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Neonatal morbidity occurs despite pulmonary maturity prior to 39 weeks gestation.
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PMID:  24434777     Owner:  NLM     Status:  Publisher    
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Objective:To compare outcomes among late-preterm or early-term neonates according to fetal lung maturity (FLM) status.Study Design:We conducted a retrospective cohort study of 234 eligible singletons delivered after FLM testing before 39 weeks gestation at our center over a 2-year time period. A primary composite neonatal outcome included death and major morbidities.Result:The overall rate of primary composite morbidity was 25/46 (52.2%) and 61/188 (32.4%) in the immature/transitional and mature groups, respectively. After adjustment for confounders including gestational age, the composite outcome was not significantly different; adjusted odds ratio (aOR)=1.4 (confidence interval (CI)=0.7-3.0). The rate of respiratory distress syndrome was significantly higher in the immature/transitional group; odds ratio=3.4 (CI=1.1-10.3) as expected.Conclusion:FLM status did not correlate with the spectrum of neonatal morbidities in late-preterm and early-term births. Neonatal complications remained common in both groups.Journal of Perinatology advance online publication, 16 January 2014; doi:10.1038/jp.2013.173.
Authors:
J P Vanderhoeven; S E Peterson; E E Gannon; D E Mayock; H S Gammill
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Type:  JOURNAL ARTICLE     Date:  2014-1-16
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Title:  Journal of perinatology : official journal of the California Perinatal Association     Volume:  -     ISSN:  1476-5543     ISO Abbreviation:  J Perinatol     Publication Date:  2014 Jan 
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Nlm Unique ID:  8501884     Medline TA:  J Perinatol     Country:  -    
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Journal Information
Journal ID (nlm-journal-id): 8501884
Journal ID (pubmed-jr-id): 5061
Journal ID (nlm-ta): J Perinatol
Journal ID (iso-abbrev): J Perinatol
ISSN: 0743-8346
ISSN: 1476-5543
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nihms-submitted publication date: Day: 30 Month: 1 Year: 2014
Electronic publication date: Day: 16 Month: 1 Year: 2014
Print publication date: Month: 4 Year: 2014
pmc-release publication date: Day: 01 Month: 10 Year: 2014
Volume: 34 Issue: 4
First Page: 322 Last Page: 325
PubMed Id: 24434777
ID: 3969761
DOI: 10.1038/jp.2013.173
ID: NIHMS546496

Neonatal morbidity occurs despite pulmonary maturity prior to 39 weeks gestation
Jeroen P Vanderhoeven, MD
Suzanne E Peterson, MD
Elizabeth E Gannon, MD
Dennis E Mayock, MD
Hilary S Gammill, MD
Department of Obstetrics and Gynecology (Drs Vanderhoeven, Peterson, Gammill, and Gannon), and the Department of Pediatrics (Dr Mayock), University of Washington, Seattle, WA
Correspondence: Corresponding Author: Jeroen Vanderhoeven, 1959 NE Pacific St, Seattle, WA98195, (206) 598-4070 (work), (215) 680-7411 (cell), (206) 598-4694 (fax), hoeven@uw.edu

Introduction

Fetal lung maturation (FLM) studies often dictate obstetrical decision making in late preterm and early term pregnancies. In clinically appropriate circumstances, the status of FLM can provide an estimate of risk of neonatal respiratory distress syndrome and thus inform the timing of delivery.1 However, recent evidence suggests that despite mature FLM testing, neonates born before 39 weeks gestation have more adverse outcomes than those born subsequent to 39 weeks.2-6

