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Pharmacological management of hypertension and outcome among patients on hemodialysis at Muhimbili National Hospital, Tanzania: a cross-sectional study

Pharmacological management of hypertension and outcome among patients on hemodialysis at Muhimbili National Hospital, Tanzania: a cross-sectional study

Devis Mhagama1, Manase Kilonzi2, Peter Kunambi3, Deus Buma4, Fredrick Kalokola5, Paschal Ruggajo6, Ritah Francis Mutagonda2,&

 

1Dodoma Christian Medical Center Trust, Dodoma, Tanzania, 2Department of Clinical Pharmacy and Pharmacology, School of Pharmacy, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania, 3Department of Clinical Pharmacology, School of Biomedical Sciences, College of Medicine, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania, 4Department of Pharmacy, Muhimbili National Hospital, Dar es Salaam, Tanzania, 5Department of Internal Medicine, Weill Bugando School of Medicine, Mwanza, Tanzania,6Directorate of Curative Services, Ministry of Health, Dodoma, Tanzania

 

 

&Corresponding author
Ritah Francis Mutagonda, Department of Clinical Pharmacy and Pharmacology, School of Pharmacy, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania

 

 

Abstract

Introduction: hypertension is prevalent among patients attending hemodialysis. However, published information on hypertension management among patients on hemodialysis in African countries is scarce. This study assessed antihypertensive medication prescribing patterns and blood pressure control among patients with hypertension on hemodialysis in Tanzania.

 

Methods: an analytical cross-sectional study was conducted at Muhimbili National Hospital in Dar es Salaam from April to June 2022. The study population consisted of patients with hypertension undergoing hemodialysis. Data on demographic, clinical characteristics and the antihypertensive medications used by the patients was collected using a structured questionnaire. Analysis was performed using Statistical Package for the Social Sciences software version 26. Uncontrolled pre-dialysis blood pressure determinants were assessed using a modified Poisson regression model. A p-value < 0.05 was considered statistically significant.

 

Results: out of 314 participants, the majority (68.2%, n= 214) were male, and the median age was 52 (interquartile range: 42, 60) years. Only 16.9% (n= 53) of patients had their pre-dialysis blood pressure controlled. The most frequent antihypertensive medications prescribed were calcium channel blockers (73.2%, n= 230). Patients with less than three dialysis sessions were 20% more likely to have uncontrolled blood pressure than those with three sessions in a week (adjusted prevalence ratio = 1.2).

 

Conclusion: most patients on hemodialysis with hypertension had poor blood pressure control, according to the study. Patients with hypertension should be strongly encouraged to adhere to at least three hemodialysis treatments to achieve optimal blood pressure control.

 

 

Introduction    Down

Patients with severe and irreversible chronic renal disease or end-stage renal disease (ESRD) require routine dialysis. Dialysis patients frequently have hypertension because the kidneys are less efficient in maintaining blood pressure (BP) homeostasis [1]. In patients with ESRD getting renal replacement therapy with hemodialysis (HD), hypertension is a relatively common condition ranging from 72% to 88% of patients. It is often ineffectively treated, with only 30% to 50% reporting having well-controlled BP [2-5]. Poor BP management is a well-established risk factor for cardiovascular diseases (CVDs) and shorter survival in HD patients [6]. Volume overload and sodium excess are the primary factors exacerbating hypertension in HD patients [7]. To maintain hypertensive HD patients' BP at target levels (i.e. -dialysis BP 140/90 mmHg and post-dialysis BP 130/80 mmHg), non-pharmacological management techniques like dietary sodium restriction, gradual dry weight loss, and customized dialysate sodium prescriptions are advised as initial strategies [8]. However, it is recommended to consider antihypertensive drugs for HD patients who do not achieve adequate BP control using non-pharmacological approaches [8]. According to previously published studies, antihypertensive drugs have been positively associated with lower cardiovascular morbidity and mortality in HD patients [9,10]. Based on a recent consensus, all major antihypertensive classes effectively treat hypertension in HD patients except for diuretics [8]. Diuretics are not recommended for treating hypertension in HD patients due to the potential for ototoxicity in anuric persons and the minimal alteration in central hemodynamic parameters [8,11-13]. Beta-blockers (BBs) are preferable for treating hypertension in HD patients because of their cardioprotective effects [14,15]. Using Angiotensin-Converting Enzyme Inhibitors (ACEIs) is linked to improved survival, according to the findings of the Efrati et al. 2002 study [16]. Combining ACEIs and Angiotensin receptor blockers (ARBs) can enhance BP control and cardiovascular outcomes [8]. Nevertheless, patients with volume overload frequently take calcium channel blockers (CCBs) and other vasodilators because they efficiently control BP [17]. According to studies, amlodipine could drop systolic BP by about 10mmHg less than placebo without causing intradialytic hypotension [18]. The guidelines recommend managing HD patients using a combination of antihypertensive agents to achieve adequate BP control [13]. Despite the reported high proportion (96%) of hypertension in HD patients globally, including sub-Saharan African countries [19], there is scarce information on which antihypertensive medications have a better outcome and the overall BP control among this population in an African context. Therefore, this study assessed antihypertensive medications prescribing patterns and BP control among patients with hypertension on HD in Tanzania.

