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      An update review of intradialytic hypotension: concept, risk factors, clinical implications and management

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          Abstract

          Intradialytic hypotension (IDH) is a frequent and serious complication of chronic haemodialysis, linked to adverse long-term outcomes including increased cardiovascular and all-cause mortality. IDH is the end result of the interaction between ultrafiltration rate (UFR), cardiac output and arteriolar tone. Thus excessive ultrafiltration may decrease the cardiac output, especially when compensatory mechanisms (heart rate, myocardial contractility, vascular tone and splanchnic flow shifts) fail to be optimally recruited. The repeated disruption of end-organ perfusion in IDH may lead to various adverse clinical outcomes affecting the heart, central nervous system, kidney and gastrointestinal system. Potential interventions to decrease the incidence or severity of IDH include optimization of the dialysis prescription (cool dialysate, UFR, sodium profiling and high-flux haemofiltration), interventions during the dialysis session (midodrine, mannitol, food intake, intradialytic exercise and intermittent pneumatic compression of the lower limbs) and interventions in the interdialysis period (lower interdialytic weight gain and blood pressure–lowering drugs). However, the evidence base for many of these interventions is thin and optimal prevention and management of IDH awaits further clinical investigation. Developing a consensus definition of IDH will facilitate clinical research. We review the most recent findings on risk factors, pathophysiology and management of IDH and, based on this, we call for a new consensus definition of IDH based on clinical outcomes and define a roadmap for IDH research.

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          Most cited references128

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          US Renal Data System 2018 Annual Data Report: Epidemiology of Kidney Disease in the United States

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            Hemodialysis-induced cardiac injury: determinants and associated outcomes.

            Hemodialysis (HD)-induced myocardial stunning driven by ischemia is a recognized complication of HD, which can be ameliorated by HD techniques that improve hemodynamics. In nondialysis patients, repeated ischemia leads to chronic reduction in left ventricular (LV) function. HD may initiate and drive the same process. In this study, we examined the prevalence and associations of HD-induced repetitive myocardial injury and long-term effects on LV function and patient outcomes. Seventy prevalent HD patients were assessed for evidence of subclinical myocardial injury at baseline using serial echocardiography and followed up after 12 mo. Intradialytic blood pressure, hematologic and biochemical samples, and patient demographics were also collected at both time points. Sixty-four percent of patients had significant myocardial stunning during HD. Age, ultrafiltration volumes, intradialytic hypotension, and cardiac troponin-T (cTnT) levels were independent determinants associated with its presence. Myocardial stunning was associated with increased relative mortality at 12 mo (P = 0.019). Cox regression analysis showed increased hazard of death in patients with myocardial stunning and elevated cTnT than in patients with elevated cTnT alone (P < 0.02). Patients with myocardial stunning who survived 12 mo had significantly lower LV ejection fractions at rest and on HD (P < 0.001). HD-induced myocardial stunning is common, and may contribute to the development of heart failure and increased mortality in HD patients. Enhanced understanding of dialysis-induced cardiac injury may provide novel therapeutic targets to reduce currently excessive rates of cardiovascular morbidity and mortality.
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              Hemodialysis-associated hypotension as an independent risk factor for two-year mortality in hemodialysis patients.

              The relationship between blood pressure (BP) and mortality in hemodialysis patients has remained controversial. Some studies suggested that a lower pre- or postdialysis BP was associated with excess mortality, while others showed poorer outcome in patients with uncontrolled hypertension. We conducted a multicenter prospective cohort study to evaluate the impact of hemodialysis-associated hypotension on mortality. We recruited 1244 patients (685 males; mean age, 60 +/- 13 years) who underwent hemodialysis in 28 units during the two-year study period beginning in December 1999. Pre-, intra-, and postdialysis BP, and BP upon standing soon after hemodialysis, were measured in all patients at entry. Logistic regression analysis was used to assess the effect on mortality of pre-, intra-, and postdialysis BP, a fall in BP during hemodialysis, and a fall in BP upon standing soon after hemodialysis. During the study period, 149 patients died. Logistic models identified the lowest intradialysis systolic blood pressure (SBP) and degree of fall in SBP upon standing soon after hemodialysis as significant factors affecting mortality, but not pre- or postdialysis SBP and diastolic BP. The adjusted odds ratio for death was 0.79 (95% CI 0.64-0.98) when the lowest intradialysis SBP was analyzed in increments of 20 mm Hg, and was 0.82 (95% CI 0.67-0.98) when the fall in SBP upon standing soon after hemodialysis was analyzed in increments of 10 mm Hg. These results suggest that intradialysis hypotension and orthostatic hypotension after hemodialysis are significant and independent factors affecting mortality in hemodialysis patients.
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                Author and article information

                Journal
                Clin Kidney J
                Clin Kidney J
                ckj
                Clinical Kidney Journal
                Oxford University Press
                2048-8505
                2048-8513
                December 2020
                08 July 2020
                08 July 2020
                : 13
                : 6
                : 981-993
                Affiliations
                [1 ] Department of Medicine, Division of Nephrology, Koc University School of Medicine , Istanbul, Turkey
                [2 ] Department of Medicine, Koc University School of Medicine , Istanbul, Turkey
                [3 ] Department of Internal Medicine, Division of Nephrology , Suleyman Demirel University School of Medicine, Isparta, Turkey
                [4 ] Nephrology Clinic, Dialysis and Renal Transplant Center, ‘C.I. PARHON’ University Hospital , ‘Grigore T. Popa’ University of Medicine, Iasi, Romania
                [5 ] Division of Nephrology, Miulli General Hospital, Acquaviva delle Fonti , Italy
                [6 ] Associazione Nefrologica Gabriella Sebastio , Martina Franca, Italy
                [7 ] Dialysis Unit, School of Medicine, IIS-Fundacion Jimenez Diaz, Universidad Autónoma de Madrid , Madrid, Spain
                Author notes
                Correspondence to: Mehmet Kanbay; E-mail: drkanbay@ 123456yahoo.com ; mkanbay@ 123456ku.edu.tr ; Twitter handle: @CKJ_EiC
                Author information
                http://orcid.org/0000-0002-1297-0675
                Article
                sfaa078
                10.1093/ckj/sfaa078
                7769545
                33391741
                64040ccd-8b92-4cdc-8db8-9084bdb929d9
                © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 13 November 2019
                : 30 April 2020
                Page count
                Pages: 13
                Funding
                Funded by: Ministry of Research and Innovation, CNCS-UEFISCDI;
                Award ID: PN-III-P4-ID-PCE-2016-0908
                Award ID: 167/2017
                Award ID: PNCDI III
                Award ID: ISCIII FIS PI16/02057
                Award ID: PI19/00588
                Award ID: PI19/00815
                Award ID: DTS18/00032
                Award ID: AC18/00064
                Award ID: PERSTIGAN AC18/00071
                Award ID: ISCIII-RETIC REDinREN RD016/0009
                Funded by: FEDER, DOI 10.13039/501100002924;
                Funded by: Fundacion Renal Iñigo Álvarez de Toledo (FRIAT);
                Funded by: Comunidad de Madrid, DOI 10.13039/100012818;
                Award ID: CIFRA2 B2017/BMD-3686
                Categories
                CKJ Reviews
                AcademicSubjects/MED00340

                Nephrology
                cardiovascular event,haemodialysis,intradialytic hypotension,roadmap,ultrafiltration
                Nephrology
                cardiovascular event, haemodialysis, intradialytic hypotension, roadmap, ultrafiltration

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