Although adverse respiratory outcomes are among the most common complications in the late preterm and early term populations, recent studies highlight the importance of neonatal maturation including outcomes not directly assessed by FLM testing.2-7 Other common neonatal complications in the late preterm period include jaundice, feeding difficulties, temperature dysregulation, susceptibility to infection, and metabolic abnormalities. Notably, there is now a large body of evidence suggesting the late preterm period as a time for significant brain maturation. Cerebral cortex continues to develop anatomic complexity and to increase in volume throughout gestation. Half of cerebral cortex volume accumulates in the final 6 weeks of gestation.8-10 Recent observations regarding the relationship between even subtle differences in gestational age with neonatal outcomes have led to reconsideration of criteria for timing delivery.2

While ample evidence shows that the risk of adverse outcomes differs between a neonate born prior to 39 weeks with mature FLM testing and a neonate born after 39 weeks, the ability of FLM testing to predict overall neonatal outcomes at a given gestational age is less clear. We hypothesized that among neonates at similar late-preterm or early-term gestational ages, mature pulmonary testing would not serve as a surrogate of overall fetal maturity. Specifically, we sought to investigate overall neonatal outcomes through a direct comparison of those neonates with mature fetal lung status to those with immature or transitional status in the critical gestational age where FLM testing is routinely performed.


Materials and Methods

We conducted a retrospective cohort study of all women with a singleton, non-anomalous pregnancy undergoing FLM testing after amniocentesis and delivery at a single tertiary care center from January 2004 to December 2004 and January 2006 to December 2006. This time period was selected based on data available to the authors from detailed chart abstraction at the predetermined analysis point. This study was approved by the Human Subjects Division of the University of Washington. Data were derived from direct review of the electronic medical records of women and their newborns as detailed below. All chart abstraction was performed by one of the authors (JV, SP, or EG). Discrepancies regarding abstraction outcomes were resolved in consultation with a fourth author (HG). Exclusion criteria were multiple gestation, delivery at or after 39 weeks gestation, fetal anomalies, vaginal sample collection, or collection interval greater than seven days prior to delivery.

All FLM testing was performed with a previously validated in-house fluorescence polarization assay using a commercial clinical laboratory TDx analyzer (Abbott Laboratories).11 Pregnancy outcomes for two groups of women with FLM testing within one week of delivery were compared: 1) immature or transitional FLM status and 2) mature FLM status. Both groups were identified from laboratory records and verified by direct chart review.

FLM indices were abstracted including the gestational age at the time of testing. Maternal characteristics including age, parity, race, dating criteria, comorbidities including (pregestational and gestational) diabetes and chronic hypertension, medications, delivery indication, and mode of delivery were abstracted. All subjects underwent first- or second-trimester sonographic confirmation of gestational age by criteria recommended by the American College of Obstetricians and Gynecologists.12

Extensive information was gathered from neonatal charts including daily progress notes, laboratory and radiologic studies, transfer and discharge summaries with the goal to identify any outcome that required clinical intervention. A broad range of clinically relevant neonatal morbidities was considered, excluding outcomes without direct impact on clinical management. Neonatal outcomes examined included death, respiratory outcomes, infectious complications, neurologic abnormalities, gastrointestinal outcomes, metabolic abnormalities, cardiovascular complications, and hematologic problems. Specifically, respiratory outcomes included respiratory distress syndrome (RDS), transient tachypnea of the newborn, bronchopulmonary dysplasia, persistent pulmonary hypertension, need for respiratory support (including ventilatory support or any other mode of oxygen supplementation), and use of surfactant. Infectious outcomes included proven sepsis and pneumonia. Evaluation for possible infection, including antibiotic administration, was examined but not included in the composite outcome as this is the highest incidence intervention in late preterm births.3 Neurologic outcomes included intraventricular hemorrhage, generalized seizures requiring treatment, hypoxic ischemic encephalopathy, and periventricular leukomalacia. Gastrointestinal outcomes included feeding difficulties requiring hyperalimentation or enteral tube feeding. Hepatobiliary outcome included jaundice requiring phototherapy. Cardiovascular outcomes included arrhythmia or need for neonatal echocardiography. Hematologic outcomes included blood transfusion and thrombocytopenia requiring treatment. The metabolic outcome examined was hypoglycemia requiring intravenous glucose administration.

