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to describe neonatal intensive care unit (NICU) medical interventions and NICU mortality by birth weight and major anomaly types for infants with trisomy 13 (T13) or 18 (T18).
retrospective cohort analysis of infants with T13 or T18 from 2005–12 in the Pediatrix Medical Group. We classified infants into 3 groups by associated anomaly type: neonatal surgical, non-neonatal surgical, and minor. Outcomes were NICU medical interventions and mortality.
841 infants were included from 186 NICUs. NICU mortality varied widely by anomaly type and birth weight, from 70% of infants <1500g with neonatal surgical anomalies to 31% of infants ≥2500g with minor anomalies. Infants ≥1500g without a neonatal surgical anomaly comprised 66% of infants admitted to the NICU; they had the lowest rates of NICU medical interventions and NICU mortality.
Risk stratification by anomaly type and birth weight may help provide more accurate family counseling for infants with T13 and T18.
There is ongoing debate about the extent of neonatal intensive care unit (NICU) interventions that should be provided for infants with trisomy 13 (T13) or trisomy 18 (T18), and whether providing more interventions impacts survival.(1–21) Multi-center studies are limited to very-low-birth-weight (VLBW) infants (1) or to older survivors for whom information on neonatal management is lacking.(22) Parent surveys report many infants who survive past 1 year, but there is no denominator of how many infants received neonatal intervention or what kinds of intervention they received.(4, 14, 23) Single-center case series report 1-year survival among infants receiving intensive treatment and cardiac surgeries, but these are limited by small numbers.(3, 6, 24) Due to lack of multi-center data on neonatal management of infants with T13 or T18, it is challenging for families and physicians to have informed discussions on medical interventions for infants with these diagnoses. (3, 5, 6, 23–27)
The impact of NICU medical interventions on survival may be influenced by coexisting major anomalies or birth weight.(3, 28–30) While rates of anomalies for infants with T13 or T18 are well-documented, not all anomalies impact survival equally.(11, 12, 29, 31) For example, infants with limb anomalies may not require immediate inpatient care, whereas infants with ductal-dependent cardiac lesions require immediate decisions about surgical intervention. In addition, many infants with T13 or T18 are born with significant growth restriction; birth weight influences feasibility of some surgical interventions.(32) For families pursuing a goal of discharge home from the NICU, it would be helpful to understand how many infants survived to discharge home after birth, and how coexisting anomalies, birth weight, and receipt of medical interventions affect their infant’s chance of discharge home.
Our specific objectives were to use a multi-center NICU dataset to 1) evaluate the rates of coexisting major anomalies in infants with T13 or T18, categorized by whether or not those anomalies are life-threatening without surgical intervention during the neonatal period; 2) describe the use of NICU medical interventions by anomaly type and birth weight; 3) compare NICU mortality by anomaly type, birth weight, and receipt of medical interventions.
We conducted a retrospective cohort analysis of infants with T13 or T18 admitted to the NICU from 2005–12 using the Pediatrix Clinical Data Warehouse (CDW). The CDW contains de-identified electronic medical record data on all infants from 270 NICUs in 34 states, including academic and private NICUs of all levels of care, and representing 15–20% of NICU admissions in the U.S. Data are automatically extracted from the medical record generated prospectively by clinicians, de-identified, and stored in the CDW. Information includes maternal history, birth information, demographics, medications, laboratory values, diagnoses, and respiratory support. The CDW includes all diagnoses that are made throughout a patient’s hospitalization, not just admission diagnoses. All diagnoses are recorded as entered by the provider; major and minor anomaly diagnoses are flagged within the CDW. T13 and T18 are coded discretely.
We manually reviewed all diagnoses flagged as major or minor anomalies in the CDW, and consolidated them similarly to reports from the Vermont Oxford Network (32) and National Institutes of Child Health and Development Neonatal Research Network.(33) We further classified major anomalies into those that are neonatal surgical or non-neonatal surgical. A neonatal surgical anomaly was defined as: a) incompatible with life without surgical intervention during the neonatal period, and/ or b) an anomaly that prohibits enteral feeding unless surgically repaired during the neonatal period. Accordingly, the following anomalies were counted as ‘neonatal surgical’: gastrointestinal anomalies such as bowel atresias and gastroschisis; diaphragmatic hernia; meningomyelocele, and ductal-dependent cardiac lesions (hypoplastic left heart syndrome (HLHS), interrupted aortic arch, total anomalous pulmonary venous return, transposition of the great vessels, pulmonary atresia, tricuspid atresia, truncus arteriosus)(Supplemental Information (1)). Since the CDW does not systematically require details about surgical intervention, we were not able to determine with certainty whether patients with neonatal surgical anomalies received neonatal surgical intervention, only that such an anomaly was present.
