Home About Us Contact Us

 

Table of Content - Volume 8 Issue 2 - November 2017



Varied etiology of ARF among patients attending teaching hospital: Descriptive clinical study

 

Raghukanth Reddy G1, Shivaputrappa Ghanti2*

 

1Assistant Professor, Department of General Medicine, Raichur Institute of Medical sciences, Raichur, Karnataka

2Senior Resident, Department of General Medicine, Oxford Medical college, Bangalore, Karnataka

Email: raghukanth45@gmail.com

 

Abstract              Over the past decade, the term Acute Kidney Injury (AKI) had replaced the older term Acute Renal Failure (ARF). The term ARF suggests a dichotomous relationship between normal kidney function and overt organ failure; in contrast, the term AKI attempts to encompass the growing body of data associating small acute and transient decrements in kidney function with serious adverse outcomes. All the study subjects were followed up on daily basis, till discharge, death or return of their renal function to baseline. Socio-Demographic, biochemical and clinical profiles of all patients were recorded. Malaria was found positive in 11 patients (10.6%), while Leptospirosis in 3(2.9%) patients and Dengue in 13(12.5%) patients. Blood culture for Staph. pseudomonas and E.coli was found positive in 5,2 and 1 patients respectively. Abnormal echo findings were observed in 7.7% patients.

Key Word: Acute Kidney Injury, E.coli, ARF

 

INTRODUCTION

Acute renal failure is sudden and sustained decrease in the Glomerular Filtration Rate (GFR) occurring over a period of hours to days and resulting in the failure of kidney to excrete nitrogenous waste products and maintain fluid and electrolytes homeostasis.1 Depending on the severity and duration of the renal dysfunction, this accumulation is accompanied by metabolic disturbances, such as metabolic acidosis and hyperkalemia, changes in body fluid balance, and effects on many other organ systems. ARF range from severe (that is requiring dialysis) to slight increase in serum creatinine concentration.1 Recent evidences has shown that relatively small changes in renal function are associated with substantial increase in mortality.2,3 Over the past decade, the term Acute Kidney Injury (AKI) had replaced the older term Acute Renal Failure (ARF). The term ARF suggests a dichotomous relationship between normal kidney function and overt organ failure; in contrast, the term AKI attempts to encompass the growing body of data associating small acute and transient decrements in kidney function with serious adverse outcomes.4 In May 2004, a new classification, the ‘’RIFLE” (Risk, Injury, Failure, Loss of kidney function and End stage kidney disease) classification, was proposed by the Acute Dialysis and Quality Initiative Group (ADQI) in order to define and stratify the severity of AKI.5 Three years later in March 2007, the Acute Kidney Injury Network (AKIN) classification, a modified version of the RIFLE was released in order to increase the sensitivity and specificity of AKI diagnosis.6 Unfortunately, despite major advances in management of acute renal failure, the mortality in these patients is still high due to severe underlying illnesses and complications. It is rare for a patient to die directly as a result of renal failure, but ARF is an independent risk factor for death. Factors other than loss of renal function probably determine the outcome and their identification is necessary to improve the prognosis of AKI.7-10 The burden of AKI is most significant in developing countries due to limited resources for the care of the patients, once the disease has progressed to kidney failure necessitating Renal Replacement Therapy (RRT)11. AKI is common, harmful, treatable and largely preventable but there are very few studies available on this subject from India using various serum creatinine values.12,13 Hence we carried out this study to look into the varied etiology of AKI.

 

METHODOLOGY

All the study subjects were followed up on daily basis, till discharge, death or return of their renal function to baseline. Socio-Demographic, biochemical and clinical profiles of all patients were recorded. Variables assessed were: age, sex, type of primary disease (medical or surgical), type of AKI (pre-renal/renal/post-renal), risk factors, indications and type of dialysis and outcomes (recovery/death/discharge on dialysis).

Data Analysis: Association between qualitative variables was done with the help of Chi-square test. P value <0.05 was taken as significant. Quantitative data was represented using Mean±SD and median and Interquartile range (IQR).

