Research Article (Open access) |
---|
SSR
Inst. Int. J. Life. Sci., 5(6): 2428-2435, November
2019
Incidence
and Epidemiology of Acute Kidney Injury in Tertiary Care Centre in Gwalior
Chambal Region
Krishan
Kumar1, Neelima Singh2*, Sushma Trikha3, Nitin
Kr. Srivastava4, Archana Kansal3, Sutakshee Sonowani5
1Junior
Resident III, Department of Medicine, G. R. Medical College, Gwalior, India
2Associate
Professor, Department of Medicine, G. R. Medical College, Gwalior, India
3Professor,
Department of Medicine, G. R. Medical College, Gwalior, India
4Junior
Resident III, Department of Medicine, Lalit Narayan Mishra Railway Hospital,
Gorakhpur, India
5 Senior Resident, Department of Medicine, G. R. Medical College, Gwalior, India
*Address for Correspondence: Dr.
Neelima Singh, Associate Professor, Department of Medicine, G. R. Medical
College, Gwalior, Madya Pradesh-474002, India
E-mail: neelimajadon@yahoo.com
ABSTRACT- Background: Acute kidney injury (AKI)
is a commonly encountered syndrome associated with various aetiologies and
pathophysiological processes leading to decreased kidney function. This study
was designed to assess the incidence and epidemiology of AKI of patients in a
tertiary care centre in Intensive Care Unit (ICU) of Gwalior, Madhya Pradesh,
India.
Methods: This was a prospective study of AKI patients,
admitted in ICU and Internal medicine of Department of Medicine from September 2017 to February 2018. In total 100 AKI
patients, which included 54 males and 46 females,
male (44.20±8.54) and females (47.56±10.20) were collected and then subjected
to the classification and arrangements data on the basis of general
characteristics of patients; nature of disease and etiology of AKI amongst
patients reported. Statistical data was collected by using
self-administered questionnaire.
Results: 100 AKI patients with the mean age of
male (44.20±8.54) and female (47.56±10.2) cases of AKI causes were
characteristics of AKI patients most prominent of co-mortality diabetic (18%)
then hypertension (12%). Etiology of cases among the pneumonia was (13%), sepsis post trauma (12%), pylonephritis/urosepsis
(11%), acute gastrointestinal tract pathology (8%), meningitis (5%),
bacterial gastroenteritis (5%), soft tissue injury (4%), and septic arthritis
(3%) found. Female was risked to AKI majorly due to acute gastrointestinal
tract pathology (8%). Hair dye (4%) was
the first major poisonous cause of occurrence of AKI, followed by Organophosphorous (1%), celphos (3%), Datura (1%), and rat killer (1%).
Conclusion:
AKI
is an increasing concern and potentially catastrophic complication in
hospitalized patients and frequently observed in our study due to sepsis
post-truma and heart failure as well as it carries a poor prognosis.
Key Words: Acute kidney injury,
Acute kidney failure, Chronic disease, Cardiac failure, Hemorrhage
INTRODUCTION- Acute kidney injury (AKI) is a syndrome (or more accurately a
group of syndromes) [1] defined by an abrupt decrease in glomerular
filtration. AKI is a common condition in all countries of the world, regardless
of economic status. The syndrome is associated with considerable morbidity,
mortality and high costs. As an episode of AKI can lead to the development of
chronic kidney disease (CKD) or end-stage renal disease (ESRD), and the
incidence of AKI is increasing, the impact of AKI on long-term health and cost
is far greater than formerly acknowledged [2,3].
Annual prevalence of patients with AKI in need of one of the
replacement methods has been reported to be about 200 to 300 cases in 1 million
populations [4,5]. The causes of AKI are different based on various
geographical regions and there is a significant difference in its prevalence
between developing and developed countries [6]. Most affected
population was 60–79 year old men and common co-morbidities in this group of
patients include surgery, diabetes, pneumonia, cardiac failure, stroke, and
history of CKD [7].
Definitions and diagnosis of AKI- Loss of kidney function is classically defined by increases in
serum creatinine level; however, in community settings and circumstances in
which a patient’s volume status is closely monitored for example, in
ICU-oliguria or anuria might be the only recognizable sign of AKI [8].
