Antihypertensive prescribing patterns in non-dialysis dependent chronic kidney disease: Findings from the Salford

Rajkumar Chinnadurai1, Henry H L Wu2, Jones Abuomar3

  • 1Donal O'Donoghue Renal Research Centre & Department of Renal Medicine, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, United Kingdom. rajkumar.chinnadurai@nca.nhs.uk.

PubMed

Insights

Patients with chronic kidney disease (CKD) on three or more antihypertensive medications showed poorer outcomes. This highlights the need for optimized hypertension management in CKD patients.

Area of Science:

  • Nephrology
  • Cardiology
  • Clinical Pharmacy

Background:

  • Hypertension is a common comorbidity in chronic kidney disease (CKD) patients.
  • The relationship between hypertension and CKD is complex and bidirectional, complicating treatment.
  • Current antihypertensive treatment practices for CKD patients exhibit variability.

Purpose of the Study:

  • To analyze antihypertensive prescribing patterns in CKD patients using the Salford Kidney Study database.
  • To investigate the association between the number of antihypertensive agents prescribed and clinical outcomes in CKD.

Main Methods:

  • Analysis of prospective data from the Salford Kidney Study (recruiting since 2002).
  • Evaluation of antihypertensive prescription patterns relative to eGFR, urine albumin-creatinine ratio, CKD aetiology, and cardiovascular disease.
  • Cox regression and Kaplan-Meier analyses were used to assess associations with mortality and survival.

Main Results:

  • In 3,230 CKD patients, 53% with eGFR ≤ 15 mL/min/1.73 m² received ≥3 antihypertensives vs. 26% with eGFR ≥ 60 mL/min/1.73 m² (P < 0.001).
  • Prescription of ≥3 agents increased with higher urine albumin-creatinine ratio categories (62% in A3 vs. 40% in A1, P < 0.001), notably for renin-angiotensin system blockers.
  • Using ≥3 antihypertensives was linked to all-cause mortality (HR 1.15; 95% CI: 1.04-1.27, P = 0.006), irrespective of blood pressure control.

Conclusions:

  • Antihypertensive prescribing in the Salford Kidney Study aligns with UK guidelines but shows poorer outcomes with multiple agents and uncontrolled blood pressure.
  • Further research is needed to address variations in hypertension management for CKD patients globally.
Abstract

Related Concept Videos

Antihypertensive Drugs: Potassium-Sparing Diuretics01:28

Antihypertensive Drugs: Potassium-Sparing Diuretics

Liddle syndrome is a genetically inherited form of hypertension characterized by the overactivity of epithelial sodium channels in the nephron, the functional unit of the kidney. This heightened activity leads to increased sodium reabsorption and excessive excretion of potassium. To counteract this, potassium-sparing diuretics such as amiloride are used. They function by blocking these sodium channels, thereby reducing the influx of sodium into the epithelial cells and minimizing the loss of...
563
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
384
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
432
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
631
Hypertension and Regulation of Blood Pressure01:18

Hypertension and Regulation of Blood Pressure

Hypertension, the most common cardiovascular disease, is diagnosed through repeated measurements of elevated blood pressure. Its risks, including damage to the kidney, heart, and brain, are directly proportional to blood pressure levels. Starting from 115/75 mm Hg, the risk of cardiovascular disease doubles with each increment of 20/10 mm Hg. The diagnosis relies on blood pressure measurements, not on patient symptoms, as hypertension is often asymptomatic until end-organ damage is imminent or...
2.1K
Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

In patients with renal impairment, drugs undergo significant changes in their pharmacokinetics, which require dosage adjustments to ensure safe and effective therapy.
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
92