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The relative importance of frailty, physical and cardiovascular function as exercise-modifiable predictors of falls in haemodialysis patients: a prospective cohort study
1 Abstract
Background
Stage 5 chronic kidney disease (CKD-5) patients on haemodialysis (HD) are at high risk of accidental falls. Previous research has shown that frailty is one of the primary contributors to the increased risk of falling in this clinical population. However, HD patients often present with abnormalities of cardiovascular function such as baroreflex impairment and orthostatic dysregulation of blood pressure (BP) which may also be implicated in the aetiology of falling. Therefore, we aimed to explore the relative importance of frailty and cardiovascular function as potential exercise-modifiable predictors of falls in these patients.
Methods
Ninety-three prevalent CKD-5 patients on HD from three Renal Units were recruited for this prospective cohort study, which was conducted between October 2015 and August 2018. At baseline, frailty status was assessed using the Fried’s frailty phenotype, while physical function was evaluated through timed up and go (TUG), five repetitions chair sit-to-stand (CSTS-5), objectively measured physical activity, and maximal voluntary isometric strength. Baroreflex and haemodynamic function at rest and in response to a 60° head-up tilt test (HUT-60°) were also assessed by means of the Task Force Monitor. The number of falls experienced was recorded once a month during 12 months of follow-up.
Results
In univariate negative binomial regression analysis, frailty (RR: 4.10, 95%CI: 1.60–10.51, p = 0.003) and other physical function determinants were associated with a higher number of falls. In multivariate analysis however, only worse baroreflex function (RR: 0.96, 95%CI: 0.94–0.99, p = 0.004), and orthostatic decrements of BP to HUT-60° (RR: 0.93, 95%CI: 0.87–0.99, p = 0.033) remained significantly associated with a greater number of falls. Eighty falls were recorded during the study period and the majority of them (41.3%) were precipitated by dizziness symptoms, as reported by participants.
Conclusions
This prospective study indicates that cardiovascular mechanisms implicated in the short-term regulation of BP showed a greater relative importance than frailty in predicting falls in CKD-5 patients on HD. A high number of falls appeared to be mediated by a degree of cardiovascular dysregulation, as evidenced by the predominance of self-reported dizziness symptoms.
Trial registration
ClinicalTrials.gov (trial registration ID: NCT02392299; date of registration: March 18, 2015).
Background
Stage 5 chronic kidney disease (CKD-5) patients receiving maintenance haemodialysis (HD) are at high risk of falls and fall-related injuries [1–3], with incidence rates being 1.5 to 3.5 times higher than community-dwelling older adults [4–6]. The clinical implications of an accidental fall can be devastating in this patient population who are already multi-comorbid. Several prospective cohort studies conducted in HD patients have concluded that those who fell had a 2.1 to 3.5 times higher risk of admission to nursing homes, hospitalisation, and death [7, 8]. Previous research has shown that factors such as older age, comorbidity, polypharmacy and frailty seem to be principal factors implicated in the aetiology of falls in these patients [1, 2, 4, 7].
