THE PREVALENCE OF PERIPHERAL NEUROPATHY IN HEMODIALYSIS PATIENTS AT AL-AZHAR UNIVERSITY HOSPITAL IN NEW DAMIETTA CITY

Document Type : Original Article

Authors

1 Neurology Department, Faculty of Medicine, Al-Azhar University Damiatta , Eygpt

2 Neurology Department, Faculty of Medicine, Al-Azhar University Cairo, Eygpt

Abstract

Background: Chronic kidney disease (CKD) is a worldwide public health problem. There are several etiologies for CKD. It can occur due to either primary kidney disease or as a complication of a multi-systemic disorder. Much emphasis has been placed on the increased cardiovascular risk and electrolyte abnormalities that accompany chronic kidney disease. The dreaded neurological complications are usually the uremic encephalopathy or a vascular event that accompanies hypertension.
Objectives: To study the prevalence of peripheral neuropathy in uremic patients on hemodialysis and its clinical and neurophysiological characters at Al-Azhar University Hospital in New Damietta.
Patients and Methods: This study was a cross-sectional study. This study was carried out at HemodialysisCenteratAl-AzharUniversityHospital in New Damietta.
     Fifty hemodialysis patients were investigated in the HemodialysisCenteratAl-AzharUniversityHospital in New Damietta. All patients were submitted to clinical evaluation by the Michigan Neuropathy Screening Instrument (MNSI), and Electroneuromyography (ENMG), and laboratory investigations.
Results: The results of the study revealed that there was no significant relation between dialysis mode and severity of neuropathy, and there was significant relation between duration of dialysis and neuropathy of the studied cases.
Conclusion: The present study emphasized the high prevalence of peripheral neuropathy in a group of patients with end-stage kidney disease under hemodialysis maintenance treatment. The gold standard exam for diagnosis confirmation was nerve conduction studies. Thus, before undergoing dialysis, it would be recommended to submit all patients with CKD to nerve conduction studies.

Keywords


THE PREVALENCE OF PERIPHERAL NEUROPATHY IN HEMODIALYSIS PATIENTS AT AL-AZHAR UNIVERSITY HOSPITAL IN NEW DAMIETTA CITY

By

Sherief M. Al-Shazly*, Mohammad Ali Saeed Hassan, El-Sayed Fathi Ali Hamed*, Mohammad Mahmoud Abd El-Aziz Mohammad*

Neurology Department, Faculty of Medicine, Al-AzharUniversity (Cairo and Damiatta*), Eygpt

*Corresponding author: Mohammad Mahmoud AbdElaziz Mohammad,

E-mail: drzezo531@gmail.com

ABSTRACT

Background: Chronic kidney disease (CKD) is a worldwide public health problem. There are several etiologies for CKD. It can occur due to either primary kidney disease or as a complication of a multi-systemic disorder. Much emphasis has been placed on the increased cardiovascular risk and electrolyte abnormalities that accompany chronic kidney disease. The dreaded neurological complications are usually the uremic encephalopathy or a vascular event that accompanies hypertension.

Objectives: To study the prevalence of peripheral neuropathy in uremic patients on hemodialysis and its clinical and neurophysiological characters at Al-Azhar University Hospital in New Damietta.

Patients and Methods: This study was a cross-sectional study. This study was carried out at HemodialysisCenteratAl-AzharUniversityHospital in New Damietta.

     Fifty hemodialysis patients were investigated in the HemodialysisCenteratAl-AzharUniversityHospital in New Damietta. All patients were submitted to clinical evaluation by the Michigan Neuropathy Screening Instrument (MNSI), and Electroneuromyography (ENMG), and laboratory investigations.

Results: The results of the study revealed that there was no significant relation between dialysis mode and severity of neuropathy, and there was significant relation between duration of dialysis and neuropathy of the studied cases.

Conclusion: The present study emphasized the high prevalence of peripheral neuropathy in a group of patients with end-stage kidney disease under hemodialysis maintenance treatment. The gold standard exam for diagnosis confirmation was nerve conduction studies. Thus, before undergoing dialysis, it would be recommended to submit all patients with CKD to nerve conduction studies.

