PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 9, 2025Frontiers in Medicine0 citationsOpen Access

Case Report: Rescue “awake” extracorporeal membrane oxygenation for acute respiratory failure in severe granulomatosis with polyangiitis with multisystem involvement

TKTae‐Hun KimBSByung Wook SongHSHyeong Chan Shin

Key Result

Awake venovenous extracorporeal membrane oxygenation combined with rituximab induction therapy successfully managed acute respiratory failure in a patient with severe granulomatosis with polyangiitis.

Study Design

Type

Case Report (n=1)

Multicenter

No

Structured PICO

P
Population
A 40-year-old man with severe granulomatosis with polyangiitis and acute respiratory failure who was treated with awake VV-ECMO and rituximab.
I
Intervention
"Awake" venovenous extracorporeal membrane oxygenation (VV-ECMO) without mechanical ventilation, combined with rituximab (375 mg/m2 weekly for 4 doses) and corticosteroids.
O
Outcome
Clinical recovery and successful weaning from ECMO

Rescue 'awake' VV-ECMO without mechanical ventilation, combined with rituximab, is a viable strategy for severe ARDS secondary to refractory granulomatosis with polyangiitis.

Limitations

  • Single retrospective case report limits generalizability
  • Confounding effects of multiple concurrent treatments including corticosteroids and ganciclovir

Abstract

We present the case of a 40-year-old man who developed severe acute respiratory failure along with hemoptysis and was subsequently diagnosed with granulomatosis with polyangiitis (GPA). He was initially treated with high-dose corticosteroids, cyclophosphamide, plasmapheresis, and mechanical ventilation (MV). The patient's condition deteriorated after being weaned from MV, leading to his transfer to our medical center without reintubation. Upon admission, a high-flow nasal cannula delivering FiO2 of 1.0 was immediately initiated. Despite the severity of hypoxemia, the patient exhibited neither tachypnea nor subjective dyspnea, and was subsequently initiated on "awake" venovenous extracorporeal membrane oxygenation (VV-ECMO) without MV. Anticoagulation therapy was initiated, and continuous renal replacement therapy was commenced to manage anuria associated with acute renal failure. Due to treatment failure after initial immunosuppressive therapy with cyclophosphamide, rituximab was administered as an induction agent. Following four cycles of rituximab, the patient's respiratory function showed marked improvement. Subsequently, a splenic artery hemorrhage occurred but was effectively managed through prompt embolization, resulting in immediate hemodynamic stabilization. The patient was successfully weaned off VV-ECMO support on day 22 after starting ECMO. After the transfer from the intensive care unit, the patient began active rehabilitation, during which he reported episodes of dizziness. Magnetic resonance imaging of the brain revealed multiple acute infarctions, which are presumed to be caused by vasculitis, leading to the initiation of adjunctive antiplatelet therapy. This represents the first reported case of refractory severe GPA affecting the kidneys, splenic artery, and central nervous system and resulting in respiratory failure, which was managed using "awake" VV-ECMO. The patient remains on maintenance hemodialysis and continues treatment with corticosteroids and rituximab. No disease relapse has occurred until now (June 2025), and the patient is undergoing rehabilitation for intensive care unit-acquired weakness.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Kim et al. (2025) conducted a case report in Severe granulomatosis with polyangiitis (GPA) with acute respiratory failure (n=1). Awake venovenous extracorporeal membrane oxygenation (VV-ECMO) and rituximab was evaluated on Clinical recovery and weaning from ECMO. Awake venovenous extracorporeal membrane oxygenation combined with rituximab induction therapy successfully managed acute respiratory failure in a patient with severe granulomatosis with polyangiitis.

synapsesocial.com/papers/6a3fa67684e5814408cd5dd9https://doi.org/10.3389/fmed.2025.1461269
Ask AI
Helpful
Bookmark
Share
View Full Paper