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      Clinical Correlates of Cholestasis in Preterm Infants with Surgical Necrotizing Enterocolitis

      research-article
      1 , 2 , 3 , 2 , 4 , 5 , 1 , 6 , 6 , 7 , 1 , 8 , 2 , 3 , 9
      Newborn (Clarksville, Md.)
      Anthropometric, Adhesions, Bell’s criteria, Cholestasis, Farnesoid X, Fenton growth, Fish oil-containing lipid emulsion, Fistula, Ileocecal valve, Intralipids, Infant, Intestinal failure, Liver X receptors, Logistic regression, Necrotizing enterocolitis, Neonate, Outcome, Parenteral nutrition, Perforations, Pneumoperitoneum, Pneumatosis, Portal venous gas, Preterm, Premature, Soybean oil–medium chain triglycerides–olive oil–fish oil, Surgical site infection, Stricture, Term-equivalent age, Weight-for-length, Wound dehiscence, z-scores

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          Abstract

          Background:

          We sought to investigate the clinical determinants and outcomes of cholestasis in preterm infants with surgical necrotizing enterocolitis (sNEC).

          Methods:

          Retrospective comparison of clinical information in preterm infants who developed cholestasis vs those who did not.

          Results:

          Sixty-two (62/91, 68.1%) infants with NEC developed cholestasis at any time following the onset of illness. Cholestasis was seen more frequently in those who had received ionotropic support at 24 hours following sNEC diagnosis (87.1% vs 58.6%; p = 0.002), had higher mean C-reactive protein levels 2 weeks after NEC diagnosis ( p = 0.009), had blood culture-positive sepsis [25 (40.3%) vs 4 (13.8%); p = 0.011], received parenteral nutrition (PN) for longer durations (108.4 ± 56.63 days vs 97.56 ± 56.05 days; p = 0.007), had higher weight-for-length z scores at 36 weeks’ postmenstrual age [−1.0 (−1.73, −0.12) vs −1.32 (−1.76, −0.76); p = 0.025], had a longer length of hospital stay (153.7 ± 77.57 days vs 112.51 ± 85.22 days; p = 0.024), had intestinal failure more often (61% vs 25.0%, p = 0.003), had more surgical complications (50% vs 27.6%; p = 0.044), and had >1 complication (21% vs 3.4%; p = 0.031). Using linear regression, the number of days after surgery when feeds could be started [OR 15.4; confidence interval (CI) 3.71, 27.13; p = 0.009] and the postoperative ileus duration (OR 11.9, CI 1.1, 22.8; p = 0.03) were independently associated with direct bilirubin between 2 and 5 mg/dL (mild–moderate cholestasis) at 2 months of age. The duration of PN was independently associated with direct bilirubin >5 mg/dL (severe cholestasis) at 2 months of age in these patients.

          Conclusion:

          Cholestasis was seen in 68% of infants following surgical NEC. The most likely contributive factors are intestinal failure and subsequent PN dependence for longer periods. Our data suggest that identification and prevention of risk factors such as sepsis and surgical complications and early feeds following NEC surgery may improve outcomes.

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          Most cited references27

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          • Article: not found

          Necrotizing enterocolitis.

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            • Abstract: found
            • Article: not found

            Neonatal necrotizing enterocolitis. Therapeutic decisions based upon clinical staging.

            A method of clinical staging for infants with necrotizing enterocolitis (NEC) is proposed. On the basis of assigned stage at the time of diagnosis, 48 infants were treated with graded intervention. For Stage I infants, vigorous diagnostic and supportive measures are appropriate. Stage II infants are treated medically, including parenteral and gavage aminoglycoside antibiotic, and Stage III patients require operation. All Stage I patients survived, and 32 of 38 Stage II and III patients (85%) survived the acute episode of NEC. Bacteriologic evaluation of the gastrointestinal microflora in these neonates has revealed a wide range of enteric organisms including anaerobes. Enteric organisms were cultured from the blood of four infants dying of NEC. Sequential cultures of enteric organisms reveal an alteration of flora during gavage antibiotic therapy. These studies support the use of combination antimicrobial therapy in the treatment of infants with NEC.
              • Record: found
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              Neonatal MRI to predict neurodevelopmental outcomes in preterm infants.