Accordingly, in the Improving Global Outcomes (KDIGO) guideline, AKI stages are
classified into three stages on the basis of either the increase in serum
creatinine level or the duration and extent of oliguria [9-11].
Epidemiology and risk
factors of AKI patients- The
widespread adoption of standardized criteria to define the presence of AKI have
facilitated comparisons of the epidemiology and outcomes of AKI across hospital settings [12]. However, this standardization
should not imply that AKI is a single entity. Rather, AKI is a syndrome that
encompasses a multitude of clinical scenarios, underlying etiologies,
co-morbidities, drug exposures and severities of renal dysfunction. AKI also involves several different patho-physiological processes;
in experimental models, gene expression in the kidney in response to intrinsic
renal tubular injury differs from that seen in homeostatic responses to volume
contraction, even when each mechanism results in similar changes in serum
creatinine concentration [13]. These factors are important to
consider when evaluating studies describing the epidemiology of AKI in
hospitalized patients (or indeed, in any group of patients), especially given
that most epidemiologic studies use serum creatinine criteria alone to define
AKI and generally do not report the etiology of AKI or the characteristics of
the hospitals studied [14]. Therefore, the present study was done
with the aim of evaluating the incidence and epidemiology of AKI in patients
presenting to emergency department as a sample of ICU.
MATERIALS AND METHODS- A prospective study was done from September 2017 to February 2018 in a
1200 bed strength tertiary care centre (G. R. Medical College) located in Gwalior, Madya Pradesh, India. The
study protocol was approved by the Institute Ethics Committee. Total numbers of 100 AKI patients (i.e. 54 male and 46 female) were collected for this study. Obtained data was then
subjected to the classification and arrangements on the basis of general
characteristics of patients; nature of
disease, etiology of septisemic cause of AKI amongst patients, nephrotoxins, and poisonous causes of AKI amongst
population reported.
Inclusion
criteria
Ø
Presence of uremic symptoms
or oliguria or anuria of recent onset,
Ø
AKI as defined using the kidney disease- KDIGO criteria based on serum creatinine (increase in serum
creatinine by ≥0.3 mg/dL within 48 h or increase in serum creatinine to
≥1.5 times baseline), which is known or presumed to have occurred within
the prior 7 days. Staging of AKI was serum creatinine 1.5 to 1.9 times
base-line or ≥0.3 mg/dL increase (stage 1); 2.0 to 2.9 times baseline
(stage 2) and 3.0 time baseline or increase in serum creatinine to ≥4.0
mg/dL or initiation of renal replacement therapy (stage 3). It was presumed
that the patient had normal renal function, if the serum creatinine was 1.5
mg/dL.
Exclusion criteria
Ø
Pre-existing kidney disease
(serum creatinine >1.5 mg/dL or ultrasonography of the abdomen suggestive of
bilateral small kidneys/loss of corticomedullary differentiation (CMD)/obstructive
nephropathy/other renal pathology)
Ø Patients with AKI on CKD.
Statistical Analysis- The results were presented in mean±SD and percentage. Chi-square
test was used to compare the categorical variables between cases and controls.
Unpaired t-test was used to compare the study parameters between cases and
controls. The Pearson correlation coefficient was calculated among the study
parameters. The p-value<0.05 was considered significant. All the analysis
was carried out by using SPSS (IBM) 21.0 version (Chicago, Inc., USA).
RESULTS- A
total of 1795 patients admitted in ICU of the Department of Medicine at G. R. Medical
College, Gwalior during the study period were screened for inclusion
into the study. In which, total of 100 patients were suffered from AKI and the
incidence rate of AKI in present study was 5.57% (Table 1).
Table 1:
Incidence rate of AKI in present study cohort
|
Number |
Percentage (%) |
Total Admission at
study place |
1795 |
100 |
Incidence rate of AKI |
100 |
5.57 |
Majority
of the patients had AKI stage II (74%) followed by AKI stage I (13%) and AKI stage III
(13%) shown in Table 2.
