|Year : 2019 | Volume
| Issue : 1 | Page : 1-7
Effect of intradialytic aerobic exercise on patients with diabetic nephropathy
Abdel Raoof A Neveen1, El Nahas G Nesreen2, Marae K Nadia3, Galal M Al Shaimaa4
1 Department of Basic Science, Faculty of Physical Therapy, Cairo University, Cairo, Egypt
2 Department of Cardiovascular, Respiratory Disorder and Geriatrics, Faculty of Physical Therapy, Cairo University, Cairo, Egypt
3 Department of Internal Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt
4 Department of Physical Therapy, Cairo University, Cairo, Egypt
|Date of Web Publication||19-Mar-2019|
Galal M Al Shaimaa
61 El Tahrir street, Edfu, Aswan
Source of Support: None, Conflict of Interest: None
Background Diabetes is a major health problem in nowadays’ society, as the number of patients with diabetes is growing continuously with their diabetic complications, especially kidney diseases, which is the most feared complication because of its substantial comorbidity, cost, and mortality.
Purpose The aim of this study was to determine the effect of intradialytic aerobic exercise on kidney functions tests [serum calcium, serum creatinine, urine creatinine, urine albumin, and estimated glomerular filtration rate (GFR)] in patients with diabetic nephropathy.
Materials and methods Thirty patients of both sexes (19 male and 11 female) under hemodialysis with a mean age of 54.13±4.32 years were selected from the renal rehabilitation unit of Edfou General Hospital. They were assigned randomly to two groups of equal number. Group A received a moderate-intensity intradialytic aerobic exercise program (12–13 on rate of perceived exertion scale), and group B received their regular dialysis program only. The treatment program continued for 8 weeks (three exercise sessions per week). Laboratory investigations for serum calcium, serum creatinine, urine creatinine, urine albumin, and estimated GFR were carried out at the beginning and after the end of the treatment program in both groups.
Results The results of this study revealed a significant increase in serum calcium in group A compared with group B, and a significant decrease in serum creatinine and urine creatinine in group A compared with group B (P=0.03 and 0.04, respectively). There was no significant change in urine albumin and estimated GFR between the two groups.
Conclusion Moderate-intensity intradialytic aerobic exercise (12–13 rate of perceived exertion scale) is beneficial in modulating serum calcium, serum creatinine, and urine creatinine in diabetic nephropathy patients.
Keywords: aerobic exercise, chronic kidney disease, diabetic nephropathy, dialysis
|How to cite this article:|
Neveen AA, Nesreen EG, Nadia MK, Al Shaimaa GM. Effect of intradialytic aerobic exercise on patients with diabetic nephropathy. Bull Fac Phys Ther 2019;24:1-7
|How to cite this URL:|
Neveen AA, Nesreen EG, Nadia MK, Al Shaimaa GM. Effect of intradialytic aerobic exercise on patients with diabetic nephropathy. Bull Fac Phys Ther [serial online] 2019 [cited 2020 Feb 22];24:1-7. Available from: http://www.bfpt.eg.net/text.asp?2019/24/1/1/254615
| Introduction|| |
Chronic kidney disease (CKD) is characterized by abnormal kidney function and/or structure. It is common, and often exists together with other conditions (e.g. cardiovascular disease and diabetes) . This global epidemic of diabetes is in large part due to obesity and sedentary lifestyle. The major determinants of kidney disease and its progression to end-stage kidney failure, especially in type 2 diabetes are uncontrolled blood glucose, blood pressure, and albuminuria .
Complications of diabetes include macrovascular complications (coronary heart disease, peripheral vascular disease, and cerebrovascular accident) and microvascular complications (neuropathy, retinopathy, and nephropathy) . Diabetic nephropathy is a progressive kidney disease caused by angiopathy of capillaries in the kidney glomeruli. It is characterized by nephrotic syndrome and diffuse glomerulosclerosis. It is due to longstanding diabetes mellitus, and is a prime indication for dialysis in many developed countries. It is classified as a small blood vessel complication of diabetes .
It is established that hemodialysis (HD) patients have low levels of physical activity compared with their age-matched controls . Physical inactivity has also been associated with lower levels of self-reported physical functioning (particularly lower extremity), a higher prevalence of cardiovascular disease , and an increased level of all-cause and cardiovascular mortality .