 

 

Methods Up    Down

Study design, duration, and setting: this was a hospital-based cross-sectional study conducted between April and June 2022. The study was conducted at Muhimbili National Hospital (MNH) at Upanga and Mloganzila branches. Muhimbili National Hospital is a public national referral and teaching hospital in Tanzania attending more than >25% of HD patients (approximately 385 patients per month) all over Tanzania with more than 42 HD machines [20]. Additionally, the hospital has qualified staff and modern facilities for managing patients with hypertension receiving HD.

Study population: the study included all hypertensive adult patients (18 years or above) on maintenance HD therapy for at least three months at MNH dialysis centers. Patients with mental disorders, bedridden patients, and pregnant women were excluded.

Sample size and sampling strategy: using the cross-sectional study formula, the sample size was estimated based on the prevalence of 27.8% controlled BP reported by Ahmed et al., 2020 among HD patients in Pakistan [21]. Therefore, the minimum sample size was 314 study participants. A consecutive sampling technique was used to recruit participants in the study.

Data collection: using a structured questionnaire, the principal investigator and research assistants collected data on the sociodemographic characteristics of the patients, including their age, sex, level of education, employment status, use of tobacco products, and alcohol consumption. Clinical and laboratory data such as body mass index (BMI), anthropometric measurements, vascular access, hemoglobin level, and blood urea nitrogen were also recorded. Information on comorbidities and medication use were collected by reviewing patient files and prescriptions to reduce recall bias. Patients with heart failure, left ventricular hypertrophy, coronary artery disease, or any other chronic cardiac disease were categorized as having CVDs. Antihypertensive medications prescribed to patients were categorized under their respective pharmacological classes. Study participants on a single antihypertensive were categorized as being on monotherapy and those on more than one antihypertensive medication (either two different single drugs or a fixed-dose combination) were defined as being on multitherapy. The BP was measured and recorded by trained dialysis nurses using an oscillometer BP monitor. The average of two consecutive readings taken at 5-minute intervals of quiet rest while the patient was seated was used to determine the pre- and post-dialysis BP readings on the day of the hemodialysis session.

Data analysis: data was analyzed using IBM Statistical Package for the Social Sciences (SPSS) for Windows, Version 26.0 (IBM Corp. Released 2019. Armonk, NY). Frequency and percentages were used to summarize categorical variables, while the median and interquartile range (IR) was used for continuous variables. The Wilcoxon signed ranks test was used to measure the change in median BP before and after dialysis. Uncontrolled hypertension was diagnosed when pre-dialysis BP was ≥140/90 mmHg. A modified (robust) Poisson regression model was used to determine predictors of uncontrolled pre-dialysis BP among patients. Only variables with a univariate p-value < 0.2 were included in the multivariable regression model to be able to obtain adjusted prevalence ratio (aPR), and a p-value of < 0.05 was considered statistically significant.

