Children Kidney Injury after Hematopoietic Stem Cell Transplant: History
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor: , ,

Hematopoietic cell transplant (HCT), used for treatment of many malignant and non-malignant pediatric diseases, is associated with serious complications, limiting this therapy’s benefit. Acute kidney injury (AKI), seen often after HCT, can occur at different stages of the transplant process and contributes to morbidity and mortality after HCT. The etiology of AKI is often multifactorial, including kidney hypo-perfusion, nephrotoxicity from immunosuppressive and antimicrobial agents, and other transplant-related complications such as transplant-associated thrombotic microangiopathy and sinusoidal obstructive syndrome. Early recognition of AKI is crucial to prevent further AKI and associated complications. Initial management includes identifying the etiology of AKI, preventing further kidney hypo-perfusion, adjusting nephrotoxic medications, and preventing fluid overload. Some patients will require further support with kidney replacement therapy to manage fluid overload and AKI.

  • hematopoietic cell transplant
  • kidney injury
  • renal replacement therapy
  • thrombotic microangiopathy
  • continuous kidney replacement therapy

1. Acute Kidney Injury

Acute kidney injury (AKI) is a relatively common complication after hematopoietic cell transplant (HCT), with a reported incidence rate of 21–84% [1][2].  Common risk factors for kidney injury include myeloablative conditioning, older age, acute graft versus host disease (GVHD), and sinusoidal obstruction syndrome (SOS). Satwani et al. observed a significant increase in the incidence of kidney injury in children who received myeloablative conditioning versus reduced intensity conditioning (45.7% and 17.1% respectively) [3]. In addition to its contribution to a higher rate of mortality, previous AKI predisposes patients to chronic kidney disease (CKD). In a cohort of 158 adult allogeneic HCT survivors, the risk of chronic kidney disease (CKD) ≥ stage 3 was approximately 10-fold higher in patients in whom AKI developed following HCT [4]. AKI is encountered at any stage in the transplant process, although often at the earlier stages. Early in the pre-transplant phase, many children receive myeloablative conditioning regimen with or without total body irradiation (TBI) that can induce kidney injury. Shortly after transplant, nephrotoxic immunosuppressive medications such as calcineurin inhibitors are given to mitigate the risk of GVHD. In addition, children are at a higher risk of infection and subsequent sepsis due to their immune-compromised status. In many instances, the etiology of AKI is multifactorial and includes hypoperfusion in the setting of capillary leak or sepsis resulting in acute tubular necrosis, drug induced nephrotoxicity, thrombotic microangiopathy (TMA), and sinusoidal obstruction syndrome (SOS) (Figure 1) [1]. Drug induced nephrotoxicity is relatively common in HCT patients. Antimicrobials that are often used to treat infections post HCT such as aminoglycoside, vancomycin, or amphotericin can induce direct kidney injury. Nephrotoxicity is also encountered with calcineurin inhibitors such as cyclosporin or tacrolimus that can cause kidney arteriolar vasoconstriction via activation of the renin–angiotensin–aldosterone system [5]. In addition, calcineurin inhibitors may trigger endothelial injury and subsequent thrombotic microangiopathy (TMA) [6]. Moreover, kidneys can be a target of GVHD, although less described than other organs like skin, liver, and lungs. Kidney injury related to GVHD is mediated by donor T-cells as well as proinflammatory cytokines. Kidney GVHD can present as AKI, nephrotic syndrome, glomerulonephritis, and TMA [7]. However, the most common presentation is nephrotic syndrome with a high degree of proteinuria, hypoalbuminemia, and edema. Hemorrhagic cystitis can cause obstructive kidney injury when clots in the bladder obstruct the outflow tract. The etiology of hemorrhagic cystitis is usually multifactorial, but often encountered with the use of cyclophosphamide or in the context of reactivation of virus infections such as BK virus, adenovirus, and cytomegalovirus. Treatment include hyperhydration, diuresis, and bladder irrigation with a three-way bladder catheter.
/media/item_content/202305/6473fb940bf66curroncol-30-00253-g001.png
Figure 1. Etiologies of AKI in children following HCT. SOS, sinusoidal obstructive syndrome; TMA, thrombotic microangiopathy; aGVHD, acute graft versus host disease; CART, Chimeric antigen receptor (CAR) T-cell therapy.

