Case report: Extracorporeal life support as a successful bridge to recovery in an incident case of pulmonary arterial hypertension

被引:0
|
作者
Pequignot, Benjamin [1 ,2 ]
Chaouat, Ari [2 ,3 ]
Chabot, Francois [2 ,3 ]
Levy, Bruno [1 ,2 ]
Valentin, Simon [3 ,4 ]
机构
[1] Univ Lorraine, Hop Brabois, CHRU Nancy, Serv Medecine Intens & Reanimat, Nancy, France
[2] Univ Lorraine, Fac Med Nancy, Inserm UMR S1116, Nancy, France
[3] Univ Lorraine, CHRU Nancy, Pole Special Med, Dept Pneumol, Nancy, France
[4] Univ Lorraine, IADI, INSERM U1254, Nancy, France
关键词
PAH; ECMO; pulmonary hypertension; prostacyclin; ECLS; cardiac failure; TRIPLE COMBINATION THERAPY;
D O I
10.3389/fmed.2024.1283065
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:7
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