We defined a ‘non-neonatal surgical’ anomaly as a major life-limiting anomaly that does not necessarily require surgery during the neonatal period. For example, an AV canal typically does not cause symptoms until several weeks of life. Thus, it does not prohibit discharge home if feedings and respiratory status are stable. Similarly, neurologic anomalies such as holoprosencephaly impact survival, but cannot be surgically repaired, and therefore were also classified as ‘non-neonatal surgical.’ Infants with multiple anomalies (such as HLHS and coarctation of the aorta) were classified under the more severe category (in this case HLHS).
Infants without major anomalies were classified as having ‘minor’ anomalies, since they were likely to have characteristic facial, musculoskeletal, or skin anomalies but would not necessarily require neonatal intensive care for those specific conditions.
We defined ‘NICU medical interventions’ as interventions generally only offered in an intensive care setting. We recorded respiratory supports including mechanical ventilation, surfactant, and inhaled nitric oxide (iNO); cardiovascular medications including prostaglandins, vasopressors, and systemic corticosteroids; and neuromuscular blocking agents.
Information on anomalies and medical interventions was merged with patient data including gender, gestational age by obstetric estimate, birth weight, multiple gestations, maternal age, maternal race/ethnicity, delivery method, Apgar scores, and inborn status.
All infants with a diagnosis of T13 or T18 admitted to a Pediatrix NICU between 2005 and 2012 were included. Rates of missing demographic data were assessed (infants with missing data were retained in the dataset). For calculation of mortality rates, infants who were transferred were retained in the denominator. Our primary outcome of interest was mortality before NICU discharge.
First, we evaluated demographic characteristics of infants with T13 or T18 to compare our data to prior reports in the literature. Second, we identified major anomalies in infants with T13 or T18, and calculated the proportion of infants with T13 or T18 who had neonatal surgical anomalies, non-neonatal surgical anomalies, or minor anomalies. Third, we compared differences in the use of NICU medical interventions among infants with T13 or T18 by coexisting anomalies and birth weight. We analyzed use of prostaglandin only for infants with neonatal surgical cardiac anomalies. Univariate comparisons were made using chi-squared and Wilcoxon rank-sum tests, as appropriate. Finally, we calculated differences in NICU mortality by birth weight, major anomalies, and receipt of medical intervention.
The Mantel-Haenszel test was used to evaluate temporal trends in admissions, inborn status, receipt of mechanical ventilation, and mortality over the study period. A p-value of 0.05 was accepted for statistical significance. Stata version 13 was used for all analyses. The study was approved by the Medical College of Wisconsin institutional review board; the Clinical Data Warehouse was approved for research use by the Western institutional review board.
Out of 615,200 neonates admitted to the Pediatrix NICUs from 2005–12, 273 had T13 and 568 had T18, representing 0.13% of all admissions and 11% of all infants with a recognized chromosomal anomaly. These infants were admitted to one of 186 NICUs. There was no significant clustering of infants with T13 or T18 within NICUs; 132 (71%) of the NICUs had ≤5 patients with T13 or T18, 33 (18%) of NICUs had 6–10 patients, and 21 (11%) had >10 patients. All but two infants with T13 or T18 were cared for in a center that provided mechanical ventilation, and 94% were cared for in a center that discharged at least one patient with a neonatal surgical condition.
Demographic characteristics are shown in Supplemental Information (2) (online). Three-fourths of infants were born after 34 weeks’ gestation. VLBW was uncommon, but low birth weight occurred in over half of the infants. Three-fourths of infants were inborn and born to mothers under 35 years of age. Half of infants were delivered via cesarean section. Less than 10% of infants had a 5-minute Apgar score < 3. There were no significant temporal trends from 2005–2012 in number of NICU admissions, although more infants were inborn over time (67% inborn in 2005–06 increasing to 80% inborn in 2011–12; Mantel-Haenzel test for trend p=0.003).