2. Special Disease Conditions Post HCT That Are Associated with AKI

2.1. Transplant-Associated Thrombotic Microangiopathy

Transplant-associated thrombotic microangiopathy (TA-TMA) is a life-threatening complication that is encountered early in the post-HCT phase. The incidence of TA-TMA in children is 16%, with a median onset of 47 days post-transplant [8]. Risk factors for TA-TMA include acute GVHD, infectious process (especially viral), mismatched donor, multiple HCTs, and myeloablative conditioning [8]. The pathophysiology of TA-TMA involves an initial endothelial injury triggered by factors such as chemotherapy or infection that results in an increase in the proinflammatory cytokines, procoagulant factors, and soluble adhesion molecules. This combination promotes further endothelial injury and initiates and propagates the complement cascade, resulting in platelet aggregation, fibrin deposition, and microthrombi formation.
Eculizumab is a monoclonal antibody against the complement component C5, which blocks the formation of the membrane attack complex (MAC or C5b-9) and thus prevents endothelial damage. In a cohort of 64 pediatric HCT patients with high-risk TA-TMA and multiorgan dysfunction, the survival rate improved dramatically with the use of eculizumab (66% in 1-year post HCT in treated vs 16.7% in a previously reported untreated cohort) [9].

2.2. Sinusoidal Obstruction Syndrome

Sinusoidal obstruction syndrome (SOS) is associated with multiorgan dysfunction and a high mortality rate [10]. SOS occurs in the early stage post HCT secondary to cytotoxic therapy or radiotherapy [11]. The incidence rate is 20–60%. Diagnosis of SOS is based on the following criteria (two or more criteria present) [12]:
  • Consumptive and transfusion-refractory thrombocytopenia;
  • Weight gain on 3 consecutive days despite the use of diuretics, or a weight gain of >5% above baseline weight within 72 h;
  • Increase in bilirubin from baseline on 3 consecutive days, or bilirubin ≥ 2 mg/dL within 72 h;
  • Hepatomegaly (best if supported by imaging) above baseline value;
  • Ascites (best if supported by imaging) above baseline.
Kidney injury in SOS is attributed to hypoperfusion and vasoconstriction and is associated with fluid overload. Managing the kidney injury requires fluid restriction and use of diuretics to reduce fluid overload. Renal replacement therapy may be necessary if fluid overload persists, and urine output remains inadequate despite diuretic treatment [13].

2.3. Fluid Overload

Fluid overload (FO) is common in critically ill children and negatively affects outcome [14][15]. Additionally, FO can exacerbate kidney injury by worsening kidney venous hypertension, impairing perfusion pressure capacity of the glomerular capillaries. Cumulative fluid balance is often used interchangeably with fluid overload and is calculated as follows: Fluid intake – Fluid output (L)/ICU admission weight (kg) × 100 [16]. FO can also be calculated by comparing current weight to admission weight if fluid balance information is not available. FO > 10% is common in critically ill children and was observed in 33% of a large cohort of 1017 critically ill children [14]. FO was associated with higher risk of mortality, kidney adverse events, and increased duration of mechanical ventilation (MV) and ICU stay. A metanalysis including 44 pediatric studies showed a 6% increase in odds of mortality with each 1% increase in FO [15]. The adverse effect of FO is also prevalent in the pediatric HCT population [17][18].

2.4. CAR T-Cell Therapy

Chimeric antigen receptor (CAR) T-cell therapy, used for treatment of hematologic malignancies, involves the utilization of engineered cytotoxic T-cell to recognize specific tumor antigen. AKI occurs with this therapy secondary to cytokine release syndrome (CRS), a well described complication of this therapy which can lead to organ dysfunction. Hypoperfusion secondary to capillary leak and proinflammatory cytokines contribute to AKI encountered post CAR-T cell therapy. AKI is usually mild in these cases [19].