The prevalence of physical frailty in the CKD-5 population is 36.8% and is approximately five-fold higher than in community-dwelling older adults [9, 10]. From a preventive and rehabilitative point of view, this syndrome is a potentially modifiable risk factor, as previous studies conducted in HD populations have shown that single frailty components, such as low physical activity, muscle strength, and slow gait speed can be improved following exercise-based interventions [11]. Although frailty has been consistently shown to be associated with falls in HD patients [4, 12, 13], few studies have explored the relationship between objective frailty-related physical function measures and falls [1, 2, 4, 12, 14, 15]. Results from these studies seem to indicate that, in predicting falls, composite indices of physical function [14, 15] may be more useful than single component assessments [2]. However, the identification of which individual frailty/physical function components may be more closely associated with falls is of paramount importance, as this would eventually allow exercise-based rehabilitation programs to be tailored to reduce the occurrence of falls in CKD-5 patients on HD. Along with frailty, cardiovascular disease (CVD) is also highly prevalent in CKD-5 patients and impaired cardiovascular function is associated with multiple adverse clinical outcomes [16]. A few studies have also begun to better explore the link between clinical outcomes such as falls and cardiovascular dysregulation in this patient group [5, 17, 18]. In particular, it appears that the CKD-5 population on dialysis may be at risk of hypotension that can lead to postural dizziness, and potentially falls. This is further exacerbated by the combined effect of autonomic failure and the significant fluid shifts associated with dialysis [17]. Two studies reported that low pre-dialysis blood pressure (BP) was associated with increased odds of falling [2, 19], and a recent investigation by Kono et al. [15] highlighted a significant relationship between intra-dialytic hypotension and falls in HD patients. In addition, we recently postulated that a drop in BP in response to a passive orthostatic challenge, as well as impaired baroreflex function may be linked to an increased risk of falling in HD patients [18]. All of these observations seem to indirectly suggest that impaired BP control, to maintain haemodynamic stability, might be implicated as an additional factor in the aetiology of falls in the CKD-5 population on dialysis, due to the CKD-related autonomic failure and/or the dialysis-related hypotension. From a rehabilitation/therapeutic perspective, this could have important translational impact, since the short-term regulation of BP, as assessed by means of baroreflex function, has been shown to improve following active interventions such as exercise [20].
The objective of this investigation was to explore the relative importance of frailty and cardiovascular function as potential exercise-modifiable predictors of falls in CKD-5 patients on HD. We hypothesised that 1) frailty and cardiovascular function would be associated with a higher number of falls, and that 2) modelling the risk of falling by adding a cardiovascular function variable to frailty would improve the prediction of falls sustained and recorded over a 12-month period in CKD-5 patients on HD.
Methods
Study design
An observational prospective study design was used to investigate the association between potential predictors of falls (e.g. frailty, cardiovascular function) and the number of falls sustained over a 12-month follow-up period in CKD-5 patients on HD.
Study setting
The study was conducted in three National Health Service (NHS) Renal Units located in North Lanarkshire and Fife, United Kingdom, between October 2015 and August 2018. Recruitment started in October 2015 and continued on a rolling basis until December 2017. All potential predictors and clinical variables were assessed (during a single session of 2 hours duration) at baseline for each participant between October 2015 and December 2017, while the follow-up period ran from November 2015 to August 2018.
This research project abided by the ethical principles for medical research involving human participants, as set out by the world medical association declaration of Helsinki, and received ethical approval by the West of Scotland NHS and Queen Margaret University Research Ethics Committees (NHS REC reference number: 15/WS/0079). This research project was prospectively registered in ClinicalTrials.gov (trial registration ID: NCT02392299; date of registration: March 18, 2015).
Study participants
Prevalent ambulatory CKD-5 patients stable on HD therapy for at least 3 months, fluent in spoken and written English, and ≥ 18 years of age were considered eligible to participate in the study.
Exclusion criteria were lower limb amputation without prosthesis, unstable dialysis and medication treatment, unstable cardiac condition, clinically severe left ventricular outflow obstruction, suspected or known aneurysm, critical mitral stenosis, critical cerebrovascular stenosis, critical proximal coronary artery stenosis, pregnancy and severe cognitive impairment.
All patients who agreed to take part in the study provided written informed consent.
Measurements
Demographic and clinical characteristics
Patient demographics (age, gender, height, weight, body mass index), and clinical characteristics (dialysis vintage, Charlson comorbidity index, medications) were extracted from the patients’ medical records. Height and weight were measured on the assessment day.
Falls
A fall was operationally defined as an unexpected event in which the participant comes to rest on the ground, floor, or lower level [21]. One researcher (TZ) and two research nurses (KC and NA) administered a customised falls questionnaire to all study participants during dialysis, once a month following baseline assessment, for a period of 12 months. Information recorded included number of falls experienced (if any), circumstances surrounding these falls (i.e. location, activities undertaken at the time of fall, precipitating factors), and their consequences (i.e. hospitalisation, injuries, emergency services etc.). A patient was classified as a “faller” if he/she reported at least one fall during the 12-month longitudinal follow-up.
