Outcomes of Juvenile Myasthenia Gravis: A Comparison of Robotic Thymectomy With Medication Treatment
The study aimed to compare the clinical outcomes of patients with juvenile myasthenia gravis (MG) who underwent robotic thymectomy with that of those who only received medication therapy. We retrospectively reviewed patients who visited our institution for the diagnosis or treatment of MG with an ag...
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Published in | The Annals of thoracic surgery Vol. 113; no. 1; pp. 295 - 301 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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01.01.2022
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Abstract | The study aimed to compare the clinical outcomes of patients with juvenile myasthenia gravis (MG) who underwent robotic thymectomy with that of those who only received medication therapy.
We retrospectively reviewed patients who visited our institution for the diagnosis or treatment of MG with an age at onset younger than 18 years. Patients who underwent thymectomy comprised the surgical group and those who received only medication therapy comprised the nonsurgical group. The clinical outcomes were assessed according to the Myasthenia Gravis Foundation of America Post-Intervention Status.
Forty-seven patients (35 female, 12 male) were included as the surgical group and 20 patients (15 female, 5 male) comprised the nonsurgical group. Significant differences were observed between the surgical and nonsurgical groups in antibody against acetylcholinesterase receptor (91.5% vs 65%; P = .012), disease duration (median 16 [interquartile range, 7-25] months vs 96 [interquartile range, 42-480] months; P < .001), and corticosteroids requirement (53.2% vs 15%; P = .004) at baseline. Kaplan-Meier analysis showed a higher cumulative probability of complete stable remission in the surgical group (P = .002) compared with the nonsurgical group. Moreover, thymectomy (hazard ratio, 3.842; 95% confidence interval, 1.116-13.230; P = .033) and age at onset (hazard ratio, 0.89; 95% confidence interval, 0.80-0.99; P = .037) were still associated with the achievement of complete stable remission in the multivariable analysis. Furthermore, a significant steroid-sparing effect was observed in the surgical group but not in the nonsurgical group.
Robotic thymectomy seems to be more effective than medication therapy on juvenile MG in terms of inducing remission and reducing the use of corticosteroids. |
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AbstractList | The study aimed to compare the clinical outcomes of patients with juvenile myasthenia gravis (MG) who underwent robotic thymectomy with that of those who only received medication therapy.
We retrospectively reviewed patients who visited our institution for the diagnosis or treatment of MG with an age at onset younger than 18 years. Patients who underwent thymectomy comprised the surgical group and those who received only medication therapy comprised the nonsurgical group. The clinical outcomes were assessed according to the Myasthenia Gravis Foundation of America Post-Intervention Status.
Forty-seven patients (35 female, 12 male) were included as the surgical group and 20 patients (15 female, 5 male) comprised the nonsurgical group. Significant differences were observed between the surgical and nonsurgical groups in antibody against acetylcholinesterase receptor (91.5% vs 65%; P = .012), disease duration (median 16 [interquartile range, 7-25] months vs 96 [interquartile range, 42-480] months; P < .001), and corticosteroids requirement (53.2% vs 15%; P = .004) at baseline. Kaplan-Meier analysis showed a higher cumulative probability of complete stable remission in the surgical group (P = .002) compared with the nonsurgical group. Moreover, thymectomy (hazard ratio, 3.842; 95% confidence interval, 1.116-13.230; P = .033) and age at onset (hazard ratio, 0.89; 95% confidence interval, 0.80-0.99; P = .037) were still associated with the achievement of complete stable remission in the multivariable analysis. Furthermore, a significant steroid-sparing effect was observed in the surgical group but not in the nonsurgical group.