3. Continuous Kidney Replacement Therapy

Nearly one-third of patients with AKI require kidney replacement therapy (KRT) [1]. Continuous kidney replacement therapy (CKRT) is used often in the ICU to deliver KRT because it is tolerated better than intermittent hemodialysis (IHD) in hemodynamically unstable critically ill children. During CKRT, fluid removal and solute clearance occur continuously, promoting better control of fluid status. Solute clearance occurs by either convection, diffusion, or both, whereas fluid is removed via ultrafiltration. Hemofiltration modes of CKRT can increase removal of small and medium-sized solutes by convection (solute drag); in contrast, hemodialysis modes mainly remove small-sized molecules by diffusion (concentration gradient).
No consensus exists on the optimal time for initiation of CKRT and whether early initiation can improve outcome. Most evidence is from adult randomized trials that compared the early initiation of CKRT to using a standard strategy. One of the largest adult trials, the STARRT-AKI trial, randomized 3019 critically ill adults with AKI to either an accelerated RRT strategy (initiated within 12 h in adult critically ill patients with Stage 2 or Stage 3 AKI) or a standard strategy. The accelerated RRT strategy did not reduce mortality compared to the standard strategy, and survivors of the accelerated RRT strategy had a higher risk of adverse events and dependence on kidney replacement therapy [20]. In contrast, in the ELAIN trial that included 231 critically ill patients with AKI, a lower mortality in the early RRT group compared to the delayed initiation group was observed (39% versus 54% respectively) [21]

4. Transition from CKRT to IHD/Discontinuation of CKRT

The optimal timing for successful discontinuation of CKRT or switch to IHD is difficult to predict. Renal recovery is usually preceded by an increase in urine output. Urine output > 500 cc/day is used in some adult patients as a criterion to discontinue KRT [22]. Factors that have been shown to predict successful liberation include the hourly urine output within 12 h before CKRT discontinuation, serum creatinine level within 24 h before liberation, and the cumulative fluid balance (from ICU admission to CKRT discontinuation) [23]. In general, children are switched from CKRT to IHD when FO is resolved and they are hemodynamically stable.

5. Outcomes of KRT

ICU mortality in children post HCT requiring CKRT is estimated to be 52–65% [2][24]. The 1-year overall survival rate is also poor (27.4% (95% CI: 16–40.5%, p < 0.0001)) [1]. Reported factors that are associated with mortality include FO > 10%, mechanical ventilation, vasoactive support, and neutropenia at the end of CKRT [2].

6. Biomarkers of AKI in Children with HCT

Given the potential shortcomings of sCr as a marker of AKI, several additional biomarkers of AKI have been developed and studied. These biomarkers measure either glomerular function or renal tubular damage and can aid in early detection of AKI (Table 1).
Table 1. Biomarkers in AKI.
Biomarker Characteristic Detection Time Peak AUC for AKI Detection Limitations
Glomerular injury
Cystatin C 13-kDa protein that is present in all nucleated cells, protease inhibitor 2–48 h 6–8 h   Influenced by inflammation, muscle mass, and high-dose steroids
Renal tubular injury
NGAL 25-kDa protein of the family of lipocalins with bacteriostatic function 2–24 h 6–12 h 0.8 (0.72–0.87) False elevation in sepsis and malignancy
NAG >130-kDa proximal tubular lysosomal enzyme 2–4 h   0.6 Elevated in diabetes and albuminuria
KIM 1 38.7-kDa type I transmembrane glycoprotein 1–24 h   0.85 Slow rise and non-specific
May be elevated in the settings of chronic proteinuria and inflammatory diseases
Interleukin-18 24-kDa cytokine 4–48 h 12 h 0.75 Low sensitivity/specificity
L-FABP 14-kDa lipid binding protein 12–72 h     May lose its specificity when liver disease is present
TIMP 2 21-kDa protein, endogenous inhibitor of metalloproteinase activities, involved in G1 cycle arrest 1–12 h   0.8 Proteinuria interferes with the test results
Elevated in diabetes
IGFBP7 29-kDa protein, IGF-1 receptor antagonist, involved in G1 cycle arrest     0.76  
NGAL, Neutrophil gelatinase-associated lipocalin; KIM-1, Kidney injury molecule-1; L-FABP, Liver type fatty acid binding protein; TIMP 2, Tissue inhibitor of metalloproteinase 2; IGFBP7, insulin-like growth factor-binding protein-7.

