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Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy

OBJECTIVES: The postoperative wound infection rate for canal wall reconstruction (CWR) tympanomastoidectomy with mastoid obliteration in the treatment of chronic otitis media with cholesteatoma has been reported to be 3.6%. Postoperative administration of 24–48 hours of intravenous antibiotics has b...

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Autores principales: Kao, Richard, Wannemuehler, Todd, Yates, Charles W., Nelson, Rick F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743161/
https://www.ncbi.nlm.nih.gov/pubmed/29299507
http://dx.doi.org/10.1002/lio2.116
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author Kao, Richard
Wannemuehler, Todd
Yates, Charles W.
Nelson, Rick F.
author_facet Kao, Richard
Wannemuehler, Todd
Yates, Charles W.
Nelson, Rick F.
author_sort Kao, Richard
collection PubMed
description OBJECTIVES: The postoperative wound infection rate for canal wall reconstruction (CWR) tympanomastoidectomy with mastoid obliteration in the treatment of chronic otitis media with cholesteatoma has been reported to be 3.6%. Postoperative administration of 24–48 hours of intravenous antibiotics has been recommended. We aim to determine the infection rate of CWR with postoperative outpatient oral antibiotics. STUDY DESIGN: Institutional review board—approved retrospective case review. SETTING: Tertiary referral center. Patients: Retrospective review of consecutive patients who underwent CWR tympanomastoidectomy with mastoid obliteration at a single institution from 2014 to 2016. Main Outcome Measure: Patient characteristics (age, sex) were calculated. Rate of postoperative complications and infections within 1 month of surgery were calculated. Comparison to previous published infection rates with postoperative intravenous antibiotics. RESULTS: 51 patients underwent CWR followed by outpatient oral antibiotics with a mean age of 25.9 years (16 patients were less than 10 years old). There were no postoperative wound infections. Outpatient antibiotics showed non‐inferiority to IV antibiotic historic controls (0% vs. 3.6%; 95% confidence interval [CI], 0–6.09%; p = 0.03). One patient had small postoperative wound dehiscence with CSF leak that was managed conservatively. One patient developed Clostridium difficile colitis on postoperative day 2. CONCLUSIONS: The infection rate after CWR tympanomastoidectomy with use of outpatient antibiotics is low and is non‐inferior to a historic cohort treated with inpatient intravenous antibiotics. A larger randomized controlled trial is warranted. LEVEL OF EVIDENCE: 4.
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spelling pubmed-57431612018-01-03 Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy Kao, Richard Wannemuehler, Todd Yates, Charles W. Nelson, Rick F. Laryngoscope Investig Otolaryngol Otology, Neurotology, and Neuroscience OBJECTIVES: The postoperative wound infection rate for canal wall reconstruction (CWR) tympanomastoidectomy with mastoid obliteration in the treatment of chronic otitis media with cholesteatoma has been reported to be 3.6%. Postoperative administration of 24–48 hours of intravenous antibiotics has been recommended. We aim to determine the infection rate of CWR with postoperative outpatient oral antibiotics. STUDY DESIGN: Institutional review board—approved retrospective case review. SETTING: Tertiary referral center. Patients: Retrospective review of consecutive patients who underwent CWR tympanomastoidectomy with mastoid obliteration at a single institution from 2014 to 2016. Main Outcome Measure: Patient characteristics (age, sex) were calculated. Rate of postoperative complications and infections within 1 month of surgery were calculated. Comparison to previous published infection rates with postoperative intravenous antibiotics. RESULTS: 51 patients underwent CWR followed by outpatient oral antibiotics with a mean age of 25.9 years (16 patients were less than 10 years old). There were no postoperative wound infections. Outpatient antibiotics showed non‐inferiority to IV antibiotic historic controls (0% vs. 3.6%; 95% confidence interval [CI], 0–6.09%; p = 0.03). One patient had small postoperative wound dehiscence with CSF leak that was managed conservatively. One patient developed Clostridium difficile colitis on postoperative day 2. CONCLUSIONS: The infection rate after CWR tympanomastoidectomy with use of outpatient antibiotics is low and is non‐inferior to a historic cohort treated with inpatient intravenous antibiotics. A larger randomized controlled trial is warranted. LEVEL OF EVIDENCE: 4. John Wiley and Sons Inc. 2017-10-31 /pmc/articles/PMC5743161/ /pubmed/29299507 http://dx.doi.org/10.1002/lio2.116 Text en © 2017 The Authors Laryngoscope Investigative Otolaryngology published by Wiley Periodicals, Inc. on behalf of The Triological Society This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Otology, Neurotology, and Neuroscience
Kao, Richard
Wannemuehler, Todd
Yates, Charles W.
Nelson, Rick F.
Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title_full Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title_fullStr Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title_full_unstemmed Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title_short Outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
title_sort outpatient management of cholesteatoma with canal wall reconstruction tympanomastoidectomy
topic Otology, Neurotology, and Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743161/
https://www.ncbi.nlm.nih.gov/pubmed/29299507
http://dx.doi.org/10.1002/lio2.116
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