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Meconium-Related Obstruction and Clinical Outcomes in Term and Preterm Infants
Jordan M Rook1,2, Nikhil Chervu1,3, Kara L Calkins4
1Department of Surgery, UCLA David Geffen School of Medicine, Los Angeles, California.
Insights
Meconium-related obstruction (MRO) most commonly affects preterm infants without cystic fibrosis or Hirschsprung disease. These infants experienced increased surgery rates, longer hospital stays, and higher costs, highlighting a need for targeted interventions.
Area of Science:
- Neonatalogy
- Pediatric Surgery
- Gastroenterology
Background:
- Textbook estimates suggest cystic fibrosis and Hirschsprung disease cause most meconium-related obstructions (MRO).
- The incidence and outcomes of MRO, especially in preterm infants with immature bowels, are not well-established.
- Current understanding may not accurately reflect the etiology and impact of MRO in diverse infant populations.
Purpose of the Study:
- To determine the incidence of MRO by specific causes in live-born infants.
- To evaluate the association between MRO and key clinical outcomes, including mortality, surgery, hospitalization duration, and cost.
- To investigate the specific risk and outcomes of MRO in preterm infants.
Main Methods:
- Retrospective cohort study utilizing the National Inpatient Sample (NIS) from 2016-2020.
- Survey weighting methods were employed to estimate national MRO incidence by etiology.
- Multivariable regression models analyzed factors associated with MRO and its impact on clinical outcomes, adjusting for covariates.
Main Results:
- Out of 3,550,796 infants, 1844 (0.1%) were treated for MRO.
- Cystic fibrosis and Hirschsprung disease accounted for only 2.2% and 3.3% of MRO cases, respectively; 94.5% had neither condition.
- Preterm infants without CF or Hirschsprung disease had the highest MRO incidence (187.3 per 100,000 births) and experienced increased surgery, longer hospital stays, and higher costs, without increased mortality.
Conclusions:
- Meconium-related obstruction (MRO) is predominantly observed in preterm infants lacking cystic fibrosis or Hirschsprung disease.
- MRO in this population is linked to significantly higher rates of abdominal surgery, prolonged hospitalizations, and increased healthcare costs.
- The findings underscore the necessity for developing specialized prevention and treatment strategies for MRO in understudied preterm infant populations.
Importance:
Textbooks attribute 80% of meconium-related small bowel obstructions to cystic fibrosis and 15% of colonic obstructions to Hirschsprung disease. It is unknown whether these estimates are accurate, particularly among preterm infants, whose immature bowel predisposes them to meconium-related obstruction (MRO).
Objective:
To estimate the incidence of MRO by type and to assess its association with clinical outcomes.
Design, Setting, And Participants:
This retrospective cohort study of live-born infants included in the National Inpatient Sample from January 1, 2016, to December 31, 2020, used survey weighting methods to estimate the national incidence of MRO by etiology. Data were analyzed from November 27, 2023, to November 12, 2024.
Exposure:
MRO.
Main Outcomes And Measures:
The primary outcome was diagnosis with MRO. Secondary outcomes included mortality, need for abdominal surgery, hospitalization duration, and cost. Multivariable regression models were developed to evaluate characteristics associated with MRO and to assess the association of MRO of prematurity with clinical outcomes after adjusting for demographic and clinical covariates.
Results:
Of 3 550 796 infants, 51.2% were male and 46.7% were privately insured. Overall, 9.1% (n = 322 499) were born preterm. Of 1844 (0.1%) infants treated for MRO, 41 (2.2%) had cystic fibrosis, 60 (3.3%) had Hirschsprung disease, and 1743 (94.5%) had neither predisposing condition. Preterm infants were at highest risk for MRO, with 4.7 MRO cases per 100 000 births associated with cystic fibrosis, 4.7 MRO cases per 100 000 births associated with Hirschsprung disease, and 187.3 MRO cases per 100 000 births associated with neither predisposing condition. Among infants with neither cystic fibrosis nor Hirschsprung disease, those with gestational ages from 28 weeks to 31 weeks 6 days were most likely to develop MRO compared with term infants (adjusted odds ratio, 6.08 [95% CI, 4.27-8.67]). Among preterm infants, having an MRO was associated with a 4.2 percentage point increase in the probability of abdominal surgery (95% CI, 3.1-5.4 percentage points), a 7.3-day increase in length of stay (95% CI, 5.8-8.8 days), and a $23 215 increase in hospitalization costs (95% CI, $17 739-$28 690) compared with infants who did not have an obstruction, with no change in mortality rate (0.1 percentage point change [95% CI, -0.6 to 0.8 percentage points]).
Conclusions And Relevance:
In this cohort study of over 3.5 million infants, MRO was most likely to occur among preterm infants without cystic fibrosis or Hirschsprung disease. These infants more frequently required surgery and had longer and more costly hospitalizations, indicating a need for dedicated prevention and treatment pathways for this understudied disease.
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