Ethical considerations: the study was done after obtaining authority from Muhimbili University of Health and Allied Sciences (MUHAS) Institutional Review Board with reference number DA.282/298/01C/1085. Muhimbili National Hospital´s administration gave permission to enroll patients at the facility during the study period and a written informed consent was provided by the patients prior to being enrolled.

 

 

Results Up    Down

Sociodemographic and clinical characteristics of the study participants: a total of 314 participants were included in the final analysis, with a median age of 52 years. Of all participants, 68.2% (n= 214) were male, and 66.9% (n= 210) had health insurance schemes. The participants' median BMI was 22.5kg/m2, and the median hemoglobin level was 9.0g/dL. Moreover, 77.7% (n= 244) of participants had been hypertensive for over 12 months. Most (66.6%, n = 209) patients attended three sessions weekly. The characteristics are further described in Table 1.

Antihypertensive medications prescribing pattern: the most prescribed antihypertensive classes, either alone or in combination, were CCBs (73.2%, n= 230), followed by vasodilators (55.1%, n= 173), BBs (36.3%, n= 114), diuretics (24.9%, n= 78), ARBs (4.8%, n= 15), and ACEIs (1.3%, n= 4) (Table 2).

Pre- and post-dialysis BP of the study participants: the findings showed that only 16.9% (n= 53) of the 314 patients on HD had attained a controlled pre-dialysis BP target, based on the definition of controlled BP (i.e. pre-dialysis BP <140/90 mmHg). The median pre-dialysis systolic BP was 160.0 (147.0 - 173.0) mmHg, while the median post-dialysis systolic BP was 155.0 (142.0 - 172.0) mmHg. The difference in systolic BP between pre- and post-dialysis BP was statistically significant (p= 0.004). The median (IQR) pre-dialysis diastolic BP was 76 (69.0 - 86.0) mmHg, and the median post-dialysis BP was 78.0 (69.0 - 88.0) mmHg. The diastolic BP difference between pre- and post-dialysis was not statistically significant (p= 0.879) Figure 1.

Predictors of uncontrolled pre-dialysis BP in patients on hemodialysis: after adjusting for confounders, the multivariable model showed that participants on monotherapy had a 36% lower risk of having uncontrolled BP compared to those taking multiple medications (≥3) (aPR) 0.64: 95% confidence interval (CI), (0.45 - 0.82); p = 0.001). Participants taking BBs had a 23% lower risk of having uncontrolled BP (aPR 0.77: 95% CI (0.65 - 0.91); p = 0.002) compared to patients who were not on BBs. Moreover, participants who had hypertension for more than 120 months and those who had it for 61 to 120 months had a 24% lower probability of having uncontrolled BP than those with hypertension for more than 120 months. Participants who had dialysis less than three times per week were 20% more likely to have uncontrolled BP than those who had dialysis at least three times per week (aPR 1.20: 95% CI, (1.04 - 1.38); p = 0.011). Table 3 presents the univariate and multivariate analysis results for the predictors of uncontrolled BP among patients on dialysis.

 

 

Discussion Up    Down

This study assessed BP control and antihypertensive medications prescribing pattern among patients with hypertension on HD in Tanzania. The findings showed that the magnitude of pre-dialysis BP control is low. The CCBs were the most prescribed antihypertensive medications. The use of CCBs, monotherapy, the number of dialysis sessions, and the duration of hypertension diagnosis were determinants of BP control among patients with hypertension on HD. The proportion of patients with hypertension on HD who attained controlled pre-dialytic BP in this study is slightly low (16.9%, n = 53) compared to what was reported previously in the United States (30%, n= 659), Pakistan (28.7%, n= 68) and Malaysia (28.9%, n= 42) [3,21,22]. Differences in the thresholds used to define BP control, as noted by Workgroup KDet al. 2003 who defined hypertension as pre-dialysis systolic BP >150 mmHg or diastolic BP >85 mmHg [23], or the use of antihypertensive medications, could account for the discrepancies in the results of these studies [3]. However, differences in ethnicity of the study population could also account for the difference observed. Nevertheless, the findings signify that control of BP among patients with hypertension on HD is of concern for both developed and developing countries. Our study demonstrated that CCBS, BBs, loop diuretics, and ARBs are the most prescribed antihypertensive medications, while ACEIs are the least used. Several studies reported that CCBs are significantly prescribed because of their efficiency in reducing BP even in a volume overload state and have the advantage of once-daily dosing [8,24,25]. In USA and Japan, ACEIs and ARBs are reported to be widely used as first-line antihypertensives due to their safety and efficacy in controlling cardiovascular events among chronic kidney disease patients and in the general population [12,26-28]. The observed infrequent use of ACEIs could be associated with their risk of inducing hyperkalemia caused by blockage of the renin-angiotensin-aldosterone pathway [29,30].