Frailty
A modified version of the Fried’s frailty phenotype was used to assess frailty [10]. Patients were classified as frail if they met at least three of the following conditions: 1) low self-reported levels of physical activity (PA), assessed by means of the short-form international physical activity questionnaire (IPAQ-SF) [22] (total Kcal/week below an established threshold [10]); 2) low gait speed, assessed as walking time of 15 ft above an established threshold [10]; 3) low strength, assessed by means of an isometric handgrip test below an established threshold [10]; 4) self-reported exhaustion, assessed by means of the SF-36 questionnaire (vitality score <55) [23]; 5) unintentional weight loss ≥10 lbs. in the previous 12 months (ascertained through medical records).
Additional objective physical function and physical activity measures
1) The 3-m timed up and go (TUG) test was used to assess dynamic balance [24]. 2) The 5 repetitions chair sit to stand test (CSTS-5) was used to assess lower extremity muscle power [25]. 3) Maximal voluntary isometric handgrip and leg extension strength were assessed using a hydraulic hand dynamometer (Jamar Patterson Medical Ltd., USA) and a digital myometer (MIE, Medical Research Ltd., Leeds, UK): participants performed three trials interspersed by a one-minute rest and the average of these was taken for analysis purposes [26–28]. 4) Objective measures of PA patterns were obtained using the activPal monitor (PAL Technologies Ltd., Glasgow, UK). Participants wore this device on the anterior aspect of the thigh for seven consecutive days and the average daily time spent standing, number of daily steps, and number of daily sit to stands were recorded and summarised using the manufacturer’s proprietary software [29].
Cardiovascular function
The arterial baroreflex was assessed during quiet rest (in supine position) and in response to a five-minute head-up tilt test at 60° (HUT-60°) [18]. The Task Force Monitor 3040i (CNSystems, Graz, Austria), was used for the non-invasive measurement of all haemodynamic and baroreflex variables [30–32]. Stroke volume (SV), cardiac output (CO), and total peripheral resistance (TPR) were recorded by means of impedance cardiography (ICG). Heart rate (HR), R-R interval (RRI), continuous systolic (contSBP) and diastolic (contDBP) BP were measured by means of 6-lead electrocardiography (ECG) and continuous photoelectric plethysmography.
Baroreflex function variables taken for the analysis were i) number of up (up-events) and down (down-events) baroreceptor events, defined as the simultaneous coupling of a contSBP ramp (+/− 1 mmHg for 3 consecutive beats) with either an increase or decrease of the RRI of at least 4 ms. The total number of baroreceptor events (total-events) were then calculated as the sum of all down-events and up-events, ii) the down/up/total baroreceptor effectiveness index (BEI), representing the ratio of occurred down/up/total baroreceptor events and detected down/up/total BP ramps expressed as a percentage [33], and iii) baroreflex sensitivity (BRS), the average slope of the regression lines between the RRIs and the contSBP values resulting from every baroreceptor event [34]. All baroreflex and haemodynamic assessments were performed on a non-dialysis day, during the midweek interval, in order to minimise the influence of fluid and electrolyte shifts on data collected.
Statistical analysis
Statistical analyses were performed with SPSS (Version 23.0 for Windows, SPSS Inc., Chicago, IL). The Kolmogorov-Smirnov Test (K-S) was used to assess whether data were normally distributed. Differences between fallers and non-fallers in demographic, clinical, frailty, and cardiovascular characteristics were analysed by means of a Chi-Squared test for categorical variables, and by either Mann-Whitney U or independent t-tests, as appropriate, for continuous variables.
