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Some studies suggest that volume loading, pressor agents, and early identification with hemodynamic optimization can protect kidneys, while other studies highlight the potential benefits of medications like candesartan, SGLT2 inhibitors, dihydroquercetin, and PDE5 inhibitors for chronic conditions.
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Kidney protection, especially in patients undergoing surgery or those with chronic kidney disease (CKD), is a critical area of medical research. Various pharmacological agents and interventions have been explored to mitigate renal damage and improve outcomes. This article synthesizes findings from multiple studies to provide an overview of effective medications and strategies for kidney protection.
Dopamine and its analogues have been extensively studied for their potential renal protective effects during the perioperative period. However, the evidence remains inconclusive. Several reviews have indicated that while dopamine may show some benefits in animal models, its efficacy in human trials is not well-supported .
Diuretics, including mannitol and frusemide, have been evaluated for their renal protective properties. Despite some positive outcomes in renal transplantation settings, their routine use in critically ill patients or during surgery is not recommended due to a lack of consistent evidence supporting their benefits .
Calcium channel blockers and angiotensin-converting enzyme (ACE) inhibitors are other classes of drugs investigated for renal protection. While some studies suggest potential benefits, the overall evidence is mixed, and no definitive conclusions can be drawn regarding their effectiveness in preventing acute kidney injury (AKI) during surgery .
NAC and other antioxidants have been explored for their ability to reduce oxidative stress and protect renal function. However, similar to other interventions, the results are heterogeneous, and more high-quality studies are needed to establish their efficacy.
SGLT2 inhibitors, primarily used for diabetes management, have shown promising renal protective effects. Studies indicate that SGLT2i can reduce the progression of CKD, lower the urine albumin/creatinine ratio, and maintain estimated glomerular filtration rate (eGFR) over time. These benefits appear to be independent of their glycemic effects, making them a potential therapeutic option for CKD patients.
DHQ, a natural dihydroflavone, has demonstrated significant antioxidant, anti-inflammatory, and antifibrotic properties in diabetic nephropathy models. It reduces urine microalbumin excretion, hyperglycemia, and lipid metabolism disorders, suggesting its potential as a renal protective agent.
PDE5 inhibitors, commonly used for erectile dysfunction, have shown reno-protective properties in animal studies. These drugs improve renal function and histopathological outcomes in various forms of AKI by enhancing regional hemodynamics and reducing oxidative stress and inflammation. However, human data are limited and inconclusive.
The use of balanced crystalloid fluids over hyperchloremic solutions has been shown to reduce the incidence of AKI. This approach, along with aggressive hemodynamic stabilization, is crucial for renal protection in perioperative and critical care settings.
Avoiding nephrotoxic drugs and ensuring adequate hydration are fundamental strategies for preventing AKI. These measures, combined with careful monitoring and early intervention, can significantly improve renal outcomes .
While numerous pharmacological agents have been investigated for kidney protection, the evidence remains mixed, and no single intervention has emerged as definitively effective. Emerging therapies like SGLT2 inhibitors and DHQ show promise, but further research is needed. Hemodynamic optimization and avoidance of nephrotoxic drugs remain critical components of renal protection strategies. Continued high-quality research is essential to develop effective interventions for kidney protection.
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