Giovanna Sophia Manzano, James Eaton, Michael Levy, Justin R Abbatemarco, Allen J Aksamit, Pria Anand, Denis T Balaban, Paula Barreras, Robert P Baughman, Shamik Bhattacharyya, Roberto Bomprezzi, Tracey A Cho, Bart Chwalisz, Stacey Lynn Clardy, David B Clifford, Eoin P Flanagan, Jeffrey M Gelfand, George Kyle Harrold, Spencer K Hutto, Siddharama Pawate, Noellie Rivera Torres, Lama Abdel-Wahed, Steven Richard Dunham, Rajesh Kumar Gupta, Brandon Moss, Carlos A Pardo, Rohini D Samudralwar, Nagagopal Venna, Aram Zabeti, Ilya Kister
{"title":"神经结节病管理的共识建议:美国专家德尔菲调查。","authors":"Giovanna Sophia Manzano, James Eaton, Michael Levy, Justin R Abbatemarco, Allen J Aksamit, Pria Anand, Denis T Balaban, Paula Barreras, Robert P Baughman, Shamik Bhattacharyya, Roberto Bomprezzi, Tracey A Cho, Bart Chwalisz, Stacey Lynn Clardy, David B Clifford, Eoin P Flanagan, Jeffrey M Gelfand, George Kyle Harrold, Spencer K Hutto, Siddharama Pawate, Noellie Rivera Torres, Lama Abdel-Wahed, Steven Richard Dunham, Rajesh Kumar Gupta, Brandon Moss, Carlos A Pardo, Rohini D Samudralwar, Nagagopal Venna, Aram Zabeti, Ilya Kister","doi":"10.1212/CPJ.0000000000200429","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>Neurosarcoidosis poses a diagnostic and management challenge due to its rarity, phenotypic variability, and lack of randomized controlled studies to guide treatment selection. Recommendations for management based on expert opinion are useful in clinical practice and provide a framework for designing prospective studies.</p><p><strong>Methods: </strong>In this Delphi survey study, specialists with experience in managing patients with neurosarcoidosis were invited to anonymously complete 2 surveys about key elements of evaluation, diagnosis, treatment, monitoring, and long-term management of neurosarcoidosis. Expert consensus recommendations were adopted if >80% threshold of agreement was reached.</p><p><strong>Results: </strong>Of the 41 invited expert clinicians across the United States, 32 (78%) participated in the study. All round 1 respondents self-identified as neuroimmunologists (except for 1 pulmonologist). Consensus was reached regarding the need to consider neurosarcoidosis phenotype and severity to guide the choice of initial immunosuppression in both the acute (relapse) and maintenance phases. Experts endorsed the use of TNF-α inhibitors as first-line agents in selected phenotypes with poor prognosis. Neuroimaging was recommended to complement clinical surveillance for treatment response.</p><p><strong>Discussion: </strong>There was agreement on several key issues, most importantly on the need to consider neurosarcoidosis phenotype and severity when deciding initial treatment. No consensus was achieved on the dosing and duration of specific immunosuppressants, nor regarding the management of the peripheral nervous system manifestation of neurosarcoidosis. These topics warrant further investigation.</p>","PeriodicalId":19136,"journal":{"name":"Neurology. 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Recommendations for management based on expert opinion are useful in clinical practice and provide a framework for designing prospective studies.</p><p><strong>Methods: </strong>In this Delphi survey study, specialists with experience in managing patients with neurosarcoidosis were invited to anonymously complete 2 surveys about key elements of evaluation, diagnosis, treatment, monitoring, and long-term management of neurosarcoidosis. Expert consensus recommendations were adopted if >80% threshold of agreement was reached.</p><p><strong>Results: </strong>Of the 41 invited expert clinicians across the United States, 32 (78%) participated in the study. All round 1 respondents self-identified as neuroimmunologists (except for 1 pulmonologist). Consensus was reached regarding the need to consider neurosarcoidosis phenotype and severity to guide the choice of initial immunosuppression in both the acute (relapse) and maintenance phases. Experts endorsed the use of TNF-α inhibitors as first-line agents in selected phenotypes with poor prognosis. Neuroimaging was recommended to complement clinical surveillance for treatment response.</p><p><strong>Discussion: </strong>There was agreement on several key issues, most importantly on the need to consider neurosarcoidosis phenotype and severity when deciding initial treatment. No consensus was achieved on the dosing and duration of specific immunosuppressants, nor regarding the management of the peripheral nervous system manifestation of neurosarcoidosis. These topics warrant further investigation.</p>\",\"PeriodicalId\":19136,\"journal\":{\"name\":\"Neurology. 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Consensus Recommendations for the Management of Neurosarcoidosis: A Delphi Survey of Experts Across the United States.
Background and objectives: Neurosarcoidosis poses a diagnostic and management challenge due to its rarity, phenotypic variability, and lack of randomized controlled studies to guide treatment selection. Recommendations for management based on expert opinion are useful in clinical practice and provide a framework for designing prospective studies.
Methods: In this Delphi survey study, specialists with experience in managing patients with neurosarcoidosis were invited to anonymously complete 2 surveys about key elements of evaluation, diagnosis, treatment, monitoring, and long-term management of neurosarcoidosis. Expert consensus recommendations were adopted if >80% threshold of agreement was reached.
Results: Of the 41 invited expert clinicians across the United States, 32 (78%) participated in the study. All round 1 respondents self-identified as neuroimmunologists (except for 1 pulmonologist). Consensus was reached regarding the need to consider neurosarcoidosis phenotype and severity to guide the choice of initial immunosuppression in both the acute (relapse) and maintenance phases. Experts endorsed the use of TNF-α inhibitors as first-line agents in selected phenotypes with poor prognosis. Neuroimaging was recommended to complement clinical surveillance for treatment response.
Discussion: There was agreement on several key issues, most importantly on the need to consider neurosarcoidosis phenotype and severity when deciding initial treatment. No consensus was achieved on the dosing and duration of specific immunosuppressants, nor regarding the management of the peripheral nervous system manifestation of neurosarcoidosis. These topics warrant further investigation.
期刊介绍:
Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.