The association between baseline factors and the number of falls recorded during follow-up was analysed by means of negative binomial regression with an overdispersion parameter estimated on the actual distribution of the dependent variable (i.e. number of falls). All frailty and cardiovascular factors were initially entered in a univariate negative binomial regression model, and those factors reaching statistical significance (p-value ≤ .05) were taken forward to the multivariate stage. The multivariate analysis consisted of a first model (Model 1), in which all factors were adjusted for clinical confounders, while a second model was designed to assess the second research hypothesis. In this second model (Model 2), frailty and physical function factors were adjusted for all variables in Model 1 and for the cardiovascular function variable showing the highest correlation (R2) with number of falls, while cardiovascular factors were adjusted for all variables in Model 1 and for frailty. In a further analysis, we calculated the relative change in Akaike’s Information criterion (AIC) to explore the goodness of fit of negative binomial regression models where only frailty and cardiovascular function variables were entered simultaneously.
Sensitivity analyses were undertaken using the receiver operating characteristic (ROC) analysis of those potential factors associated with falls (yes or no), and the area under the curve (AUC) was used to compare the predictive ability of frailty alone with a model composed of frailty and a cardiovascular predictor. Statistical limits for significance were set at an alpha level of p ≤ .05.
Results
Study participants
Ninety-three patients undergoing outpatient HD therapy at the Renal Units provided written informed consent. Seventeen patients (18.3%) did not complete baseline assessments due to i) change of mind or inability to schedule an assessment appointment within a couple of months from consent (n = 7; 7.5%), ii) deterioration of health conditions (n = 6; 6.5%) and iii) death (n = 4; 4.3%). The remaining 76 patients completed all baseline assessments and were enrolled in the study. Seven participants (9.2%) were lost to follow-up due to renal transplantation (n = 4; 5.3%) and death (n = 3; 3.9%). Therefore, 69 patients were entered in the final analysis.
Demographic and clinical characteristics
The demographic and clinical characteristics of study participants are summarised in Table 1. Fallers were more likely to be prescribed antidepressants, and had significantly higher CRP compared to non-fallers. No statistically significant differences in other clinical characteristics were detected.
Table 1
Demographic and clinical characteristics of study participants: results are expressed as percentages for categorical variables and mean ± standard deviation for continuous data
| Variables | All patients (69) | Fallers (26) | Non-fallers (43) | P-value |
|---|---|---|---|---|
| Sociodemographic characteristics | ||||
| Sex (% M) | 55.1 | 42.3 | 62.8 | 0.097 |
| Age (years) | 61.7 ± 13.3 | 58.3 ± 14.1 | 63.8 ± 12.6 | 0.151 |
| Weight (kg) | 80.3 ± 18.7 | 75.7 ± 18.6 | 83.1 ± 18.5 | 0.114 |
