Effect of inborn vs. outborn delivery on neurodevelopmental outcomes in infants with hypoxic–ischemic encephalopathy: secondary analyses of the NICHD whole-body cooling trial

Abstract

BACKGROUND

The effect of birth location on hypothermia-related outcomes has not been rigorously examined in the literature. In this study, we determined whether birth location had an impact on the benefits of whole-body cooling to 33.5 °C for 72 h in term infants (n = 208) with hypoxic–ischemic encephalopathy (HIE) who participated in the Neonatal Research Network (NRN) randomized controlled trial.

METHODS

Heterogeneity by birth location was examined with respect to cooling treatment for the 18-mo primary outcomes (death, moderate disability, severe disability) and secondary outcomes (death, components of disability), and in-hospital organ dysfunction. Logistic regression models were used to generate adjusted odds ratios.

RESULTS

Infants bom at a location other than an NRN center (outborn) (n = 93) experienced significant delays in initiation of therapy (mean (SD): 5.5 (1.1) vs. 4.4 (1.2) h), lower baseline temperatures (36.6 (1.2) vs. 37.1 (0.9) °C), and more severe HIE (43 vs. 29%) than infants born in an NRN center (inborn) (n = 115). Maternal education <12 y (50 vs. 14%) and African-American ethnicity (43 vs. 25%) were more common in the inborn group. When adjusted for NRN center and HIE severity, there were no significant differences in 18-mo outcomes or in-hospital organ dysfunction between inborn and outborn infants.

CONCLUSION

Although limited by sample size and some differences in baseline characteristics, the study showed that birth location does not appear to modify the treatment effect of hypothermia after HIE.

Hypoxic–ischemic encephalopathy (HIE) caused by acute perinatal asphyxia remains an important cause of neonatal mortality and neurodevelopmental deficit in childhood. The Cochrane meta-analysis of eight randomized controlled trials (RCTs) of therapeutic hypothermia in newborns with HIE demonstrated a beneficial effect for this treatment, with a statistically significant and clinically important reduction in the combined outcome of mortality and major neurodevelopmental disability up to the age of 18 mo (relative risk 0.76; 95% confidence interval (CI) 0.65–0.89) (1). Large published RCTs have shown a reduction in death or major developmental disability among infants with HIE who had undergone hypothermia therapy as compared with controls (Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Neonatal Research Network (NRN) trial and the Infant Cooling Evaluation trial), a reduction in death or disability among infants with less severe amplitude-integrated electroencephalogram changes at randomization (CoolCap trial), and an increase in survival without disability (TOBY trial) (2–5). With the widespread adoption of therapeutic hypothermia for HIE, it has become important to ascertain factors that could modulate its effectiveness and safety.

In an early pilot study by Eicher and colleagues, infants transported into the participating centers (outborn) were found to be significantly more likely to die than those born in the participating centers (inborn), after controlling for treatment group (6,7). There is scarcity of data on the effects of birth location on outcomes related to hypothermia therapy in neonatal HIE. We undertook a secondary analysis of data from the NICHD NRN whole-body hypothermia RCT to test the interaction between the hypothermia treatment and the location of birth (inborn or outborn), so as to determine whether the benefits and potential adverse effects of whole-body cooling vary in these subgroups. In addition, factors that may contribute to a difference in outcomes, if any, between the groups were examined.

RESULTS

Data on the primary outcome were available for 205 (98.5%) of the 208 infants enrolled. The three infants for whom data were missing were in the control group. The baseline characteristics of outborn (n = 93) and inborn (n = 115) infants are compared in Table 1. Maternal education <12 y (14 vs. 50%), African-American ethnicity (25 vs. 43%), and maternal intrapartum fever (4 vs. 15%) were significantly less frequent in outborn infants as compared to inborn ones. Outborn infants had (i) significantly delayed age at study entry (mean (± SD): 5 (0.9) vs. 3.7 (1.1) h); (ii) a greater proportion with time to onset of spontaneous respiration >10min (79 vs. 64%); (iii) a greater need for continued resuscitation at 10min (99 vs. 90%); and (iv) more severe HIE (44 vs. 29%) than inborn infants (P < 0.05). Comparable proportions (48 vs. 53%) in the two groups of infants were randomized to receive whole-body cooling. Outborn infants had lower baseline temperatures (36.6 (1.2) vs. 37.1 (0.9) °C) when placed on the cooling blanket, a greater delay in the initiation of cooling (mean (± SD): 5.5 (1.1) vs. 4.4 (1.2) h), and higher age at target temperature (mean (± SD): 6.4 (1.2) vs. 5.6 (1.3) h) than inborn infants.