In this study, 24.9 % (n=78) of our patients were using diuretics as one of their antihypertensive medications. The findings do not align with several studies that reported that diuretics are ineffective for BP control in patients with ESRD [11-13,31]. However, studies by Lemes et al. 2011, and Flythe et al. 2020, support the use of diuretics in patients on HD [32,33]. The use of diuretics in this population may be justified by the fact that they are helpful to patients on dialysis with residual diuresis to enhance urine output and prevent fluid overload [32]. In addition, loop diuretics in patients with residual renal function are associated with lower interdialytic weight gain and potassium levels [34]. Lastly, this study observed that patients with hypertension on HD using BBs, CCBs, and antihypertensive monotherapy,, and those attending at least 3 dialysis sessions per week are more likely to have adequate BP control. Moreover, recently diagnosed patients with hypertension on HD can also attain adequate BP control. Several studies have also reported similar factors contributing to adequate pre-dialysis BP control in this population [25,35-40]. Other studies reported that using BBs is associated with better hypertension control and reduced cardiovascular events and death incidence in HD patients [14,15]. Specifically, carvedilol has been useful in patients with intradialytic hypertension due to its ability to improve endothelium-dependent flow-mediated vasodilatation [41]. The use of monotherapy is favored because of minimal drug-drug interaction and good adherence [42-44]. Our study should be interpreted in light of some limitations. The selection of stable patients may have excluded those with severe CVDs, thus overestimating the prevalence and treatment while underestimating the control of BP. Lower BP values in persons with HD are related to cardiovascular illnesses. As a result, treatment outcomes might be even better. Additionally, the non-pharmacological management of the participants, such as salt and fluid restriction, was not evaluated in our investigation, which could have improved the value of our findings.

 

 

Conclusion Up    Down

The study found that most patients with hypertension on HD have poor pre-dialysis BP control. Several antihypertensive medications are used to manage patients with hypertension undergoing HD; however, CCBs are the most prescribed. The number of dialysis sessions per week and the duration since diagnosis with hypertension were associated with uncontrolled pressure. We recommend further studies be conducted in bothpublic and privately owned health facilities to be able to design proper interventions that will be suitable for our population.

What is known about this topic

  • Blood pressure is poorly controlled among patients with hypertension undergoing hemodialysis;
  • Different antihypertensive medications have been reported to work best in different populations.

What this study adds

  • This is among a few studies conducted on the African population known to have a diverse response to therapy, co-morbidities, and poor healthcare system, significantly affecting the management of patients with hypertension undergoing hemodialysis;
  • This study shows a very small proportion of patients with adequate BP control compared to studies conducted in the middle- or high-income countries;
  • We have also been able to describe the common antihypertensive medications used in our settings; determinants of inadequate blood pressure control have also been described, which provide baseline information on how we can improve the management of these patients.

 

 

Competing interests Up    Down

The authors declare no competing interests.

 

 

Authors' contributions Up    Down

The study's concept design, data collection, and data interpretation were performed by Devis Mhagama, Ritah Francis Mutagonda and Paschal Ruggajo; the statistical analysis was carried out by Devis Mhagama and Peter Kunambi; from the initial draft of the manuscript through the final approval of the version to be published, Devis Mhagama, Ritah Francis Mutagonda, Paschal Ruggajo, Deus Buma, Manase Kilonzi, Peter Kunambi, and Fredrick Kalokola all made significant contributions. All the authors have read and agreed to the final manuscript.

 

 

Acknowledgments Up    Down

The Muhimbili University of Health and Allied Sciences, Muhimbili National Hospital Administration, research assistants, and patients all contributed to making this study possible, and for that, the authors, would like to express their profound gratitude.

