Results of a multidisciplinary strategy to improve the management of cardiovascular risk factors after liver transplantation.


Journal

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
ISSN: 1527-6473
Titre abrégé: Liver Transpl
Pays: United States
ID NLM: 100909185

Informations de publication

Date de publication:
08 2022
Historique:
revised: 15 02 2022
received: 10 01 2022
accepted: 18 02 2022
pubmed: 1 3 2022
medline: 19 7 2022
entrez: 28 2 2022
Statut: ppublish

Résumé

Although liver transplantation (LT) recipients are at high cardiovascular risk (CVR), the management of CVR factors (CVRF) after LT is far from optimal and needs to be improved. For this reason, we developed a multidisciplinary protocol to standardize the identification, risk stratification, management, and targets of therapy of CVRF during the first post-LT year. The grade of identification and control of CVRF 12 months after LT in the postintervention cohort (LT January 2018-January 2020, n = 150) were compared with a control cohort who underwent LT between July 2015 and December 2016 (n = 100). Before LT, the prevalence of metabolic-associated fatty liver disease as the indication of LT and the presence of obesity were significantly higher in the postintervention cohort, whereas the prevalence of other CVRF and renal dysfunction tended to be higher. Cyclosporine A was used less frequently in the postintervention cohort, whereas everolimus tended to increase. At 12 months after LT, the proportion of patients with measured blood pressure (88% vs. 56%), glycosilated hemoglobin (HbA1c; 96% vs. 72%), and high-density lipoprotein/low-density lipoprotein cholesterol (67% vs. 33%) was higher in the postintervention than in the control cohort (all p < 0.001). Blood pressure (64% vs. 36%, p = 0.02) and HbA1c (85% vs. 70%, p = 0.1) were within target in more individuals with hypertension and diabetes mellitus, respectively, in the postintervention cohort. Median total cholesterol levels were lower in the postintervention (184 mg/dl; interquartile range [IQR], 160-210 mg/dl) than in the control cohort (212 mg/dl; IQR, 186-240 mg/dl; p = 0.02). At 2 years after LT, the incidence of cardiovascular events was 14% in the control cohort and 6% in the postintervention cohort (p = 0.063). In conclusion, a multidisciplinary, multiprofessional strategy can achieve a higher grade of assessment and management of post-LT CVR despite a worsening metabolic profile of LT recipients.

Identifiants

pubmed: 35224857
doi: 10.1002/lt.26443
pii: 01445473-202208000-00011
doi:

Substances chimiques

Cholesterol, LDL 0
Glycated Hemoglobin A 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1332-1344

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 American Association for the Study of Liver Diseases.

Références

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Auteurs

Lydia Sastre (L)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.
Department of Gastroenterology and HepatologyHospital Son EspasesPalma de MallorcaSpain.

Raquel García (R)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.

Clara Viñals (C)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Antonio J Amor (AJ)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Gema Yago (G)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Alicia Hervás (A)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.

Lorena Sánchez (L)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Joan Trabal (J)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Judit Molero (J)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.

Laia Escudé (L)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.

Giulia Pagano (G)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.

Miquel Blasco (M)

Nephrology and Kidney Transplant DepartmentHospital ClinicBarcelonaSpain.

Rosa Gilabert (R)

Radiology DepartmentHospital ClinicBarcelonaSpain.

Pablo Ruiz (P)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS)BarcelonaSpain.
Centro de Investigación Biomédica en Red-Enfermedades Hepáticas y Digestivas (CIBERehd)MadridSpain.

Jordi Colmenero (J)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS)BarcelonaSpain.
Centro de Investigación Biomédica en Red-Enfermedades Hepáticas y Digestivas (CIBERehd)MadridSpain.
University of BarcelonaBarcelonaSpain.

Miquel Navasa (M)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS)BarcelonaSpain.
Centro de Investigación Biomédica en Red-Enfermedades Hepáticas y Digestivas (CIBERehd)MadridSpain.
University of BarcelonaBarcelonaSpain.

Emilio Ortega (E)

Endocrinology and Nutrition DepartmentHospital ClinicBarcelonaSpain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS)BarcelonaSpain.
Centro de Investigación Biomédica en Red-Fisiopatología de la Obesidad y Nutrición (CIBERobn)MadridSpain.

Gonzalo Crespo (G)

Hepatology and Liver Transplant UnitHospital ClinicBarcelonaSpain.
Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS)BarcelonaSpain.
Centro de Investigación Biomédica en Red-Enfermedades Hepáticas y Digestivas (CIBERehd)MadridSpain.
University of BarcelonaBarcelonaSpain.

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