Keywords: Dialysis, neuropathy, severity, CKD, case-control, motor, sensory.

 

 

INTRODUCTION

     Chronic Kidney Disease (CKD) is a major public health problem in developed and developing countries, leading to decreased quality of life across the globe. It is a well-known fact that patients of CKD are at increased risk of mortality as well as morbidity due to the myriad complications associated with this disease entity (AbdElHafeez et al., 2018).

     Neurological complications, secondary to the uremic state, contribute largely to the morbidity and mortality in patients with renal failure. Despite continuous therapeutic advances, many neurological complications of uremia, like uremic encephalopathy, atherosclerosis, neuropathy, and myopathy fail to respond completely to these treatment modalities (Rizzo et al., 2012).

     Studies of neuropathy in the end-stage renal disease have demonstrated that 70–100% of patients on dialysis experience neuropathic symptoms despite attaining current targets of dialysis adequacy (Aggarwalet al., 2013).

     Although the prevalence of severe neuropathy may appear to have decreased to a certain extent, a significant cohort of end-stage renal disease patients still report symptoms which are considered functionally disabling, and even patients who meet accepted guidelines for dialysis adequacy may complain of neuropathic symptoms, Renal transplantation remains the only known cure for uremic neuropathy, with clinical improvement in sensory and, to a lesser extent, motor function occurring within a few days of transplantation (Arun et al., 2009).

     The present work aimed to study the prevelance of peripheral neuropathy in uremic patients on hemodyialysis

SUBJECTS AND METHODS

     Permission from The Faculty of Medicine Ethical Committee was obtained, and approval from the institutional review board was taken.

     The researcher introduced himself to all participants included in this study and asked them to participate after illustrating the goal of the study.

     All selected participants received comprehensive information regarding the objective and the expected benefit of the study. All ethical considerations were taken throughout the whole work.  Informed verbal consents from all participants were taken and confidentiality of information was assured.

     This study was a cross-sectional study. This study was carried out at the hemodialysis center at Al-AzharUniversityHospital in New Damietta (Fifty hemodialysis patients).

Inclusion criteria:

     All patients irrespective of age and sex, and patients with end-stage chronic kidney disease on hemodialysis 4 hours’ duration and 3cycles per week.

Exclusion criteria:

     Patients denying Consent, patients on peritoneal dialysis, patients who had a renal transplant, patient with other known cause of peripheral neuropathy such as hypothyroidism, alcohol, diabetes mellitus, patients on drugs having peripheral neuropathy as established toxicity, malignancy, and vitamin B6 deficiencies.

History: This included Socio-demographic factors, with special emphasis on the cause, onset, duration of kidney disease, duration of hemodialysis, detailed neurological history with particular reference to the presence of risk factors for polyneuropathy and the occurrence of symptoms indicating peripheral neurological damage.

Diagnosis of UN (Uremic Neuropathy): This was investigated by the Michigan Neuropathy Screening Instrument questionnaire (MNSI_Q), and physical assessment (Duraisamy and Parthasarathy, 2018).

     Neurological examination was done with special emphasis on peripheral nerve examination.

     Laboratory investigations were performed for every patient before the electrophysiological examination. The Parameters included CBC, S. creatinine, and fasting blood glucose.

     Electrophysiological studies were performed by using Mihonkohden Machine for motor nerve conductions, sensory nerve conduction, late responses, and EMG Protocol.

Statistical analysis:

     Analysis of data was done using the Statistical Package for Social Science version 20 (SPSS Inc., Chicago, IL, USA). Quantitative variables were described in the form of mean and standard deviation, and range. Qualitative variables were described as number and percentage. To compare parametric quantitative variables between two groups, the Student t-test was performed.  Qualitative variables were compared using the chi-square (X2) test or Fisher’s exact test when frequencies were below five. P-value < 0.05 was considered significant.


 

RESULTS

 

 

     The cause of chronic kidney disease was chronic glomerulonephritis in 38%, chronic interstitial nephritis in 26%, hypertension in 6%, obstructive chronic kidney disease in 10%, congenital in 10% and others in 10% (Table 1).


