Invasive ventilation at enrolment, n (%)	34 (89%)	36 (82%)	0.33
Mean airway pressure at enrolment (cmH2O)	10.9 (3.1)	11.1 (3.0)	0.68
Percentage of invasive ventilation days at enrolment	100 (95, 100)	93 (70, 100)	<0.01
Pulmonary haemorrhage, n (%)	9 (24%)	7 (16%)	0.38
Inotrope or vasopressor treatment, n (%)	10 (26%)	15 (34%)	0.45
Grade 3/4 intraventricular haemorrhage or cystic periventricular leukomalacia, n (%)	8 (21%)	16 (36%)	0.13
Necrotising enterocolitis ≥ stage 2, n (%)	6 (16%)	7 (16%)	0.98
Sepsis, n (%)	10 (26%)	15 (34%)	0.45
Systemic corticosteroids, n (%)	2 (5%)	4 (9%)	0.51
Echocardiography characteristics
PDA diameter (mm)	2.4 (2.2, 2.8)	2.6 (2.2, 3.2)	0.05
Left ventricular output (ml/kg/min)	426 (130)	404 (74)	0.43
Left atrium: Aortic root ratio	1.9 (1.6, 2.2)	2.0 (1.8, 2.2)	0.56
Neonatal outcomes
Death before discharge, n (%)	5 (13%)	4 (9%)	0.73
Moderate-severe bronchopulmonary dysplasia, n (%)b	22 (65%)	34 (81%)	0.11
Severe retinopathy of prematurity, n (%)c	4 (12%)	6 (15%)	0.72

Data shown for infants for whom complete outcome information was available (death or neurodevelopmental impairment). Five infants in each group were lost to neurodevelopmental follow-up.

Continuous data presented as mean (SD) or median (IQR).

COXI cyclooxygenase inhibitors, CPAP continuous positive airway pressure, PDA patent ductus arteriosus.

aFor infants treated with ibuprofen, the total dose of ibuprofen was converted to an equivalent total dose of indomethacin using the following calculation (20 mg/kg ibuprofen [representing the dosing regimen used in our unit of a 10 mg/kg initial dose followed by two daily doses of 5 mg/kg = 0.6 mg/kg indomethacin [representing three doses of 0.2 mg/kg administered every 12 h).

bModerate-severe bronchopulmonary dysplasia defined as the need for oxygen or positive pressure support at 36 weeks corrected gestational age.

cSevere retinopathy of prematurity (ROP) defined as stage 3 ROP combined with treatment with laser surgery and/or an intravitreal vascular endothelial growth factor inhibitor.

Treatment with PDA ligation

Compared with infants in the immediate surgical ligation group, infants in the acetaminophen group had decreased surgical ligation (53% vs. 72%, aOR 0.30, 95% CI: 0.11, 0.87; p = 0.03) (Table 3). In epoch 1, all infants (n = 43) were referred for ligation, though 12 did not ultimately undergo PDA surgery (3 infants died from sepsis; 4 infants experienced spontaneous ductal constriction prior to surgery; and for 5 infants, referral for ligation was cancelled in favour of conservative management due to clinical improvement in respiratory support [successful endotracheal extubation] despite a persistently large PDA on echocardiography). (Fig. 1) Among the 49 infants in epoch 2, 9 were immediately referred for PDA surgery (and did not receive acetaminophen treatment) owing to increased illness severity or contraindications for acetaminophen treatment, of whom 7 underwent ligation and 2 infants experienced spontaneous ductal constriction prior to PDA surgery. Among the 40 infants in epoch 2 who were treated with acetaminophen, 19 underwent PDA ligation after the treatment with acetaminophen was unsuccessful in facilitating ductal constriction. Among the 21 (out of 40) acetaminophen-treated infants who were not treated with ligation, 15 experienced significant improvement in ductal size and shunt volume (either PDA closure or reduction to a small shunt on echocardiography) while 4 experienced improvements in clinical respiratory stability only (without improvement in echocardiography indices of ductal size or shunt volume). (Fig. 1) Two acetaminophen-treated infants died prior to PDA ligation (one died from sepsis on the fifth day of acetaminophen treatment and the other died after withdrawal of life-sustaining intensive care due to intracranial injury). Surgically treated infants in the acetaminophen group underwent ligation at a later age compared with ligated infants in the earlier epoch (38 [23,32] vs. 28 [27,52] days after birth, p < 0.01) and had longer duration of exposure to large PDA (41 vs. 28 days, p < 0.01). No infants underwent PDA ligation after discharge home from the NICU.

Table 3

Outcomes in early childhooda.

