Evidence map›Paper›PMID 25385115›Full record

Trial reportAntimicrobial agents and chemotherapy2015

Pharmacokinetics, microbial response, and pulmonary outcomes of multidose intravenous azithromycin in preterm infants at risk for Ureaplasma respiratory colonization.

L Marcela Merchan, Hazem E Hassan, Michael L Terrin, Ken B Waites, David A Kaufman, Namasivayam Ambalavanan, Pamela Donohue, Susan J Dulkerian, Robert Schelonka, Laurence S Magder and 3 more

Open access · bronzeAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
1.7field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Azithromycin for eradication ofArchives of disease in childhood. Fetal and neonatal edition · 2026
    Pooled it
  2. Pooled it
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  4. Trial
  5. Trial
  6. Randomised trial of azithromycin to eradicateArchives of disease in childhood. Fetal and neonatal edition · 2020
    Trial
  7. Trial
  8. Trial
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Predicting the likelihood of lower respiratory tractArchives of disease in childhood. Fetal and neonatal edition · 2023
    Article
  15. Review
  16. Azithromycin for Eradication ofThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2023
    Article
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

L Marcela MerchanDepartment of Pediatrics, University of Maryland, Baltimore School of Medicine, Baltimore, Maryland, USA.
Hazem E HassanUniversity of Maryland School of Pharmacy, Baltimore, Maryland, USA Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Helwan University, Cairo, Egypt.
Michael L TerrinDepartment of Epidemiology and Preventive Medicine, University of Maryland, Baltimore School of Medicine, Baltimore, Maryland, USA.
Ken B WaitesDepartments of Pathology and Pediatrics, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, USA.
David A KaufmanDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
Namasivayam AmbalavananDepartments of Pathology and Pediatrics, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, USA.
Pamela DonohueDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Susan J DulkerianDepartment of Pediatrics, University of Maryland, Baltimore School of Medicine, Baltimore, Maryland, USA.
Robert SchelonkaDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon, USA.
Laurence S MagderDepartment of Epidemiology and Preventive Medicine, University of Maryland, Baltimore School of Medicine, Baltimore, Maryland, USA.
Sagar ShuklaUniversity of Maryland School of Pharmacy, Baltimore, Maryland, USA.
Natalie D EddingtonUniversity of Maryland School of Pharmacy, Baltimore, Maryland, USA.
Rose M ViscardiDepartment of Pediatrics, University of Maryland, Baltimore School of Medicine, Baltimore, Maryland, USA rviscard@umaryland.edu.
University of Maryland, Baltimore · USUniversity of Alabama at Birmingham · USJohns Hopkins University · USOregon Health & Science University · USUniversity of Virginia · US

Funding

Azithromycin To Prevent BPD In Ureaplasma-Infected PretermsR01HD067126 · NICHD · UNIVERSITY OF MARYLAND BALTIMORE · PI DAVIS, NATALIE LOUISE, TERRIN, MICHAEL L · 2011 to 2019
$4.7M
NICHD NIH HHS R01 HD067126NICHD NIH HHS R01HD067126
6 · The paper itself

Abstract

The study objectives were to refine the population pharmacokinetics (PK) model, determine microbial clearance, and assess short-term pulmonary outcomes of multiple-dose azithromycin treatment in preterm infants at risk for Ureaplasma respiratory colonization. Fifteen subjects (7 of whom were Ureaplasma positive) received intravenous azithromycin at 20 mg/kg of body weight every 24 h for 3 doses. Azithromycin concentrations were determined in plasma samples obtained up to 168 h post-first dose by using a validated liquid chromatography-tandem mass spectrometry method. Respiratory samples were obtained predose and at three time points post-last dose for Ureaplasma culture, PCR, antibiotic susceptibility testing, and cytokine concentration determinations. Pharmacokinetic data from these 15 subjects as well as 25 additional subjects (who received either a single 10-mg/kg dose [n = 12] or a single 20-mg/kg dose [n = 13]) were analyzed by using a nonlinear mixed-effect population modeling (NONMEM) approach. Pulmonary outcomes were assessed at 36 weeks post-menstrual age and 6 months adjusted age. A 2-compartment model with all PK parameters allometrically scaled on body weight best described the azithromycin pharmacokinetics in preterm neonates. The population pharmacokinetics parameter estimates for clearance, central volume of distribution, intercompartmental clearance, and peripheral volume of distribution were 0.15 liters/h · kg(0.75), 1.88 liters · kg, 1.79 liters/h · kg(0.75), and 13 liters · kg, respectively. The estimated area under the concentration-time curve over 24 h (AUC24)/MIC90 value was ∼ 4 h. All posttreatment cultures were negative, and there were no drug-related adverse events. One Ureaplasma-positive infant died at 4 months of age, but no survivors were hospitalized for respiratory etiologies during the first 6 months (adjusted age). Thus, a 3-day course of 20 mg/kg/day intravenous azithromycin shows preliminary efficacy in eradicating Ureaplasma spp. from the preterm respiratory tract.

Indexed as

Administration, IntravenousAnti-Bacterial AgentsAzithromycinBronchopulmonary DysplasiaCytokinesHumansInfantInfant, NewbornInfant, PrematureInflammationMicrobial Sensitivity TestsNonlinear DynamicsRespiratory Tract InfectionsTreatment OutcomeUreaplasmaUreaplasma InfectionsAnti-Bacterial AgentsAzithromycinCytokines

Identifiers

PMID25385115
PMCPMC4291400
OpenAlexW2091155248

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.