 

Table (1) Causes of chronic kidney disease in studied cases

Causes of chronic kidney disease

N

%

Chronic glomerulonephritis

19

38

Chronic interstitial nephritis

13

26

Obstructive chronic kidney disease

5

10

Congenital

5

10

Hypertention

3

6

Others

5

10

 

 

     The mean Session length per week was 11.7 ± 1.1 with range of 8-13 hours, Low-flux was present in 56.0% and High-flux was in 44%, hemodialysis in 88 % and Hemodiafiltration in 12%, and demyelination was present in 21% of cases, axonal in 39.5% and combined in 39.5% (Table 2).


 

 

 

 

 

 

 

Table (2) Types of neuropathy and dialysis characteristics of the studied cases

Types of Neuropathy

N

%

Demyelination

Axonal

Combined

8

15

15

21.0

39.5

39.5

Session length per week (Hours)

Mean ± SD

Range

11.7 ± 1.1

8-13

Dialyzer type

N

%

Low-flux

High-flux

28

22

56.0

44.0

Dialysis mode

N

%

Hemodialysis

Hemodiafiltration

44

6

88.0

12.0

 

 

     76% of cases have ENMG evidence of polyneuropathy, and 36% have scored MNSI scores between 5-10 out of 10 and 58% have scored MNSI scores between 3-5.5 out of 10 and 2% have scored MNSI scores between 1-2.5 and 4% not have any point of MNSI scores (Table 3).


 

Table (3): ENMG evidence of polyneuropathy and MNSI score among studied cases

Variables

Present

Absent

ENMG evidence

 of polyneuropathy

N

%

N

%

38

76

12

24

Cases:

N

%

MNSI score:

5-10

3-5.5

1-2.5

No point

18

29

1

2

36.0

58.0

2.0

4.0

 

     There was a significant relation between the duration of dialysis and neuropathy of the studied cases (Table 4).

 

Table (4): Relation between duration of dialysis and neuropathy of the studied cases

Variables

Duration

of dialysis

With neuropathy

N=38

Without neuropathy

N=12

P-value

Mean ± SD

5.11±1.75

3.01±0.95

< 0.001

(S)

 

     There was no significant relation between Dialysis mode and severity of neuropathy (Table 5).

 

 

 

 

Table (5) Relation between Dialysis mode and severity of neuropathy

Parameters

Dialysis

mode

Severe neuropathy

N=18

Moderate

N=10

Mild

N=10

P-value

 

NO.

%

NO.

%

NO.

%

 

Hemodialysis

Hemodiafiltration

16

2

88.9

11.1

8

2

80.0

20.0

9

1

90.0

10.0

0.453

 

 

     In patients with neuropathy there was a predominant decrease in CMAP amplitudes with relatively decreased conduction velocity, and prolonged distal latency (Table 6).

 

 

Table (6): Motor nerve conduction studies in the study

Parameters

 

Variables

Decrease in CMAP

amplitude

Decrease Conduction

velocity

Prolonged distal latency

 

No

%

No

%

No

%

Peroneal

 

34

68.0

33

66.0

21

42.0

Tibial

 

33

66.0

30

60.0

19

38.0

Ulnar

 

15

30.0

15

30.0

2

10.0

Median

 

14

28.0

14

28.0

2

10.0

 

 

     Patients with neuropathy were showed decreased SNAP amplitudes with relatively decreased conduction velocity (Table 7).


Table (7): Sensory nerve conduction studies in the study.

Parameters

Variables

Decrease SNAP amplitude

Decreased conduction velocity

 

No

%

No

%

Sural

 

38

76.0

35

70.0

Median 

 

20

40.0

22

44.0

Ulnar

 

17

34.0

20

40.0

 

 

     2.6% of patients have motor weakness, and 50% have sensory symptoms, and 44.7% have autonomic symptoms, No patient have wasting of limbs, and 78.9% have absent ankle jerk, and 31.6% have impaired pain and temperature, 44.7 % have impaired vibration and joint position sense (Table 8).


