Clinical outcomes and follow-up after thymectomy in patients with myasthenia gravis: A Colombian cohort study

<h2>Abstract</h2><h3>Objective</h3> To describe 5-year clinical outcomes after thymectomy in patients with myasthenia gravis (MG). <h3>Methods</h3> We retrospectively analyzed patients who underwent thymectomy for MG between 2010 and 2023. Preoperative and annual postoperative assessments (up to 5 years) used the Myasthenia Gravis Foundation of America classification. Outcomes were stratified as complete stable remission (CSR), pharmacologic remission, or minimal manifestations, with additional evaluation by patient-reported changes in symptoms. Kaplan-Meier analyses were conducted for time-to-event data. <h3>Results</h3> Eighty-six patients were included (median age, 42 years; 60.5% female). The median duration of symptoms was 480 days (interquartile range, 28-56 days). Most patients (n = 70; 81.4%) had a low comorbidity burden. Preoperatively, 34% were Myasthenia Gravis Foundation of America class I. Acetylcholinesterase inhibitors were used in 95% of patients. Right video-assisted thoracoscopic thymectomy was the most common approach (76%), with a 2.3% intraoperative complication rate. Thymic hyperplasia was present in 87%; thymoma, in 13%. Postoperative intensive care was required in 96.5%, with myasthenic crisis the most frequent complication (8%). The median hospital length of stay was 4 days, and there was no 30-day mortality. At 1 year, 81.7% were Myasthenia Gravis Foundation of America class I. Kaplan-Meier analysis showed 50% reported symptom improvement by 360 days (95% confidence interval, 350-375 days). By 5 years, 8% achieved CSR. Although a decline in acetylcholinesterase inhibitor dosage was observed, this was not significant (<i>P</i> = .225). <h3>Conclusions</h3> Thymectomy is associated with favorable long-term symptom control in MG, with low perioperative morbidity. However, rates of complete stable remission remain low, underscoring the need for further investigation into post-thymectomy outcomes and predictors of remission.

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Journal
JTCVS Open
Published
2025-11-20
DOI
https://doi.org/10.1016/j.xjon.2025.11.007
Primary Topic
Myasthenia Gravis and Thymoma
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article

Clinical outcomes and follow-up after thymectomy in patients with myasthenia gravis: A Colombian cohort study

Natalia Padilla-Londoño, Nicolás Felipe Torres-España, Á. Sánchez, José Alejandro Posso-Nuñez et al.
JTCVS Open
Myasthenia Gravis and Thymoma
article

Clinical outcomes and follow-up after thymectomy in patients with myasthenia gravis: A Colombian cohort study

Natalia Padilla-Londoño, Nicolás Felipe Torres-España, Á. Sánchez, José Alejandro Posso-Nuñez, Josué Daniel Gómez-Martínez, Astrid Carolina Álvarez-Ortega, Jairo Alonso Quiñones-Bautista, Mauricio Velasquez-Galvis
article en

Abstract

<h2>Abstract</h2><h3>Objective</h3> To describe 5-year clinical outcomes after thymectomy in patients with myasthenia gravis (MG). <h3>Methods</h3> We retrospectively analyzed patients who underwent thymectomy for MG between 2010 and 2023. Preoperative and annual postoperative assessments (up to 5 years) used the Myasthenia Gravis Foundation of America classification. Outcomes were stratified as complete stable remission (CSR), pharmacologic remission, or minimal manifestations, with additional evaluation by patient-reported changes in symptoms. Kaplan-Meier analyses were conducted for time-to-event data. <h3>Results</h3> Eighty-six patients were included (median age, 42 years; 60.5% female). The median duration of symptoms was 480 days (interquartile range, 28-56 days). Most patients (n = 70; 81.4%) had a low comorbidity burden. Preoperatively, 34% were Myasthenia Gravis Foundation of America class I. Acetylcholinesterase inhibitors were used in 95% of patients. Right video-assisted thoracoscopic thymectomy was the most common approach (76%), with a 2.3% intraoperative complication rate. Thymic hyperplasia was present in 87%; thymoma, in 13%. Postoperative intensive care was required in 96.5%, with myasthenic crisis the most frequent complication (8%). The median hospital length of stay was 4 days, and there was no 30-day mortality. At 1 year, 81.7% were Myasthenia Gravis Foundation of America class I. Kaplan-Meier analysis showed 50% reported symptom improvement by 360 days (95% confidence interval, 350-375 days). By 5 years, 8% achieved CSR. Although a decline in acetylcholinesterase inhibitor dosage was observed, this was not significant (<i>P</i> = .225). <h3>Conclusions</h3> Thymectomy is associated with favorable long-term symptom control in MG, with low perioperative morbidity. However, rates of complete stable remission remain low, underscoring the need for further investigation into post-thymectomy outcomes and predictors of remission.

JTCVS OpenVol. 29
Universidad El Bosque (CO), Fundación Valle del Lili (CO), Icesi University (CO)
Openalex Percentile: Top 51%
Myasthenia Gravis and Thymoma
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