Arogundade Fatiu A, Omotoso Bolanle Aderonke, Sanusi Abubakr Abefe, Balogun Rasheed A
Clin Nephrol. 2020 Supplement-Jan;93(1):8-16. doi: 10.5414/CNP92S102.
Acute kidney injury (AKI) is prevalent and is associated with high morbidity and mortality globally. The epidemiology differs remarkably between developing and developed economies. Infections, diarrheal illnesses, obstetric causes and nephrotoxins are very rampant in the tropics. Even though the etiologies are different, the final common pathway in the pathogenesis is similar - tubular damage or necrosis, tubular blockage, and back leak of glomerular filtrate. The mechanism of AKI in infections could be through ischemic insult consequent to hypovolemia and/or hemoglobinuria, as seen in malaria and viral hemorrhagic fevers, interstitial inflammation, or nephrotoxicity. On the contrary, the mechanism of nephrotoxin-induced AKI includes direct toxic effect on the renal tubules, intratubular precipitation of substances like djenkolic and oxalic acids (crystalluria) as well as intratubular obstruction and AKI. Toxicity could also be indirect by interacting with the pharmacokinetic profile of other coadministered medications. Bites and envenomation as well as obstetric complications also induce AKI through hypovolemia, interstitial nephritis, and other unclear mechanisms in eclampsia and preeclampsia. Outcome is variable and dependent on etiology. Prognosis appears to be significantly better in hypovolemic or prerenal and/or obstructive AKI compared to intrarenal or intrinsic AKI.
急性肾损伤(AKI)在全球范围内普遍存在,且与高发病率和死亡率相关。发展中经济体和发达经济体的流行病学情况差异显著。感染、腹泻性疾病、产科病因和肾毒素在热带地区非常猖獗。尽管病因不同,但发病机制中的最终共同途径相似——肾小管损伤或坏死、肾小管阻塞以及肾小球滤过液的回漏。感染性AKI的机制可能是由于低血容量和/或血红蛋白尿导致的缺血性损伤,如在疟疾和病毒性出血热中所见,也可能是间质炎症或肾毒性。相反,肾毒素诱导的AKI机制包括对肾小管的直接毒性作用、管腔内物质如豆科酸和草酸的沉淀(结晶尿)以及管腔内阻塞和AKI。毒性也可能通过与其他同时使用药物的药代动力学特征相互作用而间接产生。咬伤和中毒以及产科并发症也通过低血容量、间质性肾炎以及子痫和先兆子痫中其他不明机制诱发AKI。结局各不相同,且取决于病因。与肾内或固有性AKI相比,低血容量性或肾前性和/或梗阻性AKI的预后似乎明显更好。