 

 

 

 

Table (8): Symptoms and signs in Cases in the study

Variables

Cases

 

No

%

Motor weakness :

 

1

2.6

Sensory symptoms :

 

19

50.0

Autonomic symptoms:

 

17

44.7

Wasting of limbs:

 

0

0.0

Absent ankle jerk:

 

30

78.9

Impaired pain and temperature :

 

12

31.6

Impaired vibration and joint position sense :

 

17

44.7

 

 

DISCUSSION

     The present study showed that the cause of CKD was CGN in 38%, CIN in 26%, hypertension in 6%, obstructive CKD in 10%, congenital in 10%, and others in 10%.Our results were supported by the study of Macárioet al. (2011) as they reported that in Portugal the main etiologies for CKD in the patients under hemodialysis treatment are DM (33.6%), undetermined (20.7%), and arterial hypertension (15.5%).

     The current study showed that demyelination was present in 21% of cases, axonal in 39.5% and combined in 39.5. A patient has motor weakness 2.6%, and 50% have sensory symptoms, and 44.7% have autonomic symptoms, and 0% have wasting of limbs, and 78.9% have absent ankle jerk, and 31.6%have impaired pain and temperature, and 44.7 % have impaired vibration and joint position sense. Our results were supported by the study of Kolli et al. (2018) who reported that positive sensory symptoms were seen in 48.5%, while negative sensory symptoms were seen in 38.5%. Autonomic symptoms were seen in 8.5%.  80.5% had absent ankle jerk. Impaired pain and temperature sensation were noted in 30.5%, while impaired vibration and joint position sense was noted in 43%. Motor weakness was noted in 3% of patients. According to Anbarasu and Prathiba (2018) 71.6% of patients were diagnosed as having clinical peripheral neuropathy, and 28.33% had not satisfied the diagnosis of clinical peripheral neuropathy.

     Furthermore, Santos (2012) observed that all the patients with motor symptoms also had sensory symptoms, but not all the patients with sensory symptoms had motor symptoms.

     As regard MNSI scores, 36% have scored MNSI scores between 5-10 out of 10, and 58% have scored MNSI scores between 3-5.5 out of 10, and 2% have scored MNSI scores between 1-2.5, and 4% did not have any point of MNSI scores Mambelli, et al. (2012) concluded the study by saying that MNSI could represent a valid and simple clinical-instrumental screening test for the early diagnosis of UN because of an early therapeutic approach. The course of neuropathy is variable in patients undergoing hemodialysis. Routine hemodialysis has found not to improve neuropathy in patients with CKD despite the decrease in urea and creatinine levels, this was emphasized by Borire et al.  (2017).

     As regard hemodialysis characteristics, the mean session length per week was 11.7 ± 1.1 with a range of 8-13 hours. Low-flux was present in 56.0% and high-flux was in 44%. Hemodialysis was in 88 % and hemodiafiltration was at 12%. Our results showed that 76% of cases have ENMG evidence of polyneuropathy. 58% of them had 3-5.5 of MNSI score. Our results are supported by the study of Anbarasu and Prathiba (2018) as they reported that the smallest MNSI score obtained in the study population was 2 and the largest score was 7 with a mean score of 2.580 with a standard deviation of 2.069.

     The current study showed that there was no significant relation between demographic data and neuropathy. Anbarasu and Prathiba (2018) reported that males were significantly more affected by peripheral neuropathy when compared to females. Concerning age, in their study, it was found that patients aged ≥60 years were predominantly affected by uremic neuropathy which was statistically very significant.

     Our results showed that there was a significant relation between neuropathy and urea level, while there was no significant relation between other renal functions and neuropathy. There was no significant relation between neuropathy and the etiology of CKD in the study of the studied cases. There was a significant relation between the duration of hemodialysis and neuropathy of the studied cases.