Table 1.

Baseline characteristics of outborn and inborn groups of infants

Characteristic, mean (SD) or%	Outborn (n = 93)	Inborn (n=115)	P value
Maternal age (y)	27.9 (5.7)	26.8 (6.3)	0.17
Maternal education < 12 y (%)	14.1	50	<0.0001*
Ethnicity (%)
Black	24.7	42.6	0.007*
Caucasian	54.8	18.3	<0.0001*
Other	20.4	39.1	0.006*
Prenatal care (%)	94.6	93.9	1.0
Pregnancy complications (%)
Antepartum hemorrhage	18.3	11.3	0.19
Chronic hypertension	8.6	15.6	0.22
Diabetes	4.3	11.3	0.11
Intrapartum complications (%)
Fetal decelerations	72.8	74.8	0.87
Cord prolapse	23.7	13.0	0.07
Uterine rupture	11.8	15.6	0.55
Shoulder dystocia	7.6	11.3	0.51
Maternal fever (%)	4.3	14.8	0.02*
Maternal antibiotics for suspected/confirmed infection (%)	16.3	20.2	0.59
Rupture of membranes >18 h (%)	8.6	9.2	1.00
Maternal hemorrhage (%)	3.2	9.6	0.12
Emergency cesarean delivery (%)	77.4	69.6	0.27
Birth weight (grams)	3,422 (594)	3,341 (658)	0.36
Gestational age (wk)	38.8 (1.5)	38.9 (1.7)	0.62
Male gender (%)	57	56	0.96
Apgar score <5 (%)
At 5 min	88.0	79.1	0.13
At 10 min	75.9	65.4	0.16
Age at admission (h)	5.0 (0.9)	3.7 (1.1)	<0.0001*
Age therapy started (h)	5.5 (1.0)	4.3 (1.2)	<0.0001*
Age at target temperature (h)	6.4 (1.2)	5.6 (1.3)	0.002*
Temperature at randomization (°C)	36.6 (1.2)	37.1 (0.9)	0.002*
Temperature >37.5°C at randomization (%)	17.0	26.6	0.15
DR intubation (%)	94.6	93.0	0.86
Continued resuscitation at 10 min (%)	98.9	89.6	0.01*
Time of spontaneous respiration >10 min (%)	79.5	64.2	0.03*
Cord pH	6.82 (0.19)	6.88 (0.21)	0.11
Base deficit	19.9 (7.6)	18.9 (7.8)	0.49
Severity of encephalopathy (%)			0.04*
Moderate	56.5	71.3
Severe	43.5	28.7
Cooling group (%)	48.4	53	0.60
Septicemia/meningltis/encephalitis (%)	5.4	5.2	1.0

DR, delivery room.

^*Significant difference at 5% level.

Figure 1 reflects the outcomes related to hypothermia in outborn and inborn infants. The rates of adverse outcomes, namely, (i) death or moderate or severe disability, (ii) death, (iii) Mental Developmental Index (MDI) < 70, and (iv) Psychomotor Developmental Index < 70, were all higher in the outborn population than in the inborn population, in both hypothermia-treated and control subgroups. Table 2 shows the odds ratios (OR) with corresponding 95% CI and P values for interaction for each outcome in outborn and inborn subgroups after adjustment for study center and for the severity of HIE. There was no significant heterogeneity of treatment effect for any outcome assessed as shown by unadjusted analysis, by analysis after adjustment for study center, or by analysis after adjustment for both study center and severity of HIE.

Figure 1.

Rates of 18- to 22-mo outcomes related to hypothermia treatment in outborn and inborn groups of infants. The dark gray bar represents outborn control infants, the black bar represents outborn hypothermia-treated infants, the medium-gray bar represents inborn controls, and the light-gray outlined bar represents the inborn hypothermia-treated infants. MDI, Mental Developmental Index; PDI, Psychomotor Developmental Index.

Table 2.

ORs with corresponding 95% CIs and P values for interaction for each outcome in outborn and inborn subgroups after adjustment for center and severity of encephalopathy

