Intravenous Versus Oral Antibiotics for Postdischarge Treatment of Complicated Pneumonia

Postdischarge treatment of complicated pneumonia includes antibiotics administered intravenously via a peripherally inserted central venous catheter (PICC) or orally. Antibiotics administered via PICC, although effective, may result in serious complications. We compared the effectiveness and treatme...

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Published inPediatrics (Evanston) Vol. 138; no. 6
Main Authors Shah, Samir S, Srivastava, Rajendu, Wu, Susan, Colvin, Jeffrey D, Williams, Derek J, Rangel, Shawn J, Samady, Waheeda, Rao, Suchitra, Miller, Christopher, Cross, Cynthia, Clohessy, Caitlin, Hall, Matthew, Localio, Russell, Bryan, Matthew, Wu, Gong, Keren, Ron
Format Journal Article
LanguageEnglish
Published United States 01.12.2016
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Abstract Postdischarge treatment of complicated pneumonia includes antibiotics administered intravenously via a peripherally inserted central venous catheter (PICC) or orally. Antibiotics administered via PICC, although effective, may result in serious complications. We compared the effectiveness and treatment-related complications of postdischarge antibiotics delivered by these 2 routes. This multicenter retrospective cohort study included children ≥2 months and <18 years discharged with complicated pneumonia between 2009 and 2012. The main exposure was the route of postdischarge antibiotic administration, classified as PICC or oral. The primary outcome was treatment failure. Secondary outcomes included PICC complications, adverse drug reactions, other related revisits, and a composite of all 4 outcomes, termed "all related revisits." Among 2123 children, 281 (13.2%) received antibiotics via PICC. Treatment failure rates were 3.2% among PICC and 2.6% among oral antibiotic recipients and were not significantly different between the groups in across-hospital-matched analysis (matched odds ratio [OR], 1.26; 95% confidence interval [CI], 0.54 to 2.94). PICC complications occurred in 7.1%. Adverse drug reactions occurred in 0.6% of children; PICC antibiotic recipients had greater odds of adverse drug reaction in across hospital matched analysis (matched OR, 19.1; 95% CI, 4.2 to 87.3). The high rate of PICC complications and differences in adverse drug reactions contributed to higher odds of the composite outcome of all related revisits among PICC antibiotic recipients (matched OR, 4.71; 95% CI, 2.97 to 7.46). Treatment failure rates between PICC and oral antibiotics did not differ. Children with complicated pneumonia should preferentially receive oral antibiotics at discharge when effective oral options are available.
AbstractList Postdischarge treatment of complicated pneumonia includes antibiotics administered intravenously via a peripherally inserted central venous catheter (PICC) or orally. Antibiotics administered via PICC, although effective, may result in serious complications. We compared the effectiveness and treatment-related complications of postdischarge antibiotics delivered by these 2 routes. This multicenter retrospective cohort study included children ≥2 months and <18 years discharged with complicated pneumonia between 2009 and 2012. The main exposure was the route of postdischarge antibiotic administration, classified as PICC or oral. The primary outcome was treatment failure. Secondary outcomes included PICC complications, adverse drug reactions, other related revisits, and a composite of all 4 outcomes, termed "all related revisits." Among 2123 children, 281 (13.2%) received antibiotics via PICC. Treatment failure rates were 3.2% among PICC and 2.6% among oral antibiotic recipients and were not significantly different between the groups in across-hospital-matched analysis (matched odds ratio [OR], 1.26; 95% confidence interval [CI], 0.54 to 2.94). PICC complications occurred in 7.1%. Adverse drug reactions occurred in 0.6% of children; PICC antibiotic recipients had greater odds of adverse drug reaction in across hospital matched analysis (matched OR, 19.1; 95% CI, 4.2 to 87.3). The high rate of PICC complications and differences in adverse drug reactions contributed to higher odds of the composite outcome of all related revisits among PICC antibiotic recipients (matched OR, 4.71; 95% CI, 2.97 to 7.46). Treatment failure rates between PICC and oral antibiotics did not differ. Children with complicated pneumonia should preferentially receive oral antibiotics at discharge when effective oral options are available.