Exercise plays an important part in diabetes prevention and management . Previous studies found that exercise can reduce hemoglobulin A1C levels in patients with type 2 diabetes mellitus and improve cardiovascular fitness, reduce blood pressure, and improve lipid profile . Oxidative stress and inflammation were also improved after exercise .
According to the American College of Sports Medicine and American Heart Association, to the reduce risk for cardiovascular events, individuals with chronic illnesses should perform moderate-intensity physical activity for 30 min, five times weekly . In addition, Stack and Murthy  reported that physical exercises performed four-to-five times a week reduced the risk for death of physically active patients under HD by about 30%, when compared with sedentary patients; this is in agreement with the recommended features of this study.
As glycemic control, blood pressure control, and oxidative stress are believed to play an integral role in the pathogenesis of diabetic nephropathy, it is logical to hypothesize that exercise has beneficial effects against diabetic nephropathy. However, few studies ,,, have focused on this topic, and their results were inconclusive.
Being physically active on a regular basis will promote a range of health benefits, including reduced likelihood of cardiovascular disease, diabetes, and some cancers, strengthened heart and cardiovascular system, increased muscle strength, stronger bones, especially if the activity is weight bearing, improved stamina, lowered blood cholesterol levels, reduced blood pressure, and loss of excess body fat . Exercise for renal patients with diabetes is very important, and studies reported that staying active is the best choice to be healthy and being active every day in many ways, such as walking, cycling, and doing things by themselves . Daily physical exercise of moderate-intensity physical activity for 30 min is important for patients with renal dialysis, such as a brisk walk or cycling. The 30 min need not be continuous and can be combined with short sessions of different activities of around 10–15 min each .
It is known that inactivity, muscle wasting, and reduced physical functioning, especially for those on long-term dialysis, are associated with increased mortality in CKD. Exercise in patients receiving regular dialysis as a treatment for end-stage renal disease was first introduced 3 decades ago, but is still only offered in a minority of renal units around the world, despite a significant body of evidence to support its use. Work is needed to increase awareness of the potential benefits of increased physical activity for patients with advanced CKD .
Thus, the aim of this study was to determine the effect of intradialytic aerobic exercise on renal function tests in patients with kidney disease secondary to diabetic nephropathy.
| Materials and methods|| |
The sample size was estimated as per work of research methods and reporting . Totally, 54 patients were assessed for eligibility to participate in this study (n=54) from Edfu General Hospital for being under dialysis as a complication of diabetes and not any other cause ([Figure 1],[Figure 2],[Figure 3],[Figure 4],[Figure 5]). Totally, 16 patients were excluded for not meeting the inclusion criteria (n=16), four patients declined to participate (n=4), and four patients died during the study (n=4). Totally, 30 patients (n=30) of both sexes (19 male and 11 female) under renal HD for more than 3 months and with a mean age of 54.13±4.32 years were enrolled in this study. All patients gave their written informed consent for the participation in the study that had been preceded by the explanation of the aim of the study and its course, their role in it with regard to time and money, assurance of protection of the obtained data, and information about free willingness to participate in the study and the possibility to withdraw from the study at any time. This study was approved by the Ethics Committee for scientific research of the Faculty of Physical Therapy, Cairo University.
|Figure 1 Flow diagram of the progress through the phases of a parallel randomized trial of two groups (i.e. enrollment, intervention allocation, follow-up, and data analysis) ,,|
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Patients were included if they were diagnosed as having type 2 diabetes for more than 10 years. They were diagnosed as having CKD secondary to diabetic nephropathy. It is differentiated from acute kidney disease (acute kidney injury) in that the reduction in kidney function must be present for over 3 months . The patients were on HD for more than 3 months. Their ages ranged between 40 and 60 years. The study included both sexes (male and female) and BMI ranged from 29 to 36. All of the patients had a sedentary lifestyle.
Patients were excluded if they had poorly controlled hypertension, uncompensated heart failure, cardiac arrhythmia requiring treatment, recent unstable angina, persistent hyperkalemia before dialysis, significant valvular heart disease, myocardial infarction within the past 6 months, significant cerebral or peripheral arteriosclerosis, bone disease with a risk for fracture, orthopedic, or musculoskeletal limitations, a recent significant change in the resting echocardiography, third-degree atroventricular heart block without pacemaker, severe aortic stenosis, suspected or known dissecting aneurysm, active or suspected myocarditis or pericarditis thrombophlebitis or intracardiac thrombi, and recent systemic or pulmonary embolus and acute infection.
