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      Randomised trial of azithromycin to eradicate Ureaplasma in preterm infants

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          Abstract

          Objective

          To test whether azithromycin eradicates Ureaplasma from the respiratory tract in preterm infants.

          Design

          Prospective, phase IIb randomised, double-blind, placebo-controlled trial.

          Setting

          Seven level III–IV US, academic, neonatal intensive care units (NICUs).

          Patients

          Infants 24 0–28 6 weeks’ gestation (stratified 24 0–26 6; 27 0–28 6 weeks) randomly assigned within 4 days following birth from July 2013 to August 2016.

          Interventions

          Intravenous azithromycin 20 mg/kg or an equal volume of D5W (placebo) every 24 hours for 3 days.

          Main outcome measures

          The primary efficacy outcome was Ureaplasma-free survival. Secondary outcomes were all-cause mortality, Ureaplasma clearance, physiological bronchopulmonary dysplasia (BPD) at 36 weeks’ postmenstrual age, comorbidities of prematurity and duration of respiratory support.

          Results

          One hundred and twenty-one randomised participants (azithromycin: n=60; placebo: n=61) were included in the intent-to-treat analysis (mean gestational age 26.2±1.4 weeks). Forty-four of 121 participants (36%) were Ureaplasma positive (azithromycin: n=19; placebo: n=25). Ureaplasma-free survival was 55/60 (92% (95% CI 82% to 97%)) for azithromycin compared with 37/61 (61% (95% CI 48% to 73%)) for placebo. Mortality was similar comparing the two treatment groups (5/60 (8%) vs 6/61 (10%)). Azithromycin effectively eradicated Ureaplasma in all azithromycin-assigned colonised infants, but 21/25 (84%) Ureaplasma-colonised participants receiving placebo were culture positive at one or more follow-up timepoints. Most of the neonatal mortality and morbidity was concentrated in 21 infants with lower respiratory tract Ureaplasma colonisation. In a subgroup analysis, physiological BPD-free survival was 5/10 (50%) (95% CI 19% to 81%) among azithromycin-assigned infants with lower respiratory tract Ureaplasma colonisation versus 2/11 (18%) (95% CI 2% to 52%) in placebo-treated infants.

          Conclusion

          A 3-day azithromycin regimen effectively eradicated respiratory tract Ureaplasma colonisation in this study.

          Trial registration number

          NCT01778634.

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          Most cited references40

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          Models for Longitudinal Data: A Generalized Estimating Equation Approach

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            Prediction of bronchopulmonary dysplasia by postnatal age in extremely premature infants.

            Benefits of identifying risk factors for bronchopulmonary dysplasia in extremely premature infants include providing prognostic information, identifying infants likely to benefit from preventive strategies, and stratifying infants for clinical trial enrollment. To identify risk factors for bronchopulmonary dysplasia, and the competing outcome of death, by postnatal day; to identify which risk factors improve prediction; and to develop a Web-based estimator using readily available clinical information to predict risk of bronchopulmonary dysplasia or death. We assessed infants of 23-30 weeks' gestation born in 17 centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network and enrolled in the Neonatal Research Network Benchmarking Trial from 2000-2004. Bronchopulmonary dysplasia was defined as a categorical variable (none, mild, moderate, or severe). We developed and validated models for bronchopulmonary dysplasia risk at six postnatal ages using gestational age, birth weight, race and ethnicity, sex, respiratory support, and Fi(O(2)), and examined the models using a C statistic (area under the curve). A total of 3,636 infants were eligible for this study. Prediction improved with advancing postnatal age, increasing from a C statistic of 0.793 on Day 1 to a maximum of 0.854 on Day 28. On Postnatal Days 1 and 3, gestational age best improved outcome prediction; on Postnatal Days 7, 14, 21, and 28, type of respiratory support did so. A Web-based model providing predicted estimates for bronchopulmonary dysplasia by postnatal day is available at https://neonatal.rti.org. The probability of bronchopulmonary dysplasia in extremely premature infants can be determined accurately using a limited amount of readily available clinical information.
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              Impact of a physiologic definition on bronchopulmonary dysplasia rates.

