Is survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients

被引:79
|
作者
Burkhardt, Christian [1 ]
Neuwirth, Christoph [1 ]
Sommacal, Andreas [2 ]
Andersen, Peter M. [3 ]
Weber, Markus [1 ]
机构
[1] Kantonsspital St Gallen, Neuromuscular Dis Unit, ALS Clin, St Gallen, Switzerland
[2] Kantonsspital St Gallen, Dept Pathol, St Gallen, Switzerland
[3] Umea Univ, Inst Pharmacol & Clin Neurosci, Umea, Sweden
来源
PLOS ONE | 2017年 / 12卷 / 05期
基金
瑞士国家科学基金会;
关键词
QUALITY STANDARDS SUBCOMMITTEE; NONINVASIVE VENTILATION; RESPIRATORY-FAILURE; PRACTICE PARAMETER; AMERICAN ACADEMY; FRENCH PATIENTS; DEATH; CARE; DIAGNOSIS; CRITERIA;
D O I
10.1371/journal.pone.0177555
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Non-invasive ventilation (NIV) and percutaneous gastrostomy (PEG) are guideline-recommended interventions for symptom management in amyotrophic lateral sclerosis (ALS). Their effect on survival is controversial and the impact on causes of death is unknown. Objective To investigate the effect of NIV and PEG on survival and causes of death in ALS patients. Methods Eighty deceased ALS patients underwent a complete post mortem analysis for causes of death between 2003 and 2015. Forty-two of these patients consented for genetic testing. Effects of NIV and PEG on survival and causes of death were analyzed in a multivariable Cox proportional hazard regression. Results Six patients, who requested assisted suicide causing drug-induced hypoxia, were excluded from final analysis. Respiratory failure was the main cause of death in 72 out of 74 patients. Fifteen out of 74 died of aspiration pneumonia 23/74 of bronchopneumonia and 8/74 of a combination of aspiration pneumonia and bronchopneumonia. Twenty died of hypoxia without concomitant infection, and six patients had pulmonary embolism alone or in combination with pneumonia. NIV (p = 0.01) and PEG (p<0.01) had a significant impact on survival. In patients using NIV bronchopneumonia was significantly more frequent (p <0.04) compared to non-NIV patients. This effect was even more pronounced in limb onset patients (p<0.002). Patients with C9orf72 hexanucleotide repeat expansions showed faster disease progression and shorter survival (p = 0.01). Conclusion The use of NIV and PEG prolongs survival in ALS. This study supports current AAN and EFNS guidelines which recommend NIV and PEG as a treatment option in ALS. The risk of bronchopneumonia as cause of death may be increased by NIV.
引用
收藏
页数:12
相关论文
共 39 条
  • [1] Impact of Percutaneous Endoscopic Gastrostomy (PEG) on the Evolution of Disease in Patients with Amyotrophic Lateral Sclerosis (ALS)
    Lopez-Gomez, Juan J.
    Ballesteros-Pomar, Maria D.
    Torres-Torres, Beatriz
    De la Maza, Begona
    Penacho-Lazaro, Maria A.
    Palacio-Mures, Jose M.
    Abreu-Padin, Cristina
    Sanz-Gallego, Irene
    De Luis-Roman, Daniel A.
    NUTRIENTS, 2021, 13 (08)
  • [2] Use of Muscle Ultrasonography in Morphofunctional Assessment of Amyotrophic Lateral Sclerosis (ALS)
    Lopez-Gomez, Juan J.
    Izaola-Jauregui, Olatz
    Almansa-Ruiz, Laura
    Jimenez-Sahagun, Rebeca
    Primo-Martin, David
    Pedraza-Hueso, Maria I.