All patients were initially assessed for their weight and height using weight and height scale to calculate BMI, and assessed for their vital signs as well. Laboratory investigations (kidney functions) were carried out for both groups before and after 8 weeks of aerobic exercise program. Blood and urine samples were taken to measure urine albumin and creatinine levels, serum creatinine level, serum calcium level, and estimated glomerular filtration rate (GFR) using the following formula ,:
Patients were randomly assigned (simple randomization) to two groups of equal number, group A and group B. Each group consisted of fifteen patients: group A included 10 male and five female patients, and group B included nine male and six female patients. Group A received treatment program consisting of intradialytic aerobic exercise for 8 weeks, whereas group B did not receive any exercise program and acted as the control group. Group A received a program of moderate-intensity aerobic exercise  [12–13 rate of perceived exertion scale (RPE)] using Bicycle ergometer Zhejiang pedal exerciser, Zhejiang Todo Hardware Manufacture Co. Ltd, Zhejiang China (Mainland), with an exercise period of 30 min. The exercise period comprised the following: the warming up phase (3–5 min), which included aerobic movement exercise of range of motion joints: rotating the wrist (20 rpm clockwise and 20 rpm counter clockwise), wrist up and down (up to 20 moves on the forearm), ankle twisting motion (40 rotations clockwise and counterclockwise around the ankles), and ankles up and down (20 times); the actual phase (20–30 min), which included cycle ergometer exercise with 12–13 RPE; and finally the cooling down phase (3–5 min) in the form of the same aerobic movements as performed in the warming up phase. Because of the study aims and design, the use of VO2 max was not an option. In addition, the use of target heart rates in dialysis patients is unreliable as they have abnormal exercise heart rate responses, because of frequently prescribed medications that affect their heart rate response, especially if they are hypertensive (e.g. β-blockers). Furthermore, an individual’s heart rate response may be influenced by fluid status. Therefore, the RPE scale was used to detect exercise intensity.
The unwanted events during exercise were controlled by performing the exercise in the first 2 h of the dialysis session to avoid the cardiovascular decompensation and by following the precautions and contraindications to exercise in renal patients. Moreover, we stopped the exercise session and called for medical supervision if unwanted events occurred.
Descriptive analysis was used for all measured parameters in the form of mean and SD. Level of significance for all tests was set at P-value of 0.05. Paired and unpaired t-test was used to compare the results of serum calcium, serum creatinine, urine creatinine urine albumin, and GFR within and between the two groups.
| Results|| |
Independent t-tests showed no significant differences between the two groups in the age, weight, height, BMI, blood pressure, glucose level, and duration of diabetes ([Table 1]). In group A, there was a significant increase in Ca and GFR after treatment compared with pretreatment values (P=0.0001 for both), whereas there was no significant difference in Ca or GFR between pretreatment and post-treatment values (P=0.42 and 0.22, respectively) in group B ([Table 2] and [Table 3]). In group A, there was a significant decrease in serum creatinine and urine creatinine after treatment compared with that before treatment (P=0.0001 for both) ([Table 2]). In group B, there was no significant difference in serum creatinine or urine creatinine between pretreatment and post-treatment levels (P=0.07 and 0.27, respectively) ([Table 3]). There was no significant difference in urine albumin before and after treatment in both groups (group A, P=0.1 and group B, P=0.16) ([Table 2] and [Table 3]).
|Table 1 Descriptive statistics and t-test for the mean age, weight, height, BMI, systolic blood pressure, diastolic blood pressure, blood glucose level, and duration of diabetes of both groups (study and control)|
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|Table 2 Paired t-test for comparison between pretreatment and post-treatment mean values of group A|
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|Table 3 Paired t-test for comparison between pretreatment and post-treatment mean values of group B|
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A significant difference between the two groups in serum calcium, serum creatinine, and urine creatinine was found. Serum calcium increased significantly by 15.11% in group A compared with group B at the end of the treatment program. Moreover, serum creatinine and urine creatinine decreased significantly by 11.53 and 15.39%, respectively, in group A compared with group B at the end of the treatment program ([Table 4] and [Table 5]).