7. Tubular Injury Markers

Several tubular injury markers have been described and investigated for their utility in early recognition of AKI. Neutrophil gelatinase-associated lipocalin (NGAL) levels are elevated in the urine early after ischemic, septic, or toxic injury and precede the rise in serum creatinine levels by 48 h [25]. In addition, urine NGAL can differentiate intrinsic renal damage (where it is elevated) from prerenal acute injury related to hemodynamic alterations due to hypovolemia [26]. N-acetyl-beta-D-glycosaminidase (NAG) urine level is highly specific to tubular injury [27]. Kidney injury molecule-1 (KIM-1) participates in both kidney injury and healing processes [28].
Fatty acid-binding protein 1 is another early biomarker of AKI and can predict the need for dialysis [29]. An increased level of L-FABP at the time of ICU admission is associated with higher risk of AKI and mortality rate [30][31]. The NGAL and L-FABP combination can predict renal recovery after AKI (higher levels associated with non-recovery) [32]. Urinary IL-18 level can predict the initiation of RRT and mortality [33][34]. The combined product of tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulin-like growth factor–binding protein-7 (IGFBP-7), expressed as [TIMP-2] [IGFBP7], predicts the risk of AKI as well as the need for CKRT and death in critically ill adults [35][36].

8. Chronic Kidney Disease

CKD in children post HCT has a reported incidence of 48%. CKD is defined by estimated GFR < 90 mL/min/1.73 BSA or presence of markers of kidney damage for >3 months [37]. CKD can develop as early as 6 months and up to 10 years following transplant. Incidence of CKD in this population is 10-fold higher than in the healthy population. In a cohort of 1635 adult and pediatric HCT patients, CKD developed in 23% [38].
The most common etiologies and risk factors for CKD development are TMA, total body irradiation, nephrotic syndrome, AKI, acute GVHD, and drug toxicity (calcineurin inhibitors) [39]. Estimated GFR at the time of AKI is an important risk factor for the development of CKD. In a cohort of 275 children post allogeneic HCT, CKD developed in 69.5% and 69.8% at 1 and 3 years if GFR was < 80 mL/min/1.73 m2 at the initial AKI episode [40].
Albuminuria (albumin-to-creatinine ratio over 30 mg/g) is an important parameter to monitor in children post HCT during long-term follow-up for early recognition of CKD. Albuminuria is relatively common (detected in 50% of patients one-year post HCT) [41]. Furthermore, albuminuria at day 100 was associated with CKD at 1 year (OR = 4.0; 95% CI = 1.1 to 14.6). Proteinuria at day 100 conveyed a six-fold increase in the risk of non-relapse mortality by 1 year post HCT. Moreover, hypertension seen in 20–70% of patients post HCT can contribute to the development and progression of CKD [42]. Close monitoring for the development of hypertension is warranted for children post HCT and should follow similar guidelines for the detection and management of hypertension in children in other settings, including obtaining 24-h ambulatory blood pressure monitoring when available [43].

