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Respiratory phenotypes in amyotrophic lateral sclerosis as determined by respiratory questions on the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised and their relation to respiratory tests

Pinto, Susana (författare)
Uppsala universitet,Rehabiliteringsmedicin,Univ Lisbon, Inst Physiol, Ctr Estudos Egas Moniz, Inst Med Mol Joao Lobo Antunes,Fac Med, Lisbon, Portugal.
Santos, Miguel Oliveira (författare)
Univ Lisbon, Inst Physiol, Ctr Estudos Egas Moniz, Inst Med Mol Joao Lobo Antunes,Fac Med, Lisbon, Portugal.;Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Lisbon, Portugal.
Gromicho, Marta (författare)
Univ Lisbon, Inst Physiol, Ctr Estudos Egas Moniz, Inst Med Mol Joao Lobo Antunes,Fac Med, Lisbon, Portugal.
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Swash, Michael (författare)
Univ Lisbon, Inst Physiol, Ctr Estudos Egas Moniz, Inst Med Mol Joao Lobo Antunes,Fac Med, Lisbon, Portugal.;Queen Mary Univ London, Barts & London Sch Med, Dept Neurol & Neurosci, London, England.
de Carvalho, Mamede (författare)
Univ Lisbon, Inst Physiol, Ctr Estudos Egas Moniz, Inst Med Mol Joao Lobo Antunes,Fac Med, Lisbon, Portugal.;Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Dept Neurosci & Mental Hlth, Lisbon, Portugal.
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 (creator_code:org_t)
2023-03-22
2023
Engelska.
Ingår i: European Journal of Neurology. - : John Wiley & Sons. - 1351-5101 .- 1468-1331. ; 30:6, s. 1594-1599
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
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  • Background and purpose Respiratory insufficiency and its complications are the main cause of death in amyotrophic lateral sclerosis (ALS). Respiratory symptoms are scored in questions Q10 (dyspnoea) and Q11 (orthopnoea) of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R). The association of respiratory test alterations with respiratory symptoms is unclear. Methods Patients with ALS and progressive muscular atrophy were included. We retrospectively recorded demographic data, ALSFRS-R, forced vital capacity (FVC), maximal inspiratory (MIP) and expiratory (MEP) pressures, mouth occlusion pressure at 100 ms, nocturnal oximetry (SpO(2)mean), arterial blood gases, and phrenic nerve amplitude (PhrenAmpl). Three groups were categorized: G1, normal Q10 and Q11; G2, abnormal Q10; and G3, abnormal Q10 and Q11 or only abnormal Q11. A binary logistic regression model explored independent predictors. Results We included 276 patients (153 men, onset age = 62.6 +/- 11.0 years, disease duration = 13.0 +/- 9.6 months, spinal onset in 182) with mean survival of 40.1 +/- 26.0 months. Gender, onset region, and disease duration were similar in G1 (n = 149), G2 (n = 78), and G3 (n = 49). Time to noninvasive ventilation (NIV) was shorter in G3 (p < 0.001), but survival was similar. ALSFRS-R subscores were significantly different (G1>G2>G3, p < 0.001), except for lower limb subscore (p = 0.077). G2 and G3 patients were older than G1 (p < 0.001), and had lower FVC, MIP, MEP, PhrenAmpl, and SpO(2)mean. Independent predictors for G2 were MIP and SpO(2)mean; for G3, the only independent predictor was PhrenAmpl. Conclusions These three distinct ALS phenotypic respiratory categories represent progressive stages of ventilatory dysfunction, supporting ALSFRS-R clinical relevance. Orthopnoea is a severe symptom that should prompt NIV, phrenic nerve response being an independent predictor. Early NIV promotes similar survival for G2 and G3.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

amyotrophic lateral sclerosis
nocturnal pulsed oximetry
phrenic nerve
respiratory function
respiratory tests

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Av författaren/redakt...
Pinto, Susana
Santos, Miguel O ...
Gromicho, Marta
Swash, Michael
de Carvalho, Mam ...
Om ämnet
MEDICIN OCH HÄLSOVETENSKAP
MEDICIN OCH HÄLS ...
och Klinisk medicin
och Neurologi
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European Journal ...
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Uppsala universitet

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