Loading…

Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim of this review was to assess in “real world” studi...

Full description

Saved in:
Bibliographic Details
Published in:Children (Basel) 2022-08, Vol.9 (8), p.1207
Main Authors: Panagiotou, Panagiota, Kanaka-Gantenbein, Christina, Kaditis, Athanasios G
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3
cites cdi_FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3
container_end_page
container_issue 8
container_start_page 1207
container_title Children (Basel)
container_volume 9
creator Panagiotou, Panagiota
Kanaka-Gantenbein, Christina
Kaditis, Athanasios G
description Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim of this review was to assess in “real world” studies, whether novel treatments would have a positive impact on the mechanical ventilatory support requirements of SMA patients, already initiated on ventilatory support prior to treatment administration. A literature search was performed in Pubmed using multiple combinations of MESH terms and the snowball procedure. A total of 14 publications were discussed in this review. Considering all patients included in the published studies who were on ventilatory support and were treated with Nusinersen, 13/172 (7.5%) had reduced needs for ventilatory support, 1/172 (0.6%) did not need ventilation post-treatment, and 122/172 (70.9%) were maintained on the same ventilator settings. Moreover, 2/41 (4.9%) children who were offered gene therapy had no need for further ventilatory support and 12/41 (29.2%) had reduced requirements. In conclusion, available evidence suggests that among children with SMA, who are on mechanical respiratory support either noninvasively or via tracheostomy at the time of gene-based treatment, only a few will be weaned off the ventilator or have reduced ventilator needs per 24 h. Children will usually require the same level of support as before treatment.
doi_str_mv 10.3390/children9081207
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_561a740c3bfd4c69badd941e05f1f419</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A744375821</galeid><doaj_id>oai_doaj_org_article_561a740c3bfd4c69badd941e05f1f419</doaj_id><sourcerecordid>A744375821</sourcerecordid><originalsourceid>FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3</originalsourceid><addsrcrecordid>eNptkk1rGzEQhpfS0oQ0514FvaSHTfSxK60uBdekaSChoU57FVppZMusVxtpt-B_X9kOJQ5FB4mZZ97hHU1RfCT4kjGJr8zKdzZCL3FDKBZvilNKqSgl5uLti_dJcZ7SGmNMGK1pI94XJ4xjgrEUp0WYr3S_hIR8j35DP_pOjyFu0WIahhBH9BOeJh9hk1MJBYcWg-91h-6nZKZORzQbYxhWW3SxuJ99Rg969HvyIaQR3UAP5VedwKLHFUQ9eEgfindOdwnOn--z4te368f59_Lux83tfHZXmpqRsWwoccwx2rRaSuKsbHkDjjoqbStr0ECYwAJqW_MGW4tbazltMisJk7UFdlbcHnRt0Gs1RL_RcauC9mofCHGpdBy96UDVnGhRYcNaZyvDZautlRUBXDviKiKz1peD1jC1G7AmO4y6OxI9zvR-pZbhj5IV5lLUWeDiWSCGpwnSqDY-Geg63UOYkqLZC8__wUVGP71C12GKeeR7iu9s0xfUUmcDvnch9zU7UTUTVcVEnQeYqcv_UPlY2HgTenA-x48Krg4FJoaUIrh_HglWu5VTr1aO_QVdacje</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2706137027</pqid></control><display><type>article</type><title>Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><creator>Panagiotou, Panagiota ; Kanaka-Gantenbein, Christina ; Kaditis, Athanasios G</creator><creatorcontrib>Panagiotou, Panagiota ; Kanaka-Gantenbein, Christina ; Kaditis, Athanasios G</creatorcontrib><description>Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim of this review was to assess in “real world” studies, whether novel treatments would have a positive impact on the mechanical ventilatory support requirements of SMA patients, already initiated on ventilatory support prior to treatment administration. A literature search was performed in Pubmed using multiple combinations of MESH terms and the snowball procedure. A total of 14 publications were discussed in this review. Considering all patients included in the published studies who were on ventilatory support and were treated with Nusinersen, 13/172 (7.5%) had reduced needs for ventilatory support, 1/172 (0.6%) did not need ventilation post-treatment, and 122/172 (70.9%) were maintained on the same ventilator settings. Moreover, 2/41 (4.9%) children who were offered gene therapy had no need for further ventilatory support and 12/41 (29.2%) had reduced requirements. In conclusion, available evidence suggests that among children with SMA, who are on mechanical respiratory support either noninvasively or via tracheostomy at the time of gene-based treatment, only a few will be weaned off the ventilator or have reduced ventilator needs per 24 h. Children will usually require the same level of support as before treatment.