Lipid profile of patients treated with evolocumab in Spanish hospital nephrology units (RETOSS NEFRO)

To describe the clinical characteristics, the reasons for initiating therapy and the effects of treatment in the initial phase of evolocumab availability in the Nephrology Units of Spain. Retrospective, observational and multicentric study that included patients initiating treatment with evolocumab...

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Veröffentlicht in:Nefrología 2022-05, Vol.42 (3), p.301-310
Hauptverfasser: Goicoechea, Marian, Álvarez, Vicente, Segarra, Alfonso, Polaina, Manuel, Martín-Reyes, Guillermo, Robles, Nicolás Roberto, Escudero, Verónica, Orellana, Cristhian, Bea Granell, Sergio, de Juan-Ribera, Joaquín, Fernández Lucas, Milagros, Graña, Jose Maria, Reque, Javier, Sánchez Hernández, Rosa, Villamayor, Santiago, Górriz, Jose Luis
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Sprache:eng
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Zusammenfassung:To describe the clinical characteristics, the reasons for initiating therapy and the effects of treatment in the initial phase of evolocumab availability in the Nephrology Units of Spain. Retrospective, observational and multicentric study that included patients initiating treatment with evolocumab (from February 2016 to August 2018), in 15 Nephrology Units in Spain. The demographic and clinical characteristics of the patients, the lipid lowering treatment and the evolution of the lipid profiles between 24 weeks pre-initiation and 12±4 weeks post-initiation of evolocumab were reviewed. 60 patients were enrolled: 53.3% women; mean (SD) age, 56.9 (12.8) years, 45.0% with familial hypercholesterolemia (FH) (5.0% homozygous and 40.0% heterozygous) and 65.0% with atherosclerotic cardiovascular disease. The mean (SD) eGFR was 62.6 (30.0) ml/min/1.73m2 (51.7% of patients had eGFR 2]), 50.0% had proteinuria (>300mg/g) and 10.0% had nephrotic syndrome. Other CV risk factors were hypertension (75.0%), diabetes (25.0%), and smoking (21.7%). A 40.0% of patients were statin intolerant. At evolocumab initiation, 41.7% of patients were on a high intensity statin, 18.3% on moderate intensity statin and 50.0% were receiving ezetimibe. Mean (SD) LDL-c at evolocumab initiation was 179.7 (62.9) mg/dL (53.4% of patients with LDL-c ≥160mg/dL and 29.3% ≥190mg/dL). After 12 weeks, evolocumab resulted in LDL-c reductions of 60.1%. At week 12, 90.0% of patients reached LDL-c levels
ISSN:2013-2514
2013-2514
DOI:10.1016/j.nefroe.2022.05.005