     In the present study, there was no significant relation between hemodialysis mode and severity of neuropathy. There was a significant relation between renal function and neuropathy severity of the studied cases. In patients with neuropathy, there were a predominant decrease in compound motor action potential (CMAP) amplitudes with relatively decreased conduction velocity, and prolonged distal latency.  Abnormalities were found in the peak latency, sensory nerve action potential (SNAP) amplitude and conduction velocity (CV) of the sural, median, ulnar nerves. In patients with neuropathy, SNAP amplitudes decreased with relatively decreased conduction velocity. Aggarwal et al. (2013) showed that mean nerve conduction velocities (m/sec), which were almost similar to this study. Tilki et al. (2009) reported that the prevalence of uremic neuropathy is 60%- 100% of patients on hemodialysis. Neuropathy generally only develops at glomerular filtration rates of less than 12 mL/min/1.73 m2. In stage V CKD (on HD), the prevalence of clinical uremic peripheral neuropathy was 71.6% which was clinically and statistically significant.

CONCLUSION

     The present study emphasized the high prevalence of peripheral neuropathy in a group of patients with end-stage kidney disease under hemodialysis maintenance treatment. Despite the short period, the study was conducted and, consequently, small sample size, the obtained results allowed us to highlights the huge importance of having neurologists and nephrologists as well as other specialists working all together to better diagnose and manage neurological complications of end-stage kidney disease in those patients. The standard exam for diagnosis confirmation is nerve conduction studies. Thus, before undergoing hemodialysis, it would be recommended to submit all patients with CKD to nerve conduction studies.

REFERENCES

  1. Aggarwal HK, Sood S, Jain D, Kaverappa  v and Yadav S. (2013): Evaluation of spectrum of peripheral neuropathy in predialysis patients with chronic kidney disease. Renal failure, 35:1-7.
  2. Anbarasu D., and Prathiba P. (2018): Study on prevalence of peripheral neuropathy among patients on hemodialysis.IAIM, 5(10): 73-80.
  3. AbdElHafeez S,  Bolignano D, 'Arrigo G, Dounousi E,Tripepi G ,and  Zoccali C. (2018): Prevalence and burden of chronic kidney disease among the general population and high-risk groups in Africa: a systematic review BMJ Open, 8:e015069.
  4. Kolli, S. (2018): A Clinical and Electrophysiological Study of Peripheral Neuropathies in Predialysis and Dialysis Patients: Our Experience from South India. Journal of The Association of Physicians of India, 66(6):31-37.
  5. Macário F, Filipe R, Carvalho MJ, Galvão A, Lopes JA, Amoedo M. (2011): Diálise Domiciliária. SPNews - Sociedade Portuguesa de Neurologia, VII (24):1–20.
  6. Mambelli E, Barrella M, Facchini MG, Mancini E, Sicuso C, Bainotti S, Formica M and Santoro A. (2012): The prevalence of peripheral neuropathy in hemodialysis patients. Clinical Nephrology, 77(6): 468-75.
  7. Rizzo MA, Frediani F, Granata A, Ravasi B, Cusi D, and Gallieni M. (2012): Neurological complications of hemodialysis: J Neph., 25(02): 170-182.
  8. Santos, A. O. P. (2012): Peripheral neuropathy in patients in haemodialysis treatment Doctoral dissertation, Universidade da Beira Interior.‏
  9. Tilki HE, Akpolat T, Coşkun M, and Stålberg E. (2009): Clinical and electrophysiologic findings in dialysis patients. Journal of Electromyography and Kinesiology, 19(3): 500-8.


انتشاراعتلال الاعصاب الطرفیة عند مرضى غسیل الکلى الدموى بمستشفى جامعة الازهر بدمیاط الجدیدة

شریف محمود الشاذلى*, محمد على سعید حسن, السید فتحى على حامد*, محمد محمود عبد العزیز محمد *

قسم طب المخ والاعصاب بکلیة الطب جامعة الازهر, (القاهرة و دمیاط*), مصر

خلفیة البحث: مرض الکلى المزمن هو مشکلة صحیة عامة فی جمیع أنحاء العالم. هناک العدید من مسببات مرض الکلى المزمن. یمکن أن یحدث بسبب مرض الکلى الأولی أو کمضاعفات لاضطراب الانظمه المتعدده. وقد تم الترکیز کثیرا على زیادة مخاطر القلب والأوعیة الدمویة وتشوهات المعادن التی تصاحب أمراض الکلى المزمنة. المضاعفات العصبیة عادة ما تکون اعتلال الدماغ االبولى أو احداث الأوعیة الدمویة التی ترافق ارتفاع ضغط الدم.

