Primary prevention

The evidence for the prevention of CKD is lacking as compared with large-scale randomised trials for cardiovascular disease. Most trials have focused on modifiable diseases and risk factors that have been associated with CKD, namely diabetes and hypertension. Clinical evidence supports the recommendation for a goal HbA1c <7%, blood pressure target of <140/90 mmHg, tobacco cessation, and ideal body weight with BMI <27 to prevent the development of CKD.[30][27][43] Due to the lack of widespread screening guidelines with serum creatinine or urinary albumin, often patients are diagnosed after CKD has developed.[44]

Secondary prevention

Prevention of further kidney function loss is the primary goal in conservative management of people with CKD.[145] Kidney-preserving care includes non-pharmacological (e.g., dietary and lifestyle adjustments) and pharmacological strategies.[145] Underlying risk factors associated with disease states should be treated, including optimisation of glycaemic control in diabetes and achievement of the goal blood pressure of <140/90 mmHg with ACE inhibitors or angiotensin-II receptor antagonists. Consideration can be given to a lower blood pressure goal in those with proteinuria of >500 mg per 24 hours.[79][80][86] Although data are limited in the CKD population as compared with the general population, tobacco cessation, weight loss, salt restriction, and optimal lipid management with statin therapy are indicated. Protein restriction is recommended in late-stage (GFR category G4 or G5) disease, as a management strategy to delay the initiation of dialysis; however, severe protein restriction may result in malnourishment and impact on quality of life.[120] Aspirin use has also been beneficial for cardioprotection in those with CKD, although there is a higher risk for minor bleeding than in the general population.

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