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The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis

INTRODUCTION: There is very limited published experience with intravenous (IV) antituberculosis (anti-TB) and antiretroviral therapy (ART) especially in children. We have described a human immunodeficiency virus (HIV)-infected child with complicated abdominal tuberculosis who was initially treated w...

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Autores principales: Enimil, Anthony K., Eley, Brian, Nuttall, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479423/
https://www.ncbi.nlm.nih.gov/pubmed/32934837
http://dx.doi.org/10.4102/sajhivmed.v21i1.1121
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author Enimil, Anthony K.
Eley, Brian
Nuttall, James
author_facet Enimil, Anthony K.
Eley, Brian
Nuttall, James
author_sort Enimil, Anthony K.
collection PubMed
description INTRODUCTION: There is very limited published experience with intravenous (IV) antituberculosis (anti-TB) and antiretroviral therapy (ART) especially in children. We have described a human immunodeficiency virus (HIV)-infected child with complicated abdominal tuberculosis who was initially treated with IV anti-TB and a partially IV ART regimen before transitioning to oral therapy. PATIENT PRESENTATION: A 3-year-old boy presented with hypovolaemic shock with a 3-day history of inability to pass stools, abdominal distension and bile-stained vomiting. Abdominal ultrasound and X-ray showed small-bowel obstruction. Human immunodeficiency virus antibody testing was positive, and Cluster of Differentiation (CD)4+ lymphocyte count was 56 cells/mL (15%). Xpert Mycobacterium tuberculosis (MTB)/Rifampicin (RIF) Ultra and TB culture on induced sputum detected MTB complex sensitive to rifampicin and isoniazid. MANAGEMENT AND OUTCOME: Following laparotomy and closure of bowel perforations, the child was commenced on IV rifampicin, moxifloxacin and amikacin. Amikacin was stopped after 3 days because of nephrotoxicity, and meropenem and IV linezolid were added. After 20 days, ART comprising IV zidovudine, oral lamivudine solution, oral lopinavir/ritonavir solution and additional oral ritonavir solution for super boosting was commenced. By day 40, the patient was well established on oral feeds and was switched to standard oral anti-TB medications. Sputum examined 1 month after starting the treatment was found culture-negative for MTB. After 4 months of treatment, the HIV viral load was < 100 copies/mL. He completed a total of 12 months of anti-TB treatment. CONCLUSION: Despite limited experience and few available IV formulations of standard anti-TB and ARV medications, initial IV therapy may be beneficial for patients in whom oral medication is not an option.
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spelling pubmed-74794232020-09-14 The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis Enimil, Anthony K. Eley, Brian Nuttall, James South Afr J HIV Med Case Report INTRODUCTION: There is very limited published experience with intravenous (IV) antituberculosis (anti-TB) and antiretroviral therapy (ART) especially in children. We have described a human immunodeficiency virus (HIV)-infected child with complicated abdominal tuberculosis who was initially treated with IV anti-TB and a partially IV ART regimen before transitioning to oral therapy. PATIENT PRESENTATION: A 3-year-old boy presented with hypovolaemic shock with a 3-day history of inability to pass stools, abdominal distension and bile-stained vomiting. Abdominal ultrasound and X-ray showed small-bowel obstruction. Human immunodeficiency virus antibody testing was positive, and Cluster of Differentiation (CD)4+ lymphocyte count was 56 cells/mL (15%). Xpert Mycobacterium tuberculosis (MTB)/Rifampicin (RIF) Ultra and TB culture on induced sputum detected MTB complex sensitive to rifampicin and isoniazid. MANAGEMENT AND OUTCOME: Following laparotomy and closure of bowel perforations, the child was commenced on IV rifampicin, moxifloxacin and amikacin. Amikacin was stopped after 3 days because of nephrotoxicity, and meropenem and IV linezolid were added. After 20 days, ART comprising IV zidovudine, oral lamivudine solution, oral lopinavir/ritonavir solution and additional oral ritonavir solution for super boosting was commenced. By day 40, the patient was well established on oral feeds and was switched to standard oral anti-TB medications. Sputum examined 1 month after starting the treatment was found culture-negative for MTB. After 4 months of treatment, the HIV viral load was < 100 copies/mL. He completed a total of 12 months of anti-TB treatment. CONCLUSION: Despite limited experience and few available IV formulations of standard anti-TB and ARV medications, initial IV therapy may be beneficial for patients in whom oral medication is not an option. AOSIS 2020-08-24 /pmc/articles/PMC7479423/ /pubmed/32934837 http://dx.doi.org/10.4102/sajhivmed.v21i1.1121 Text en © 2020. The Authors https://creativecommons.org/licenses/by/4.0/ Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Case Report
Enimil, Anthony K.
Eley, Brian
Nuttall, James
The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title_full The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title_fullStr The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title_full_unstemmed The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title_short The initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
title_sort initial intravenous treatment of a human immunodeficiency virus-infected child with complicated abdominal tuberculosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479423/
https://www.ncbi.nlm.nih.gov/pubmed/32934837
http://dx.doi.org/10.4102/sajhivmed.v21i1.1121
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