Author Rao, Suchitra
Shah, Samir S
Clohessy, Caitlin
Williams, Derek J
Bryan, Matthew
Rangel, Shawn J
Srivastava, Rajendu
Wu, Gong
Keren, Ron
Wu, Susan
Colvin, Jeffrey D
Miller, Christopher
Hall, Matthew
Localio, Russell
Samady, Waheeda
Cross, Cynthia
Author_xml – sequence: 1
  givenname: Samir S
  surname: Shah
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  organization: Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio
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  givenname: Rajendu
  surname: Srivastava
  fullname: Srivastava, Rajendu
  organization: Institute for Healthcare Delivery Research and Primary Children's Hospital, Intermountain Healthcare, Salt Lake City, Utah
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  givenname: Susan
  surname: Wu
  fullname: Wu, Susan
  organization: Department of Pediatrics, University of Southern California Keck School of Medicine, Los Angeles, California
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  givenname: Jeffrey D
  surname: Colvin
  fullname: Colvin, Jeffrey D
  organization: Division of General Academic Pediatrics, Children's Mercy Hospitals and Clinics, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri
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  givenname: Derek J
  surname: Williams
  fullname: Williams, Derek J
  organization: Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee
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  givenname: Shawn J
  surname: Rangel
  fullname: Rangel, Shawn J
  organization: Harvard Medical School, Boston, Massachusetts
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  givenname: Waheeda
  surname: Samady
  fullname: Samady, Waheeda
  organization: Northwestern Feinberg School of Medicine, Chicago, Illinois
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  givenname: Suchitra
  surname: Rao
  fullname: Rao, Suchitra
  organization: Department of Pediatrics, Children's Hospital Colorado, Aurora, Colorado
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  givenname: Christopher
  surname: Miller
  fullname: Miller, Christopher
  organization: Division of Inpatient Medicine, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah
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  givenname: Cynthia
  surname: Cross
  fullname: Cross, Cynthia
  organization: Department of Pediatrics, University of Tennessee College of Medicine, Memphis, Tennessee
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  surname: Clohessy
  fullname: Clohessy, Caitlin
  organization: Divisions of Hospital Medicine and
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  surname: Hall
  fullname: Hall, Matthew
  organization: Children's Hospital Association, Overland Park, Kansas
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  givenname: Russell
  surname: Localio
  fullname: Localio, Russell
  organization: Department of Biostatistics and Epidemiology, Perlman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
– sequence: 14
  givenname: Matthew
  surname: Bryan
  fullname: Bryan, Matthew
  organization: Department of Biostatistics and Epidemiology, Perlman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
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  givenname: Gong
  surname: Wu
  fullname: Wu, Gong
  organization: Division of General Pediatrics, Center for Pediatric Clinical Effectiveness, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; and
– sequence: 16
  givenname: Ron
  surname: Keren
  fullname: Keren, Ron
  organization: Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
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Snippet Postdischarge treatment of complicated pneumonia includes antibiotics administered intravenously via a peripherally inserted central venous catheter (PICC) or...
SourceID pubmed
SourceType Index Database
SubjectTerms Administration, Intravenous
Administration, Oral
Adolescent
Anti-Bacterial Agents - administration & dosage
Anti-Bacterial Agents - adverse effects
Catheterization, Peripheral - adverse effects
Child
Child, Preschool
Cohort Studies
Humans
Infant
Patient Discharge
Pneumonia - drug therapy
Retrospective Studies
Treatment Failure
Title Intravenous Versus Oral Antibiotics for Postdischarge Treatment of Complicated Pneumonia
URI https://www.ncbi.nlm.nih.gov/pubmed/27940695
Volume 138
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