</description><identifier>ISSN: 2227-9067</identifier><identifier>EISSN: 2227-9067</identifier><identifier>DOI: 10.3390/children9081207</identifier><identifier>PMID: 36010097</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Airway management ; Algorithms ; Atrophy ; Diaphragm (Anatomy) ; Gene therapy ; gene-based therapies ; Hypoventilation ; Infections ; Neuromuscular diseases ; noninvasive ventilation ; Nusinersen ; Onasemnogene abeparvovec ; Ostomy ; Pediatrics ; Physiological aspects ; Proteins ; Respiration ; respiratory care ; Respiratory diseases ; Respiratory failure ; Review ; Sleep ; Spinal muscular atrophy ; Ventilators</subject><ispartof>Children (Basel), 2022-08, Vol.9 (8), p.1207</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3</citedby><cites>FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3</cites><orcidid>0000-0002-3544-167X ; 0000-0003-3592-0037 ; 0000-0001-6942-6470</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2706137027/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2706137027?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Panagiotou, Panagiota</creatorcontrib><creatorcontrib>Kanaka-Gantenbein, Christina</creatorcontrib><creatorcontrib>Kaditis, Athanasios G</creatorcontrib><title>Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies</title><title>Children (Basel)</title><description>Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim of this review was to assess in “real world” studies, whether novel treatments would have a positive impact on the mechanical ventilatory support requirements of SMA patients, already initiated on ventilatory support prior to treatment administration. A literature search was performed in Pubmed using multiple combinations of MESH terms and the snowball procedure. A total of 14 publications were discussed in this review. Considering all patients included in the published studies who were on ventilatory support and were treated with Nusinersen, 13/172 (7.5%) had reduced needs for ventilatory support, 1/172 (0.6%) did not need ventilation post-treatment, and 122/172 (70.9%) were maintained on the same ventilator settings. Moreover, 2/41 (4.9%) children who were offered gene therapy had no need for further ventilatory support and 12/41 (29.2%) had reduced requirements. In conclusion, available evidence suggests that among children with SMA, who are on mechanical respiratory support either noninvasively or via tracheostomy at the time of gene-based treatment, only a few will be weaned off the ventilator or have reduced ventilator needs per 24 h. Children will usually require the same level of support as before treatment.</description><subject>Airway management</subject><subject>Algorithms</subject><subject>Atrophy</subject><subject>Diaphragm (Anatomy)</subject><subject>Gene therapy</subject><subject>gene-based therapies</subject><subject>Hypoventilation</subject><subject>Infections</subject><subject>Neuromuscular diseases</subject><subject>noninvasive ventilation</subject><subject>Nusinersen</subject><subject>Onasemnogene abeparvovec</subject><subject>Ostomy</subject><subject>Pediatrics</subject><subject>Physiological aspects</subject><subject>Proteins</subject><subject>Respiration</subject><subject>respiratory care</subject><subject>Respiratory diseases</subject><subject>Respiratory failure</subject><subject>Review</subject><subject>Sleep</subject><subject>Spinal muscular atrophy</subject><subject>Ventilators</subject><issn>2227-9067</issn><issn>2227-9067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1rGzEQhpfS0oQ0514FvaSHTfSxK60uBdekaSChoU57FVppZMusVxtpt-B_X9kOJQ5FB4mZZ97hHU1RfCT4kjGJr8zKdzZCL3FDKBZvilNKqSgl5uLti_dJcZ7SGmNMGK1pI94XJ4xjgrEUp0WYr3S_hIR8j35DP_pOjyFu0WIahhBH9BOeJh9hk1MJBYcWg-91h-6nZKZORzQbYxhWW3SxuJ99Rg969HvyIaQR3UAP5VedwKLHFUQ9eEgfindOdwnOn--z4te368f59_Lux83tfHZXmpqRsWwoccwx2rRaSuKsbHkDjjoqbStr0ECYwAJqW_MGW4tbazltMisJk7UFdlbcHnRt0Gs1RL_RcauC9mofCHGpdBy96UDVnGhRYcNaZyvDZautlRUBXDviKiKz1peD1jC1G7AmO4y6OxI9zvR-pZbhj5IV5lLUWeDiWSCGpwnSqDY-Geg63UOYkqLZC8__wUVGP71C12GKeeR7iu9s0xfUUmcDvnch9zU7UTUTVcVEnQeYqcv_UPlY2HgTenA-x48Krg4FJoaUIrh_HglWu5VTr1aO_QVdacje</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Panagiotou, Panagiota</creator><creator>Kanaka-Gantenbein, Christina</creator><creator>Kaditis, Athanasios G</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3544-167X</orcidid><orcidid>https://orcid.org/0000-0003-3592-0037</orcidid><orcidid>https://orcid.org/0000-0001-6942-6470</orcidid></search><sort><creationdate>20220801</creationdate><title>Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies</title><author>Panagiotou, Panagiota ; Kanaka-Gantenbein, Christina ; Kaditis, Athanasios G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Airway