Pulmonology is the specialty that learned what everyone does is not always what works.
In May 2000, the New England Journal of Medicine published a trial about ventilators. Ventilators then gave patients with badly injured lungs large breaths, 10 to 15 ml per kilogram of body weight. Those large breaths may have stretched and damaged the lungs further. The trial gave 861 patients either 12 ml per kilogram or 6 ml per kilogram. It stopped early. Death rates were 31.0% with the small breaths and 39.8% with the large ones. The small-breath patients also spent more days off the ventilator. A gentler machine setting had saved lives.
Eleven years later, in August 2011, the field turned to lung cancer. Earlier screening had not cut deaths from it. The National Lung Screening Trial tested a new scan, low-dose CT. It enrolled 53,454 people at high risk. Each person had three yearly scans, either CT or a chest X-ray. CT found more cancers than the X-ray, 1,060 against 941. It cut deaths from lung cancer by 20.0%, and deaths from any cause by 6.7%. The price was false alarms. Across the three rounds, 24.2% of CT scans came back positive, and 96.4% of those positives were not cancer. For the first time, a screening test had cut deaths from lung cancer.
Nine months after that, in May 2012, a trial tested a treatment doctors already widely used. For idiopathic pulmonary fibrosis, doctors gave three drugs together: prednisone, azathioprine and N-acetylcysteine. Nobody knew if the combination was safe or if it worked. The trial compared it with placebo and stopped the combination early. On the combination, 8 patients died and 23 went to hospital. On placebo, 1 patient died and 7 went to hospital. The combination showed no benefit. A routine treatment had been harming the patients it was meant to help.
These are three of the thousands of studies that shaped modern pulmonology. They taught pulmonology that smaller breaths on a ventilator save lives, that a CT scan can cut deaths from lung cancer, and that a common fibrosis treatment was doing harm, and each time the answer was in a paper years before it was in a textbook.
It is still happening. Recently, in June 2025, the New England Journal of Medicine published a trial in idiopathic pulmonary fibrosis, the scarring lung disease of the 2012 paper above. The trial gave 1,177 patients a new pill, nerandomilast, or placebo for a year. Most were already on one of the two existing drugs. Over the year, lung capacity fell by 114.7 ml on the higher dose, against 183.5 ml on placebo. The cost was diarrhoea, in 41.3% against 16.0%. Serious side effects were no more common on the pill. A disease with two drugs had a third, and it worked on top of them. Practice follows the literature as it goes. It is a good culture. It has exactly one cost.
The literature grows faster than anyone can read it.
Across the medical topics a pulmonologist needs to stay up to date on, from asthma and COPD to lung fibrosis and pulmonary hypertension, around 550 full-text papers now arrive every week. That is about 2,400 a month, and more than 20,000 a year. Pneumonia treatment alone is 132 of each week’s 550. Lung cancer screening is 86. These are not press releases or opinion pieces. They are the same kind of paper as the ventilation trial and the screening trial, and somewhere in each week’s 550 are the handful that will change a prescription.
It is tempting to believe that experience closes the gap, that twenty years of clinic teach what the papers teach. The evidence points the other way. A systematic review of 62 studies found that in most of them, more years in practice went with lower adherence to current standards of care. Experience is not what keeps a pulmonologist current. Reading is. And reading is the one thing the week does not have room for.
So we built the tool you need to stay up to date.
We summarise the latest research for you and send it directly to your email inbox, every week, or whenever you choose.
Nerandomilast slowed the loss of lung function in idiopathic pulmonary fibrosis
TakeawayIn 1,177 patients with idiopathic pulmonary fibrosis, nerandomilast 18 mg twice daily cut the 52-week loss of forced vital capacity to 114.7 ml, against 183.5 ml on placebo.
Nerandomilast is a pill that preferentially blocks phosphodiesterase 4B, with antifibrotic and immune-modulating effects. FIBRONEER-IPF, a phase 3 double-blind trial, randomised 1,177 patients to 18 mg or 9 mg twice daily, or placebo. Most patients, 77.7%, were already taking nintedanib or pirfenidone.
- •Change in FVC at week 52: -114.7 ml (18 mg), -138.6 ml (9 mg), -183.5 ml (placebo).
- •Difference from placebo: 68.8 ml with 18 mg (P < 0.001), 44.9 ml with 9 mg (P = 0.02).