    Ramos-Bachiller, Beatriz
    Gonzalez-Gutierrez, Jaime
    De Luis-Roman, Daniel
    NUTRIENTS, 2024, 16 (07)
  • [3] Improvements in the multidisciplinary care are beneficial for survival in amyotrophic lateral sclerosis (ALS): experience from a tertiary ALS center
    Klavzar, Polona
    Koritnik, Blaz
    Leonardis, Lea
    Groselj, Leja
    Kirbis, Mojca
    Kovacic, Stanka Ristic
    Klinar, Polona
    Perme, Maja Pohar
    Zidar, Janez
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2020, 21 (3-4) : 203 - 208
  • [4] Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based study
    Calvo, Andrea
    Chio, Adriano
    Pagani, Marco
    Cammarosano, Stefania
    Dematteis, Francesca
    Moglia, Cristina
    Solero, Luca
    Manera, Umberto
    Martone, Tiziana
    Brunetti, Maura
    Balma, Michele
    Castellano, Giancarlo
    Barberis, Marco
    Cistaro, Angelina
    Artusi, Carlo Alberto
    Vasta, Rosario
    Montanaro, Elisa
    Romagnolo, Alberto
    Iazzolino, Barbara
    Canosa, Antonio
    Carrara, Giovanna
    Valentini, Consuelo
    Li, Tie-Qiang
    Nobili, Flavio
    Lopiano, Leonardo
    Rizzone, Mario G.
    JOURNAL OF NEUROLOGY, 2019, 266 (07) : 1633 - 1642
  • [5] Evaluation of the application of the European guidelines for the diagnosis and clinical care of amyotrophic lateral sclerosis (ALS) patients in six French ALS centres
    Marin, B.
    Beghi, E.
    Vial, C.
    Bernard, E.
    Lautrette, G.
    Clavelou, P.
    Guy, N.
    Lemasson, G.
    Debruxelles, S.
    Cintas, P.
    Antoine, J. C.
    Camdessanche, J. P.
    Logroscino, G.
    Preux, P. M.
    Couratier, P.
    EUROPEAN JOURNAL OF NEUROLOGY, 2016, 23 (04) : 787 - 795
  • [6] Factors related to respiration influencing survival and respiratory function in patients with amyotrophic lateral sclerosis: a retrospective study
    Leonardis, L.
    Groselj, L. Dolenc
    Vidmar, G.
    EUROPEAN JOURNAL OF NEUROLOGY, 2012, 19 (12) : 1518 - 1524
  • [7] Decision-making for tracheostomy in amyotrophic lateral sclerosis (ALS): a retrospective study
    Ceriana, Piero
    Surbone, Sara
    Segagni, Daniele
    Schreiber, Annia
    Carlucci, Annalisa
    AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2017, 18 (7-8) : 492 - 497
  • [8] Validation of the DYALS (dysphagia in amyotrophic lateral sclerosis) questionnaire for the evaluation of dysphagia in ALS patients
    Diamanti, Luca
    Borrelli, Paola
    Dubbioso, Raffaele
    Capasso, Margherita
    Morelli, Claudia
    Lunetta, Christian
    Petrucci, Antonio
    Mora, Gabriele
    Volanti, Paolo
    Inghilleri, Maurizio
    Tremolizzo, Lucio
    Mandrioli, Jessica
    Mazzini, Letizia
    Vedovello, Marcella
    Siciliano, Gabriele
    Filosto, Massimiliano
    Mata, Sabrina
    Montomoli, Cristina
    NEUROLOGICAL SCIENCES, 2022, 43 (05) : 3195 - 3200
  • [9] Association between nutritional status and disease severity using the amyotrophic lateral sclerosis (ALS) functional rating scale in ALS patients
    Park, Yongsoon
    Park, Jinhee
    Kim, Yeonsun
    Baek, Heejoon
    Kim, Seung Hyun
    NUTRITION, 2015, 31 (11-12) : 1362 - 1367
  • [10] Healthcare Needs of Patients with Amyotrophic Lateral Sclerosis (ALS) in Singapore: A patient-centred qualitative study from multiple perspectives
    Ang, Kexin
    Umapathi, Thirugnanam
    Tong, Jieli
    Ng, Justin
    Tseng, Liang Jun
    Woo, Ivan Mun Hong
    JOURNAL OF PALLIATIVE CARE, 2015, 31 (03) : 150 - 157