|Table 4 t-Test for comparison of pretreatment mean values between the two groups|
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|Table 5 t-Test for comparison between post-treatment mean values of both groups (group A and group B)|
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However, there was no significant change in urine albumin between the two groups (P=0.85). Although the estimated GFR was increased in group A, compared with group B, there was no significant difference (P=0.87) between the two groups ([Table 4] and [Table 5]).
| Discussion|| |
In the present study, the results revealed a significant increase in serum calcium in group A compared with group B. Furthermore, there were significant decreases in serum creatinine and urine creatinine in group A compared with group B in response to the designed exercise program. However, there was no significant change in urine albumin between the two groups. Although the estimated GFR was increased in group A compared with group B, there was no significant difference between the two groups.
The results of this study are in agreement with a study by Yu et al. , who studied the effect of physical activity on diabetic nephropathy in particular in a long study continued for more than 1 year, in that they could not identify physical activity as an important factor for reducing albuminurea and estimated GFR.
Although the effect of physical activity on diabetic nephropathy remains controversial, patients with diabetic nephropathy are at a high risk of developing cardiovascular disease . Physical activity improves the glycemic index, blood pressure, and lipid control . These are all important cardiovascular risk factors. Physical activity can improve patient’s quality of life as well . Thus, increased physical activity should be encouraged among patients with diabetes mellitus.
Moreover, Kurdak et al.  reported that, after 8 weeks of aerobic exercise in streptozotocin-induced diabetic rats, there was no significant difference in albumin in urine level between the study and the control group, whereas GFR value was lower in the exercise group, which coincides with our study result. This is contradictory to our study results but these rats were only diabetic and did not have a renal failure.
In addition to these results, the results of Yuji et al.  were in line with this study in that, after 8 weeks of exercise on mice with diabetic nephropathy, there was no significant difference in urine albumin level or GFR value between the study and the control group (despite a slight increase in GFR in the study group and a slight decrease in urine albumin level, but not statistically significant).
The result of this study coincides with the results of a study by El-Nahas et al. , who studied the effects of different exercise intensities on serum electrolyte level in HD patients. The study showed that moderate-intensity aerobic exercise increases serum calcium level (improvement of 12.29%) and seems to induce positive calcium balance more than light-intensity exercise (improvement of 4.23%). This point was approved by Zaher et al. as well .
The results of the present study as regards serum calcium level coincide with the data presented by Vaithilingham et al. , who suggested that an aerobic exercise regimen for 15 min during HD sessions improves serum calcium levels in a period of 8 weeks. This observation might be attributed to the direct beneficial effects of aerobic exercise or general effects of regular intradialytic exercise.
Although many studies agree with the results of the present study, Makhlough et al.  reported that 15 min of intradialytic aerobic exercise could not induce a significant difference in serum calcium level. This is contradictory to our study results. In this study, they investigated the effect of low-intensity (not moderate-intensity) intradialytic aerobic exercise on serum electrolyte level in HD patients, which may be a factor explaining this contradiction. Azra et al.  agreed with this and reported that there was no significant difference in serum electrolytes between active and passive pedaling intradialytic exercise. This result differs from present study results; this may be due to the small sample size in the study by Azra (16 participants only).
The present study is in agreement with the study by Afshar et al. , who compared between the effects of aerobic and resistance training in patients on maintenance HD. They reported that there was a significant reduction in serum creatinine for the aerobic type of exercise. However, there was no effect on serum albumin and body weight.
Parsons et al.  reported that combined program of aerobic and resistance training using cycle ergometer thrice weekly for 45 min (3–5 min bouts) did not induce a significant difference in serum creatinine, and the only significant changes observed were the increase in dialysate urea removal. This discrepancy may be due to the small sample size of the study by Parson.
Some results of the present study warrant further investigations. In addition to the need to study the effect of exercise on some other parameters (e.g. urea, glucose levels, quality of life, and psychological status) in patients with diabetic nephropathy, the most important is to conduct the research with a large sample size and a study duration of more than 6 months, which is needed to eliminate large discrepancies between different study results. To achieve this large number of samples, multiple researchers in multiple rental units should work together on the same topic.
The high dropout rate of end-stage renal disease was the main limitation that we faced in this study. In addition to this, lack of motivation, psychological status, and connecting needles were other limitations.
| Conclusion|| |
Intradialytic aerobic exercise with moderate intensity showed a significant increase in serum calcium and a significant decrease in serum creatinine and creatinine in urine in group A compared with group B, which was beneficial in modulating renal function tests for patients with diabetic nephropathy who received the exercise program.