              Bronchopulmonary dysplasia (BPD) is the endpoint of many intervention trials in neonatology, yet the outcome measure when based solely on oxygen administration may be confounded by differing criteria for oxygen administration between physicians. We previously reported a technique to standardize the definition of BPD between sites by using a timed room-air challenge in selected infants. We hypothesized that a physiologic definition of BPD would reduce the variation in observed rates of BPD among different neonatal centers. Methodology. A total of 1598 consecutive inborn premature infants (501-1249 g birth weight) who remained hospitalized at 36 weeks' postmenstrual age were prospectively assessed and assigned an outcome with both a clinical definition and physiologic definition of BPD. The clinical definition of BPD was oxygen supplementation at exactly 36 weeks' postmenstrual age. The physiologic definition of BPD was assigned at 36 +/- 1 weeks' postmenstrual age and included 2 distinct subpopulations. First, neonates on positive pressure support or receiving >30% supplemental oxygen with saturations between 90% and 96% were assigned the outcome BPD and not tested further. Second, those receiving 30% with saturations >96% underwent a room-air challenge with continuous observation and oxygen-saturation monitoring. Outcomes of the room-air challenge were "no BPD" (saturations > or =90% during weaning and in room air for 30 minutes) or "BPD" (saturation <90%). At the conclusion of the room-air challenge, all infants were returned to their baseline oxygen levels. Safety (apnea, bradycardia, increased oxygen use) and outcomes of the physiologic definition versus the clinical definition were assessed. A total of 560 (35.0%) neonates were diagnosed with BPD by the clinical definition of oxygen use at 36 weeks' postmenstrual age. The physiologic definition diagnosed BPD in 398 (25.0%) neonates in the cohort. All infants were safely studied. There were marked differences in the impact of the definition on BPD rates between centers (mean reduction: 10%; range: 0-44%). Sixteen centers had a decrease in their BPD rate, and 1 center had no change in their rate. The physiologic definition of BPD reduced the overall rate of BPD and reduced the variation among centers. Significant center differences in the impact of the physiologic definition were seen, and differences remained even with the use of this standardized definition. The magnitude of the change in BPD rate is comparable to the magnitude of treatment effects seen in some clinical trials in BPD. The physiologic definition of BPD facilitates the measurement of BPD as an outcome in clinical trials and the comparison between and within centers over time.
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                Author and article information

                Journal
                Arch Dis Child Fetal Neonatal Ed
                Arch Dis Child Fetal Neonatal Ed
                fetalneonatal
                fnn
                Archives of Disease in Childhood. Fetal and Neonatal Edition
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                1359-2998
                1468-2052
                November 2020
                13 March 2020
                : 105
                : 6
                : 615-622
                Affiliations
                [1 ] departmentDepartment of Pediatrics , University of Maryland School of Medicine , Baltimore, Maryland, USA
                [2 ] departmentDepartment of Epidemiology and Preventive Medicine , University of Maryland School of Medicine , Baltimore, Maryland, USA
                [3 ] departmentDepartment of Pediatrics , University of Maryland Baltimore , Baltimore, Maryland, USA
                [4 ] departmentDepartment of Pathology , University of Alabama at Birmingham , Birmingham, Alabama, USA
                [5 ] departmentDepartment of Pediatrics , University of Alabama at Birmingham , Birmingham, Alabama, USA
                [6 ] departmentDepartment of Pediatrics , University of Virginia School of Medicine , Charlottesville, Virginia, USA
                [7 ] departmentDepartment of Pediatrics , Johns Hopkins Medicine , Baltimore, Maryland, USA
                [8 ] departmentDepartment of Pediatrics , Christiana Care Health System , Newark, Delaware, USA
                [9 ] departmentDepartment of Pediatrics , Vanderbilt University Medical Center , Nashville, Tennessee, USA
                [10 ] University of Maryland School of Pharmacy , Baltimore, Maryland, USA
                Author notes
                [Correspondence to ] Dr Rose Marie Viscardi, Pediatrics, University of Maryland School of Medicine, Baltimore, MD 21201, USA; rviscard@ 123456som.umaryland.edu
                Author information
                http://orcid.org/0000-0001-7451-6059
                Article
                fetalneonatal-2019-318122
                10.1136/archdischild-2019-318122
                7592356
                32170033
                aec7472c-527d-49fb-83f5-b5d5b3e3cfe0
                © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 20 August 2019
                : 26 January 2020
                : 25 February 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100009633, Eunice Kennedy Shriver National Institute of Child Health and Human Development;
                Award ID: R01 HD067126
                Categories
                Original Research
                1506
                Custom metadata
                unlocked

                Neonatology
                neonatology,ureaplasma parvum,ureaplasma urealyticum,prematurity,bronchopulmonary dysplasia

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