الهدف من البحث: دراسة مدى انتشار الاعتلال العصبی الطرفى لدى مرضى غسیل الکلى الدموى وتشخصیاته السریریة والعصبیة الفسیولوجیة فی مستشفى جامعة الأزهر بدمیاط الجدیدة.

المرضى وطرق البحث: کانت هذه الدراسة دراسة مقطعیة. أجریت هذه الدراسة فی مرکز غسیل الکلى الدموى بمستشفى جامعة الأزهر بدمیاط الجدیدة.

         تم ادراج 50 مریضاً بغسیل الکلى بمرکز غسیل الکلى الدموى بمستشفى جامعة الأزهر بدمیاط الجدیدة. وتم تقدیم جمیع المرضى للتقییم السریری باستخدام وسیلة میشیغان فى  فحص الاعتلال العصبی، ودراسة فسیولوجیا الاعصاب، والتحقیقات المختبریة.

النتائج: کشفت نتائج الدراسة أنه لم تکن هناک علاقة کبیرة بین أسلوب غسیل الکلى الدموى وشدة الاعتلال العصبی، وکانت هناک علاقة کبیرة بین مدة غسیل الکلى والاعتلال العصبی للحالات المدروسة.

الاستنتاج: أکدت هذه الدراسة على ارتفاع معدل انتشار الاعتلال العصبی الطرفى فی مجموعة من المرضى الذین یعانون من مرض الکلى فی المرحلة النهائیة تحت علاج غسیل الکلى الدموى. کان اختبار المعیار الذهبی لتأکید التشخیص هو دراسات التوصیل العصبی. وهکذا، قبل الخضوع لغسیل الکلى الدموى، یوصى بتقدیم جمیع المرضى المصابین بمرض الکلى المزمن إلى دراسات التوصیل العصبی.

 

  1. REFERENCES

    1. Aggarwal HK, Sood S, Jain D, Kaverappa  v and Yadav S. (2013): Evaluation of spectrum of peripheral neuropathy in predialysis patients with chronic kidney disease. Renal failure, 35:1-7.
    2. Anbarasu D., and Prathiba P. (2018): Study on prevalence of peripheral neuropathy among patients on hemodialysis.IAIM, 5(10): 73-80.
    3. AbdElHafeez S,  Bolignano D, 'Arrigo G, Dounousi E,Tripepi G ,and  Zoccali C. (2018): Prevalence and burden of chronic kidney disease among the general population and high-risk groups in Africa: a systematic review BMJ Open, 8:e015069.
    4. Kolli, S. (2018): A Clinical and Electrophysiological Study of Peripheral Neuropathies in Predialysis and Dialysis Patients: Our Experience from South India. Journal of The Association of Physicians of India, 66(6):31-37.
    5. Macário F, Filipe R, Carvalho MJ, Galvão A, Lopes JA, Amoedo M. (2011): Diálise Domiciliária. SPNews - Sociedade Portuguesa de Neurologia, VII (24):1–20.
    6. Mambelli E, Barrella M, Facchini MG, Mancini E, Sicuso C, Bainotti S, Formica M and Santoro A. (2012): The prevalence of peripheral neuropathy in hemodialysis patients. Clinical Nephrology, 77(6): 468-75.
    7. Rizzo MA, Frediani F, Granata A, Ravasi B, Cusi D, and Gallieni M. (2012): Neurological complications of hemodialysis: J Neph., 25(02): 170-182.
    8. Santos, A. O. P. (2012): Peripheral neuropathy in patients in haemodialysis treatment Doctoral dissertation, Universidade da Beira Interior.‏
    9. Tilki HE, Akpolat T, Coşkun M, and Stålberg E. (2009): Clinical and electrophysiologic findings in dialysis patients. Journal of Electromyography and Kinesiology, 19(3): 500-8.