The primary outcome was a composite of any of these neonatal outcomes that required clinical intervention. In addition, NICU admission and NICU length of stay were examined. The primary outcome was compared between subjects with mature FLM status versus those subjects with immature/transitional FLM indices.

A power analysis was not feasible due to unknown proportions with specifically defined composite outcomes. Descriptive characteristics were compared using χ2 for dichotomous variables. Student t tests or Mann Whitney U were used for comparison of continuous variables as appropriate. We made an a priori decision to adjust for the following confounders using logistic regression: maternal age, race/ethnicity, gestational age, and mode of delivery.


Results

There were a total of 388 recorded births with FLM testing in the study period. After applying exclusion criteria (Figure 1), a total of 234 mother-neonate dyads were available for analysis. Of these, 46/234 (19.7%) had immature/transitional FLM results within one week of delivery, and 188/234 (80.3%) had mature FLM results within one week of delivery.

Maternal pregnancy characteristics in the mature and immature/transitional testing groups are presented in Table 1. Mean gestational age at time of fetal lung maturity testing was 36.8 ± 1.3 weeks in the mature group compared to 35.7 ± 2.1 weeks in the immature/transitional group. Mean birthweight for the mature group was 3036 ± 673 grams compared to 2486 ± 691 grams in the immature/transitional group. The mean latency from time of testing until delivery was 3.1 ± 2.3 days in the immature/transitional group compared to 1.3 ± 1.2 days in the mature group.

Among the immature/transitional group, 14/46 (30.4%) were delivered between 37 and 38 6/7 weeks gestation, 23/46 (50%) were delivered between 34 and 36 6/7 weeks gestation, and 9/46 (19.6%) were delivered prior to 34 weeks gestation. Among the mature testing group, 105/188 (55.9%) were delivered between 37 and 38 6/7 weeks gestation, 78/188 (41.5%) were delivered between 34 and 36 6/7 weeks gestation, and only 5/188 (2.7%) were delivered prior to 34 weeks gestation.

There were no perinatal deaths. The primary composite adverse neonatal outcome occurred more often in the immature/transitional group (25/46, 52.2%) than in the mature group (61/188, 32.4%). Prior to adjustment for confounders, the odds of experiencing the primary outcome in the immature/transitional group was approximately two-fold greater than that of the mature group; unadjusted odds ratio (OR) 2.3 (95% confidence interval [CI] 1.2-4.4). However, after adjusting for confounding variables including gestational age, maternal age, maternal race, and mode of delivery, the odds of experiencing the primary composite neonatal adverse outcome was not significantly different among the groups; adjusted OR 1.4 (CI 0.7-3.0) (Table 2).

There was a significant inverse relationship between gestational age and the composite outcome (p<0.001). In the group with immature/transitional testing results, the composite outcome occurred in 77.8%, 65.2%, and 14.3% of neonates born prior to 34 weeks, 34 to 36 6/7 weeks, and 37 to 38 6/7 weeks gestation, respectively. In the group with mature testing results, the composite outcome occurred in 80%, 44.9%, and 20.9% of neonates, respectively. The sample size and composite morbidity for each group by gestational age are represented in Figure 2.

Prior to adjustment, there was a significant difference in the percentage of NICU admissions; 46.7% in the immature/transitional group admitted and 21.3% in the mature, OR 3.0 (CI 1.5-5.9). After adjustment, this finding was no longer significant, aOR 1.9 (CI 0.9-4.1). Similarly, median length of stay was not significantly different between the two groups: median 7 days (range 1-48 days) in the mature group and median 9 days (range 1-34 days) immature/transitional.