Table 2: Distribution of acute kidney injury classification
AKI
classification |
Frequency |
Percentage (%) |
Stage I |
13 |
13 |
Stage II |
74 |
74 |
Stage III |
13 |
13 |
Fig. 1: Distribution
according to AKI classification
General characteristics of AKI
patients- In the total
studied population male were in majority. The average age of AKI patients was
found 45.74±9.45 years whereas, male was found 3 years younger with
average age of 44.20±8.54 and female with average age of 47.56±10.20 (Fig. 3).
Fig. 2: Comparing mean of age
between Gender
Total 20% of patients were
subjected to internal medicine ward whereas, 80% were found to be admitted into
ICU. The majority of patients were in ICU ward, which indicated that patients
were being treated for some chronic diseases. Total 8% patients were suffering
from hypertension as co-morbidity of which 14.81% were male and 8.69% were
female. Diabetes mellitus was found to one of the major chronic disease in 18%
of total population, in which 16.66% were male and 19.56% were female. Blood
pressure recordings indicated that of the total population 24% were suffering
from hypotension, 14% were normal and 8% had hypertension. It was observed that
occurrence of the 8% of the population was suffering from HIV, 6% with cancer,
4% with hepatitis B and hepatitis C, 4% with heart failure and 2% with CKD
(Table 3).
Table 3: General characteristics of AKI patients
Variables |
Total (%) N=100 |
Male (%) N=54 |
Female (%) N=46 |
Age (years) |
45.74±9.45 |
44.20±8.54 |
47.56±10.20 |
Unit of hospitalization Internal medicine ICU |
20(20) 80(80) |
12(22.22) 42(77.77) |
08(17.39) 38(82.60) |
Co-morbidity Hypertension Diabetes
mellitus |
12(12) 18(18) |
08 (14.81) 9(16.66) |
04(8.69) 9(19.56) |
Blood pressure (mmHg) Hypotension Normal Hypertension |
24(24) 14(14) 8(8) |
18(33.33) 9(16.66) 6(11.11) |
6(13.04) 5(10.86) 2(4.34) |
HIV |
8(8) |
5(9.25) |
3(6.52) |
Cancer |
6(6) |
4(7.47) |
2(4.34) |
Hepatitis B/C |
4(4) |
3(5.55) |
1(2.17) |
Heart failure Known CKD |
4(4) 2(2) |
3(5.55) 1(1.85) |
1(2.17) 1(2.17) |
Etiology of AKI amongst patients- Among the studied population the
septicemic cause of occurrence of AKI was different amongst different patients.
Sepsis post trauma was one of the biggest causes of AKI in the study population followed by the pneumonia (13%), pylonephritis/urosepsis (11%), meningitis (5%), soft tissue (4%), bacterial gastroenteritis (5%)
and septic arthritis (3%). Female was risked to AKI majorly due to acute
gastrointestinal tract pathology (8%) (Table 4).
Nephrotoxins causes of AKI
amongst patients-
The hair dye (4%) was the first major
poisonous cause of occurrence of AKI, followed by Organophosphorous (1%),
celphos (3%), Datura (1%) and rat killer (1%) in this study population. It was
also found that the males were at higher risk of poisoning than that of female
almost in all the enlisted poisoning cases (Table 4).
Table 4: Nature and etiology
of AKI amongst participants
Variables Etiologies (Septicemia) |
Total (%) N=100 |
Male (%) N=54 |
Female (%) N=46 |
Pneumonia |
13(13) |
8(14.81) |
5(10.86) |
Acute gastrointestinal
tract pathology |
8(8) |
3(5.55) |
5(10.86) |
Meningitis |
5(5) |
2(3.70) |
3(6.52) |
Pyelonephritis/Urosepsis |
11(11) |
7(15.21) |
4(8.69) |
Sepsis post trauma |
12(12) |
10(18.51) |
2(4.34) |
Septic arthritis |
3(3) |
1(1.85) |
2(4.34) |
Soft tissue
injury |
4(4) |
3(5.55) |
1(2.17) |
Bacterial
gastroenteritis |
5(5) |
4(7.40) |
1(2.17) |
Post-operative
cases |
7(7) |
4(7.40) |
3(6.52) |
Sepsis
abortion |
6(6) |
0(0.00) |
6(13.04) |
Post parter
hemorrhage |
5(5) |
0(0.00) |
5(10.86) |
Congestive
cardiac failure |
4(4) |
2(3.70) |
2(4.34) |
Acute
pancreatitis |
4(4) |
3(5.55) |
1(2.17) |
Nephrotoxins Hair
dye Organophosphorous Rat
killer Celphos Datura |
4(4) 1(1) 1(1) 3(3) 1(1) |
1(1.85) 1(1.85) 0(0.00) 2(3.70) 1(1.85) |
3(6.52) 0(0.00) 1(2.17) 1(2.17) 0(0.00) |
Others |
3(3) |
9(16.66) |
4(8.69) |
Fig.
