Pulmonology & Critical Care Clinical Practice Updates

We summarize recent practice-changing research in pulmonary and critical care medicine from peer-reviewed journals. Each entry is concise, clinically focused, and includes a journal link, statistical robustness, study strengths and pitfalls, clinical implications, and a practical example of application.

On this page

  1. Dupilumab for COPD with Type 2 Inflammation
  2. Early Mobilization in Mechanically Ventilated ICU Patients
  3. Nintedanib for Progressive Pulmonary Fibrosis
  4. High-Flow Nasal Oxygen for Acute Hypoxemic Respiratory Failure
  5. ECMO for Severe ARDS: ELSO Guidance & Key Trial
  6. Corticosteroids in Severe Community-Acquired Pneumonia

1. Dupilumab for COPD with Type 2 Inflammation

Phase 3 trials in NEJM (BOREAS, NOTUS) show dupilumab reduces moderate/severe exacerbations and improves lung function in COPD with eosinophilic/type-2 inflammation.

Statistical Robustness

Large, multicenter RCTs with prespecified endpoints and significant reductions in exacerbation rates; lung-function and symptom benefits maintained through 52 weeks.

Strengths

Targeted endotype; consistent efficacy across confirmatory trials.

Pitfalls

Indicated for patients with elevated eosinophils; cost/access and injection adverse events to consider.

Clinical Implication

Consider dupilumab in COPD with blood eosinophils ≥300/µL and frequent exacerbations despite triple therapy.

Practical Example

A 65-year-old with 3+ exacerbations/year on LABA/LAMA/ICS and eosinophils 350/µL: refer for biologic eligibility and payer review.

Reference: Bhatt SP, et al. Dupilumab for COPD with type 2 inflammation. N Engl J Med. 2023.
Confirmatory: NOTUS trial. N Engl J Med. 2024.

2. Early Mobilization in Mechanically Ventilated ICU Patients

In the TEAM RCT (NEJM 2022), increased early mobilization did not improve the primary outcome (days alive and out of hospital at 180 days) versus usual care and was associated with more mobilization-related adverse events.

Statistical Robustness

Multicenter RCT (n=750) with prespecified primary endpoint; neutral primary result; safety events higher with aggressive mobilization.

Strengths

Pragmatic, international; detailed mobilization dosing captured.

Pitfalls

Implementation heterogeneity; requires careful safety screening and sedation minimization.

Clinical Implication

Adopt structured, safety-screened activity (ABCDEF bundle) rather than aggressive targets; integrate PT/OT with sedation lightening.

Practical Example

Day 2 on ventilation: screen hemodynamics, minimize sedation, begin in-bed cycling/active-assisted movement; escalate as tolerated.

Reference: Hodgson CL, et al. Early active mobilization during mechanical ventilation in the ICU. N Engl J Med. 2022.

3. Nintedanib for Progressive Pulmonary Fibrosis

INBUILD (NEJM 2019) showed nintedanib slows FVC decline across progressive fibrosing ILDs beyond IPF; INBUILD-ON (2025) supports long-term safety and durability.

Statistical Robustness

Placebo-controlled RCT with significant FVC benefit; open-label extension with descriptive long-term outcomes and expected GI adverse events.

Strengths

Broad PPF etiologies; consistent effect on lung-function decline.

Pitfalls

Diarrhea common; dose interruptions may be needed.

Clinical Implication

Consider nintedanib for non-IPF PPF with objective progression; coordinate monitoring for GI tolerance and LFTs.

Practical Example

RA-associated PPF with declining FVC: start 150 mg bid and educate on diarrhea management; reassess FVC at 3–6 months.

Reference: Flaherty KR, et al. Nintedanib in PPF. N Engl J Med. 2019.
Extension: INBUILD-ON. Lung. 2025.

4. High-Flow Nasal Oxygen for Acute Hypoxemic Respiratory Failure

In the landmark RCT by Frat et al. (NEJM 2015), high-flow nasal oxygen reduced intubation rates and improved survival versus standard oxygen in acute hypoxemic respiratory failure.

Statistical Robustness

Randomized, three-arm trial (HFNO vs standard O2 vs NIV); significant survival advantage and lower intubation with HFNO in predefined analyses.

Strengths

Clinically meaningful endpoints; pragmatic inclusion; widely generalizable.

Pitfalls

Requires equipment/RT support; avoid delays to intubation in non-responders.

Clinical Implication

Use HFNO early for moderate hypoxemia with close monitoring (ROX index) and a clear intubation threshold.

Practical Example

COVID/viral pneumonia with SpO2 88% on 6 L: initiate HFNO 40–50 L/min, titrate FiO2, reassess ROX at 2–6 h.

Reference: Frat JP, et al. High-flow oxygen through nasal cannula in acute hypoxemic respiratory failure. N Engl J Med. 2015.

5. ECMO for Severe ARDS: ELSO Guidance & Key Trial

ELSO’s VV-ECMO consensus guideline (2021) outlines indications, management, and weaning; the EOLIA RCT (NEJM 2018) showed no significant 60-day mortality benefit for early ECMO versus conventional strategies with rescue ECMO, informing referral/timing decisions.

Statistical Robustness

Guideline synthesizes RCTs/observational data; EOLIA underpowered for modest effects but pivotal for practice.

Strengths

Standardized criteria and circuit management; supports regional referral pathways.

Pitfalls

Resource-intensive; outcomes vary with center experience and patient selection.

Clinical Implication

For refractory hypoxemia (e.g., PaO2/FiO2 <80 despite optimal care), initiate rapid ECMO center consultation; consider transport on high-flow/prone as appropriate.

Practical Example

Young ARDS patient failing proning/paralysis: notify ECMO hub early, share ventilator/ABG data and contraindications checklist.

Reference: ELSO VV-ECMO adult management guideline. 2021.  |  Combes A, et al. EOLIA trial. NEJM. 2018.

6. Corticosteroids in Severe Community-Acquired Pneumonia

CAPE COD (NEJM 2023) found that early hydrocortisone reduced 28-day mortality in ICU patients with severe CAP versus placebo.

Statistical Robustness

Multicenter, double-blind RCT with significant mortality reduction; subsequent reviews suggest hydrocortisone drives the mortality benefit in severe CAP.

Strengths

Hard outcomes; protocolized steroid dosing; early initiation.

Pitfalls

Monitor for hyperglycemia/secondary infection; applicability to non-ICU CAP limited.

Clinical Implication

For severe CAP in ICU, consider hydrocortisone per CAPE COD protocol alongside guideline-directed antibiotics and source control.

Practical Example

Shock with lobar CAP on admission: start hydrocortisone 200 mg/day (continuous or divided), titrate vasopressors, monitor glucose and cultures.

Reference: Dequin PF, et al. Hydrocortisone in severe CAP (CAPE COD). N Engl J Med. 2023.

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