As expected, the rate of respiratory distress syndrome was significantly higher in the immature/transitional group; OR 3.4 (CI 1.1-10.3). Grouping neonatal morbidities by system (results summarized in Table 2) revealed significant differences prior to adjustment in gastroenterological complications (primarily feeding difficulties requiring treatment), OR 4.4 (CI 2.0-9.8). After adjustment for confounders, this difference was no longer significant. No significant differences were noted for overall adverse hepatobiliary, respiratory, infectious disease, neurologic, cardiac, metabolic, and hematologic outcomes.

In the subset of mothers with diabetes (52/234, 22%), after adjustment for confounders, fetal lung maturity status was not associated with composite neonatal morbidity.


Comment

Both mature and immature FLM groups had high levels of composite adverse neonatal outcomes. While the unadjusted rate of clinically significant complications was increased among the transitional/immature group, this difference was not present after adjustment for potentially confounding variables including gestational age. Our findings validate previously published studies demonstrating a significant decrease in the rate of RDS in the setting of mature FLM testing but also demonstrate that this decrease does not extend to broader morbidity.11, 13, 14

Prior work by Bates, Dola, and others has provided important information regarding outcomes of late preterm/early term neonates with mature FLM compared to those delivered after 39 weeks gestation.2-6 To add to this literature, we sought to assess outcomes by FLM status among neonates at similar gestational ages in the late preterm and early term time periods. We believe our findings help place RDS within a larger context of short and long-term adverse outcomes associated with late preterm birth.7, 15-17 In our population, both RDS and composite adverse neonatal outcomes decreased as gestational age increased. Our data add to the evolving literature that supports delaying delivery until 39 weeks gestation when no immediate maternal or fetal risk is present.2-6,13,14

While the strength of our study design lies in the ability to directly compare subjects with different FLM status at the same gestational age, this design also increases the likelihood that subjects with immature/transitional status were delivered due to an incident maternal or fetal indication. While this may introduce a bias toward amplification of morbidity in the immature/transitional group, the direction of such a bias would be against our hypothesis that general morbidity would not differ between groups.

Other major strengths of our study include a large and representative sample size, a clinically diverse population potentially allowing for generalizability of our results to other populations, and an a priori defined primary outcome which limits the potential for multiple comparisons. We also acknowledge several limitations. A retrospective study design limits the ability to identify and correct potential misclassification of neonatal outcomes and maternal characteristics. Confounding remains a possibility in the absence of a randomized study design. As term uncomplicated newborns receive care in a newborn nursery whereas preterm infants often receive care in a neonatal intensive care unit, the distribution of intervention may reflect recording bias or practice variation between services. Additionally, our study was not powered to specifically analyze singular adverse outcomes such as stillbirth. Finally, we were unable to study long-term neonatal outcomes associated with the use of FLM studies, notably neurodevelopmental consequences. FLM testing was performed by fluorescence polarization. We would expect similar results with comparable FLM tests.1,11

Overall, we found that mature and transitional/immature FLM status was not correlated with the spectrum of neonatal morbidities in late preterm and early term births. In our population, neonatal complications requiring clinical intervention remained common despite mature FLM testing. As our knowledge of the complexity of fetal and neonatal maturation evolves, the limitations of the singular focus of FLM testing are clear. Thus, our study supports the idea that FLM status should be one consideration amongst many complex, sometimes unmeasurable, markers of global maturation. The obstetric balance between continued in utero gestation versus delivery should continue to give us pause.

Future studies may identify specific patient populations where a significant difference in outcome with documented FLM exists. Biomarkers predictive of non-respiratory adverse events, including neurodevelopmental outcomes, in late preterm/early term birth represent an important area of future research focus.


Notes

FN2Presented at the 31st Annual Meeting of The Pregnancy Meeting (Society for Maternal-Fetal Medicine), San Francisco, CA. February 11, 2011. (Poster #488)

FN3Conflict of interest: The authors declare no conflicts of interest.

We gratefully acknowledge the mothers who have entrusted University of Washington Medical Center with their care, the Department of Laboratory Medicine in constructing a list of FLM testing results, Evangelyn Nkwopara and Andrea Felt for research support, and WRHR (NICHD HD01264).

