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Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study

BACKGROUND: In Bangladesh, most patients with Guillain-Barré syndrome (GBS) cannot afford standard treatment with intravenous immunoglobulin (IVIG) or a standard plasma exchange (PE) course, which partly explains the high rate of mortality and residual disability associated with GBS in this country....

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Autores principales: Islam, Md. Badrul, Islam, Zhahirul, Rahman, Shafiqur, Endtz, Hubert P., Vos, Margreet C., van der Jagt, Mathieu, van Doorn, Pieter A., Jacobs, Bart C., Mohammad, Quazi D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622586/
https://www.ncbi.nlm.nih.gov/pubmed/28975040
http://dx.doi.org/10.1186/s40814-017-0185-0
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author Islam, Md. Badrul
Islam, Zhahirul
Rahman, Shafiqur
Endtz, Hubert P.
Vos, Margreet C.
van der Jagt, Mathieu
van Doorn, Pieter A.
Jacobs, Bart C.
Mohammad, Quazi D.
author_facet Islam, Md. Badrul
Islam, Zhahirul
Rahman, Shafiqur
Endtz, Hubert P.
Vos, Margreet C.
van der Jagt, Mathieu
van Doorn, Pieter A.
Jacobs, Bart C.
Mohammad, Quazi D.
author_sort Islam, Md. Badrul
collection PubMed
description BACKGROUND: In Bangladesh, most patients with Guillain-Barré syndrome (GBS) cannot afford standard treatment with intravenous immunoglobulin (IVIG) or a standard plasma exchange (PE) course, which partly explains the high rate of mortality and residual disability associated with GBS in this country. Small volume plasma exchange (SVPE) is an affordable and potentially effective alternative form of plasma exchange. SVPE is the repeated removal of small volumes of supernatant plasma over several days via sedimentation of patient whole blood. The aim of this study is to define the clinical feasibility and safety of SVPE in patients with GBS in resource poor settings. METHODS: A total of 20 adult patients with GBS will be enrolled for SVPE at a single center in Bangladesh. Six daily sessions of whole blood sedimentation and plasma removal will be performed in all patients with GBS with a target to remove an overall volume of at least 8 liters (L) of plasma over a total of 8 days. Serious adverse events (SAE) are defined as the number of patients developing severe sepsis associated with the central venous catheter or deep venous thrombosis in the limb where the catheter is placed for SVPE. Based upon a predictive success rate of 75%, the SVPE procedure will be considered safe if less than 5 of 20 SVPE-treated GBS patients have a SAE. The procedure will be considered feasible if 8 L of plasma can be removed in at least 15 of 20 patients with GBS who receive SVPE. In addition, detailed clinical and neurological outcome assessments will be performed until discharge of the patient from the hospital and up to 4 weeks after study entry. DISCUSSION: This is the first clinical study to evaluate the feasibility and safety of SVPE as a potential alternative low-cost treatment for the patients with GBS in resource poor settings. TRIAL REGISTRATION: Clinicaltrials.gov NCT02780570 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40814-017-0185-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-56225862017-10-03 Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study Islam, Md. Badrul Islam, Zhahirul Rahman, Shafiqur Endtz, Hubert P. Vos, Margreet C. van der Jagt, Mathieu van Doorn, Pieter A. Jacobs, Bart C. Mohammad, Quazi D. Pilot Feasibility Stud Study Protocol BACKGROUND: In Bangladesh, most patients with Guillain-Barré syndrome (GBS) cannot afford standard treatment with intravenous immunoglobulin (IVIG) or a standard plasma exchange (PE) course, which partly explains the high rate of mortality and residual disability associated with GBS in this country. Small volume plasma exchange (SVPE) is an affordable and potentially effective alternative form of plasma exchange. SVPE is the repeated removal of small volumes of supernatant plasma over several days via sedimentation of patient whole blood. The aim of this study is to define the clinical feasibility and safety of SVPE in patients with GBS in resource poor settings. METHODS: A total of 20 adult patients with GBS will be enrolled for SVPE at a single center in Bangladesh. Six daily sessions of whole blood sedimentation and plasma removal will be performed in all patients with GBS with a target to remove an overall volume of at least 8 liters (L) of plasma over a total of 8 days. Serious adverse events (SAE) are defined as the number of patients developing severe sepsis associated with the central venous catheter or deep venous thrombosis in the limb where the catheter is placed for SVPE. Based upon a predictive success rate of 75%, the SVPE procedure will be considered safe if less than 5 of 20 SVPE-treated GBS patients have a SAE. The procedure will be considered feasible if 8 L of plasma can be removed in at least 15 of 20 patients with GBS who receive SVPE. In addition, detailed clinical and neurological outcome assessments will be performed until discharge of the patient from the hospital and up to 4 weeks after study entry. DISCUSSION: This is the first clinical study to evaluate the feasibility and safety of SVPE as a potential alternative low-cost treatment for the patients with GBS in resource poor settings. TRIAL REGISTRATION: Clinicaltrials.gov NCT02780570 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40814-017-0185-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-29 /pmc/articles/PMC5622586/ /pubmed/28975040 http://dx.doi.org/10.1186/s40814-017-0185-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Islam, Md. Badrul
Islam, Zhahirul
Rahman, Shafiqur
Endtz, Hubert P.
Vos, Margreet C.
van der Jagt, Mathieu
van Doorn, Pieter A.
Jacobs, Bart C.
Mohammad, Quazi D.
Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title_full Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title_fullStr Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title_full_unstemmed Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title_short Small volume plasma exchange for Guillain-Barré syndrome in resource poor settings: a safety and feasibility study
title_sort small volume plasma exchange for guillain-barré syndrome in resource poor settings: a safety and feasibility study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622586/
https://www.ncbi.nlm.nih.gov/pubmed/28975040
http://dx.doi.org/10.1186/s40814-017-0185-0
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