INVESTIGATIONS

The following investigations were done (as and when required)

  1. Complete urine examination, 24 hour urine protein estimation, urine albumin.
  2. Biochemical tests including
  3. Complete hematological tests including coagulation profile,
  4. Bacterial and fungal (in patients with indication) cultures of blood, urine, venous catheters, and endotracheal secretions.
  5. Radiological tests include x-ray of chest and abdomen and ultrasonography/computer tomography (CT) of abdomen and pelvis.
  6. HIV, HBs Ag, HCV
  7. Ophthalmology- Fundoscopy
  8. Renal biopsy
  9. ABG

 

RESULTS

In this study there were 96 (92.3%) of patients due to medical causes. Out of this 33 (31.7%) due to Gastroentiritis, 18(17.3%) due to UTI, 13(12.5%) due to VHF. Other causes were malaria 10(9.6%), CCF 7(6.7%),Pneumonia 5(4.8%), Leptospirosis3(2.9%), Pyelonephritis 3(2.9%), Snake Bite 2(1.9%), NSAID induced AKI and Diabetic ketoacidosis 1(1.0%) each.8 patients (7.7%), were of medico-surgical cases out of this 5(4.8%) cases were of cellulitis, 2(1.9%) were of obstructive-uropathy and 1(1.0%) were perforation.

 

Table 1: Distribution based on Etiology

ETIOLOGY

No. of cases

Percent

Medical

96

92.3

CCF

7

6.7

Diabetic ketoacidosis

1

1.0

Gastroentritis

33

31.7

Leptospirosis

3

2.9

Malaria

10

9.6

NSAID induced AKI

1

1.0

Pneumonia

5

4.8

Pyelonephritis

3

2.9

Snake bite

2

1.9

UTI

18

17.3

VHF

13

12.5

Medico-surgical

8

7.7

Cellulitis

5

4.8

Obstructive uropathy

2

1.9

post lscsileal perforation

1

1.0

Total

104

100.0

Malaria was found positive in 11 patients (10.6%), while Leptospirosis in 3(2.9%) patients and Dengue in 13(12.5%) patients. Blood culture for Staph. pseudomonas and E.coli was found positive in 5,2 and 1 patients respectively.

 

Table 2: Distribution based on Investigation Findings

Investigation Findings

No of cases

%

 

 

Yes

11

10.6%

Malaria

 

P. Vivax

4

3.8%

 

P. Falci

7

6.7%

Dengue

No

91

87.5%

 

 

Yes

13

12.5%

Lepto

No

101

97.1%

 

 

Yes

3

2.9%

 

Not done/ Negative

96

92.3%

Blood Culture

Staph.

5

4.8%

 

 

Pseudomonas

2

1.9%

 

E. Coli

1

1.0%

 

Not done/ Negative

85

81.7%

 

Staph.

8

7.7%

Urine Culture

 

 

 

Pseudomonas

2

1.9%

 

E. Coli

7

6.7%

 

Klebsiella

2

1.9%

ARDS was observed in 8(7.7%) while pulmonary oedema in 6 (5.8%) patients. Abnormal echo findings were observed in 8(7.7%) patients.

Table 3: Distribution based on Radiological Investigation

Radiological Investigation

No of cases

%

 

Normal

87

83.7%

Chest X-Ray

 

ARDS

8

7.7%

 

Pul. Oedema

6

5.8%

Echo

Normal

96

92.3%

 

 

Abnormal

8

7.7%

 

DISCUSSION

Imaging of the urinary tract with renal ultrasound or CT should be undertaken to investigate obstruction in individuals with AKI unless an alternate diagnosis is apparent. Findings of obstruction include dilation of the collecting system and hydroureteronephrosis. Obstruction can be present without radiologic abnormalities in the setting of volume depletion, retroperitoneal fibrosis, encasement with tumor, and also early in the course of obstruction. Imaging may also provide additional helpful information about kidney size and echogenicity to assist in the distinction between acute versus CKD. Large kidneys observed in these studies suggest the possibility of diabetic nephropathy, HIV-associated nephropathy, infiltrative diseases, or occasionally acute interstitial nephritis. In present study deranged LFT was observed in 16.3% patients of Acute Kidney Injury. In a study by Bouchard et al. deranged liver functions were observed in 27% of patients with Acute Kidney Injury. Most common etiology for AKI was gastroenteritis (31.7%) and UTI (17.3%) followed by Dengue (12.5), Malaria(9.6) and CCF (7.7% each). Other diagnosis included pneumonia(4.8%), cellulitis(4.8%), lepto(2.9%), pyelonephritis (2.9%), snake bite(1.9%), obstructive uropathy(1,9%), Diabetic ketoacidosis(1%),NSAID induced AKI (1%) and perforation(1%). In present study out of total patients, 44 (42.3% %) had FAILURE stage of AKI, while 32 (30.8 %) had INJURY stage of AKI and 28(26.9) had RISK according to RIFLE staging. No gender difference was observed in the distribution of patients according to AKI stage. in the study. Commonly noted co morbidities in our patients were Type 2 diabetes mellitus, hypertension and coronary artery disease of which diabetes was predominant (14.38%). However the association was not statistically significant with regard to outcome. Mehta RL et al14in the PICARD experience, have reported an incidence of comorbidity in excess of 30%.J Prakash et al noted comorbidity in 52.17%15. In our study, AKI due to medical causes was contributory in 94.18%. The remaining 5.82% was contributed by surgical causes. J Prakash et al15showed results of 71.7% due to medical causes, 23.9% due to surgical cause and 4.3% due to obstetrical causes. According to Cenzig et al16 59% had medical causes, 25% had surgical cause and 16% had obstetric cause contributing to ARF. The overall mortality in our study was 13.5% of which mortality in the medical group was 12.54% and the remaining 0.96% was contributed by medico-surgical group. According to the study done by Kennedy et al17, mortality in medical group was 24%, medico-surgical group was 28.5% and in obstetric was 1%. Incidence of prerenal failure was less in our study as most of the patients who presented to us had already progressed to acute tubular necrosis. The percentage of 81prerenal, intrinsic renal and post renal AKI was 38%, 60% and 2% respectively and mortality in the prerenal and intrinsic renal groups being 20% and 10% with no mortality in the postrenal AKI group. According to Mehta et al18, prerenal ARF was seen in 50% of patients, 48% had intrinsic renal failure and 2% had postrenal ARF. Kaufman et al19, showed a mortality of only 7% in prerenal AKI. The group with intrinsic renal failure had the highest mortality of 55%. In our study hypotension was the predominant presenting features which was seen in 30.7% of the patients followed by metabolic acidosis- 20.2%, encephalopathy was seen in 13.5%, oliguria in 19.3% and fluid overload was seen in 6.7%. J Prakash et al noted hypotension, altered sensorium and respiratory distress as the commonest features in the ICU. 65% of patients were oliguric and 36.9% of patients had evidence of fluid overload. Similarly, Mehta et al, in Spectrum of ARF in ICU: The PICARD experience, 2004 have noted hypotension in 20% of patients as the presenting feature which is comparable to that in our study In our study sepsis (33%) and MODS (10.6%) were the main complications. Highest mortality was found in patients with sepsis 9 patients. Patients with MODS were 8 patients J Prakash et al15, reported evidence of sepsis in 69.2% patients and mortality of 84%. MODS was noted in 63% of cases and 83% of those had mortality. An S. De Vriese et al reported that mortality was higher in patients with septic ARF (74.5%) than in those whose renal failure did not result from sepsis (45.2%). In the study done by Marlies Ostermann et al, the incidence of MODS of patients in ICU was 23.1% with an overall mortality of 78.85%. In our study, out of 104 patients, 96(92.3%) had conservative line of management and 8(7.7%) underwent haemodialysis, J Prakash et al showed mortality of 80% in dialysed group and 42% in non-dialysed group. Metcalfe et al in his study showed 73.5% of patients receiving RRT for ARF expired. This seems to be due to confounding effects of severity of underlying disease process, sepsis.