Outcome	Immediate surgical ligation epoch	Acetaminophen epoch	Crude OR (95% CI)	Adjusted OR (95% CI)b	p value
Death or Any NDI, n/N (%)	25/38 (66%)	31/44 (70%)	1.24 (0.49, 3.15)	1.03 (0.30, 3.56)	0.96
Death or Severe NDI, n/N (%)	17/38 (45%)	20/44 (45%)	1.03 (0.43, 2.46)	0.86 (0.30, 2.51)	0.78
Any NDI, n/N (%)c	20/33 (61%)	27/40 (67%)	1.35 (0.52, 3.53)	1.02 (0.28, 3.65)	0.98
Severe NDI, n/N (%)c	12/33 (36%)	16/40 (40%)	1.17 (0.45, 3.02)	0.86 (0.27, 2.76)	0.81
Autism Spectrum Disorder, n/N (%)c	1/33 (1%)	4/40 (5%)	3.55 (0.38, 33.5)	3.49 (0.24, 50.78)	0.36
Death before 18-24 months, n/N (%)	5/43 (12%)	4/49 (8%)	0.68 (0.17, 2.70)	0.91 (0.17, 4.97)	0.92
Ligation before 18-24 months, n/N (%)	31/43 (72%)	26/49 (53%)	0.44 (0.18, 1.05)	0.30 (0.11, 0.87)	0.03

CI confidence interval, NDI neurodevelopmental impairment, OR odds ratio.

aReference is the Immediate surgical ligation epoch (epoch 1). Ten infants (five infants per epoch) did not undergo neurodevelopmental evaluation and denominators for outcomes that include neurodevelopmental impairment include only infants for which complete outcomes were known.

bAdjusted for sex, outborn status, maternal exposure to magnesium sulfate for foetal neuroprotection, delivery room intubation, SNAP-II score, and the following postnatal confounders representing illness severity/acquired morbidity prior to or at the time of enrolment: treatment with inotropic drugs, culture-negative sepsis, culture-positive sepsis.

cIncluded only infants who survived and completed neurodevelopmental follow-up (five infants died, and five infants did not complete a neurodevelopmental evaluation in the Immediate surgical ligation epoch; four infants died, and five infants did not complete a neurodevelopmental evaluation in the Acetaminophen epoch).

Outcomes in early childhood

There was no difference in the primary composite outcome of death or any NDI at 18-24 months (70% vs. 66%; adjusted odds ratio (aOR) 1.03, 95% confidence interval (CI): 0.30, 3.56). (Table 3) There was no difference in any of the secondary outcomes, including death or severe NDI (45% vs. 45%; aOR 0.86, 95% CI: 0.30, 2.51), NDI alone (67% vs. 61%; aOR 1.02, 95% CI: 0.28, 3.65) or autism spectrum disorder (5% vs. 1%, aOR 3.49, 95% CI: 0.24, 50.78; p = 0.36).

The incidence of cerebral palsy was similar among both epochs (Epoch 1: 21% vs. Epoch 2: 13%, p = 0.34), as were the BSID III cognitive (median [IQR] 90 [80, 100] vs. 85 [70,90], p = 0.06), language (79 [65,94] vs. 77 [60.5, 90.5], p = 0.54) and motor (88 [82,97] vs. 85 [73,94], p = 0.17) scores.

Among infants in epoch 2 who were treated with acetaminophen (n = 40), there were no differences in early childhood outcomes among those treated vs. not treated with surgical ligation. (Supplementary Table 3).

Discussion

In this retrospective comparative epoch study of ELGANs with persistent large PDA who were being considered for surgical ligation, treatment with a relatively prolonged course of oral acetaminophen was associated with decreased odds of PDA surgery and no difference in death or neurodevelopmental impairment in early childhood. These results suggest that late acetaminophen treatment may be effective and safe in facilitating PDA closure and avoiding surgical ligation without adverse neurodevelopmental effects in early childhood.

While treatment with acetaminophen has been demonstrated to be efficacious for facilitating ductal closure [10, 22, 28], few studies have evaluated the impact on neurodevelopmental outcomes. Follow-up studies of pilot clinical trials of acetaminophen prophylaxis [20] (vs. placebo) and early treatment in the first 3 days after birth (vs. ibuprofen) [21] have reported no differences in neurodevelopmental impairment in early childhood. Knowledge of the long-term safety of acetaminophen for symptomatic PDA treatment is important as it is being increasingly prescribed by clinicians worldwide, who in contemporary practice may be seeking to avoiding treatment with surgical ligation and/or as an alternative to COXI [6-9]. Acetaminophen treatment among ELGANs with PDA in the Canadian Neonatal Network increased from 7% in 2014 to over 25% in 2019 [12, 29]. Similarly, in 2018, 1/3 of neonatal units in the United Kingdom administered acetaminophen for PDA treatment, mostly as second-line therapy after unsuccessful COXI therapy [30]. To the best of our knowledge, no prior studies have evaluated the long-term safety of later (beyond the first week after birth) or prolonged (>3 days) courses of acetaminophen. In our study, longer courses (median 7 days) of acetaminophen treatment and a modestly prolonged exposure to large PDA (41 vs. 28 days) were not associated with NDI among ELGANs with persistent PDA compared with immediate referral for surgical ligation.