| Height (cm) | 166.2 ± 9 | 166 ± 9 | 166.3 ± 9 | 0.892 |
| BMI (kg * m−2) | 29.1 ± 6.4 | 27.6 ± 7 | 30 ± 5.9 | 0.144 |
| Clinical history | ||||
| Dialysis vintage (days) | 713 ± 714 | 732 ± 636 | 701 ± 765 | 0.465 |
| CCI (score) | 5.3 ± 2.2 | 5.1 ± 2.1 | 5.4 ± 2.3 | 0.639 |
| Primary renal disease (%) | ||||
| Diabetic nephropathy | 25 | 26.9 | 23.8 | 0.773 |
| Glomerulonephritis | 19.1 | 19.2 | 19 | 1.000 |
| Polycystic kidney | 8.8 | 0 | 14.3 | 0.075 |
| Renovascular or hypertensive | 8.8 | 0 | 14.3 | 0.075 |
| Other | 20.6 | 23.1 | 19 | 0.690 |
| Uncertain aetiology | 17.6 | 30.8 | 9.5 | 0.046 |
| Type of vascular access (%) | ||||
| Arteriovenous fistula | 64.7 | 61.5 | 66.7 | 0.667 |
| Central-venous | 35.3 | 38.5 | 33.3 | 0.667 |
| Inter-dialytic weight gain (kg) | 1.6 ± 1.2 | 1.6 ± 1 | 1.6 ± 1.4 | 0.923 |
| Ultrafiltration rate (mL/kg/h) | 6.5 ± 2.4 | 7.1 ± 2.5 | 6.1 ± 2.3 | 0.095 |
| HD treatment time (h) | 4.1 ± 0.5 | 4.1 ± 0.4 | 4.2 ± 0.5 | 0.395 |
| Prescribed medications | ||||
| Medications (n°) | 11.8 ± 3.4 | 12.4 ± 3.3 | 11.5 ± 3.5 | 0.262 |
| Beta blockers use (%) | 50 | 42.3 | 54.8 | 0.318 |
| ACE-inhibitors use (%) | 7.4 | 7.7 | 7.1 | 1.000 |
| Ca-channel blockers use (%) | 57.4 | 50 | 61.9 | 0.335 |
| AngII-receptor antagonists use (%) | 16.2 | 11.5 | 19 | 0.512 |
| Alpha blockers use (%) | 32.4 | 38.5 | 28.6 | 0.397 |
| Antihypertensive use (%) | 83.8 | 80.8 | 85.7 | 0.737 |
| > 1 antihypertensive use (%) | 51.5 | 42.3 | 57.1 | 0.234 |
| Opiates use (%) | 19.1 | 11.5 | 23.8 | 0.342 |
| Antidepressants use (%) | 33.8 | 50 | 23.8 | 0.027 |
| Diuretics use (%) | 33.8 | 23.1 | 40.5 | 0.141 |
| Laboratory values | ||||
| Hb (g/dL) | 11.2 ± 1.2 | 11 ± 1 | 11.2 ± 1.2 | 0.317 |
| CRP (mg/L) | 25.8 ± 45.4 | 37.6 ± 59.2 | 18.3 ± 32.7 | 0.027 |
| Bicarbonate (mmol/L) | 21.2 ± 3.2 | 21.5 ± 3.1 | 21.1 ± 3.4 | 0.546 |
| Na (mmol/L) | 139 ± 2.8 | 138.4 ± 3.3 | 139.4 ± 2.4 | 0.388 |
| K (mmol/L) | 4.6 ± 0.7 | 4.6 ± 0.7 | 4.6 ± 0.6 | 0.992 |
| Urea (mg/dL) | 16.4 ± 5.1 | 15.7 ± 6.1 | 16.7 ± 4.5 | 0.276 |
| Phosphate (mmol/L) | 1.5 ± 0.6 | 1.5 ± 0.6 | 1.5 ± 0.5 | 0.978 |
| PTH (ρmol/L) | 27.2 ± 32.1 | 28.9 ± 43.4 | 26.2 ± 23.1 | 0.586 |
| Albumin (g/L) | 37.1 ± 4.3 | 36.1 ± 5.2 | 37.7 ± 3.7 | 0.146 |
| Adjusted calcium (mmol/L) | 2.4 ± 0.1 | 2.3 ± 0.1 | 2.4 ± 0.1 | 0.511 |
| URR (%) | 71.1 ± 6.2 | 71.1 ± 7.7 | 71 ± 5.1 | 0.994 |
| Creatinine (μmol/L) | 638.1 ± 161.3 | 592 ± 175.7 | 666 ± 147.1 | 0.064 |
Abbreviations: BMI body mass index, CCI Charlson comorbidity index, HD haemodialysis, ACE angiotensin-converting enzyme, Ca calcium, AngII angiotensin II, Hb hemoglobin, CRP C-reactive protein, Na sodium, K potassium, PTH parathyroid hormone, URR urea reduction ratio
Falls
A total number of 80 falls were recorded during the 12-month observational follow-up. Figure 1 shows the distribution of number of falls while Fig. 2 displays the characteristics of the falls experienced by study participants.
Frailty and physical function
The frailty and physical function characteristics of study participants are summarised in Table 2. Fallers were more likely to meet the frailty component of self-reported exhaustion.