This entry is adapted from the peer-reviewed paper 10.3390/curroncol30030253

References

  1. Raina, R.; Abu-Arja, R.; Sethi, S.; Dua, R.; Chakraborty, R.; Dibb, J.T.; Basu, R.K.; Bissler, J.; Felix, M.B.; Brophy, P.; et al. Acute kidney injury in pediatric hematopoietic cell transplantation: Critical appraisal and consensus. Pediatr. Nephrol. 2022, 37, 1179–1203.
  2. Elbahlawan, L.; Bissler, J.; Morrison, R.R. Continuous Renal Replacement Therapy: A Review of Use and Application in Pediatric Hematopoietic Stem Cell Transplant Recipients. Front. Oncol. 2021, 11, 632263.
  3. Satwani, P.; Bavishi, S.; Jin, Z.; Jacobson, J.S.; Baker, C.; Duffy, D.; Lowe, L.; Morris, E.; Cairo, M.S. Risk factors associated with kidney injury and the impact of kidney injury on overall survival in pediatric recipients following allogeneic stem cell transplant. Biol. Blood Marrow Transplant. 2011, 17, 1472–1480.
  4. Ando, M.; Ohashi, K.; Akiyama, H.; Sakamaki, H.; Morito, T.; Tsuchiya, K.; Nitta, K. Chronic kidney disease in long-term survivors of myeloablative allogeneic haematopoietic cell transplantation: Prevalence and risk factors. Nephrol. Dial. Transplant. 2010, 25, 278–282.
  5. Prókai, Á.; Csohány, R.; Sziksz, E.; Pap, D.; Balicza-Himer, L.; Boros, S.; Magda, B.; Vannay, Á.; Kis-Petik, K.; Fekete, A.; et al. Calcineurin-inhibition Results in Upregulation of Local Renin and Subsequent Vascular Endothelial Growth Factor Production in Renal Collecting Ducts. Transplantation 2016, 100, 325–333.
  6. Wanchoo, R.; Bayer, R.L.; Bassil, C.; Jhaveri, K.D. Emerging Concepts in Hematopoietic Stem Cell Transplantation-Associated Renal Thrombotic Microangiopathy and Prospects for New Treatments. Am. J. Kidney Dis. 2018, 72, 857–865.
  7. Catherine Joseph, J.R.A.; Benjamin, L. Laskin, sangeeta hingorani. Hematopoietic cell transplant associated kidney injury. In Onco-Nephrology; Elsevier: Amsterdam, The Netherlands, 2020; pp. 89–98.
  8. Van Benschoten, V.; Roy, C.; Gupta, R.; Ouellette, L.; Hingorani, S.; Li, A. Incidence and Risk Factors of Transplantation-Associated Thrombotic Microangiopathy: A Systematic Review and Meta-Analysis. Transplant. Cell Ther. 2022, 28, 266.e261–266.e268.
  9. Jodele, S.; Dandoy, C.E.; Lane, A.; Laskin, B.L.; Teusink-Cross, A.; Myers, K.C.; Wallace, G.; Nelson, A.; Bleesing, J.; Chima, R.S.; et al. Complement blockade for TA-TMA: Lessons learned from a large pediatric cohort treated with eculizumab. Blood 2020, 135, 1049–1057.
  10. Coppell, J.A.; Richardson, P.G.; Soiffer, R.; Martin, P.L.; Kernan, N.A.; Chen, A.; Guinan, E.; Vogelsang, G.; Krishnan, A.; Giralt, S.; et al. Hepatic veno-occlusive disease following stem cell transplantation: Incidence, clinical course, and outcome. Biol. Blood Marrow Transplant. 2010, 16, 157–168.
  11. Bonifazi, F.; Barbato, F.; Ravaioli, F.; Sessa, M.; Defrancesco, I.; Arpinati, M.; Cavo, M.; Colecchia, A. Diagnosis and Treatment of VOD/SOS After Allogeneic Hematopoietic Stem Cell Transplantation. Front. Immunol. 2020, 11, 489.
  12. Mohty, M.; Malard, F.; Abecassis, M.; Aerts, E.; Alaskar, A.S.; Aljurf, M.; Arat, M.; Bader, P.; Baron, F.; Bazarbachi, A.; et al. Sinusoidal obstruction syndrome/veno-occlusive disease: Current situation and perspectives-a position statement from the European Society for Blood and Marrow Transplantation (EBMT). Bone Marrow Transplant. 2015, 50, 781–789.
  13. Mahadeo, K.M.; McArthur, J.; Adams, R.H.; Radhi, M.; Angelo, J.; Jeyapalan, A.; Nicol, K.; Su, L.; Rabi, H.; Auletta, J.J.; et al. Consensus Report by the Pediatric Acute Lung Injury and Sepsis Investigators and Pediatric Blood and Marrow Transplant Consortium Joint Working Committees on Supportive Care Guidelines for Management of Veno-Occlusive Disease in Children and Adolescents: Part 2-Focus on Ascites, Fluid and Electrolytes, Renal, and Transfusion Issues. Biol. Blood Marrow Transplant. 2017, 23, 2023–2033.
