Sniff nasal inspiratory pressure as a prognostic factor of tracheostomy or death in amyotrophic lateral sclerosis

被引:47
作者
Capozzo, Rosa [1 ]
Quaranta, Vitaliano N. [2 ]
Pellegrini, Fabio [3 ,4 ]
Fontana, Andrea [3 ]
Copetti, Massimiliano [3 ]
Carratu, Pierluigi [2 ]
Panza, Francesco [1 ,5 ]
Cassano, Anna [2 ]
Falcone, Vito A. [2 ]
Tortelli, Rosanna [1 ,5 ]
Cortese, Rosa [1 ]
Simone, Isabella L. [1 ]
Resta, Onofrio [2 ]
Logroscino, Giancarlo [1 ,5 ]
机构
[1] Univ Bari Aldo Moro, Neurosci & Sense Organs, Dept Basic Med Sci, Neurodegenerat Dis Unit, Bari, Italy
[2] Univ Bari Aldo Moro, Pulm Dis Inst, Bari, Italy
[3] IRCCS Casa Sollievo Sofferenza, Biostat Unit, San Giovanni Rotondo, FG, Italy
[4] Ist Ric Farmacol Mario Negri, Consorzio Mario Negri Sud, Biostat Unit, I-66030 Santa Maria Imbaro, CH, Italy
[5] Univ Bari Aldo Moro, Dept Clin Res Neurol, Pia Fdn Cardinale G Panico, Tricase, LE, Italy
关键词
SNIP; FVC; Prognosis; Respiratory function; ALS; RESPIRATORY MUSCLE STRENGTH; PULMONARY-FUNCTION; PREDICT SURVIVAL; DIAGNOSIS; EPIDEMIOLOGY; ALS;
D O I
10.1007/s00415-014-7613-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Forced vital capacity (FVC) shows limitations in detecting respiratory failure in the early phase of amyotrophic lateral sclerosis (ALS). In fact, mild-to-moderate respiratory muscle weakness may be present even when FVC is normal, and ALS patients with bulbar involvement might not be able to perform correctly the spirometry test. Sniff nasal inspiratory pressure (SNIP) is correlated with transdiaphragmatic strength. We evaluated SNIP at baseline as a prognostic factor of tracheostomy or death in patients with ALS. In a multidisciplinary tertiary care center for motorneuron disease, we enrolled 100 patients with ALS diagnosed with El Escorial criteria in the period between January 2006 and December 2010. Main outcome measures were tracheostomy or death. RECursive Partitioning and AMalgamation (RECPAM) analysis was also used to identify subgroups at different risks for the tracheostomy or death. Twenty-nine patients with ALS reached the outcome (12 died and 17 had tracheostomy). Using a multivariate model SNIP correctly classified the risk of the composite event within 1 year of follow-up with a continuous Net Reclassification Improvement cNRI of 0.58 (p = 0.03). Sex, Amyotrophic Lateral Sclerosis Functional Rating Scale revisited, site of onset, and FVC did not improve the classification of prognostic classes. SNIP a parts per thousand currency sign18 cmH(2)O identified the RECPAM class with the highest risk (Class 1, hazard ratio = 9.85, 95 % confidence interval: 2.67-36.29, p < 0.001). SNIP measured at baseline identified patients with ALS with initial respiratory failure. Finally, using only ALS patients with spinal onset of the disease, our findings were mostly overlapping with those reported in the models including the whole sample. At baseline, SNIP appeared to be the best predictor of death or tracheostomy within 1 year of follow-up. The measurement of SNIP in the early phase of the disease may contribute to identify patients with high risk of mortality or intubation. SNIP may also provide an additional tool for baseline stratification of patients with ALS in clinical trials.
引用
收藏
页码:593 / 603
页数:11
相关论文
共 37 条
  • [1] Electrophysiologic techniques for the assessment of respiratory muscle function
    Aldrich, TK
    Sinderby, C
    McKenzie, DK
    Estenne, M
    Gandevia, SC
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (04) : 548 - +
  • [2] Allen C, 2013, LANCET NEUROL, V12, P339, DOI [10.1016/S1474-4422(13)700374, 10.1016/S1474-4422(13)70037-1]
  • [3] EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force
    Andersen, Peter M.
    Abrahams, Sharon
    Borasio, Gian D.
    de Carvalho, Mamede
    Chio, Adriano
    Van Damme, Philip
    Hardiman, Orla
    Kollewe, Katja
    Morrison, Karen E.
    Petri, Susanne
    Pradat, Pierre-Francois
    Silani, Vincenzo
    Tomik, Barbara
    Wasner, Maria
    Weber, Markus
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2012, 19 (03) : 360 - E24
  • [4] Good practice in the management of amyotrophic lateral sclerosis: Clinical guidelines. An evidence-based review with good practice points. EALSC Working Group
    Andersen, Peter Munch
    Borasio, Gian Domenico
    Dengler, Reinhard
    Hardiman, Orla
    Kollewe, Katja
    Leigh, Peter Nigel
    Pradat, Pierre-Francois
    Silani, Vincenzo
    Tomik, Barbara
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2007, 8 (04): : 195 - 213
  • [5] Use of respiratory function tests to predict survival in amyotrophic lateral sclerosis
    Baumann, Fusun
    Henderson, Robert D.
    Morrison, Stephen C.
    Brown, Michael
    Hutchinson, N.
    Douglas, James A.
    Robinson, Peter J.
    McCombe, Pamela A.
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2010, 11 (1-2): : 194 - 202
  • [6] BLACK LF, 1971, AM REV RESPIR DIS, V103, P641
  • [8] Brown RH, 2017, NEW ENGL J MED, V377, P1602, DOI [10.1056/NEJMra1603471, 10.1016/S0140-6736(17)31287-4, 10.1016/S0140-6736(10)61156-7, 10.1056/NEJMc1710379, 10.1038/nrdp.2017.85]
  • [9] Association between low sniff nasal-inspiratory pressure (SNIP) and sleep disordered breathing in amyotrophic lateral sclerosis: Preliminary results
    Carratu, Pierluigi
    Cassano, Anna
    Gadaleta, Felice
    Tedone, Mariangela
    Dongiovanni, Salvatore
    Fanfulla, Francesco
    Resta, Onofrio
    [J]. AMYOTROPHIC LATERAL SCLEROSIS, 2011, 12 (06): : 458 - 463
  • [10] The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function
    Cedarbaum, JM
    Stambler, N
    Malta, E
    Fuller, C
    Hilt, D
    Thurmond, B
    Nakanishi, A
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 169 (1-2) : 13 - 21