 

 

Tables and figure Up    Down

Table 1: socio-demographic and clinical characteristics of the participants (n= 314)

Table 2: antihypertensive medications prescribing pattern (n= 314)

Table 3: predictors of uncontrolled pre-dialysis BP among the patients on dialysis (n=314)

Figure 1: A,B) the median values and the association of pre-and post-dialysis BP (n= 314)

 

 

References Up    Down

  1. Agarwal R. Hypertension in chronic kidney disease and dialysis: pathophysiology and management. Cardiol Clin. 2005 Aug;23(3):237-48. PubMed | Google Scholar

  2. Bucharles SG, Wallbach KK, Moraes TP, Pecoits-Filho R. Hypertension in patients on dialysis: diagnosis, mechanisms, and management. J Bras Nefrol. 2019 Jul-Sep;41(3):400-411. PubMed | Google Scholar

  3. Agarwal R, Nissenson AR, Batlle D, Coyne DW, Trout JR, Warnock DG. Prevalence, treatment, and control of hypertension in chronic hemodialysis patients in the United States. Am J Med. 2003 Sep;115(4):291-7 PubMed | Google Scholar

  4. Salem MM. Hypertension in the hemodialysis population: a survey of 649 patients. Am J Kidney Dis. 1995 Sep;26(3):461-8. PubMed | Google Scholar

  5. Agarwal R. Supervised atenolol therapy in the management of hemodialysis hypertension. Kidney Int. 1999 Apr;55(4):1528-35. PubMed | Google Scholar

  6. Botdorf J, Chaudhary K, Whaley-Connell A. Hypertension in cardiovascular and kidney disease. Cardiorenal Med. 2011;1(3):183-192. PubMed | Google Scholar

  7. Sarafidis PA, Mallamaci F, Loutradis C, Ekart R, Torino C, Karpetas A et al. Prevalence and control of hypertension by 48-h ambulatory blood pressure monitoring in haemodialysis patients: a study by the European Cardiovascular and Renal Medicine (EURECA-m) working group of the ERA-EDTA. Nephrol Dial Transplant. 2019 Sep 1;34(9):1542-1548. PubMed | Google Scholar

  8. Sarafidis PA, Persu A, Agarwal R, Burnier M, De Leeuw P, Ferro CJ et al. Hypertension in dialysis patients: a consensus document by the European Renal and Cardiovascular Medicine (EURECA-m) working group of the European Renal Association-European Dialysis and Transplant Association (ERA-EDTA) and the Hypertension and the Kidney working group of the European Society of Hypertension (ESH). Nephrol Dial Transplant. 2017 Apr 1;32(4):620-640. PubMed | Google Scholar

  9. Agarwal R, Sinha AD. Cardiovascular protection with antihypertensive drugs in dialysis patients: systematic review and meta-analysis. Hypertension. 2009 May;53(5):860-6. PubMed | Google Scholar

  10. Heerspink HJ, Ninomiya T, Zoungas S, de Zeeuw D, Grobbee DE, Jardine MJ et al. Effect of lowering blood pressure on cardiovascular events and mortality in patients on dialysis: a systematic review and meta-analysis of randomised controlled trials. Lancet. 2009 Mar 21;373(9668):1009-15. PubMed | Google Scholar

  11. Agarwal R, Flynn J, Pogue V, Rahman M, Reisin E, Weir MR. Assessment and management of hypertension in patients on dialysis. J Am Soc Nephrol. 2014 Aug;25(8):1630-46. PubMed | Google Scholar

  12. Denker MG, Cohen DL. Antihypertensive Medications in End-Stage Renal Disease. Semin Dial. 2015 Jul-Aug;28(4):330-6. PubMed | Google Scholar

  13. Inrig JK. Antihypertensive agents in hemodialysis patients: a current perspective.Semin Dial. 2010 May-Jun;23(3):290-7 PubMed | Google Scholar

  14. Weir MA, Herzog CA. Beta blockers in patients with end-stage renal disease-Evidence-based recommendations. Semin Dial. 2018 May;31(3):219-225. PubMed | Google Scholar