Figure 1 shows the common anomalies in infants with T13 or T18. The majority of infants had a coexisting major anomaly; however, most were non-neonatal surgical anomalies. Although there were differences between T13 and T18 in prevalence of specific anomalies, overall the most common neonatal surgical anomaly was tracheo-esophageal fistula. Cardiac neonatal surgical anomalies were recognized in only 5% of patients.
Figure 2 shows NICU medical interventions in infants with T13 or T18, stratified by major anomaly and birth weight. Infants with T13 or T18 were likely to receive mechanical ventilation, with those receiving ventilation having a median 5 days on the ventilator (IQR 2–10 days). Vasopressors and iNO were infrequently used. Of the 42 infants with cardiac neonatal surgical anomalies, 19 (45%) received prostaglandin.
Overall, receipt of NICU medical intervention was most common in infants with neonatal surgical anomalies, occurring in 96/142 (67%) infants with neonatal surgical anomalies, 274/545 (50%) infants with non-neonatal surgical anomalies, and 33/154 (21%) infants with only minor anomalies. VLBW infants were more likely to receive mechanical ventilation, vasopressors, and surfactant. Infants with minor anomalies were least likely to receive medical interventions across all birth weight categories.
There were no temporal trends in receipt of mechanical ventilation from 2005–2012 (Mantel-Haenzel test for trend p=0.759). There were no differences in receipt of medical intervention between infants with T13 and infants with T18, except that infants with T13 were more likely to receive postnatal steroids (8% vs 3%, p<0.001).
47% of infants with T13 or T18 died in the NICU; 40% survived to home discharge; 13% were transferred to another facility before discharge. The proportion of infants transferred was similar to infants without T13 or T18 (13%; p=0.593), and was not different among the anomaly groups (11–13%, p=0.707). For surviving infants discharged home, the median length of stay (LOS) was 10 days (IQR 6–23 days). For infants who died, median LOS was 4 days (IQR 1–12). There were no temporal trends in survival to NICU discharge, transfer before discharge or LOS for infants who died in the NICU or survived to discharge from 2005–2012.
Figure 3 shows that infants’ birth weight and anomaly category were associated with significant differences in mortality before NICU discharge among infants with T13 or T18. NICU mortality varied widely by birth weight and anomaly category, ranging from 70% of infants <1500g with neonatal surgical anomalies to 31% of infants ≥2500g with only minor anomalies. VLBW infants had the highest mortality in every anomaly category. Among larger birth weight infants, neonatal surgical anomalies were associated with higher mortality. When analyzed separately, infants with T13 had higher NICU mortality than infants with T18 in the lower-risk groups of infants ≥1500gm (54% vs 36%, p<0.001) and infants without neonatal surgical anomalies (51% vs 36%, p=0.001). There were no differences in mortality between infants with T13 and T18 among those with neonatal surgical anomalies (69% vs 59%, p=0.317) or those <1500gm (71% vs 68%, p=0.719).
Table 1 shows the association between receipt of NICU medical intervention and NICU mortality in subgroups of anomaly category and birth weight. Overall, infants receiving NICU medical intervention had similar or higher NICU mortality compared to infants who did not receive NICU medical intervention. Of the 14 infants with neonatal surgical anomalies that were discharged home without NICU medical interventions, 9 infants had a cardiac anomaly, 2 infants had TEF/EA, and 1 infant each had imperforate anus, CDH, and meningomyelocele.
Infants >1500g without a neonatal surgical anomaly comprised 554/841 (66%) of the infants in the study. These infants were at lower risk for receipt of intervention and subsequent NICU mortality. Infants in these lower-risk groups who did not receive NICU medical intervention had approximately half the NICU mortality of their anomaly- and birth-weight-matched peers (21–43% versus 50–82%).
