Literature DB >> 25522696

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

Rosa Capozzo1, Vitaliano N Quaranta, Fabio Pellegrini, Andrea Fontana, Massimiliano Copetti, Pierluigi Carratù, Francesco Panza, Anna Cassano, Vito A Falcone, Rosanna Tortelli, Rosa Cortese, Isabella L Simone, Onofrio Resta, Giancarlo Logroscino.   

Abstract

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 ≤18 cmH2O 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.

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Year:  2014        PMID: 25522696     DOI: 10.1007/s00415-014-7613-3

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  36 in total

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Journal:  Eur J Neurol       Date:  2011-09-14       Impact factor: 6.089

Review 6.  Pulmonary function testing in neuromuscular disease.

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7.  Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial.

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Review 9.  Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues.

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Review 10.  Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group.

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  18 in total

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Authors:  Benoît Marin; Philippe Couratier; Simona Arcuti; Massimiliano Copetti; Andrea Fontana; Marie Nicol; Marie Raymondeau; Giancarlo Logroscino; Pierre Marie Preux
Journal:  J Neurol       Date:  2015-10-30       Impact factor: 4.849

2.  Respiratory Muscle Assessment in Acute Guillain-Barré Syndrome.

Authors:  S Walterspacher; A Kirchberger; J Lambeck; D J Walker; A Schwörer; W D Niesen; W Windisch; F Hamzei; H J Kabitz
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4.  Prognostic role of slow vital capacity in amyotrophic lateral sclerosis.

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Journal:  J Neurol       Date:  2020-02-12       Impact factor: 4.849

Review 5.  Sleep disordered breathing in motor neurone disease.

Authors:  Rebecca F D'Cruz; Patrick B Murphy; Georgios Kaltsakas
Journal:  J Thorac Dis       Date:  2018-01       Impact factor: 2.895

6. 

Authors:  Harrison N Jones; Maragatha Kuchibhatla; Kelly D Crisp; Lisa D Hobson Webb; Laura Case; Milisa T Batten; Jill A Marcus; Richard M Kravitz; Priya S Kishnani
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7.  Pattern of Respiratory Deterioration in Sporadic Amyotrophic Lateral Sclerosis According to Onset Lesion by Using Respiratory Function Tests.

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8.  The ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onset.

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9.  Hospitalizations due to respiratory failure in patients with Amyotrophic Lateral Sclerosis and their impact on survival: a population-based cohort study.

Authors:  Federica Edith Pisa; Giancarlo Logroscino; Paolo Giacomelli Battiston; Fabio Barbone
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Review 10.  Recent advances in amyotrophic lateral sclerosis.

Authors:  Nilo Riva; Federica Agosta; Christian Lunetta; Massimo Filippi; Angelo Quattrini
Journal:  J Neurol       Date:  2016-03-30       Impact factor: 4.849

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