  15. Maruyama T, Takashima H, Abe M. Blood pressure targets and pharmacotherapy for patients with hypertension on hemodialysis. Expert Opin Pharmacother. 2020 Jul;21(10):1219-1240. PubMed | Google Scholar

  16. Efrati S, Zaidenstein R, Dishy V, Beberashvili I, Sharist M, Averbukh Z et al. ACE inhibitors and survival of hemodialysis patients. Am J Kidney Dis. 2002 Nov;40(5):1023-9. PubMed | Google Scholar

  17. London GM, Marchais SJ, Guerin AP, Metivier F, Safar ME, Fabiani F et al. Salt and water retention and calcium blockade in uremia. Circulation 1990 Jul;82(1):105-13. PubMed | Google Scholar

  18. Kestenbaum B, Gillen DL, Sherrard DJ, Seliger S, Ball A, Stehman-Breen C. Calcium channel blocker use and mortality among patients with end-stage renal disease. Kidney Int. 2002 Jun;61(6):2157-64. PubMed | Google Scholar

  19. Bramania P, Ruggajo P, Bramania R, Mahmoud M, Furia F. Nutritional status of patients on maintenance hemodialysis at Muhimbili National Hospital in Dar es Salaam, Tanzania: a cross-sectional study. J Nutr Metab. 2021 May 22;2021:6672185. PubMed | Google Scholar

  20. Furia FF, Shoo J, Ruggajo PJ, Kilonzo K, Basu G, Yeates K et al. Developing nephrology services in low-income countries: a case of Tanzania. BMC Nephrol. 2019 Oct 17;20(1):378. PubMed | Google Scholar

  21. Ahmad N, Wahid A, Khan A, Atif M, Khan A. Evaluation of management and factors associated with hypertension control in hemodialysis patients at a tertiary care hospital in Pakistan. Drugs & Therapy Perspectives. 2020 Sep;36:396-403. Google Scholar

  22. Khan A, Khan AH, Adman AS, Suleiman SA, Mehta S, Ahmad N et al. Hypertension control among euvolemic hypertensive hemodialysis patients in Malaysia: a prospective follow-up study. J Pharm Policy Pract. 2019 May 14;12:10. PubMed | Google Scholar

  23. Workgroup KD. K/DOQI clinical practice guidelines for cardiovascular disease in dialysis patients. Am J Kidney Dis. 2005 Apr;45(4 Suppl 3):S1-153. PubMed | Google Scholar

  24. Tepel M, Hopfenmueller W, Scholze A, Maier A, Zidek W. Effect of amlodipine on cardiovascular events in hypertensive haemodialysis patients. Nephrol Dial Transplant. 2008 Nov;23(11):3605-12. PubMed | Google Scholar

  25. Mallappallil MC, Fishbane S, Wanchoo R, Lerma E, Roche-Recinos A, Salifu M. Practice patterns in transitioning patients from chronic kidney disease to dialysis: a survey of United States nephrologists. BMC Nephrol. 2018 Jun 22;19(1):147. PubMed | Google Scholar

  26. Ichihara A, Hayashi M, Kaneshiro Y, Takemitsu T, Homma K, Kanno Y et al. Low doses of losartan and trandolapril improve arterial stiffness in hemodialysis patients. Am J Kidney Dis. 2005 May;45(5):866-74. PubMed | Google Scholar

  27. Taniyama Y. Management of hypertension for patients undergoing dialysis therapy. RRT. 2016 Jun 8;2(1):21. Google Scholar

  28. Takahashi A, Takase H, Toriyama T, Sugiura T, Kurita Y, Ueda R et al. Candesartan, an angiotensin II type-1 receptor blocker, reduces cardiovascular events in patients on chronic haemodialysis-a randomized study. Nephrol Dial Transplant. 2006 Sep;21(9):2507-12. PubMed | Google Scholar

  29. Brenner BM, Cooper ME, De Zeeuw D, Keane WF, Mitch WE, Parving HH, Remuzzi G, Snapinn SM, Zhang Z, Shahinfar S. Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl J Med. 2001 Sep 20;345(12):861-9 PubMed | Google Scholar