	Delivery site	Rate (%)		Adjusted OR (95% CI)	P value (interaction)
		Hypothermia	Control		Unadjusted	Center, HIE severity adjusted
Death/moderate or severe disability, %	Outborn	50	68.2	0.81 (0.29–2.24)	0.91	0.87
	Inborn	38.9	58.3	0.91 (0.33–2.45)
Death, %	Outborn	27.1	43.2	0.85 (0.27–2.74)	0.88	0.93
	Inborn	20.4	31.7	0.80 (0.28–2.31)
Bayley MDI score ≥ 85, %	Outborn	37.5	28.9	0.81 (0.29–2.28)	0.31	0.37
	Inborn	38.9	19.7	0.44 (0.15–1.25)
Bayley MDI score 70–84, %	Outborn	18.5	21.3	1.21 (0.29–4.96)	0.94	0.93
	Inborn	14.6	0	0
Bayley MDI score <70, %	Outborn	47.9	71.1	1.1 (0.41–3.02)	0.63	0.57
	Inborn	42.6	59.1	0.77 (0.29–2.02)
Bayley PDI ≥ 85, %	Outborn	35.4	24.4	1.95 (0.67–5.65)	0.76	0.92
	Inborn	53.7	37.7	1.82 (0.64–5.14)
Bayley PDI score 70–84, %	Outborn	12.5	4.4	0.23 (0.03–1.56)	0.15	0.21
	Inborn	3.7	6.6	1.15 (0.17–7.90)
Bayley PDI score < 70, %	Outborn	52.1	71.1	0.83 (0.30–2.31)	0.67	0.57
	Inborn	42.6	55.7	0.57 (0.21–1.53)
Cerebral palsy, %	Outborn	31.4	45.8	0.21 (0.04–0.96)	0.60	0.40
	Inborn	9.5	22.5	0.48 (0.13–1.83)
Blindness, %	Outborn	5.9	20.8	1.44 (0.17–12.4)	0.38	0.46
	Inborn	7.3	10.2	0.55 (0.09–3.36)
Severe hearing impairment, %	Outborn	2.9	12.5	0.12 (0.01–1.03)	0.10	0.06
	Inborn	4.8	2.5	1.75 (0.25–12.4)
Organ dysfunction
Pulmonary	Outborn	12.5	20	1.26 (0.37–4.25)	0.41	0.41
	Inborn	24.1	22.9	0.66 (0.22–1.96)
Cardiac	Outborn	57.5	43.2	0.50 (0.22–1.11)	0.41	0.38
	Inborn	39.2	37.7	0.80 (0.36–1.75)
Renal	Outborn	16.7	28.9	2.11 (0.58–7.71)	0.16	0.16
	Inborn	22.6	18	0.69 (0.21–2.22)
Hematologic	Outborn	20.8	17.8	0.62 (0.16–2.43)	0.40	0.45
	Inborn	15.1	6.6	0.30 (0.06–1.41)
GI, metabolic, or infectious	Outborn	20.8	8.9	1.16 (0.27–4.96)	0.18	0.06
	Inborn	18.9	19.7	7.32 (1.40–38.2)

CI, confidence interval; GI, gastrointestinal; HIE, hypoxic-ischemic encephalopathy; MDI, Mental Developmental Index; OR, odds ratio; PDI, Psychomotor Developmental Index.

DISCUSSION

Therapeutic hypothermia for neonatal HIE has been demonstrated to have a consistent benefit without major adverse effects (1,8–10). We utilized data from the NICHD NRN whole-body cooling RCT to determine whether the safety and efficacy of hypothermia varied between a group of infants who were inborn and a group of infants transported from a referral center to an NRN site. The unadjusted rates of adverse outcomes (death or moderate or severe disability; death; MDI < 70; and psychomotor developmental index < 70) were higher in the outborn population as compared with the inborn population in both hypothermia-treated and control subgroups. After adjusting for NRN center and severity of encephalopathy, we were unable to detect an independent effect of birth location on outcome.

In an early pilot study by Eicher and colleagues, outborn infants, who formed 75% of the study population, were found to be significantly more likely to die than inborn infants (OR 10.7; 95% CI 1.3–90), after controlling for treatment group. However, severity of HIE was not controlled for in this analysis (7). Approximately 77% of the study cohort had severe HIE (Sarnat stage III). Of 24 deaths, 22 occurred in the outborn population. Active cooling was undertaken during transport for all outborn infants. Of note, in the infants who received hypothermia treatment, the mean time to target temperature (32.5–33.5 °C) in outborn infants (n = 23) tended to be shorter than in inborn ones (n = 6) (111 ± 78 vs. 156 ± 116min). The authors speculated that the adverse outcomes among outborn infants may have been due to lack of experienced personnel, difficulties in resuscitation, or problems with postresuscitation stabilization. In the recent ICE trial there was no significant finding to suggest that the effects of hypothermia differed within the outborn subgroup (5). The ICE trial also included cooling at the birth hospital and passive and active cooling during transport, along with rectal temperature monitoring (5). However, in the current NICHD NRN data set, cooling was not undertaken for the infants during transport.

