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Hemodynamic response to orthostatic stress immediately after dialysis session in chronic hemodialysis patients

Renal Replacement Therapy20184:49

https://doi.org/10.1186/s41100-018-0189-0

  • Received: 31 August 2018
  • Accepted: 29 October 2018
  • Published:

Abstract

Orthostatic hypotension is a risk factor for falls among chronic hemodialysis (HD) patients. This study aimed to investigate the hemodynamic response to orthostatic stress immediately after an HD session. Twenty-one HD patients (mean age, 70.2 ± 8.1 years; HD duration, 7.5 ± 6.4 years) participated in this study. Each 5-min hemodynamic monitoring was performed in the supine, semi-recumbent, and sitting positions immediately after an HD session. Hemodynamic variables were measured using a noninvasive beat-to-beat monitoring device during the test. Patients were divided into an intradialytic hypotension (IDH) group and a non-IDH group according to the presence or absence of IDH on the day of the measurements, and intra- and intergroup comparisons were performed. In the IDH group, the nadir values of systolic blood pressure in the semi-recumbent and sitting positions were significantly lower than those in the supine position and the last systolic blood pressure in the semi-recumbent position. The nadir of stroke volume in the sitting position was significantly lower than that in the supine position. There were no statistically significant intergroup differences in the changes for any positions. These results suggest that patients with IDH require special attention when getting out of bed to prevent post-dialytic falls.

Keywords

  • Hemodialysis
  • Hypotension
  • Noninvasive continuous hemodynamic monitoring
  • Postural change

Background

Orthostatic hypotension (OH) is caused by an excessive decrease in cardiac output (CO) and/or compensatory vasoconstrictor mechanisms such as autonomic failure and age-related physiologic changes [1]. OH is a risk factor for falls among chronic hemodialysis (HD) patients. The cross-sectional prevalence of OH in HD patients is reportedly higher than that in the general population. Previous studies reported a 42% prevalence of OH in the introductory phase of HD [2] versus 5–30% in unselected individuals aged ≥ 65 years [3].

In the post-dialysis period, there are several HD-related risk factors for OH such as the rapid removal of intravascular volume and several hours of bed rest during HD therapy, in addition to other common risk factors such as advanced age, autonomic failure, and frailty. Previous studies demonstrated that the incidences of OH and falls were higher in the post- than pre-dialysis. Roberts et al. reported that 69.6% of patients had post-dialysis OH versus 34.8% with pre-dialysis OH [4]. The incidences of falls pre- and post-dialysis session are reportedly 9–41% [5] and 27–73% [6], respectively. These findings suggest the risk for post-dialytic falls. Furthermore, post-HD OH and intradialytic hypotension (IDH) are significant and independent factors that affect mortality in HD patients [7]. Therefore, studying hemodynamic responses to orthostatic stress after dialysis is important to manage the fall risk in the care for HD patients. However, to our knowledge, little is known about hemodynamic response during postural change immediately after an HD session.

A manual sphygmomanometer is most frequently used to measure OH; however, this device provides only a single blood pressure value unless repeated measurements are taken to identify clinically relevant OH [8]. Continuous beat-to-beat blood pressure measurements are increasingly available in hospital settings [9]. Beat-to-beat methods have been validated against intra-arterial recordings, meet acceptable criteria for bias and precision [10], and identified a higher prevalence of OH than sphygmomanometry [11]. Furthermore, beat-to-beat technology is reportedly more effective for detecting OH and discriminating blood pressure responses in fallers and non-fallers compared to intermittent manual sphygmomanometer assessments [12].

This study aimed to investigate hemodynamic responses to orthostatic stress immediately after an HD session using continuous beat-to-beat blood pressure measurements. We hypothesized that the decreases in blood pressure upon orthostatic stress immediately after an HD session would be larger in patients with IDH than in those without IDH.

Methods

Patients

This observational study was conducted in a single dialysis center (Ibuki Clinic, Osaka, Japan). Twenty-five HD patients (mean age, 70.8 ± 8.6 years; male/female ratio, 10/15) who underwent maintenance HD three times a week at Ibuki Clinic, Osaka, Japan, participated in this study. None of the patients had common risk factors for falls such as gait disorder, visual impairment, or neurologic disease [13], and all were able to walk into the clinic unassisted and had a history of hypotensive episodes immediately after HD session within the previous year. We excluded patients with severe heart disease (New York Heart Association III or IV) or peripheral artery disease (Fontaine III or IV) as well as those with neurological diseases that induce OH.