Supported by NICHD HD-01-264


References
1. Assessment and Induction of Fetal Pulmonary MaturityCreasy RK,Resnick R,Iams JMaternal-fetal medicine: principles and practice6thPhiladelphiaWB Saunders Co.Year: 2009419431
2. Tita AT,Landon MB,Spong CY,Lai Y,Leveno KJ,Varner MW,et al. Eunice Kennedy Shriver NICHD Maternal-Fetal Medicine Units Network. Timing of elective repeat cesarean delivery at term and neonatal outcomesN Engl J MedYear: 20093601112019129525
3. Bates E,Rouse DJ,Mann ML,Chapman V,Carlo WA,Tita AT. Neonatal outcomes after demonstrated fetal lung maturity before 39 weeks of gestationObstet GynecolYear: 201011612889521099593
4. Dola C,Tran T,Linhuber AM,Cierny J,Denicola N,Chong E,et al. Preterm birth after mature fetal lung indices: is there any neonatal morbidity?J Matern Fetal Neonatal MedYear: 20112473820459338
5. Fang YMV,Guirguis P,Borgida A,Feldman D,Ingardia C,Herson V. Increased neonatal morbidity despite pulmonary maturity for deliveries occurring before 39 weeksJ Matern Fetal Neonatal MedYear: 2013261798222963341
6. Kamath BD,Marcotte MP,DeFranco EA. Neonatal morbidity after documented fetal lung maturity in late preterm birth and early term infantsAm J Obstet GynecolYear: 2011204518.e1821752754
7. Melamed N,Klinger G,Tenenbaum-Gavish K,Herscovici T,Linder N,Hod M,et al. Short-term neonatal outcome in low-risk, spontaneous, singleton, late preterm deliveriesObstet GynecolYear: 20091142536019622985
8. Kinney HC. The near-term (late preterm) human brain and risk for periventricular leukomalacia: a reviewSemin PerinatolYear: 20063081816731282
9. van Soelen IL,Brouwer RM,Peper JS,van Beijsterveldt TC,van Leeuwen M,de Vries LS,et al. Effects of gestational age and birth weight on brain volumes in healthy 9 year-old childrenJ PediatrYear: 201015689690120227719
10. Wahlvold KB,Fjell AM,Brown TT,et al. Long-term influence of normal variation in neonatal characteristics on human brain developmentPNASYear: 201210949200892009423169628
11. Talt JF,Foerder CA,Ashwood ER,Benedetti TJ. Prospective clinical evaluation of an improved fluorescence polarization assay for predicting fetal lung maturityClin ChemYear: 19873355483829389
12. American Academy of Pediatrics and the American College of Obstetricians and GynecologistsGuidelines for perinatal care6thWashington, DCACOGYear: 2007
13. Parvin CA,Kaplan LA,Chapman JF,McManamon TG,Gronowski AM. Predicting respiratory distress syndrome using gestational age and fetal lung maturity by fluorescent polarizationAm J Obstet GynecolYear: 200519219920715672025
14. Consortium on Safe LaborHibbard JU,Wilkins I,Sun L,Gregory K,Haberman S,et al. Respiratory morbidity in late preterm birthsJAMAYear: 20103044192520664042
15. McIntire DD,Leveno KJ. Neonatal mortality and morbidity rates in late preterm births compared with births at termObstet GynecolYear: 2008111354118165390
16. Talge NM,Holzman C,Wang J,Lucia V,Gardiner J,Breslau N. Late-preterm birth and its association with cognitive and socioemotional outcomes at 6 years of agePediatricsYear: 201012611243121098151
17. Woythaler MA,McCormick MC,Smith VC. Late preterm infants have worse 24-month neurodevelopmental outcomes than term infantsPediatricsYear: 2011127e622921321024

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Keywords: fetal lung maturity, late preterm birth, amniocentesis, neonatal outcomes, prematurity.

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