  14. Alobaidi, R.; Basu, R.K.; DeCaen, A.; Joffe, A.R.; Lequier, L.; Pannu, N.; Bagshaw, S.M. Fluid Accumulation in Critically Ill Children. Crit. Care Med. 2020, 48, 1034–1041.
  15. Alobaidi, R.; Morgan, C.; Basu, R.K.; Stenson, E.; Featherstone, R.; Majumdar, S.R.; Bagshaw, S.M. Association Between Fluid Balance and Outcomes in Critically Ill Children: A Systematic Review and Meta-analysis. JAMA Pediatr. 2018, 172, 257–268.
  16. Goldstein, S.L.; Currier, H.; Graf, C.; Cosio, C.C.; Brewer, E.D.; Sachdeva, R. Outcome in children receiving continuous venovenous hemofiltration. Pediatrics 2001, 107, 1309–1312.
  17. Raymakers-Janssen, P.; Lilien, M.R.; Tibboel, D.; Kneyber, M.C.J.; Dijkstra, S.; van Woensel, J.B.M.; Lemson, J.; Cransberg, K.; van den Heuvel-Eibrink, M.M.; Wosten-van Asperen, R.M. Epidemiology and Outcome of Critically Ill Pediatric Cancer and Hematopoietic Stem Cell Transplant Patients Requiring Continuous Renal Replacement Therapy: A Retrospective Nationwide Cohort Study. Crit. Care Med. 2019, 47, e893–e901.
  18. Elbahlawan, L.; Morrison, R.; Li, Y.; Huang, S.; Cheng, C.; Avent, Y.; Madden, R. Outcome of Acute Respiratory Failure Secondary to Engraftment in Children After Hematopoietic Stem Cell Transplant. Front. Oncol. 2020, 10, 584269.
  19. Gutgarts, V.; Jain, T.; Zheng, J.; Maloy, M.A.; Ruiz, J.D.; Pennisi, M.; Jaimes, E.A.; Perales, M.A.; Sathick, J. Acute Kidney Injury after CAR-T Cell Therapy: Low Incidence and Rapid Recovery. Biol. Blood Marrow Transplant. 2020, 26, 1071–1076.
  20. Bagshaw, S.M.; Wald, R.; Adhikari, N.K.J.; Bellomo, R.; da Costa, B.R.; Dreyfuss, D.; Du, B.; Gallagher, M.P.; Gaudry, S.; Hoste, E.A.; et al. Timing of Initiation of Renal-Replacement Therapy in Acute Kidney Injury. N. Engl. J. Med. 2020, 383, 240–251.
  21. Zarbock, A.; Kellum, J.A.; Schmidt, C.; Van Aken, H.; Wempe, C.; Pavenstädt, H.; Boanta, A.; Gerß, J.; Meersch, M. Effect of Early vs Delayed Initiation of Renal Replacement Therapy on Mortality in Critically Ill Patients With Acute Kidney Injury: The ELAIN Randomized Clinical Trial. Jama 2016, 315, 2190–2199.
  22. Mendu, M.L.; Ciociolo, G.R., Jr.; McLaughlin, S.R.; Graham, D.A.; Ghazinouri, R.; Parmar, S.; Grossier, A.; Rosen, R.; Laskowski, K.R.; Riella, L.V.; et al. A Decision-Making Algorithm for Initiation and Discontinuation of RRT in Severe AKI. Clin. J. Am. Soc. Nephrol. 2017, 12, 228–236.
  23. Liu, C.; Peng, Z.; Dong, Y.; Li, Z.; Andrijasevic, N.M.; Albright, R.C., Jr.; Kashani, K.B. Predicting successful continuous renal replacement therapy liberation in critically ill patients with acute kidney injury. J. Crit. Care 2021, 66, 6–13.
  24. Elbahlawan, L.; Morrison, R.R. Continuous renal replacement therapy in children post-hematopoietic stem cell transplantation: The present and the future. Curr. Stem. Cell Res. Ther. 2012, 7, 381–387.
  25. Charlton, J.R.; Portilla, D.; Okusa, M.D. A basic science view of acute kidney injury biomarkers. Nephrol. Dial. Transplant. 2014, 29, 1301–1311.
  26. Nickolas, T.L.; Schmidt-Ott, K.M.; Canetta, P.; Forster, C.; Singer, E.; Sise, M.; Elger, A.; Maarouf, O.; Sola-Del Valle, D.A.; O’Rourke, M.; et al. Diagnostic and prognostic stratification in the emergency department using urinary biomarkers of nephron damage: A multicenter prospective cohort study. J. Am. Coll. Cardiol. 2012, 59, 246–255.
  27. Augustynowicz, M.; Bargenda-Lange, A.; Kałwak, K.; Zwolińska, D.; Musiał, K. Markers of acute kidney injury in children undergoing hematopoietic stem cell transplantation. Adv. Clin. Exp. Med. 2019, 28, 1111–1118.