This study was approved by the Ethics Committee of Mukogawa Women’s University, and written informed consent was obtained from each participant after a detailed explanation of the study protocol was provided.

Demographic and clinical characteristics

The demographic and clinical characteristics obtained from patients’ medical records included age, sex, body mass index, presence of underlying diabetes mellitus (DM), HD vintage, dry weight, cardiothoracic ratio, left ventricular ejection fraction (LVEF) by echocardiography, and hemoglobin (Hb), hematocrit (Ht), blood urea nitrogen, creatinine, albumin (Alb), total cholesterol, triglyceride, high-density lipoprotein cholesterol, and C-reactive protein levels in a blood sample obtained before HD. Serum B-type natriuretic peptide (BNP) level was measured before and after the HD session. Parameters concerning arterial stiffness included ankle-brachial index (ABI), toe-brachial index, brachial-ankle pulse wave velocity, and skin perfusion pressure. The body fluid removal rate (%) during the HD session was assessed according to the following equation: body fluid removal rate (%) = (pre-dialysis body weight − post-dialysis body weight)/post-dialysis body weight × 100 [14].

Study protocol

Hemodynamic monitoring was performed on the day of the HD session after a 1-day interval at the timing of getting out of the dialysis bed for returning home. Arterial blood pressure was recorded every 30 min during the HD session by the cuff method with an automatic blood pressure monitor. IDH was defined as a decrease of ≥ 20 mmHg in systolic blood pressure (SBP) during the HD session [15]. Patients were divided into an IDH group and a non-IDH group according to the aforementioned definition of IDH on the day of the measurement.

Immediately after the HD session and detachment of the dialysis circuit, subjects were maintained in the supine position in the dialysis bed for 5 min and then passively moved into a semi-recumbent position by repositioning the head of the bed to 60° and maintained the position for 5 min (semi-recumbent position phase). Next, the subjects were asked to move unassisted into a chair placed beside the dialysis bed and remain there for 5 min (chair sitting position phase). Each postural change occurred within 10 s.

Hemodynamics measurement

During the aforementioned postural changes, we continuously recorded noninvasive beat-to-beat arterial blood pressure (Portapres, Finapres Medical Systems, Amsterdam, The Netherlands) from the pointer or middle finger of the hand without vascular access. The finger cuff of the Portapres was sized to each participant per the manufacturer’s specifications after a calibration procedure. Participant height, weight, and age were entered before starting the device to ensure accurate determination of stroke volume (SV) and CO using the Modelflow algorithm (Modelflow, TNO Biomedical Instrumentation, Amsterdam, The Netherlands) [16]. A hydrostatic height correction sensor was placed at the level of the heart to compensate for any hand movements relative to the heart that could impact the blood pressure recordings.

Assessment of hemodynamics

SBP and diastolic blood pressure (DBP) were derived from the arterial pressure waveform. Heart rate (HR) was computed as the inverse of the inter-beat interval and expressed as beats per minute. Beat-to-beat left ventricular SV was estimated by modeling flow from the arterial pressure waveform (16). CO was the product of estimated SV and HR. Total peripheral resistance (TPR) was computed by mean blood pressure at the heart level divided by the computed CO.

Data processing

The data were exported to Microsoft Excel spreadsheets with BeatScope software using the 5-s average method [9], which was reported to show the best association with fall history using various mean times.

Outcome measures

SBP measurements at the following time points were analyzed:
  1. 1.

    Baseline: SBP of the final 5-s average of the supine position phase before the semi-recumbent position phase

     
  2. 2.

    Semi-recumbent nadir: the lowest 5-s average SBP obtained within the first 3 min of the semi-recumbent position phase

     
  3. 3.

    Semi-recumbent recovery: SBP of the final 5-s average of the semi-recumbent position phase before the chair sitting position phase

     
  4. 4.

    Sitting nadir: lowest 5-s average SBP obtained within the first 3 min of the chair sitting position phase

     

Values for DBP, HR, SV, CO, and TPR at the same time point of SBP obtained according to the above definition were used in the analysis. Data acquired during postural changes were excluded to avoid any effect from body motion.

