Why the study?
Few reports describe extracorporeal life support as a bridge to recovery with targeted drugs in untreated or undertreated pulmonary arterial hypertension.
Does VA-ECMO combined with PAH targeted therapy allow for clinical recovery in a patient with incident heritable PAH and refractory hypoxemia?
Does VA-ECMO combined with PAH targeted therapy allow for clinical recovery in a patient with incident heritable PAH and refractory hypoxemia?
VA-ECMO can serve as a successful bridge-to-recovery strategy in incident cases of severe heritable PAH presenting with refractory hypoxemia when combined with prompt initiation of triple PAH therapy.
Answers are grounded in this paper and cite their sources.
May support bridge-to-recovery with VA-ECMO plus triple therapy in severe heritable PAH; hypothesis-generating and requires prospective trials.
Pulmonary arterial hypertension (PAH) is characterized by a progressive increase in pulmonary vascular resistance (PVR) due to vascular remodeling of the small pulmonary arteries. In advanced RV failure or severe hypoxemia, extra corporeal life support (ECLS) is now to be considered, with the objective to bridge patients back to their baseline clinical state while waiting or right after lung transplantation, or bridge to pharmacological optimization of PAH (i.e., bridge to recovery). We describe herein a case of a 30-year-old woman ( gravida 6, para 6) with an incident case of heritable PAH revealed by refractory hypoxemia. Despite the use of mechanical ventilation and fluid optimization, the patient remained profoundly hypoxemic. ECLS was then initiated to avoid tissue hypoxia. The mechanical option chosen was peripheral femoro-femoral venoarterial extracorporeal membrane oxygen (VA-ECMO), percutaneously implanted. Due to the absence of evidence of chronic respiratory disease or chronic thromboembolic pulmonary hypertension, this severe pre-capillary pulmonary hypertension was attributed to PAH. Therefore, epoprostenol infusion and an association of oral treatments (bosentan and tadalafil) were administered. A dramatic improvement was observed, allowing decannulation 7 days after the initiation of pharmacological treatment. After 29 days, the patient was discharged from the hospital with epoprostenol, bosentan, and tadalafil. The assessment has been completed by positive research on mutations ( c.741C > G, p.Tyr247 ) corresponding to a loss of function of the bone morphogenetic protein receptor 2 ( BMPR2 ) gene. The final diagnosis was heritable PAH. The use of ECLS has been well demonstrated in patients with PAH complicated by acute RV failure or refractory hypoxemia in the “bridge-to-transplantation” strategy. Only a few reports have described the use of ECLS as a “bridge-to-recovery” with PAH drugs in untreated or undertreated PAH patients, but none has described such a rapid improvement with resolution of refractory hypoxemia. More studies are needed to assess the benefits and limitations of the “bridge-to-recovery” strategy and to identify the patients most likely to benefit from it.
No takes yet. Share an insight, caveat, or question.
Péquignot et al. (2024) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: