Home About Us Contact Us

 

Table of Content - Volume 3 Issue 3- September 2016


 


A study of clinical profile of patients with adult nephritic syndrome at department of medicine of a tertiary health care centre

 

Janrao Bhaurao Rajput1, Sanjay Pandharinath Patil2*

 

1Associate Professor, 2Assistant Professor, Department of General Medicine, Dr. Ulhas Patil Medical College and Hospital, Jalgaon, Maharashtra, INDIA.

Email: jitendrapsm@gmail.com

 

Abstract              Background: Nephrotic syndrome is a disorder characterized by proteinuria >3.5g/24hr, hypoalbuminemia <3g/dL and peripheral edema. The underlying etiology of the condition is influenced in large part by the age of the patient. In adults aged 15–65 the cause of nephrotic syndrome varies from primary kidney pathologies such as focal segmental glomerulosclerosis, membranous nephropathy, or less commonly minimal change disease. Aims and objectives: To study the clinical profile of patients with nephrotic syndrome ijnn adult at department of medicine of a tertiary health care centre. Materials and method: In the present was retrospective record based descriptive study all the patients of adult nephritic syndrome admitted during January 2015 to December 2016 were enrolled. The detailed history of all the selected patients was recorded on a prestructured proforma including demographic. Clinical examination and biochemical investigations findings wewre also recorded. Renal biopsy findings to know the lesion responsible for the proteinuria were also recorded. Results: Majority of the patients in the present study were young male with age less than 30 years (50%). Followed by 31-40 years of age (21.05%). The proportion of male patients (68.42%) suffering from nephritic syndrome was more as compared to female patients (31.58%). Edema was the most common presenting symptom (81.58%) followed by hematuria (31.58%) and hypertension (28.95%). Anemia was observed in 60.53% patients. Hypoalbuminemia was seen in 86.84% patients. Hypercholesterolemia (>200mg/Dl) was seen in 55.26%. Increased Levels of Creatinine and RBSc in urine were observed in 34.21% and 36.84% patients. The most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (44.74%) followed by Membranous Glomerulonephritis (15.79%) and Membranoproliferative glomerulonephritis (13.16%) were observed. Conclusion: Thus we conclude that the most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (FSGS) 2nd common lesion was Membranous Glomerulonephritis (MGN) and 3rd common lesion was Membranoproliferative glomerulonephritis. Adult nephrotic syndrome was seen commonly in young male. Commonest mode of presentation was edema followed by hematuria and hypertension. Hypoalbuminemia and anaemia were common laboratory findings.

Key Words: Adult Nephrotic Syndrome, edema, Focal Segmental Glomerulosclerosis.

 

INTRODUCTION

Nephrotic syndrome is a disorder characterized by proteinuria >3.5g/24hr, hypoalbuminemia <3g/dL, and peripheral edema1. The underlying etiology of the condition is influenced in large part by the age of the patient. In children under the age of 16, a large majority of cases (76.6%) are due to minimal change disease (MCD)2. However, in adults aged 15–65 the cause of nephrotic syndrome becomes more varied to include primary kidney pathologies such as focal segmental glomerulosclerosis, membranous nephropathy, or less commonly minimal change disease.3 Progressive lower extremity edema, weight gain, and fatigue are typical presenting symptoms of nephrotic syndrome. In advanced disease, patients may develop periorbital or genital edema, ascites, or pleural or pericardial effusion. Persons who present with new edema or ascites, without typical dyspnea of congestive heart failure or stigmata of cirrhosis, should be assessed for nephrotic syndrome.4 The mechanism of edema formation in Nephrotic syndrome is unclear. The primary defect seems to be increased glomerular permeability to albumin and other plasma proteins. Pri­mary renal sodium retention and decreased oncotic pressure from hypoalbuminemia lead to increased extravasation of fluid from the intravascular space into the interstitial space, resulting in edema5. Nephrotic syndrome constitutes the most recurrent revelation of about 50% of chronic kidney diseases observed as well in the United States, in Europe or in Africa6. Renal biopsy is mandatory in the identification and the characterization of lesions7.

 

MATERIALS AND METHOD

The present was retrospective record based descriptive study was conducted in the department of Medicine of Dr. Ulhas Patil Medical College and Hospital. Following inclusion and exclusion criteria was used to select the study subjects.

Inclusion Criteria

  • Adults with nephrotic syndrome age > 18yrs.
  • Urinary protein excretion more than 3.5g/24hrs. Or Urinary protein to creatinine ratio more than 3.5 on spot sample of urine. Or Heavy proteinuria on a spot sample of urine with a serum albumin of less than 2.5g/dl.

Exclusion Criteria

  • Evidence of diabetic nephropathy as suggested by other target organ such as diabetic retinopathy.
  • H/o episodes of nephrotic syndrome in childhood.

With reference to above inclusion and exclusion criteria all the patients of adult nephritic syndrome admitted during January 2015 to December 2016 (2 years) were enrolled in the present study. The detailed history of all the selected patients was recorded on a prestructured proforma including demographic. Clinical examination and biochemical investigations findings wewre also recorded. Renal biopsy findings to know the lesion responsible for the proteinuria were also recorded. According to WHO Anemia was defined as haemoglobin level <13gm% in males and <12gm% in females8. Hypertension was defined as a blood pressure either systolic BP> 140mmHg and/or diastolic BP> 90mmHg9. Nephrotic range proteinuria was defined >3gm/24hrs10,11; hypoalbuminemia <3.5gm/dL12. Hematuria as >5RBCs/hpf13. Renal failure has been defined as GFR (MDRD) <60 mL/min14. Normal levels of serum urea was defined as 15 – 45 mg/dl12 and serum creatinine was considered to be in the abnormal range when >1.4mg/dl15 and serum cholesterol was defined (NCEP-ATP III Classification) as being in the higher range when >200mg/dl12.

                                       

RESULTS

Table 1: Distribution of according to age and sex

Variable

No. of Cases

Percentage

Age group

≤30

19

50.00

31-40

8

21.05

41-50

5

13.16

51-60

5

13.16

61-70

1

2.63

Sex

Male

26

68.42

Female

12

31.58

Total 38 cases of nephritic syndrome were enrolled in the present study. It was observed that majority of the patients in the present study were young male with age less than 30 years (50%). Followed by 31-40 years of age (21.05%). The proportion of male patients (68.42%) suffering from nephritic syndrome was more as compared to female patients (31.58%).

 

Table 2: Distribution of according clinical profile

Clinical profile

No. of Cases

Percentage

Complaint

Hypertension

11

28.95

Edema

31

81.58

Hematuria

12

31.58

Laboratory findings

Anemia

23

60.53

Hypercholesterolemia

21

55.26

Hypoalbuminemia

33

86.84

Increased Levels of Creatinine

13

34.21

Urine RBCs

14

36.84

Edema was the most common presenting symptom (81.58%) followed by hematuria (31.58%) and hypertension (28.95%). Anemia was observed in 60.53% patients. Hypoalbuminemia was seen in 86.84% patients. Hypercholesterolemia (>200mg/Dl) was seen in 55.26%. Increased Levels of Creatinine and RBSc in urine were observed in 34.21% and 36.84% patients.

 

Table 3: Distribution according to Etiology of adult nephrotic syndrome

Lesion

Number

Percentage

Focal Segmental Glomerulosclerosis (FSGS)

17

44.74

Membranous Glomerulonephritis (MGN)

6

15.79

Membranoproliferative glomerulonephritis (MPGN)

5

13.16

Renal Amyloidosis

4

10.53

Lupus Nephritis (LN)

3

7.89

Minimal Change Disease (MCD)

3

7.89

 

The most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (44.74%) followed by Membranous Glomerulonephritis (15.79%) and Membranoproliferative glomerulonephritis (13.16%) were observed. Renal Amyloidosis was seen in 10.53% patients.


 

 

 


DISCUSSION

The present study was conducted among the patients of nephritic syndrome admitted in the Department of Medicine and who were of >18years of age. The Demographic profile of the adult patients who presented with nephritic range proteinuria was studied which revealed that, majority of the patients were young with age less than 30 years (50%). Followed by 31-40 years of age (21.05%). Naini EA et al15, Sanjay Dhawale16 and Rajeev Malipatil19 also observed similar findings in their study. The proportion of male patients (68.42%) suffering from nephritic syndrome was more as compared to female patients (31.58%). Sanjay Dhawale16 in their study revealed that, 64.8% of the patients were males and the mean age at presentation was 31.7±8.5 years. Haraldsson et al17 and Javed Iqbal Kazi et al18 also showed that there was male predominance in the occurrence of nephrotic syndrome in adults. Edema was the most common presenting symptom (81.58%) followed by hematuria (31.58%) and hypertension (28.95%). According to Sanjay Dhawale16 edema was the most common complaint at the time of presentation and was seen in 96.3 % cases while 33. 3% had hypertension and 37% had microscopic hematuria. Anaemia was observed in 60.53% patients. Hypoalbuminemia was seen in 86.84% patients. Hypercholesterolemia (>200mg/Dl) was seen in 55.26%. Increased Levels Of Creatinine and RBSc in urine was observed in 34.21% and 36.84% patients. Rajeev Malipatil19 in their study observed that Hypoalbuminemia was present in 92.5% of patients with an average of 1.97g/dl. Hypercholesterolemia was present in 80% of patients with an average value of 325.9mg/dl. Serum creatinine was elevated in 19 patients (47.5%). Similar findings were also observed by Sanjay Dhawale16. The most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (44.74%) followed by Membranous Glomerulonephritis (15.79%) and Membranoproliferative glomerulonephritis (13.16%) were observed. Renal Amyloidosis was seen in 10.53% patients. Sanjay Dhawale16 in their study observed that the most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (FSGS). FSGS was the lesion responsible in 37% of the cases. The next common lesion was Membranous Glomerulonephritis (MGN) which contributed to around 18.5% of the cases. The third most common lesion in our study was Renal Amyloidosis which constituted 14.8% of the total. Membranoproliferative Glomerulonephritis (MPGN) was found in 13% of the cases. Lupus Nephritis (LN) was identified as the cause of adult nephrotic syndrome in 9.3 % cases. Minimal Change Disease (MCD) was responsible for adult nephrotic syndrome in 5.5% of the cases with adult nephritic syndrome. Only one among the 54 cases studied came out to be IgA Nephropathy (IgAN) which contributed to 1.8%. Thus the findings of the present study were comparable with Sanjay Dhawale16 study. Similar findings were also observed by M. Faye et al20.

 

CONCLUSION

Thus we conclude that the most common lesion responsible for the nephrotic syndrome in adults was Focal Segmental Glomerulosclerosis (FSGS) 2nd common lesion was Membranous Glomerulonephritis (MGN) and 3rd common lesion was Membranoproliferative glomerulonephritis. Adult nephrotic syndrome was seen commonly in young male. Commonest mode of presentation was edema followed by hematuria and hypertension. Hypoalbuminemia and anemia were common laboratory findings.

 

REFERENCES

  1. Mähr N, Neyer U, Prischl F, et al. Proteinuria and hemoglobin levels in patients with primary glomerular disease. Am J Kidney Dis 2005 Sep; 46(3):424–31.
  2. Nephrotic syndrome in children: prediction of histopathology from clinical and laboratory characteristics at time of diagnosis. A report of the International Study of Kidney Disease in Children. Kidney Int 1978 Feb; 13(2):159–65.
  3. Reynolds SB, Lutz RW. Diagnosis and management of nephrotic syndrome in an adult patient: A case report. Int J Case Rep Images 2016;7(8):529–532.
  4. Charles Kodner. Nephrotic Syndrome in Adults: Diagnosis and Management. American Family Physician.2009; 80(10):1129-34.
  5. Siddall EC, Radhakrishnan J. The pathophysiology of edema formation in the nephrotic syndrome. Kidney Int. 2012; 82(6):635-642.
  6. Diallo, A.D., Nochy, D. and Niamkey, E. (1997) Etiologic Aspects of nephrotic Syndrome in Black African Adults in a Hospital Setting in Abidjan. Bulletin de la Société de pathologie exotique, 90, 342-345.
  7. Swaminathan, S., Leung, N. and Lager, D. (2000) Changing Incidence of Glomerular Disease in Olmsted County, Minnesota: A 30-Year Renal Biopsy Study. Clinical Journal of the American Society of Nephrology, 1, 483-487.
  8. Fauci, Braunwald, Kasper, Hauser, Longo, Jameson, Loscalzo. ‘Cardinal manifestation and presentation of diseases In: Harrison’s principles of internal medicine; 17th edition section 10-Hematologic alterations’; Chapter 58, I(2), 355-363
  9. Fauci, Braunwald, Kasper, Hauser, Longo, Jameson, Loscalzo. ‘Disorders of the cardiovascular system; section 5 :vascular disease; Chapter 241 :Hypertensive vascular disease’ In: Harrison’s principle of Internal Medicine;17th edition; Table 241-1 Blood pressure classification, 2(9), 1549-1562
  10. Akhtar SZ, Akbar Ali. ‘Histologacal pattern of nephritic syndrome in elderly patients’; J Ayub Med Coll Abbottabad, 2008, 20(4).
  11. Khanna UB, Nerurkar SV, Almeida AF, et al. ‘Study of hyperlipidemia in adults with nephrotic syndrome’. 1985; 31(3):140-5.
  12. Tester Ashavaid F. Index of normal values’ In: API textbook of medicine 8th edition Miscellaneous; chapter11, 2(27), 1603-1611.
  13. Melanie Kim S, Howard L. ‘Urinanalysis’ In: Corwin Diseases of the kidney and urinary tract; Lippincott Williams and Wilkins ;Robert W.Schrier,MD;7th edition; section II-Clinical Evaluation : chapter 10, I, 317-331
  14. Acharya VN. ‘Nephrology’ In: API textbook of medicine 8th edition chapter12, 1, 717-781
  15. Naini AE, Harandi AA, Ossareh S et al. ‘Prevalence and Clinical Findings of Biopsy-Proven Glomerulonephritidis in Iran’. Saudi journal of kidney diseases and transplantation. 2007; 4(18):556-564.
  16. Sanjay Dhawale, Satyam Singh jayant, Rakesh gaharwar. Study of Etiological Profile of Nephrotic Syndrome in Adults. International Journal of Applied Research 2015; 1(9): 545-549.
  17. Cohen Eric P. Nephrotic Syndrome’; <http:// emedicine. medscape.com /article/244631-overview>
  18. Javed Iqbal Kazi, Muhammed Mubarak, Ejaz Ahmed et al.’ Spectrum of glomerulonephritides in adults with nephrotic syndrome in Pakistan’. Clinical and Experimental Nephrology, 13(1), 38-43.
  19. Rajeev Malipatil, Sunita Patil, Vaibhavi Velangi. Clinical and Histopathologic Study of Nephrotic Syndrome in Adults. OSR Journal of Dental and Medical Sciences (IOSR-JDMS).2016; 15(11): 19-20.
  20. Faye, M., Lemrabott, A.T., Cisse, M.M., Nzambaza, J. De D., Dia, C.M., Seck, S.M., Fall, K., Faye, M., Ka, E.F., Niang, A. and Diouf, B. (2016) Idiopathic Adult Nephrotic Syndrome: A Clinicopathological Study and Response to Steroid in a Sub-Saharan African Country. Open Journal of Nephrology, 6, 61-65.

 

 

 

 









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.