3 Nature and Etiology of AKI amongst patients
DISCUSSION- In the present study, the average age of the population was
45.74±9.45 years, which were younger than the studies reported [15-17].
It is also reported that the AKI mostly occurs at old age or a disease of
senility [15]. In our study, AKI suffered male were also found three
years younger than the average age of female, which clearly indicates male is
at higher risk at early age than females. This may be due to rapidly changing
life style and consumption of fast food in busy lifestyle. It was reported that
consumption of fast food and increased dietary intake of foods with high
oxalate content such as cocoa will lead to CKD [18]. Such chronic disease many a times leads to
development of AKI [18]. Hypotension
was found to be the main co-morbidity in present study, which found in majority
in sample population suffering AKI. Hypotension lowers the rate of flow of
blood throughout the body which, leads to reduce in the rate of filtration of
toxic component in the kidney. Non-filtered toxic component remains in the body
majorly in accumulating in the kidney prone to AKI. It is also reported that
patients with CKD, congestive heart failure, hypertension, renovascular disease
and diabetes were more likely to develop AKI [15,19]. In our study,
4% population was found to be suffering from heart failure and 2% with CKD [16,19].
In study population, diabetes mellitus was found to one of the major chronic
disease affecting 18% of total population of which 16.66% were male and 19.56%
were female. Hypotension as well as hypertension was also observed in the AKI patients. In male population,
occurrence of AKI with normal blood pressure was higher 16.66%, as compared to
females 10.86%, which again indicative of food habits and stress [16,18].
Along with it the patient were suffering from the infectious causes like affecting
total 8% HIV was higher in 9.25% male as compared to females 6.52%, total 6% cancer
was higher 7.47% as compared to females 4.32%, 4% as well as total hepatitis B
and hepatitis C was higher 5.55% as compared to females 2.17%. Heart failure 4%
total and known CKD 2% of higher as 5.55% of male
compared than 1% of female.
It
was reported that sepsis is one of the major cause of AKI and septicemic causes
to occurrence of AKI was different amongst different patients. With respect to the observations made in the present study most
literature report a similar total Incidence of hospitalization in ICU ward
ranging from 55.60% to 84% [20-25]. Certain reports, have however
documented a highest Incidence of hospitalization in Internal medicine ward the
range 37.1% [26]. Similarly
ICU admitted patients, sepsis was one of the major causes in our finding of
with 77.77% of male and 82.60% of female were at risk, whereas, in Internal
medicine ward cases, our finding
was 22.22% of male and 17.39% of female [27]. The
majority of studied population was admitted in ICU with chronic history of
disease and prolonged intensive treatment.
Other
septicemic causes though do not directly relate to the AKI indirectly
contributing the aggravation of condition. Those includes infections like
pneumonia, pylonephritis/urosepsis, acute
gastrointestinal tract pathology, meningitis, soft tissue, bacterial
gastroenteritis, septic arthritis and other unidentified cause. In our study it
is also found that the female with infectious causes are greater risk relating
poor health and hygiene of females. Infectious causes like pneumonia, for male
was 14.81% and 10.86% for female, gastrointestinal tract pathology (10.86%) and
meningitis (6.52%) were the main disease associated with the occurrence of AKI
in females. In all the toxic origin of occurrence of AKI male population was suffered
greatly than the females, which clearly indicate the toxogenic occurrences of
AKI related to job profile [21]. Male population was found at higher
risk in all the toxic incidences. All other toxicities of hair dye, methanol,
organophosphate, paraquat, celphos, and rat killer are either industrial origin
or the risk jobs preferably performed by the male candidates at home and
socially; hence male was clearly at major risk.