Robotic thymectomy seems to be more effective than medication therapy on juvenile MG in terms of inducing remission and reducing the use of corticosteroids. The study aimed to compare the clinical outcomes of patients with juvenile myasthenia gravis (MG) who underwent robotic thymectomy with that of those who only received medication therapy.BACKGROUNDThe study aimed to compare the clinical outcomes of patients with juvenile myasthenia gravis (MG) who underwent robotic thymectomy with that of those who only received medication therapy.We retrospectively reviewed patients who visited our institution for the diagnosis or treatment of MG with an age at onset younger than 18 years. Patients who underwent thymectomy comprised the surgical group and those who received only medication therapy comprised the nonsurgical group. The clinical outcomes were assessed according to the Myasthenia Gravis Foundation of America Post-Intervention Status.METHODSWe retrospectively reviewed patients who visited our institution for the diagnosis or treatment of MG with an age at onset younger than 18 years. Patients who underwent thymectomy comprised the surgical group and those who received only medication therapy comprised the nonsurgical group. The clinical outcomes were assessed according to the Myasthenia Gravis Foundation of America Post-Intervention Status.Forty-seven patients (35 female, 12 male) were included as the surgical group and 20 patients (15 female, 5 male) comprised the nonsurgical group. Significant differences were observed between the surgical and nonsurgical groups in antibody against acetylcholinesterase receptor (91.5% vs 65%; P = .012), disease duration (median 16 [interquartile range, 7-25] months vs 96 [interquartile range, 42-480] months; P < .001), and corticosteroids requirement (53.2% vs 15%; P = .004) at baseline. Kaplan-Meier analysis showed a higher cumulative probability of complete stable remission in the surgical group (P = .002) compared with the nonsurgical group. Moreover, thymectomy (hazard ratio, 3.842; 95% confidence interval, 1.116-13.230; P = .033) and age at onset (hazard ratio, 0.89; 95% confidence interval, 0.80-0.99; P = .037) were still associated with the achievement of complete stable remission in the multivariable analysis. Furthermore, a significant steroid-sparing effect was observed in the surgical group but not in the nonsurgical group.RESULTSForty-seven patients (35 female, 12 male) were included as the surgical group and 20 patients (15 female, 5 male) comprised the nonsurgical group. Significant differences were observed between the surgical and nonsurgical groups in antibody against acetylcholinesterase receptor (91.5% vs 65%; P = .012), disease duration (median 16 [interquartile range, 7-25] months vs 96 [interquartile range, 42-480] months; P < .001), and corticosteroids requirement (53.2% vs 15%; P = .004) at baseline. Kaplan-Meier analysis showed a higher cumulative probability of complete stable remission in the surgical group (P = .002) compared with the nonsurgical group. Moreover, thymectomy (hazard ratio, 3.842; 95% confidence interval, 1.116-13.230; P = .033) and age at onset (hazard ratio, 0.89; 95% confidence interval, 0.80-0.99; P = .037) were still associated with the achievement of complete stable remission in the multivariable analysis. Furthermore, a significant steroid-sparing effect was observed in the surgical group but not in the nonsurgical group.Robotic thymectomy seems to be more effective than medication therapy on juvenile MG in terms of inducing remission and reducing the use of corticosteroids.CONCLUSIONSRobotic thymectomy seems to be more effective than medication therapy on juvenile MG in terms of inducing remission and reducing the use of corticosteroids. |
Author | Ismail, Mahmoud Zhang, Hongbin Rueckert, Jens-C. Meisel, Andreas Swierzy, Marc Li, Feng Li, Zhongmin |
Author_xml | – sequence: 1 givenname: Zhongmin surname: Li fullname: Li, Zhongmin organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 2 givenname: Feng surname: Li fullname: Li, Feng organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 3 givenname: Hongbin surname: Zhang fullname: Zhang, Hongbin organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 4 givenname: Marc surname: Swierzy fullname: Swierzy, Marc organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 5 givenname: Mahmoud surname: Ismail fullname: Ismail, Mahmoud organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 6 givenname: Andreas surname: Meisel fullname: Meisel, Andreas organization: Department of Neurology, Integrated Center for Myasthenia gravis, NeuroCure Clinical Research Center, Center for Stroke Research Berlin, Charité – Universitätsmedizin Berlin, Berlin, Germany – sequence: 7 givenname: Jens-C. surname: Rueckert fullname: Rueckert, Jens-C. email: jens-c.rueckert@charite.de organization: Department of Surgery, Competence Center of Thoracic Surgery, Charité – Universitätsmedizin Berlin, Berlin, Germany |
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Cites_doi | 10.1016/j.thorsurg.2018.12.006 10.1016/j.athoracsur.2012.11.074 10.1016/j.jpedsurg.2005.10.006 10.1055/s-0033-1364181 10.3928/01913913-20180620-01 10.1016/j.nrl.2015.09.004 10.1056/NEJMoa1602489 10.1212/WNL.0000000000002790 10.1055/s-0037-1603775 10.1016/S1474-4422(18)30392-2 10.1097/CND.0b013e318253a48e 10.1093/brain/awn092 10.1093/ejcts/ezu309 10.1111/nyas.13537 10.1016/j.athoracsur.2010.05.014 10.1016/j.spen.2017.04.003 10.1007/s10072-013-1443-4 10.1016/j.ejpn.2017.04.003 10.1093/icvts/ivv135 10.3389/fneur.2018.00077 10.1111/j.1749-6632.1998.tb11010.x 10.1007/s00383-019-04441-0 10.1016/j.ajo.2010.05.002 10.1097/MOP.0b013e328365ad16 10.1016/j.jpedsurg.2015.12.016 10.1016/S1010-7940(03)00299-9 10.1016/j.jpedsurg.2014.10.005 |
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SubjectTerms | Adolescent Child Female Humans Male Myasthenia Gravis - drug therapy Myasthenia Gravis - surgery Retrospective Studies Robotic Surgical Procedures Thymectomy - methods Treatment Outcome |
Title | Outcomes of Juvenile Myasthenia Gravis: A Comparison of Robotic Thymectomy With Medication Treatment |
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