  28. Shao, X.; Tian, L.; Xu, W.; Zhang, Z.; Wang, C.; Qi, C.; Ni, Z.; Mou, S. Diagnostic value of urinary kidney injury molecule 1 for acute kidney injury: A meta-analysis. PLoS ONE 2014, 9, e84131.
  29. Susantitaphong, P.; Siribamrungwong, M.; Doi, K.; Noiri, E.; Terrin, N.; Jaber, B.L. Performance of urinary liver-type fatty acid-binding protein in acute kidney injury: A meta-analysis. Am. J. Kidney Dis. 2013, 61, 430–439.
  30. Suzuki, G.; Ichibayashi, R.; Yamamoto, S.; Nakamichi, Y.; Watanabe, M.; Honda, M. Clinical significance of urinary L-FABP in the emergency department. Int. J. Emerg. Med. 2019, 12, 24.
  31. Suzuki, G.; Ichibayashi, R.; Yamamoto, S.; Serizawa, H.; Nakamichi, Y.; Watanabe, M.; Honda, M. Urinary liver-type fatty acid-binding protein variation as a predictive value of short-term mortality in intensive care unit patients. Ren. Fail. 2021, 43, 1041–1048.
  32. Zeng, X.F.; Li, J.M.; Tan, Y.; Wang, Z.F.; He, Y.; Chang, J.; Zhang, H.; Zhao, H.; Bai, X.; Xie, F.; et al. Performance of urinary NGAL and L-FABP in predicting acute kidney injury and subsequent renal recovery: A cohort study based on major surgeries. Clin. Chem. Lab. Med. 2014, 52, 671–678.
  33. Gauer, S.; Sichler, O.; Obermüller, N.; Holzmann, Y.; Kiss, E.; Sobkowiak, E.; Pfeilschifter, J.; Geiger, H.; Mühl, H.; Hauser, I.A. IL-18 is expressed in the intercalated cell of human kidney. Kidney Int. 2007, 72, 1081–1087.
  34. Gonzalez, F.; Vincent, F. Biomarkers for acute kidney injury in critically ill patients. Minerva Anestesiol 2012, 78, 1394–1403.
  35. Kashani, K.; Al-Khafaji, A.; Ardiles, T.; Artigas, A.; Bagshaw, S.M.; Bell, M.; Bihorac, A.; Birkhahn, R.; Cely, C.M.; Chawla, L.S.; et al. Discovery and validation of cell cycle arrest biomarkers in human acute kidney injury. Crit. Care 2013, 17, 1–12.
  36. Xie, Y.; Ankawi, G.; Yang, B.; Garzotto, F.; Passannante, A.; Breglia, A.; Digvijay, K.; Ferrari, F.; Brendolan, A.; Raffaele, B.; et al. Tissue inhibitor metalloproteinase-2 (TIMP-2) • IGF-binding protein-7 (IGFBP7) levels are associated with adverse outcomes in patients in the intensive care unit with acute kidney injury. Kidney Int. 2019, 95, 1486–1493.
  37. Levey, A.S.; Eckardt, K.U.; Dorman, N.M.; Christiansen, S.L.; Cheung, M.; Jadoul, M.; Winkelmayer, W.C. Nomenclature for Kidney Function and Disease: Executive Summary and Glossary from a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference. Kidney Dis. Basel. 2020, 6, 309–317.
  38. Hingorani, S.; Guthrie, K.A.; Schoch, G.; Weiss, N.S.; McDonald, G.B. Chronic kidney disease in long-term survivors of hematopoietic cell transplant. Bone Marrow Transplant. 2007, 39, 223–229.
  39. Hingorani, S. Chronic kidney disease after pediatric hematopoietic cell transplant. Biol. Blood Marrow Transplant. 2008, 14, 84–87.
  40. Prasad, M.; Jain, N.G.; Radhakrishnan, J.; Jin, Z.; Satwani, P. Risk factors for chronic kidney disease following acute kidney injury in pediatric allogeneic hematopoietic cell transplantation. Bone Marrow Transplant. 2021, 56, 1665–1673.
  41. Hingorani, S.R.; Seidel, K.; Lindner, A.; Aneja, T.; Schoch, G.; McDonald, G. Albuminuria in hematopoietic cell transplantation patients: Prevalence, clinical associations, and impact on survival. Biol. Blood Marrow Transplant. 2008, 14, 1365–1372.
  42. Hingorani, S. Renal Complications of Hematopoietic-Cell Transplantation. N. Engl. J. Med. 2016, 374, 2256–2267.
  43. Flynn, J.T.; Kaelber, D.C.; Baker-Smith, C.M. Subcommittee on screening and management of high blood pressure in children. Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents. Pediatrics. Pediatrics 2017, 140, e20171904.
More
This entry is offline, you can click here to edit this entry!
Video Production Service