Over the past decade, there have been concerns raised that prenatal or neonatal exposure, or both, to acetaminophen may adversely affect cerebral development. Prenatal exposure to acetaminophen has been associated with language delay, lower intelligence quotient, autism spectrum disorder and ADHD in childhood [31-34]. Longer duration of prenatal exposure has been related to increased risk, even after adjusting for indications for use, familial risk and other confounders [34]. Neonatal exposure to acetaminophen has similarly been associated with behaviour and cognitive deficits in a murine model [35]. In addition, increased autism spectrum disorder was associated with neonatal acetaminophen exposure in a human ecological study of country-specific rates of neonatal circumcision [31].

Several potential pathobiological mechanisms may explain the association of acetaminophen exposure and neurodevelopmental disorders. Acetaminophen may interrupt brain development by induction of oxidative stress, leading to neuronal death [36]. Prenatal exposure to acetaminophen has been associated, in a dose-dependent relationship, with increased DNA methylation among children with ADHD [37]. The genes affected by DNA methylation were largely those enriched in pathways involved in oxidative stress and neurological function [37]. In addition, acetaminophen may interfere with maternal and neonatal hormones (e.g. thyroid) related to brain development [38], and alter the expression of brain-derived neurotrophic factor, impacting neuronal growth, migration, and survival, and resulting in altered behaviour and reduced learning abilities [35, 39]. Although clinical toxicity has not been reported among ELGANs treated with acetaminophen for PDA, a recent review identified 22 case reports of acetaminophen-related hepatotoxicity in neonates when administered for other indications using similar dosing regimens [40]. In addition, studies of single administrations of high-dose acetaminophen have reported detectable toxic metabolites, indicating the potential for toxicity and stressing the need for careful and rigorous monitoring among ELGANs receiving repeated and prolonged courses of high-dose acetaminophen [41].

The strengths of this study include the in-depth abstraction of postnatal morbidities and indices of illness severity, such as daily respiratory support. These data collection included key covariates in the multivariable analyses to minimise confounding by indication. In addition, the proportion of infants lost to neurodevelopmental follow-up was low (10.9%) [42].

Our study has several limitations; first, as a comparative epoch cohort study, improvements in clinical care and outcomes over time may be misattributed to the exposure under investigation (i.e. acetaminophen vs. surgical ligation treatment). In addition, the secular trend toward more selective PDA treatment may have resulted in selection bias in assembling the cohort of infants in each epoch considered eligible for ligation. However, the similar proportion of eligible infants in each epoch (9.2% vs. 8.6%) may suggest against the possibility of significant selection bias. Further, our inclusion of infants in epoch 2 who were not treated with acetaminophen (and instead immediately referred for ligation) may also have mitigated the potential for selection bias, as similar infants considered ineligible for acetaminophen treatment may have been included in epoch 1. Second, the observational nature of this study means that the true causal effect of late acetaminophen treatment in avoiding surgical ligation, compared with the potential for spontaneous closure over time, cannot be definitively established. Third, neurodevelopmental follow-up occurred too early in childhood (18–24 months corrected gestational age) to permit the appropriate evaluation and diagnosis of ADHD [43], which is the disorder that has been most strongly associated with acetaminophen exposure. Fourth, this study was underpowered to detect clinically important differences in the frequency of major, but uncommon, neurodevelopmental disorders such as ASD. Finally, 18–24 month neurodevelopmental evaluation of children born preterm may have limited reliability compared with outcomes later in childhood [44]. Additional, well-powered studies are required to evaluate the association of acetaminophen treatment for PDA among preterm infants with neurodevelopmental outcomes at school-age.

Conclusion

The clinical approach of administering late treatment with oral acetaminophen among extremely preterm infants with persistent large PDA was associated with reduced surgical ligation and no difference in death or neurodevelopmental impairment in early childhood. These results support the safety and effectiveness of late acetaminophen treatment for PDA to avoid surgical ligation.

Supplementary Table 1: Classification of Neurodevelopmental Outcomes

Supplementary Table 2: Univariable Analysis of the Association of Potential Covariates with the Primary Outcome of Death or Neurodevelopmental Impairment

Supplementary Table 3: Early Childhood Outcomes among Ligated vs. Non-ligated Infants Exposed to Acetaminophen Treatment