Table 2.
Authors | Excluded Comorbidity to Define CKDu | Comorbidity Status |
---|---|---|
ChannaJayasumana et al. [20] | DM or chronic and/or severe HTN, history of snakebite, urological disease of known etiology, glomerulonephritis | Not mentioned |
VanDervort DR. [21] | Not mentioned | Not mentioned |
SA. Hamilton et al. [22] | DM, HTN, and Heavy Proteinuria | Obese = 54, HIV positive = 3, Overweight = 177 |
M Gonzalez et al. [23] | Self-reported CKD, DM, or HTN | Not mentioned |
E Siriwardhana et al. [24] | DM, long-standing HTN, glomerular nephritis, urolithiasis, congenital kidney diseases, history of snake bite and leptospirosis | Not mentioned |
N Jayatilake et al. [16] | Glomerulonephritis, pyelonephritis, renal calculi or snake bite, hypertension | Not mentioned |
S Nanayakkara [25] | History of DM and HbA1c >6.5% or HTNor other known renal diseases such as autoimmune diseases, glomerular nephritis, Fanconi syndrome or IgA nephropathy | NCDs = 43% |
L Lopez et al. [26] | HTN, DM, glomerulopathies, polycystic kidney disease and obstructive kidney disease, HIV positivity | Glomerulomegally(73.3%), Tubular atrophy(89.1%), Mono nuclear inflammatory infiltration, Intimal proliferation, thickening of the tunica media in blood vessels |
T Rango et al. [27] | Not mentioned | Normal weight =72 , Underweight = 34). Overweight = 27, and Obese= 1. |
K Gobalarajah et al. [28] | The patients’ disease history revealed that they were secondarily diagnosed with DM & HTN only after they developed CKDu. | DM & HTN, but these are secondarily developed. |
S Mascarenhas et al. [29] | DM & HTN | |
JM jayaseka ra et al. [30] | DM, HTN, UTI or other renal diseases in the history | Not mentioned |
E Siriwardhana et al. [31] | DM, long-standing HTN, glomerular nephritis, urolithiasis, and congenital kidney diseases and having a history of snake bite and leptospirosis | Not mentioned |
MA Jayasumana [32] | Not mentioned | Not mentioned |
R Osorio et al. [33] | Antecedents of renal disease, DM, HTN, UTI | Not mentioned |
X Xing et al. [34] | Secondary renal damage, chronic glomerulonephritis, nephritic syndrome, polycystic kidney disease | Hepatitis, tuberculosis, acute and chronic glomerulonephritis, respiratory infections, Urinary calculus and urinary tract infection (UTI), hydronephrosis(50 individuals) |
R Chandrajith et al. [35] | Not mentioned | Anaemia is mild in the early stage of CKD, HTN in the late stage, edema is a late feature.Tubular atrophy and glomerular sclerosis |
M Selvarajah et al. [36] | DM, chronic or severe HTN, snake bite, glomerulonephritis or urological diseases, active renal or peri-renal infection, structural and anatomical renal abnormalities of the kidney, cysts and renal masses and those with a solitary kidney, coagulopathy, and uncontrolled HTN. | Not mentioned |
Nanayakkara et al. [37] | Not clearly stated | Not mentioned |
N Athuraliya et al. [38] | HTN, DM | Co-morbidity status among CKDu: Not Mentioned |
de Silva MW et al. [39] | DM, HTN, UTI or other diseases likely toaffect renal function | Interstitial nephritis in all CKDu cases |
S Wijetunge et al. [40] | DM and long-standingessential HTN | Glomerular sclerosis (GS), Interstitial fibrosis (IF), Interstitial inflammation (II), Tubular atrophy (TA) and Hypertension associated changes in blood vessels |
Siddarth et al. [41] | DM and any other known causes of CKD such as chronic glomerulonephritis, hypertensive nephrosclerosis, autosomal dominant polycystic kidney disease, chronic tubulointerstitial nephropathy or evidence of systemic/local (UTI) infection | Not mentioned |
B Guttierrez et al. [42] | T2DM, essential HTN, glomerulonephritis, infections, drugs | Not mentioned |
S Sayanthooran et al. [43] | DM, chronic or severe HTN snake bite, glomerulonephritis or urological diseases | Asthma = 3 |
T2DM: type 2 diabetes mellitus, CKD: chronic kidney disease, HTN: hypertension, DM: diabetes mellitus, NCDs non-communicable diseases, UTI: urinary tract infection.