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All pulmonology briefings

The edition · Pulmonology

Gabapentin gets a trial in fibrotic cough, and it works

A placebo-controlled trial in idiopathic pulmonary fibrosis finds three-quarters of patients get meaningful cough relief. Also: an expert consensus on when to screen rheumatoid arthritis for lung disease, who actually progresses to severe asthma after a first exacerbation, and what wood dust does to the lungs of workers who breathe it.

The edition in brief

A randomised, double-blind, placebo-controlled trial at a single Chinese centre gave 68 patients with idiopathic pulmonary fibrosis and cough lasting over eight weeks either gabapentin titrated to a maximum 900 mg/day or placebo for 12 weeks. Cough relief — at least a 50% fall in Cough Symptom Score — was reached by 73.5% on gabapentin against 26.5% on placebo, a placebo-adjusted difference of 47.1 percentage points (95% CI 26.1 to 68.0, P < 0.001). Adverse events affected 32.4% versus 8.8%, chiefly drowsiness, fatigue and dizziness. An international expert group issued consensus statements on rheumatoid arthritis-associated interstitial lung disease, covering risk factors, screening and treatment. The group convened explicitly because high-quality studies are too scarce to support strict evidence-based guidelines, and synthesised the evidence qualitatively instead. A Danish cohort within the NORDSTAR collaboration followed 99,748 adults with mild-to-moderate asthma from their first exacerbation for five years. Overall, 4.1% progressed to severe asthma. Risk factors were exacerbation despite medium-dose inhaled corticosteroid (OR 3.72, 95% CI 3.39-4.09), blood eosinophils at or above 0.6 x 10^9/L (OR 1.97, 1.47-2.61), high short-acting beta agonist use (OR 1.76, 1.64-1.90), two or more respiratory infections (OR 1.61, 1.49-1.73) and age 40-49 (OR 1.62, 1.49-1.77). A patient with all of these had a 30.4% five-year risk. A meta-analysis of 55 studies of occupational wood dust exposure found pooled reductions of 8.57 percentage points in FEV1 % predicted (95% CI -12.07 to -5.08), 7.43 in FVC and 13.43 in PEFR, with heterogeneity above 95% and signs of publication bias.

In this edition
01Clinical update

Rheumatoid arthritis-associated lung disease: consensus where the evidence will not support a guideline

An expert group has issued consensus statements on screening for, diagnosing and treating rheumatoid arthritis-associated interstitial lung disease — useful for building a joint pathway with rheumatology, but consensus rather than trial evidence, and it says so.

2 min · The Lancet. Respiratory medicineRead →
02Research

After a first asthma exacerbation, most patients do not progress — and you can tell which ones might

Only 4.1% of adults progress to severe asthma in the five years after a first exacerbation, but exacerbating despite medium-dose inhaled corticosteroid, eosinophils at or above 0.6, high reliever use and recurrent infections together put that risk near 30%.

2 min · American journal of respiratory and critical care medicineRead →
03Research

Wood dust and the working lung: a large signal in a noisy literature

Workers exposed to wood dust had FEV1 about 8.6 percentage points and PEFR about 13.4 points lower than unexposed workers — enough to make an occupational history and spirometry, rather than an empirical inhaler, the right first step.

2 min · The National medical journal of IndiaRead →
04Pearl

Chronic cough: the three drugs and the one question people forget

In chronic cough, stop the ACE inhibitor for a full four weeks whatever the duration of use, exclude reflux and post-nasal drip, and always ask what the patient does at work and what they burn at home.

1 minRead →
05Practice changer

Gabapentin for the cough of idiopathic pulmonary fibrosis

Gabapentin at up to 900 mg daily gave at least 50% cough relief to 73.5% of patients with idiopathic pulmonary fibrosis against 26.5% on placebo — a cheap, available option for a symptom that has had none.

2 min · ChestRead →

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