Statistical analysis

Values for SBP, DBP, HR, SV, CO, and TPR between each time point were analyzed by two-way analysis of variance with the repeated measures or Kruskal-Wallis and Bonferroni test as the post hoc test in each group. The two groups in each time point were compared using an unpaired t test or the Mann-Whitney test after converting to the difference from the baseline values (i.e., ΔSBP, ΔDBP) and percentage changes relative to the baseline values (i.e., %HR, %SV, %CO, %TPR). Clinical characteristics in each group were compared using an unpaired t test or the Mann-Whitney test or chi-square test. Values are shown as mean ± SD. P values < 0.05 were considered statistically significant. All statistical analyses were performed using IBM SPSS version 19 (IBM Japan Inc., Tokyo, Japan).

Results

Clinical and demographic characteristics

We evaluated 21 patients (mean age, 70.3 ± 8.0; male/female ratio, 9/12); three patients were excluded before the hemodynamic monitoring because of discomfort including nausea just after the HD session. In the three patients, SBP decreased by ≥ 20 mmHg in two patients and by < 20 mmHg in one patient during the HD session. Another patient was excluded because of syncope with SBP decrease of ≥ 20 mmHg during the HD session. The underlying kidney diseases were diabetic nephropathy (n = 15), chronic glomerulonephritis (n = 4), polycystic kidney disease (n = 1), and chronic nephritis (n = 1). The body fluid removal rate during the HD in all participants was < 5%. No patient was administered midodrine to prevent IDH before and during the HD session or complained of hypotensive symptoms including dizziness and faintness during the hemodynamic monitoring. Eleven patients were categorized into the IDH group, and the other 10 were categorized into the non-IDH group.

Clinical and demographic characteristics for each group are shown in Table 1. Hb and Ht levels in the IDH group were significantly higher than those in the non-IDH group (P = 0.009 and P = 0.033, respectively). The mean Alb level in the IDH group was significantly lower than that in the non-IDH group (P = 0.040). There were no significant intergroup differences in cardiac function markers or body fluid removal rates (Table 2).
Table 1

Characteristics of subjects

 

IDH group

(n = 11)

Non-IDH group

(n = 10)

P value

Characteristics

 Age (years)

71.1 ± 8.7

70.4 ± 7.1

0.852

 HD vintage (years)

7.5 ± 5.6

7.4 ± 7.2

0.888

 Male/female

5/6

4/6

0.617

 DM (+/−)

8/3

7/3

0.705

 BMI

23.4 ± 2.4

22.2 ± 3.2

0.354

 CTR

51.1 ± 3.4

49.2 ± 3.4

0.246

Medications

 ACEI/ARB (%)

9.1

10.0

0.739

 β-blocker (%)

9.1

10.0

0.739

 Ca antagonist (%)

36.4

20.0

0.145

Laboratory parameters

 Hb

11.8 ± 0.6

10.6 ± 1.2

0.009

 Ht

36.3 ± 2.3

32.7 ± 4.4

0.033

 BUN

56.3 ± 17.7

59.2 ± 13.1

0.689

 Cr

9.79 ± 4.41

9.23 ± 1.23

0.369

 Alb

3.4 ± 0.3

3.6 ± 0.2

0.040

 TC

163.1 ± 43.9

171.3 ± 37.9

0.669

 TG

109.3 ± 48.8

104.3 ± 35.6

0.815

 HDL-c

42.9 ± 11.4

42.8 ± 10.6

0.983

 CRP

0.24 ± 0.23

0.09 ± 0.08

0.128

Atherosclerotic parameters

 ABI

0.95 ± 0.21

1.10 ± 0.13

0.087

 TBI

0.59 ± 0.15

0.63 ± 0.13

0.596

 ba-PWV

2233.3 ± 460.0

2087.1 ± 584.4

0.530

 SPP

63.3 ± 16.1

63.1 ± 11.9

0.979

Data are expressed as means ± SD

BMI body mass index, DM diabetes mellitus, CTR cardiothoracic ratio, ACEI angiotensin-converting-enzyme inhibitor, ARB angiotensin receptor blocker, Ca calcium, Hb hemoglobin, Ht hematocrit, BUN blood urea nitrogen, Cr creatinine, Alb albumin, TC total cholesterol, TG triglycerides, HDL-c high-density lipoprotein cholesterol, CRP C-reactive protein, ABI ankle-brachial index, TBI toe-brachial index, ba-PWV brachial-ankle pulse wave velocity, SPP skin perfusion pressure

