PTCohortArchives of physiotherapy2020

Timed immersion expiration measures in patients with muscular dystrophies.

Mariana Callil Voos, Priscila Santos Albuquerque Goya, Bruna Leal de Freitas and 3 others

PMID 32099666

WHAT IT FOUND

In patients with muscular dystrophies, mouth blowing time in water stayed similar over the follow-up year, while nose blowing time became longer.

Motor and breathing measures still worsened, so this does not show aquatic therapy stopped decline.

Key findings

01Mouth blowing time in water did not change significantly over one year, while nose blowing time was significantly longer at follow-up.

02Motor function scores and respiratory measures were significantly lower at one-year follow-up.

03In the Duchenne group, mouth blowing time and nose blowing time showed a strong correlation with each other.

STILL TO COME

How it was doneWhat they foundWhat it means for PTs

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What it does not show

There was no untreated control group, so one-year changes cannot be separated from the natural course of muscular dystrophies. Participants received physical therapy, respiratory therapy, aquatic therapy, occupational therapy, pedagogic supervision, medical supervision, nutritional supervision, air stacking, cough assist machines when needed, and steroids if they had Duchenne muscular dystrophy, so the contribution of any single component cannot be separated. The dose of conventional and aquatic exercises was not controlled; each therapist set the routine. The nose blowing improvement had a p-value of 0.049, close to the significance threshold. All participants had leg function graded 2 to 8 on the Vignos scale and were already adapted to aquatic therapy, so the findings may not apply to patients outside that range or to patients new to water.

The easy way to misread this

Do not read the longer nose blowing time as proof that aquatic therapy improved respiratory control. Participants also received physical therapy, respiratory therapy, aquatic therapy, occupational therapy, pedagogic supervision, medical supervision, nutritional supervision, air stacking, cough assist machines when needed, and steroids if they had Duchenne muscular dystrophy, and there was no untreated control group.

Read it on PubMed →