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Clinical Outcomes Among High-Risk Primary Care Patients With Diabetic Kidney Disease: Methodological Challenges and Results From the STOP-DKD Study.
Bosworth, Hayden B; Patel, Uptal D; Lewinski, Allison A; Davenport, Clemontina A; Pendergast, Jane; Oakes, Megan; Crowley, Matthew J; Zullig, Leah L; Patel, Sejal; Moaddeb, Jivan; Miller, Julie; Malone, Shauna; Barnhart, Huiman; Diamantidis, Clarissa J.
  • Bosworth HB; Department of Population Health Sciences, Duke University.
  • Patel UD; Center of Innovation to Accelerate Discovery and Practice Transformation (ADAPT), Durham Veterans Affairs Health Care System.
  • Lewinski AA; Division of General Internal Medicine, Duke University School of Medicine.
  • Davenport CA; School of Nursing.
  • Pendergast J; Department of Psychiatry and Behavioral Sciences, Duke University.
  • Oakes M; Division of Nephrology, Duke University School of Medicine, Durham, NC.
  • Crowley MJ; Gilead Sciences, Inc., Foster City, CA.
  • Zullig LL; Department of Population Health Sciences, Duke University.
  • Patel S; School of Nursing.
  • Moaddeb J; Department of Biostatistics and Bioinformatics.
  • Miller J; Department of Biostatistics and Bioinformatics.
  • Malone S; Department of Population Health Sciences, Duke University.
  • Barnhart H; Center of Innovation to Accelerate Discovery and Practice Transformation (ADAPT), Durham Veterans Affairs Health Care System.
  • Diamantidis CJ; Division of Endocrinology.
Med Care ; 2024 Jul 18.
Article en En | MEDLINE | ID: mdl-39038105
ABSTRACT
BACKGROUND/

OBJECTIVE:

Slowing the progression of diabetic kidney disease (DKD) is critical. We conducted a randomized controlled trial to target risk factors for DKD progression.

METHODS:

We evaluated the effect of a pharmacist-led intervention focused on supporting healthy behaviors, medication management, and self-monitoring on decline in estimated glomerular filtration rate (eGFR) for 36 months compared with an educational control.

RESULTS:

We randomized 138 individuals to the intervention group and 143 to control. At baseline, mean (SD) eGFR was 80.7 (21.7) mL/min/1.73m2, 56% of participants had chronic kidney disease and a history of uncontrolled hypertension with a baseline SBP of 134.3 mm Hg. The mean (SD) decline in eGFR by cystatin C from baseline to 36 months was 5.0 (19.6) and 5.9 (18.6) mL/min/1.73m2 for the control and intervention groups, respectively, with no significant between-group difference (P=0.75).

CONCLUSIONS:

We did not observe a significant difference in clinical outcomes by study arm. However, we showed that individuals with DKD will engage in a pharmacist-led intervention. The potential explanations for a lack of change in DKD risk factors can be attributed to 5 broad issues, challenges (1) associated with enrolling patients with low eGFR and poor BP control; (2) implementing the intervention; (3) limited duration during which to observe any clinical benefit from the intervention; (4) potential co-intervention or contamination; and (5) low statistical power.

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2024 Tipo del documento: Article