In this study, a significantly greater proportion of outborn infants (as compared to inborn ones) required continued resuscitation at 10min, experienced onset of spontaneous respiration at > 10 min, and had severe, rather than moderate HIE. It was not possible to determine whether these differences originated from any systematic differences in the availability of personnel or quality and effectiveness of resuscitation, or whether it reflected a referral bias, with the most severely HIE-affected infants being referred to another center for cooling.

We noted several differences in baseline characteristics between the inborn and outborn groups. Maternal fever occurred more often, and baseline infant temperatures were higher in the inborn group. Elevated temperatures > 37.5 °C were noted in 27% of inborn infants as compared to 17% of the outborn ones; however, these differences were not statistically significant. Elevated temperatures during study intervention among control infants have been previously shown to increase the odds for death or disability (11,12). On the other hand, outborn infants experienced a greater delay in initiation of cooling therapy (although still within the 6-h window of the protocol), and took longer to attain target temperatures. Experimental data in animal models suggest that cerebral hypothermia that is initiated as early as possible in the latent phase of injury is associated with neuroprotection (13). In the CoolCap trial, within the fairly narrow range of recruitment times, there was no greater improvement in those treated earliest after birth than in those treated later (4). In the NICHD study cohort, time to achieve target temperatures did not influence outcome (8). In the TOBY trial, the effect of treatment group did not vary significantly on the basis of time to randomization: among the 105 infants randomly assigned to a group at <4h after birth, the relative risk for the primary outcome (death or severe neurodevelopmental disability) with hypothermia treatment was 0.77 (95% CI 0.44–1.04), whereas among the other 220 infants who were randomly assigned to groups at 4–6 h after birth, the relative risk was 0.95 (95% CI 0.72–1.25; P = 0.21 for interaction) (3). In the ICE trial, no significant interactions were demonstrated between hypothermia and age at randomization (P = 0.22) (5). The age at randomization in the CoolCap, NICHD, TOBY, and ICE RCTs were 4.8 (range 2.6–6), mean 4.3 (SD 1.3), median 4.7 (range 3.8–5.4), and mean (SD) 4 (1.3) h, respectively. In recent years, with the premise that “time to target temperature” may be critical, there have been reports of cooling of the infants being carried out during transport to the treatment center (14–16). Passive, active, and servo-controlled cooling during transport have been performed in small numbers of infants (14–16). However, overcooling to <32°C has been reported in one-third of the infants; therefore it is critical to monitor core temperatures when carrying out cooling in infants during transport. More research is needed on safety and efficacy issues of cooling treatment during transport. Early ascertainment of encephalopathy is also essential so as to optimally disseminate therapeutic hypothermia to centers that do not currently offer this therapy (14,15).

The reason for more elevated temperatures recorded in inborn infants is unclear, although they could be secondary to higher maternal temperatures. Maternal antibiotic regimens, conditions of prolonged rupture of membranes, and clinical diagnosis of neonatal septicemia, all of which are used as surrogate measures of infection, were not different between the groups. The primary trial was completed under conditions of clinical equipoise, and cooling was not initiated prior to the trial intervention at the NRN center. It is unlikely, therefore, that the differences in temperatures were related to transport conditions. Another significant difference between the groups was in the frequency of low maternal education (<12 y) (50% in the inborn population vs. 14% among the outborn), a potential modulator of early childhood developmental outcomes.

The strengths of our study are that data were collected prospectively from infants diagnosed with HIE using stringent clinical and biochemical criteria and managed according to a consistent protocol in tertiary level centers. We had a very high follow-up rate, and a structured neurodevelopmental assessment was performed at 18–22 mo by certified trained examiners. The proportion of outborn vs. inborn infants in the trial was roughly equal (45 vs. 55%), allowing a reasonable statistical comparison. The primary trial was completed at a time when there was clinical equipoise and cooling was not initiated prior to the trial intervention at the NRN center.

The reasons for the absence of any significant interaction between birth location and the effects of cooling are complex. Baseline differences between groups, specifically the higher baseline temperatures and lower maternal education levels in inborn infants as a group, may have obscured an effect on outcomes. We may have had relatively low power to detect an interaction in this secondary analysis. Nonetheless, the value of a careful statistical exploration for heterogeneity of treatment effect, based on clinical data and biologic rationale, has been previously recognized (17). Gabler and colleagues recently found that only 29% of the RCTs that reported results had formally analyzed “heterogeneity of treatment effects” data (18). They suggest that heterogeneity of treatment effect may have important implications for individualized patient care, and that therefore the lack of such analyses represent “missed opportunities” (18).

We examined the putative association between outcomes and birth location, potentially important data for risk stratification and optimizing outcomes in perinatal HIE. In conclusion, although limited by sample size and some differences in baseline characteristics, birth location does not appear to modify the treatment effect of hypothermia treatment after HIE in newborn infants.