CONCLUSIONS- The incidence of AKI is high in ICU admitted patients and the
development of AKI is associated with poor outcome and reduced survival. AKI
significantly increases the period of hospital stay, and this is likely to
increase to the healthcare burden and morbidity. The epidemiology of present
study concluded, the risk of AKI was high among critically ill patients with
co-morbidities. Most
of the risk factors of AKI can be prevented with early diagnosis and
interventions such as health education on oral rehydration, quality prenatal
and emergency obstetric care, appropriate management of infections and taking
proper precautions, when prescribing nephrotoxic medications.
Future study may be also
benefitted by better identifying modifiable risk factors to prevent the
development of AKI from the outset and timely and aggressive management will
certainly reduce the incidence of AKI. Treatment
of AKI is largely supportive and further research is urgently needed to improve
AKI diagnosis and patient’s outcomes.
CONTRIBUTION OF AUTHORS
Research concept- Prof. Sushma Trikha, Prof. Archana Kansal, Dr. Neelima Singh
Research design- Dr. Krishan Kumar
Supervision- Prof. Sushma Trikha
Materials- Dr. Krishan Kumar
Data collection- Dr. Krishan Kumar
Data analysis and Interpretation - Dr. Krishan Kumar, Dr. Sutakshee Sonowani
Literature search- Dr. Krishan Kumar
Writing article- Dr. Krishan Kumar, Dr. Nitin Kr. Srivastava
Critical review-Prof. Sushma Trikha, Prof. Archana Kansal, Dr. Neelima Singh
Article editing- Dr. Krishan Kumar
Final approval-
Prof. Sushma Trikha
REFERENCES
1. Kellum JA. Why are patients still
getting and dying from acute kidney injury? Curr. Opin. Crit. Care, 2016;
22(6): 513–19.
2. Lameire NH, Bagga A, Cruz D, De
Maeseneer J, Endre Z, et al. Acute kidney injury: an increasing global concern.
Lancet, 2013; 382(9887): 170–79.
3. Mehta RL, Cerdá J, Burdmann EA, Tonelli M, García-García G, et al.
International Society of Nephrology’s by 25 initiative for acute kidney injury
(zero preventable deaths by 2025): a human rights case for nephrology. Lancet,
2015; 385(9987): 2616–43. doi:
10.1016/S0140-6736(15)60126-X.
4. Metcalfe W, Simpson M, Khan IH, Prescott GJ, Simpson K, et al.
Acute renal failure requiring renal replacement therapy: incidence and outcome.
QJM: An Int. J. Med., 2002; 95(9): 579-83.
5. Hoste EA, Schurgers M. Epidemiology of acute kidney injury: how
big is the problem? Crit. Care Med., 2008; 36(4): S146-S51.
6. Susantitaphong P, Cruz DN, Cerda J, Abulfaraj M, Alqahtani F, et
al. World incidence of AKI: a meta-analysis. Clinical J. Am. Soc. Nephrol.,
2013; 8(9): 1482-93.
7. Xu X, Nie S, Liu Z, Chen C, Xu G, Zha Y, et al. Epidemiology and
clinical correlates of AKI in Chinese hospitalized adults. Clin. J. Am. Soc.
Nephrol., 2015; 10(9): 1510-18. doi: 10.2215/CJN.02140215.
8. Kellum JA, Sileanu FE, Murugan R, Lucko N, Shaw AD,
et al. Classifying AKI by urine output versus serum creatinine level. J. Am.
Soc. Nephrol., 2015; 26: 2231–38. doi: 10.1681/ASN.2014070724.
9. Bellomo R, Ronco C, Kellum JA, Mehta RL,
Palevsky P, et al. Acute renal failure-definition, outcome measures, animal
models, fluid therapy and information technology needs: the Second
International Consensus Conference of the Acute Dialysis Quality Initiative (ADQI)
Group. Crit. Care, 2004; 8(4): R204–R12.
10. Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, et al. Acute Kidney
Injury Network: report of an initiative to improve outcomes in acute kidney
injury. Crit. Care; 2007; 11(2): R31.
11. Kidney Disease Improving Global Outcomes
(KDIGO). Acute Kidney Injury Work Group. KDIGO clinical practice guideline for
acute kidney injury. Kidney Int., 2012; Suppl. 2: 01–138.
12. Hsu CY, McCulloch CE, Fan D, Ordoñez JD,
Chertow GM, et al. Community- based incidence of acute renal failure. Kidney
Int., 2007; 72(2): 208–12.
13. Xu K, Rosenstiel P, Paragas N, Hinze C,
Gao X, et al. Unique transcriptional programs identify subtypes of AKI. J. Am.
Soc. Nephrol., 2017; 28(6): 1729–40. doi: 10.1681/ASN.2016090974.
14. Susantitaphong P, Cruz DN, Cerda J,
Abulfaraj M, et al. World incidence of AKI: a meta- analysis. Clin. J. Am. Soc.
Nephrol., 2013; 8(9): 1482–93.
15.
Coca SG.
Acute kidney injury in elderly persons. Am. J. Kidney Dis., 2010; 56(1): 122-31.
16.
Haynes RJ,
Read S, Collins GP, Darby SC, Winearls CG. Presentation and survival of
patients with severe acute kidney injury and multiple myeloma: a 20-year
experience from a single centre. Nephrology
Dialysis Transplantation, 2009; 25(2): 419-26.
17.
Uchino S,
Bellomo R, Goldsmith D, Bates S, Ronco C. An assessment of the RIFLE criteria
for acute renal failure in hospitalized patients. Critical care medicine, 2006; 34(7): 1913-17.
18.
Albersmeyer
M, Hilge R, Schröttle A, Weiss M, Sitter T, et al. Acute kidney injury after
ingestion of rhubarb: secondary oxalate nephropathy in a patient with type 1
diabetes. BMC nephrology, 2012;
13(1): 141.
19.
Wu VC, Wu CH, Huang TM, Wang
CY, Lai CF, Shiao CC. and Chu TS. Long-term risk of coronary events after
AKI. Journal of the American
Society of Nephrology, 2014; 25(3):
595-605.
20.
Liborio AB, Leite TT, Neves
FM, et al. AKI complications in critically ill patients: association with
mortality rates and RRT. Clin. J. Am.
Soc. Nephrol., 2015; 10: 21.
21.
Mandelbaum T, Scott DJ, Lee
J, et al. Outcome of critically ill patients with acute kidney injury using the
Acute Kidney Injury Network criteria. Crit.
Care Med., 2011; 39: 2659.
22.
Hoste EA, Bagshaw SM,
Bellomo R, et al. Epidemiology of acute kidney injury in critically ill
patients: the multinational AKI-EPI study. Intensive Care Med., 2015; 41: 1411.
23.
Hoste EA, Clermont G,
Kersten A, et al. RIFLE criteria for acute kidney injury are associated with
hospital mortality in critically ill patients: a cohort analysis. Crit. Care, 2006; 10: R73.
24.
Kellum JA, Sileanu FE,
Murugan R, et al. Classifying AKI by Urine Output versus Serum Creatinine
Level. J. Am. Soc. Nephrol.,
2015; 26: 2231.
25.
Vasanth G, Surendrakumar P,
Catherine P, Venu G. A study of factors determining outcome of acute kidney
injury patients requiring hemodialysis. Int. J. Res. Med. Sci., 2018; 6:
2974-82.
26.
Cheng X, Wu B, Liu Y, Mao H,
Xing C. Incidence and diagnosis of Acute kidney injury in hospitalized adult
patients: a retrospective observational study in a tertiary teaching Hospital
in Southeast China. BMC Nephrol., 2017: 18: 203. doi:
10.1186/s12882-017-0622-6.
27.
Schrier RW, Wang W. Acute
renal failure and sepsis. New
England J. Med., 2004; 351(2):
159-69.