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Conflicts of interests
There are no conflicts of interest.
| References|| |
NICE Clinical Guideline 73. Chronic kidney disease: early identification and management of chronic kidney disease in adults in primary and secondary care. UK: National Institute for Health and Clinical Excellence; 2008.1.
Stratton IM, Cull CA, Adler AI, Matthews DR, Neil HA, Holman RR. Additive effects of glycaemia and blood pressure exposure on risk of complications in type 2 diabetes: a prospective observational study (UKPDS 75). Diabetologia 2008; 49:1761–1769.
Bloomgarden ZT. American Diabetes Association annual meeting, more on cardiovascular disease. Diabetes Care 2000; 23:845–852.
Zamojska S, Szklarek M, Niewodniczy M, Nowicki M. Correlates of habitual physical activity in chronic hemodialysis patients. Nephrol Dial Transplant 2006; 21:1323–1327.
Longo DL, Fauci AS, Kasper DL, Hauser SL, Jameson JL, Harrison’s JL. Principles of internal medicine, 18th ed.; 2015. p. 2982.
O’Hare AM, Tawney K, Bacchetti P, Johansen KL. Decreased survival among sedentary patients undergoing dialysis: results from the dialysis morbidity and mortality study wave 2. Am J Kidney Dis 2003; 41:447–454.
Stack AG, Molony DA, Rives T, Tyson J, Murthy BVR. Association of physical activity with mortality in the US dialysis population. Am J Kidney Dis 2005; 45:690–701.
Wing RR. Long-term effects of a lifestyle intervention on weight and cardiovascular risk factors in individuals with type 2 diabetes mellitus: four-year results of the Look AHEAD trial. Arch Intern Med 2010; 170:1566–1575.
Chudyk A, Petrella RJ. Effects of exercise on cardiovascular risk factors in type 2 diabetes: a meta-analysis. Diabetes Care 2011; 34:1228–1237.
Choi KM, Han KA, Ahn HJ, Hwang SY, Hong HC, Choi HY et al.
Effects of exercise on sRAGE levels and cardiometabolic risk factors in patients with type 2 diabetes: a randomized controlled trial. J Clin Endocrinol Metab 2012; 97:3751–3758.
Nelson M, Rejeski W, Blair S, Duncan P, Judge J, King A. Physical activity and public health in older adults: recommendation from the American College of Sports Medicine and Heart Association. Med Sci Sport Med 2007; 39:1435–1445.
Stack AG, Murthy B. Exercise and limitations in physical activity levels among new dialysis patients in the United States: an epidemiologic study. Ann Epidemiol 2008; 18:880–888.
Boor P, Celec P, Behuliak M, Grančič P, Kebis A, Kukan M et al.
Regular moderate exercise reduces advanced glycation and ameliorates early diabetic nephropathy in obese Zucker rats. Metabolism 2009; 58:1669–1677.
Ishikawa Y, Gohda T, Tanimoto M, Omote K, Furukawa M, Yamaguchi S et al.
Effect of exercise on kidney function, oxidative stress, and inflammation in type 2 diabetic KK-A(y) mice. Exp Diabetes Res 2012; 2012:1–10.
Lazarevic G, Antic S, Vlahovic P, Djordjevic V, Zvezdanovic L, Stefanovic V. Effects of aerobic exercise on microalbuminuria and enzymuria in type 2 diabetic patients. Ren Fail 2007; 29:199–205.
Leehey DJ, Moinuddin I, Bast JP, Qureshi S, Jelinek CS, Cooper C et al.
Aerobic exercise in obese diabetic patients with chronic kidney disease: a randomized and controlled pilot study. Cardiovasc Diabetol 2009;8:62.
Kouidi E. Central and peripheral adaptations to physical training in patients with end-stage renal disease. Sports Med 2001; 31:651–665.
Neil A, Smart A, Andrew D, Williams B, Itamar Levinger C, Steve Selig D et al.
Exercise & Sports Science Australia (ESSA) position statement on exercise and chronic kidney disease. J Sci Med Sport 2013; 16:406–411.
Moher D, Hopewell S, Schulz KF, Montori V, Gøtzsche PC, Devereaux PJ et al.
CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials. BMJ 2010; 340:c869.
Moher D, Schulz KF, Altman DG. The CONSORT statement: revised 52 recommendations for improving the quality of reports of parallel-group randomized trials. Ann Intern Med 2001; 134:657–662.
Moher D, Schulz KF, Altman D. The CONSORT statement: revised 53 recommendations for improving the quality of reports of parallel-group randomized trials. JAMA 2001; 285:1987–1991.
Moher D, Schulz KF, Altman DG. The CONSORT statement: revised 54 recommendations for improving the quality of reports of parallel-group randomised trials. Lancet 2001; 357:1191–1194.
Martínez-Castelao A, Górriz JL, Bover J et al.
Consensus document for the detection and management of chronic kidney disease. Nefrologia 2014; 34:24362–24362.
Cockcroft DW, Gault MH. Prediction of creatinine clearance from serum creatinine. Nephron 1976; 16:31–41.
Gault MH, Longerich LL, Harnett JD, Wesolowski C. Predicting glomerular function from adjusted serum creatinine. Nephron 1992; 62:249–256.
American College of Sports Medicine. ACSM’s guidelines for exercise testing and prescription. 6th ed. Indianapolis: Lippincott Williams & Wilkins; 2000.
Yu H-I, Chiu S-T, Hua S-C, Tai T-S, Chen H-C. The effect of physical activity on diabetic nephropathy. Life Sci J 2014; 11:3.
Tanaka K, Hara S, Kushiyama A, Ubara Y, Yoshida Y, Mizuiri S et al.
Risk of macrovascular disease stratified by stage of chronic kidney disease in type 2 diabetic patients: critical level of the estimated glomerular filtration rate and the significance of hyperuricemia. Clin Exp Nephrol 2011; 15:391–397.
Boule NG, Haddad E, Kenny GP, Wells GA, Sigal RJ. Effects of exercise on glycemic control and body mass in type 2 diabetes mellitus: a meta-analysis of controlled clinical trials. J Am Med Assoc 2001; 286:1218–1227.
Nicolucci A. Improvement of quality of life with supervised exercise training in subjects with. Arch Intern Med 2011; 171:1951–1953.
Kurdak H, Sandıkçı S, Ergen N, Dogan A, Kurdak SS. The effects of regular aerobic exercise on renal functions in streptozotocin induced diabetic rats. J Sports Sci Med 2010; 9:294–299.
Yuji I, Tomohito G, Mitsuo T, Keisuke O, Masako F, Saori Y. Effect of exercise on kidney function, oxidative stress, and inflammation in type 2 diabetic KK-A mice. Exp Diabetes Res 2012; 2012:702948.
El-Nahas N, Bahey H, Aboelazm SH. Moderate versus low intensity aerobic exercise on bone mineral density in patients on hemodialysis. Glob J Med Res 2013; 13:11–17.
Zaher S, El-Nahas N, Serry Z. Effect of aerobic exercise on serum calcium and phosphorus in patients under renal haemodialysis. Faculty of Physical Therapy [master thesis]. Cairo: Cairo University; 2012.
Vaithilingham I, Polkinghorne KR, Atkins RC, Kerr PG. Time and exercise improve phosphate removal in hemodialysis patients. Am J Kidney Dis 2004; 43:85–89.
Makhlough A, Ilali E, Mohseni R, Shahmohammadi S. Effect of intradialytic aerobic exercise on serum electrolytes levels in hemodialysis patients. Iran J Kidney Dis 2012; 6:119–123.
Azra SM, Soleimani A, Alavi NM, Baseri AM, Savari M. Comparing the effects of active and passive intradialytic pedaling exercises on dialysis efficacy, electrolytes, hemoglobin, hematocrit, blood pressure and health-related quality of life. Nurs Midwifery Stud 2015; 4:e25922.
Afshar R, Shegarfy L, Shavandi N, Sanavi S. Effects of aerobic exercise and resistance training on lipid profiles and inflammation status in patients on maintenance hemodialysis. Indian J Nephrol 2010; 20:185–189.
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Parsons TL, Toffelmire EB, King-VanVlack CE. The effect of an exercise program during hemodialysis on dialysis efficacy, blood pressure and quality of life in end-stage renal disease (ESRD) patients. Clin Nephrol 2004; 61:261–274.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]