This is the first multi-center study to describe the medical management of infants with T13 or T18 admitted to U.S. NICUs. Our findings add to the literature on outcomes of infants with T13 and T18 by describing not just overall survival, but by the major risk factors of anomaly type and birth weight. A publication from the NICHD Neonatal Research Network highlighted the high mortality of VLBW infants with T13 or T18.(1) Our study extends those findings by highlighting the survival of infants larger than 1500g, who represent >75% of NICU admissions with T13 or T18. Our major conclusions are:
There is often clinical and ethical conflict between health care providers or between families and providers, over how much intervention should be offered to infants with T13 or T18.(4, 34) We found that the majority of infants with T13 or T18 admitted to a NICU in fact do not require decisions pertaining to surgical management during the neonatal period. We do not know how many of these infants were considered for medical and surgical interventions after the neonatal period. We also do not know how the distribution of coexisting anomalies differs from infants diagnosed prenatally, who may have experienced in utero demise or whose parents may have chosen pregnancy termination. The prevalence of coexisting anomalies in this study was consistent with other published reports.(29–31, 35) Although most studies on surgical intervention for infants with T13 or T18 have focused on congenital heart disease, (5, 24) we found that the most common condition associated with early neonatal surgery was tracheoesophageal fistula. Surgical decision-making for non-cardiac conditions is an important area for further research. Regardless, in counseling families on how to best advocate for their infant, encouraging a longitudinal relationship with a supportive primary care provider and relevant subspecialists is critical to addressing intervention decisions over time, not just at birth.
Despite concern that medical providers are unwilling to provide neonatal intensive care to infants with T13 or T18, (4, 34) we found that infants with T13 or T18 were offered a wide variety of medical interventions. Infants frequently received ventilation and surfactant, and those with neonatal surgical anomalies were more likely to receive medical interventions. These findings could represent two possible clinical scenarios: Some families likely received a prenatal diagnosis and were interested in pursuing NICU interventions. Other families may have received a postnatal diagnosis and made decisions about the extent of NICU interventions after a diagnosis was confirmed. We do not have data on the number of infants diagnosed prenatally with T13 or T18, but in an era of increasingly common prenatal diagnostic testing, it is likely that a significant percentage of families knew or suspected the diagnosis and opted for intervention. A survey of US neonatologists showed that about half would resuscitate an infant with T18 if parents desired.(36) Our results suggest that, consistent with the report about older infants with T13 or T18 receiving inpatient care and procedures, neonates with these conditions also receive significant NICU interventions.(22) Our finding that NICU survival, length of stay, and use of mechanical ventilation have not significantly changed over our study period may reflect that a high proportion (40%) of infants in this cohort were receiving mechanical ventilation at the onset of the study period, and suggests that the changes in the medical treatment of these infants may have occurred prior to the study period we investigated. The increasing number of inborn admissions and large proportion of infants delivered via Cesarean section in our study also suggests that many obstetricians may be willing to arrange transfer of care and offer surgical intervention to facilitate a live birth.
We found wide variation in NICU mortality by infants’ anomaly type and birth weight, with VLBW infants and those with neonatal surgical anomalies having twice the NICU mortality of other infants with T13 and T18. We suggest that physicians offering prognostic counseling could apply this type of risk stratification when offering prognostic counseling for infants with T13 and T18. A key feature of our study is that we reported mortality before NICU discharge, as opposed to the commonly-reported outcome of mortality before one year of age. Recent literature and our clinical experience both suggest that this distinction is not always clear when counseling families of infants with T13 or T18. While medical textbooks and population studies report 75–90% one-year mortality, it is important to understand that this does not necessarily mean that their infant with T13 or T18 will die during the birthing process or shortly after birth. Indeed, our results show that a majority of these infants do not have poor Apgar scores, and do not require significant resuscitation at birth. In our study we do not have the numbers of spontaneous or elective terminations of pregnancy or the numbers of infants who died in the delivery room, but we do know that at least 841 infants with T13 or T18 were admitted to a NICU, and 40% of those admitted to a NICU survived to discharge home. This is similar to a Japanese national study reporting 50% mortality within the first week of life.(37) Death after NICU discharge is certainly a strong possibility in this high-risk patient group. But if a family’s goal is to meet their baby and decide over time how much intervention makes sense, we suggest that physicians should provide counseling about survival to discharge for babies admitted to a NICU, along with longer-term survival. Inappropriate counseling regarding the timing of mortality may lead to parents’ distrust of the medical system and complicate later decision-making.