Table 2

Markers of cardiac function and removed body fluid rate

 

IDH group

(n = 11)

Non-IDH group

(n = 10)

P value

LVEF (%)

67.8 ± 7.8

71.1 ± 12.5

0.495

BNP (pre-HD session)

177.7 ± 120.4

109.4 ± 67.9

0.160

BNP (post-HD session)

83.7 ± 53.6

61.4 ± 30.8

0.297

Removed body fluid rate (%)

3.48 ± 1.07

2.96 ± 0.45

0.187

Hemodynamics during postural changes

The changes of hemodynamic parameters between each time point are shown in Fig. 1. SBP for semi-recumbent nadir in the IDH group were significantly lower than those for baseline and semi-recumbent recovery. The SBP for sitting nadir in the IDH group was significantly lower than that for semi-recumbent recovery. The SV for sitting nadir in the IDH group was significantly lower than that for baseline.
Fig. 1
Fig. 1

Hemodynamic responses to postural changes immediately after dialysis session. a SBP. b DBP. c SV. d CO. e HR. f TPR. Data are expressed as means ± SD. *P < 0.05

There were no statistically significant intergroup differences between the two groups in changes at any time point.

Discussion

In the present study, hemodynamic monitoring during postural changes was performed immediately after an HD session in both the semi-recumbent and sitting positions using noninvasive beat-to-beat blood pressure monitoring. OH has been traditionally measured on active standing or on a head-up tilt table at an angle of 60°. In patients who are unable to stand or who are at risk for symptomatic standing postural hypotension, evaluating postural hypotension in a sitting position is recommended. Advanced age, significant bed rest, and hypertension are reportedly the most important predisposing factors for seated postural hypotension [1]. The effectiveness of the orthostatic stress test in the sitting position was demonstrated in a study by Shaw et al., in which passive seated orthostatic stress and head-up tilt testing produced blood pressure responses of similar magnitudes and no difference was seen in cerebral blood flow velocity in the middle cerebral artery between the two tests in healthy volunteers [8].

In this study, patients with IDH had orthostatic intolerance upon postural change from a supine to a semi-recumbent position immediately after an HD session. This finding supports our assumption that HD therapy negatively affected orthostatic tolerance in HD patients with IDH. Furthermore, the nadir SBP in the sitting position was significantly lower than that in the semi-recumbent position in the patients with IDH, that is, the change from the semi-recumbent to the sitting position decreased the SBP.

In the IDH group, compensatory responses to orthostatic stress such as increases in HR and TPR for stabilizing arterial pressure did not reach statistical significance in spite of significant SBP and SV decrease. Since the orthostatic HR response may be a useful marker of cardiac baroreflex function [10], this result suggests that autonomic dysfunction including diabetic and/or uremic neuropathy was a possible factor for those poor responses considering the lack of a significant intergroup difference in major risk factors for orthostatic intolerance such as age, cardiac function measured by LVEF and BNP level, and body fluid removal rate. Further studies are needed to investigate the effect of those factors on orthostatic intolerance immediately after an HD session.

The post-dialysis period includes not only a higher risk for postural hypotension but also other factors that may increase the risk for accidental falls. Cook et al. revealed that HD treatment altered motor function in older HD patients, weakening their strength and decreasing their mobility after the HD session [7]. Soangra et al. reported decreased sit-to-walk test performance pre- versus post-HD session [17]. Furthermore, a greater postural sway in the post- versus pre-HD session was observed [18] in addition to poorer postural control in HD patients than in age-matched controls, which was further exacerbated by the simultaneous performance of a cognitive task [19]. These results suggest that the immediate post-HD period is particularly unsafe, so medical staff in dialysis units should be sure to provide the necessary support [18]. Accordingly, dialysis staff should consider such alterations concerning physical function post-dialysis as well as the probability of the aforementioned postural hypotension immediately after the HD session. It is likely that dialysis staff already knows about the increased risk for post-dialysis falls; however, only a few studies have reported hemodynamic data from that period. This study is the first to use beat-to-beat technology immediately after an HD session to capture rapid and transient hemodynamic fluctuations.