CONCLUSION

  • Most common etiology for AKI was medical causes with 96 patients, out of which Gastroentiritis were 33 (31.7%),UTI18(17.3%),VHF13(12.5%),malaria10(9.6%),CCF7(6.7%),Pneumonia5(4.8%), eptospirosis3(2.9%), Pyelonephritis 3(2.9%), Snake Bite 2(1.9%), NSAID induced AKI and Diabetic ketoacidosis 1(1.0%) each.
  • 8 patients (7.7%), were of medico-surgical cases out of this 5(4.8%) cases were of cellulitis, 2(1.9%) were of obstructive-uropathy and 1(1.0%) were perforation.

 

REFERENCES

  1. Lameire N, Van Biesen W, Vanholder R. Acute renal failure. Lancet 2005; 417-30.
  2. Mangano CM, Diamondstone LS, Ramsay JG,AggarwalA, Herskowitz A, Manango DT, for the multicentre Study of perioperative ischaemia research group: Renal dysfunction after myocardial revascularisation: Risk factors, adverse outcomes and utilization. Ann Inter Med 128:194-203, 1998.
  3. Shusterman N, Strom BL, Murray TG, et al. Risk factors and outcome of hospital acquired acute renal failure. Clinical epidemiologic study. Am J Med.65-71, 1987.
  4. Asif A Sharfuddin, Steven D Weisbord, Paul M Palversky, Bruce A Molitoris. Acute Kidney Injury: Brenner BM. Brenner and Rector’s- The Kidney, 9th ed. Philadelphia: Saunders- Elsevier; 2012. p1044-1099.
  5. Bellomo R, Ronco C, Kellum JA, 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: R204–212.
  6. Molitoris, Bruce A., et al. "Improving outcomes of acute kidney injury: report of an initiative." Nature clinical practice Nephrology 3.8 (2007): 439-442.
  7. Beaman M. Turney JH, Rodger RSC et al. changing pattern of acute renal failure Qj med. 1987; 62 (237): 15-23.
  8. Butkus DE. Persistent high mortality in acute renal failure. Are we asking the right question? Arch Intern Med 1983; 143: 209-212.
  9. Stott RB, Cameron JS. Why the persistently high mortality in acute renal failure? Lancet 1972; ii: 75-79.
  10. Turney JH, Marshal DH. The evolution of acute renal failure. Q J Med 1990; 74:83-104.
  11. Cerda J, Bagga A, Kher V, et al. The contrasting characteristics of acute kidney injury in developed and developing countries. Nat ClinPractNephrol 2008; 4: 138–153.
  12. HS Kohli, Madhu C Bhaskaran, Thangamani, KandavelThennarasu, Kamal Sud, VivekanandJha, KrishanL.Gupta and VinaySakhuja Treatment-related acute renal failure in the elderly: a hospital-based prospective study. NDT 2000, 15: 212-217.
  13. AnupamaKaul. Hospital Acquired acute renal insufficiency in INDIA – A tertiary centre experience. JNRT 3(1) 2011: 20–29
  14. Mehta RL, Pascual Mt, Soroko S, et al. Spectrum of acute renal failure in the intensive care unit: The PICARD experience. Kidney International 2004; 66: 161321.
  15. Prakash J, Murthy AS, Vohra R, Rajak M, Mathur SK. Acute renal failure in the intensive care unit. J Assoc Physicians India 2006 Oct; 54:784-788
  16. Cenzing et al. Acute Renal Failure in Central Anatolia, Nephrol Dial Transplant 2000; 15: 152-155.
  17. Kennedy AC, Burton JA et al .Factors affecting prognosis in acute renal failure. Q J Med 1973; 47: 73-86.
  18. Yi Fang Xiaoqiang Ding, YihongZhong, JianzhouZou, JieTeng, Ying Tang, Jing Lin, Pan Lin; Acute Kidney Injury in a Chinese Hospitalized Population : Blood Purif 2010;30:120–126
  19. Kaufmann J, Dhakal M Community acquired acute renal failure. AM J kidney disease 1991; 17: 191-8.


 



 


 


 

 


 



 



 





 




 









Policy for Articles with Open Access
Authors who publish with MedPulse International Journal of Anesthesiology (Print ISSN:2579-0900) (Online ISSN: 2636-4654) agree to the following terms:
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
Authors are permitted and encouraged to post links to their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.