management</topic><topic>Algorithms</topic><topic>Atrophy</topic><topic>Diaphragm (Anatomy)</topic><topic>Gene therapy</topic><topic>gene-based therapies</topic><topic>Hypoventilation</topic><topic>Infections</topic><topic>Neuromuscular diseases</topic><topic>noninvasive ventilation</topic><topic>Nusinersen</topic><topic>Onasemnogene abeparvovec</topic><topic>Ostomy</topic><topic>Pediatrics</topic><topic>Physiological aspects</topic><topic>Proteins</topic><topic>Respiration</topic><topic>respiratory care</topic><topic>Respiratory diseases</topic><topic>Respiratory failure</topic><topic>Review</topic><topic>Sleep</topic><topic>Spinal muscular atrophy</topic><topic>Ventilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Panagiotou, Panagiota</creatorcontrib><creatorcontrib>Kanaka-Gantenbein, Christina</creatorcontrib><creatorcontrib>Kaditis, Athanasios G</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (DOAJ)</collection><jtitle>Children (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Panagiotou, Panagiota</au><au>Kanaka-Gantenbein, Christina</au><au>Kaditis, Athanasios G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies</atitle><jtitle>Children (Basel)</jtitle><date>2022-08-01</date><risdate>2022</risdate><volume>9</volume><issue>8</issue><spage>1207</spage><pages>1207-</pages><issn>2227-9067</issn><eissn>2227-9067</eissn><abstract>Spinal muscular atrophy (SMA) is a genetic neuromuscular disease resulting in global muscular weakness and, frequently, in respiratory failure and premature death. Gene-based therapies like Nusinersen are now available for patients with SMA. The aim of this review was to assess in “real world” studies, whether novel treatments would have a positive impact on the mechanical ventilatory support requirements of SMA patients, already initiated on ventilatory support prior to treatment administration. A literature search was performed in Pubmed using multiple combinations of MESH terms and the snowball procedure. A total of 14 publications were discussed in this review. Considering all patients included in the published studies who were on ventilatory support and were treated with Nusinersen, 13/172 (7.5%) had reduced needs for ventilatory support, 1/172 (0.6%) did not need ventilation post-treatment, and 122/172 (70.9%) were maintained on the same ventilator settings. Moreover, 2/41 (4.9%) children who were offered gene therapy had no need for further ventilatory support and 12/41 (29.2%) had reduced requirements. In conclusion, available evidence suggests that among children with SMA, who are on mechanical respiratory support either noninvasively or via tracheostomy at the time of gene-based treatment, only a few will be weaned off the ventilator or have reduced ventilator needs per 24 h. Children will usually require the same level of support as before treatment.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>36010097</pmid><doi>10.3390/children9081207</doi><orcidid>https://orcid.org/0000-0002-3544-167X</orcidid><orcidid>https://orcid.org/0000-0003-3592-0037</orcidid><orcidid>https://orcid.org/0000-0001-6942-6470</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2227-9067
ispartof Children (Basel), 2022-08, Vol.9 (8), p.1207
issn 2227-9067
2227-9067
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_561a740c3bfd4c69badd941e05f1f419
source Open Access: PubMed Central; Publicly Available Content Database
subjects Airway management
Algorithms
Atrophy
Diaphragm (Anatomy)
Gene therapy
gene-based therapies
Hypoventilation
Infections
Neuromuscular diseases
noninvasive ventilation
Nusinersen
Onasemnogene abeparvovec
Ostomy
Pediatrics
Physiological aspects
Proteins
Respiration
respiratory care
Respiratory diseases
Respiratory failure
Review
Sleep
Spinal muscular atrophy
Ventilators
title Changes in Ventilatory Support Requirements of Spinal Muscular Atrophy (SMA) Patients Post Gene-Based Therapies
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T17%3A39%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Changes%20in%20Ventilatory%20Support%20Requirements%20of%20Spinal%20Muscular%20Atrophy%20(SMA)%20Patients%20Post%20Gene-Based%20Therapies&rft.jtitle=Children%20(Basel)&rft.au=Panagiotou,%20Panagiota&rft.date=2022-08-01&rft.volume=9&rft.issue=8&rft.spage=1207&rft.pages=1207-&rft.issn=2227-9067&rft.eissn=2227-9067&rft_id=info:doi/10.3390/children9081207&rft_dat=%3Cgale_doaj_%3EA744375821%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c531t-821f3f328ba991fd9b68ef2f29db95eae13707e5d5680dd0bdd628a9991395de3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2706137027&rft_id=info:pmid/36010097&rft_galeid=A744375821&rfr_iscdi=true