There were significant differences in Hb, Ht, and Alb levels between the IDH and non-IDH groups. It is known that anemia is one of the factors that aggravate OH in the general population [20]. However, Hb and Ht level measurements in both groups in this study were within the target range recommended by the Japanese Society of Dialysis Therapy guideline [21], which suggests that even patients with target Hb and Ht levels could develop OH immediately after HD. Meanwhile, the K/DOQI guidelines [15] include hypoalbuminemia as a factor related to IDH; however, whether the intergroup difference in Alb has clinically relevant significance remains unclear because of a lack of evidence.

There are several limitations to this study. First, the small sample size may have affected its ability to show a statistically significant difference in some measures. In addition, we could not evaluate the impact of DM which is the most common disease associated with peripheral damage to the autonomic nerves [22] and could not evaluate patients with hypotensive symptoms before hemodynamic monitoring, who might have had orthostatic intolerance just after HD session. Second, the correlation between IDH and orthostatic intolerance immediately after dialysis was not fully clarified. It is well known that intradialytic and orthostatic hypotension have multifactorial causes. Future studies to identify factors related to post-dialysis OH are needed to enable the earlier detection of fall risk. Third, there is a diverse pattern of orthostatic BP decay [11] such as initial and delayed OH in which a blood pressure decrease occurs within 15 s and after 3 min, respectively [23]; however, we could not investigate the blood pressure patterns and recovery times. Further studies on blood pressure decrease timing are needed to develop more effective strategies to reduce the probability of post-dialytic falls in HD patients upon returning home.

Conclusion

In patients with IDH, postural changes from the supine to the semi-recumbent position immediately after an HD session may significantly decrease SBP. Postural changes from a semi-recumbent to a sitting position may also significantly decrease SBP. These results suggest that beat-to-beat hemodynamic monitoring during HD session provides useful information to identify the patients with a potential risk for post-dialytic falls and that dialysis care team members should provide support to patients with IDH who are transferring out of bed to prevent post-dialytic falls.

Abbreviations

ABI: 

Ankle-brachial index

Alb: 

Albumin

BNP: 

B-type natriuretic peptide

CO: 

Cardiac output

DBP: 

Diastolic blood pressure

DM: 

Diabetes mellitus

Hb: 

Hemoglobin

HD: 

Hemodialysis

HR: 

Heart rate

Ht: 

Hematocrit

IDH: 

Intradialytic hypotension

LVEF: 

Left ventricular ejection fraction

OH: 

Orthostatic hypotension

SBP: 

Systolic blood pressure

SV: 

Stroke volume

TPR: 

Total peripheral resistance

Declarations

Acknowledgements

The authors thank the hospital staff and patients who participated in this study.

Funding

The authors declare that there is no funding related to this manuscript.

Availability of data and materials

The datasets analyzed during the present study are available from the corresponding author on reasonable request.

Authors’ contributions

TM and YM were involved in the study design and article writing of the manuscript. TM, MS and KM participated in the study procedure implementation and data collection. ST, TF, and IY kindly reviewed and revised the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

This study was approved by the Ethical Committee of Mukogawa Women’s University, and written informed consent was obtained from each participant after a detailed explanation of the study protocol was provided.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Authors’ Affiliations

(1)
Physical Therapy Service, Ibuki Clinic, 1-37 Kofuku-cho, Kadoma Osaka, 571-0066, Japan
(2)
Graduate School of Health and Sports Sciences, Mukogawa Women’s University, 6-46 Ikebiraki, Nishinomiya Hyogo, 663-8558, Japan
(3)
Nursing Department, Ibuki Clinic, 1-37 Kofuku-cho, Kadoma Osaka, 571-0066, Japan
(4)
Department of Internal Medicine, Ibuki Clinic, 1-37 Kofuku-cho, Kadoma Osaka, 571-0066, Japan
(5)
Department of Urology, Ibuki Clinic, 1-37 Kofuku-cho, Kadoma Osaka, 571-0066, Japan

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© The Author(s) 2018

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