  30. Lewis EJ, Hunsicker LG, Clarke WR, Berl T, Pohl MA, Lewis JB et al. Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. N Engl J Med. 2001 Sep 20;345(12):851-60. PubMed | Google Scholar

  31. Agarwal R. Epidemiology of interdialytic ambulatory hypertension and the role of volume excess. Am J Nephrol. 2011;34(4):381-90. PubMed | Google Scholar

  32. Lemes HP, Araujo S, Nascimento D, Cunha D, Garcia C, Queiroz V et al. Use of small doses of furosemide in chronic kidney disease patients with residual renal function undergoing hemodialysis. Clin Exp Nephrol. 2011 Aug;15(4):554-9. PubMed | Google Scholar

  33. Flythe JE, Chang TI, Gallagher MP, Lindley E, Madero M, Sarafidis PA et al. Blood pressure and volume management in dialysis: conclusions from a Kidney Disease: improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2020 May;97(5):861-876. PubMed | Google Scholar

  34. Ranjan A, Kolli A, Raju MR, Ansari RK. Management of Hypertension in CKD Patients Undergoing Maintenance Hemodialysis: A Prospective Cross-Sectional Study. Age. 2017;45:12-66. Google Scholar

  35. Chiu YW, Teitelbaum I, Misra M, De Leon EM, Adzize T, Mehrotra R. Pill burden, adherence, hyperphosphatemia, and quality of life in maintenance dialysis patients. Clin J Am Soc Nephrol. 2009 Jun;4(6):1089-96. PubMed | Google Scholar

  36. Stern A, Sachdeva S, Kapoor R, Singh J, Sachdeva S. High blood pressure in dialysis patients: cause, pathophysiology, influence on morbidity, mortality, and management. J Clin Diagn Res. 2014 Jun;8(6):ME01-4. PubMed | Google Scholar

  37. Hommos M, Schinstock C. Hypertension in hemodialysis patient. Hypertension: from basic research to clinical practice. Adv Exp Med Biol. 2017;956:327-340. PubMed | Google Scholar

  38. Cheigh JS, Milite C, Sullivan JF, Rubin AL, Stenzel KH. Hypertension is not adequately controlled in hemodialysis patients. Am J Kidney Dis. 1992 May;19(5):453-9. PubMed | Google Scholar

  39. Ashby D, Borman N, Burton J, Corbett R, Davenport A, Farrington K et al. Renal association clinical practice guideline on haemodialysis. BMC Nephrol. 2019 Oct 17;20(1):379. PubMed | Google Scholar

  40. Shafiee MA, Chamanian P, Shaker P, Shahideh Y, Broumand B. The impact of hemodialysis frequency and duration on blood pressure management and quality of life in end-stage renal disease patients. Healthcare (Basel). 2017 Sep 2;5(3):52. PubMed | Google Scholar

  41. Inrig JK, Van Buren P, Kim C, Vongpatanasin W, Povsic TJ, Toto R. Probing the mechanisms of intradialytic hypertension: a pilot study targeting endothelial cell dysfunction. Clin J Am Soc Nephrol. 2012 Aug;7(8):1300-9. PubMed | Google Scholar

  42. Rocco MV, Yan G, Heyka RJ, Benz R, Cheung AK. Risk factors for hypertension in chronic hemodialysis patients: baseline data from the HEMO study. Am J Nephrol. 2001 JulAug;21(4):280-8. PubMed | Google Scholar

  43. Morais JG, Pecoits-Filho R, Canziani MEF, Poli-de-Figueiredo CE, Cuvello Neto AL, Barra AB et al. Fluid overload is associated with use of a higher number of antihypertensive drugs in hemodialysis patients. Hemodial Int. 2020 Jul;24(3):397-405. PubMed | Google Scholar

  44. Salam A, Huffman MD, Kanukula R, Hari Prasad E, Sharma A, Heller DJ et al. Two-drug fixed-dose combinations of blood pressure-lowering drugs as WHO essential medicines: An overview of efficacy, safety, and cost. J Clin Hypertens (Greenwich). 2020 Oct;22(10):1769-1779. PubMed | Google Scholar