METHODS

This was a secondary post hoc analysis of data collected as part of the whole-body cooling NICHD NRN RCT (2). The safety and 18-mo neurodevelopmental outcomes of the trial have been previously reported (2,8). The original trial was approved by the institutional review board at each participating site, and written consent was obtained from the parents of eligible infants.

The study population was composed of infants with HIE, enrolled in the whole-body cooling NICHD NRN RCT (2). Eligibility criteria included pH level of ≤ 7 or a base deficit of ≥ 16 in cord blood or during the first hour after birth. If pH was between 7.01 and 7.15 during this interval and if base deficit was between 10 and 15.9 (or if blood gas data were not available), the additional criteria required included an acute perinatal event (late or variable decelerations, cord prolapse, cord rupture, uterine rupture, maternal trauma, hemorrhage, or cardio-respiratory arrest), and either a 10-min Apgar score of ≤5 or assisted ventilation initiated at birth and continued for at least 10 min (2). All the infants were moderately or severely encephalopathic (one or more signs in at least three of six categories: level of consciousness, spontaneous activity, posture, tone, primitive reflexes, and autonomic nervous system) on a standardized neurologic examination by a certified physician examiner, or had seizures. Exclusion criteria were inability to enroll the infant before 6h of life, major congenital anomaly, birth weight <1800 grams, refusal of consent by parent or attending physician, and moribund infant for whom no further aggressive treatment was planned. The infants were randomly assigned to treatment groups stratified by center. The neurodevelopmental assessments at 18–22 mo of age were performed by trained examiners who were unaware of the intervention status of the infants.

“Inborn” was defined in the original whole-body cooling trial as birth at a site performing the trial. “Outborn” included infants transferred to the clinical site where the hypothermia trial was conducted; the birth could have been in a hospital setting or outside of a hospital or healthcare setting such as delivery at home or in the ambulance. The interaction between cooling and inborn vs. outborn birth was examined using 18-mo primary outcomes (death or moderate or severe disability) and secondary outcomes (components of the primary outcome separately) of the primary trial, and organ dysfunction (safety outcome) during hospitalization. Severe disability was defined as (i) MDI < 70 on Bayley Scales of Infant Development II, (ii) gross motor functional classification scale (Palisano) level 3–5, (iii) hearing impairment requiring aids (>60 db audiometric testing), or (iv) bilateral blindness (<20/200 visual acuity). Moderate disability was defined as MDI of 70 to 84 plus one of the following: (i) gross motor functional classification scale level 2, (ii) hearing impairment requiring no amplification, or (iii) a persistent seizure disorder defined as recurrent seizures after Neonatal Intensive Care Unit discharge, requiring anti-convulsant therapy at the 18-mo examination time point. Non-central nervous system organ dysfunction was defined as follows: (i) pulmonary involvement included meconium aspiration syndrome, persistent pulmonary hypertension of the newborn (requiring inhaled nitric oxide and extra-corporeal membrane oxygenation), chronic lung disease, and/or pulmonary hemorrhage; (ii) cardiac involvement such as cardiomegaly, cardiac failure and cardiac dysfunction as determined by echocardiography, cardiac ischemia as determined by electrocardiography or elevated enzyme levels, hypotension, hypertension, and/or arrhythmia; (iii) renal involvement such as oliguria, anuria, and/or need for dialysis; (iv) gastrointestinal involvement characterized by hepatic dysfunction or necrotizing enterocolitis; (v) infections such as bloodstream infection, meningitis, or encephalitis; (vi) hematologic dysfunction, including thrombocytopenia and disseminated intravascular coagulation, and (vii) metabolic dysfunction, including hypoglycemia, hypocalcemia, and/or hypomagnesemia (8). Demographic data and baseline clinical characteristics of inborn and outborn groups were compared.

Statistical Analysis

Descriptive statistics were expressed as median (range), mean (SD), and number (percentage) as appropriate. Formal statistical comparisons of mean values or proportions between the two groups were carried out using two-sample t-test and χ², as appropriate. For each dichotomous outcome, logistic regression models were fitted for the inborn and outborn subgroups, to determine an OR and 95% CI for each subgroup. ORs were adjusted to control for NRN center and severity of HIE, two potential confounding variables that had been adjusted for in the original trial and were selected a priori. The statistical significance of the heterogeneity of treatment effect was determined using logistic regression models with treatment/subgroup interactions. A value of P < 0.05 for the test of heterogeneity (treatment X subgroup interaction) was considered a significant subgroup effect.