              Very preterm infants are at high risk for adverse neurodevelopmental outcomes. Magnetic resonance imaging (MRI) has been proposed as a means of predicting neurodevelopmental outcomes in this population. We studied 167 very preterm infants (gestational age at birth, 30 weeks or less) to assess the associations between qualitatively defined white-matter and gray-matter abnormalities on MRI at term equivalent (gestational age of 40 weeks) and the risks of severe cognitive delay, severe psychomotor delay, cerebral palsy, and neurosensory (hearing or visual) impairment at 2 years of age (corrected for prematurity). At two years of age, 17 percent of infants had severe cognitive delay, 10 percent had severe psychomotor delay, 10 percent had cerebral palsy, and 11 percent had neurosensory impairment. Moderate-to-severe cerebral white-matter abnormalities present in 21 percent of infants at term equivalent were predictive of the following adverse outcomes at two years of age: cognitive delay (odds ratio, 3.6; 95 percent confidence interval, 1.5 to 8.7), motor delay (odds ratio, 10.3; 95 percent confidence interval, 3.5 to 30.8), cerebral palsy (odds ratio, 9.6; 95 percent confidence interval, 3.2 to 28.3), and neurosensory impairment (odds ratio, 4.2; 95 percent confidence interval, 1.6 to 11.3). Gray-matter abnormalities (present in 49 percent of infants) were also associated, but less strongly, with cognitive delay, motor delay, and cerebral palsy. Moderate-to-severe white-matter abnormalities on MRI were significant predictors of severe motor delay and cerebral palsy after adjustment for other measures during the neonatal period, including findings on cranial ultrasonography. Abnormal findings on MRI at term equivalent in very preterm infants strongly predict adverse neurodevelopmental outcomes at two years of age. These findings suggest a role for MRI at term equivalent in risk stratification for these infants. Copyright 2006 Massachusetts Medical Society.

                Author and article information

                Journal
                9918418384706676
                51742
                Newborn (Clarksville)
                Newborn (Clarksville)
                Newborn (Clarksville, Md.)
                2769-514X
                22 October 2023
                Jul-Sep 2023
                26 September 2023
                15 November 2023
                : 2
                : 3
                : 191-197
                Affiliations
                [1 ]Department of Pediatrics/Neonatology, Atrium Health Wake Forest Baptist, Wake Forest School of Medicine, Winston Salem, North Carolina, United States of America
                [2 ]Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi, United States of America
                [3 ]Global Newborn Society, Clarksville, Maryland, United States of America
                [4 ]Frank Porter Graham Child Development Institute, University of North Carolina at Chapel Hill, NC, United States of America
                [5 ]Department of Regenerative Medicine, Wake Forest School of Medicine, Winston Salem, North Carolina, United States of America
                [6 ]Department of Pediatric Surgery, Atrium Health Wake Forest Baptist, Wake Forest School of Medicine, Winston Salem, North Carolina, United States of America
                [7 ]Department of Pathology, Atrium Health Wake Forest Baptist, Wake Forest School of Medicine, Winston Salem, North Carolina, United States of America
                [8 ]Texas Children Hospital, Baylor College of Medicine, Houston, Texas, United States of America
                [9 ]Louisiana State University Health Sciences Center – Shreveport, LA, United States of America
                Author notes

                Author’s Contributions

                PMG, PPG, and AM designed the study. PMG, IP, JY, VGW, RJR, ML, CW, MHP, PPG, AGM, JLL, and AM analyzed the data and wrote the paper. All the authors contributed and approved the paper.

                Corresponding Author: Parvesh Mohan Garg, Department of Pediatrics/Neonatology, Atrium Health Wake Forest Baptist, Wake Forest School of Medicine, Winston Salem, North Carolina, United States of America, Phone: +1 252 364 5800, gargparvesh@ 123456hotmail.com
                Article
                NIHMS1935669
                10.5005/jp-journals-11002-0069
                10653206
                37974929
                e1e94e35-1148-4432-ad52-801e89b6174b

                This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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                anthropometric,adhesions,bell’s criteria,cholestasis,farnesoid x,fenton growth,fish oil-containing lipid emulsion,fistula,ileocecal valve,intralipids,infant,intestinal failure,liver x receptors,logistic regression,necrotizing enterocolitis,neonate,outcome,parenteral nutrition,perforations,pneumoperitoneum,pneumatosis,portal venous gas,preterm,premature,soybean oil–medium chain triglycerides–olive oil–fish oil,surgical site infection,stricture,term-equivalent age,weight-for-length,wound dehiscence,z-scores

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