De-escalating treatment indications for patients who achieve metabolic goals.
Diabetes Res Clin Pract
; 208: 111096, 2024 Feb.
Article
en En
| MEDLINE
| ID: mdl-38244782
ABSTRACT
INTRODUCTION:
Robust evidence exists regarding initiation, intensification or modification of treatments. Recommendations to de-escalate therapy are lacking, specifically in diabetes. A successful treatment de-intensification reduces overtreatment, polypharmacy, and risk of adverse effects.OBJECTIVE:
To encompass current recommendations for deprescribing common drugs and create a consensus among health professionals.METHODS:
We reviewed four databases for deprescribing approaches published between 2010 and 2022. Articles were divided into different groups of drugs (for uric-acid, hypoglycemic, lipid-lowering, and psychotropic drugs).RESULTS:
Hypoglycemic agents strategies were limited to newer agents and insulin regimens for elderly individuals. Reducing insulin was associated with 1.1% reduction of A1c over time. SGLT2i and GLP-1RAs dose reduction depends on adverse events. Lipid-lowering agents studies show that patients with very low cholesterol have fewer cardiovascular events without associated increased risk. Antihypertensive agents Younger patients, lower systolic blood pressure, and few comorbidities are ideal characteristics for discontinuation. Uric acid therapy we found no recommendation for dose de-escalation. Poor treatment adherence is associated with episodes of gout and deforming arthritis in the long term.CONCLUSION:
Deprescribing hypoglycemic, statins, antihypertensives, and urate-lowering agents may be feasible in selected patients, but periodic surveillance is important. More evidence is necessary to support this decision entirely.Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Diabetes Mellitus
/
Objetivos
Tipo de estudio:
Guideline
/
Prognostic_studies
Límite:
Aged
/
Humans
Idioma:
En
Revista:
Diabetes Res Clin Pract
Asunto de la revista:
ENDOCRINOLOGIA
Año:
2024
Tipo del documento:
Article
País de afiliación:
México