We found that receipt of NICU medical interventions was not necessarily associated with improved survival to discharge. This again suggests two possible clinical scenarios: The first is that for some infants, interventions were started and then withdrawn, perhaps when a diagnosis was confirmed and discussions led to withdrawal. The other possibility is that for some infants, interventions were provided but the infants were too sick and the interventions were not effective. Infants with neonatal surgical anomalies who survived without medical interventions may represent infants who received surgical intervention without NICU medical support, such as coming back from the operating room extubated, or infants discharged with palliative care. In any scenario, these data support that many infants with T13 or T18 are offered NICU interventions, and it is likely that the high risk of NICU mortality is not entirely a self-fulfilling prophecy.
The majority of infants in our study did not have neonatal surgical anomalies, were not VLBW, and did not receive intervention. These infants had nearly half the rate of NICU mortality compared to their peers receiving NICU medical intervention. Again, this has two possible interpretations: The first is that many infants with T13 and T18 may not receive intervention in the neonatal period because they do not require intervention in the neonatal period. Many medical and surgical interventions are reported for infants with T13 or T18 after the neonatal hospitalization. (22) The second is that some families may choose limited interventions during the neonatal hospitalization, opting to go home with palliative care. From a practical standpoint, it is easier to arrange home discharge for babies receiving fewer NICU interventions. In both scenarios, it is important to counsel families that many infants with T13 and T18 will need a range of home care supports, which are likely to include medical and surgical considerations in addition to supportive palliative care services.
The results of this study should be interpreted in light of several limitations. Although the rate of anomalies is consistent with other publications, this is a retrospective study of data abstracted from electronic medical record documentation. We do not have information on whether the diagnosis of T13 or T18 was made prenatally or postnatally, how many families at each center may have elected terminations of pregnancy, or the exact genetic diagnosis (mosaic vs. full trisomy). We do not know how many infants received palliative care in the delivery room or were discharged home with hospice care. For infants who died, we do not know if this was due to withholding or failure of interventions. Anomalies are classified based on whether they would typically be associated with neonatal surgical intervention, but we do not know if surgery was performed. Finally, we caution against the use of the study results in counseling about long-term survival or prognosis. The outcomes of this study are limited to NICU discharge, and provide no information about long-term survival or neurodevelopmental outcomes. Despite these limitations, this is the largest study with objective data on infants with T13 or T18 cared for in multiple U.S. NICUs, providing detail on how many infants have neonatal surgical anomalies, which interventions are used, and the associations between major risk factors and survival to discharge home. This fills a major gap in honest physician-parent communication to support families’ goals.
Infants with T13 or T18 receive a wide spectrum of medical interventions in U.S. NICUs. VLBW and neonatal surgical anomalies are risk factors for higher NICU mortality. Medical interventions are not necessarily associated with improved survival to NICU discharge, and the majority of infants discharged home from the NICU receive minimal intervention. For families whose goal is to take their infant home from the NICU with full, limited, or end of life interventions, these data can be used to individualize counseling to support those goals.
Cardiac anomalies were counted with the following order of importance: Cardiac neonatal surgical, major cardiac, valve anomaly, minor cardiac anomaly (ASD, VSD, PDA) and other cardiac anomaly. For example, if a patient had a cardiac neonatal surgical anomaly (such as HLHS) along with coarctation of aorta, that patient was counted as having HLHS and not as coarctation.
Within each organ system, anomalies that usually go together were counted as one: for example, a patient with hydrocephalus and myelomeningocele was counted as myelomeningocele.
Neonatal surgical anomalies include cardiac neonatal surgical, esophageal atresia, duodenal atresia, bowel atresia, imperforate anus, congenital diaphragmatic hernia, meningomyelocele, and gastroschisis.
There were no missing values for gestational age, birth weight, race, multiple birth, Cesarean section delivery, inborn or 5-minute Apgar score <3. There were a total of 8 missing values for gender (5 for trisomy 13, 3 for trisomy 18) and 3 missing values for maternal age (trisomy 18) which were removed from the calculation of percentages.
IQR = interquartile range.
The authors have no financial disclosures or conflicts of interest.