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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...
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Published in: | Children (Basel) 2022-08, Vol.9 (8), p.1207 |
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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. |
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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. 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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 ; 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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> |
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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 |
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