Table 2
Frailty and physical function characteristics of study participants: results are expressed as percentages for categorical variables and mean ± standard deviation for continuous data
| Variables | All patients (69) | Fallers (26) | Non-fallers (43) | P-value |
|---|---|---|---|---|
| Frailty components and phenotype | ||||
| Low PA (%) | 47.8 | 46.2 | 48.8 | 0.829 |
| Low gait speed (%) | 29 | 42.3 | 20.9 | 0.058 |
| Low strength (%) | 47.8 | 46.2 | 48.8 | 0.829 |
| Exhaustion (%) | 73.5 | 92.3 | 61.9 | 0.006 |
| Unintentional weight loss (%) | 17.6 | 28 | 11.6 | 0.108 |
| Fried’s frailty phenotype (%) | 37.7 | 50 | 30.2 | 0.101 |
| Objectively measured PA | ||||
| Time spent standing (h) | 2.4 ± 1.2 | 2.1 ± 1.1 | 2.5 ± 1.2 | 0.177 |
| Daily steps (n°) | 3086 ± 1810 | 2601 ± 1325 | 3366 ± 2004 | 0.144 |
| Daily sit to stands (n°) | 37.5 ± 12.6 | 38.3 ± 16.1 | 37.1 ± 10.3 | 0.894 |
| Strength | ||||
| Handgrip (kg) | 26.9 ± 9.5 | 24.5 ± 10 | 28.4 ± 9 | 0.101 |
| Leg extension (kg) | 20.1 ± 9 | 17.4 ± 8.3 | 21.8 ± 9.1 | 0.050 |
| Functional tests | ||||
| Gait speed (m/s) | 0.85 ± 0.26 | 0.78 ± 0.26 | 0.9 ± 0.25 | 0.067 |
| TUG (s) | 11.5 ± 4.8 | 13.3 ± 6.4 | 10.4 ± 3.4 | 0.055 |
| CSTS-5 (s) | 17.1 ± 8.9 | 19.6 ± 12.3 | 15.7 ± 6.3 | 0.355 |
Abbreviations: PA physical activity, TUG timed up and go test, CSTS-5 5 repetitions chair sit to stand test
Cardiovascular function
The cardiovascular function characteristics of study participants at rest are summarised in Table 3, while the haemodynamic responses to HUT-60° are reported in Table 4.
Table 3
Cardiovascular function characteristics of study participants. Baroreflex and haemodynamic variables at rest: results are expressed as mean ± standard deviation
| Variables | All patients (69) | Fallers (26) | Non-fallers (43) | P-value |
|---|---|---|---|---|
| Baroreflex function | ||||
| Up-ramps (n°) | 20.4 ± 18.9 | 20.9 ± 22.9 | 20.1 ± 15.8 | 0.632 |
| Down-ramps (n°) | 18.4 ± 15.9 | 19.1 ± 18.3 | 17.9 ± 14.2 | 0.811 |
| Total-ramps (n°) | 38.8 ± 34.3 | 40 ± 40.7 | 38 ± 29.8 | 0.688 |
| Up-events (n°) | 4.5 ± 7.1 | 2.6 ± 3.7 | 5.7 ± 8.4 | 0.125 |
| Down-events (n°) | 4.8 ± 6.4 | 3.3 ± 4.5 | 5.7 ± 7.3 | 0.347 |
| Total-events (n°) | 9.3 ± 13 | 6 ± 7.9 | 11.4 ± 15.1 | 0.129 |
| Up-BEI (%) | 20.6 ± 25.2 | 14.6 ± 20.2 | 24.7 ± 27.7 | 0.165 |
| Down-BEI (%) | 27.9 ± 26.4 | 20.3 ± 22.7 | 32.9 ± 27.7 | 0.103 |
| Total-BEI (%) | 25.4 ± 25 | 17.7 ± 19.1 | 30.6 ± 27.4 | 0.078 |
| BRS (ms/mmHg) | 9.3 ± 7.1 | 10.3 ± 9.3 | 8.8 ± 5.9 | 0.806 |
| Haemodynamic variables | ||||
| RRI (ms) | 894.9 ± 163.1 | 867.7 ± 112.4 | 911.4 ± 186.8 | 0.240 |
| HR (bpm) | 69.5 ± 12 | 70.7 ± 9.3 | 68.8 ± 13.4 | 0.506 |
| contSBP (mmHg) | 124 ± 23.1 | 127 ± 26.2 | 122.1 ± 21.1 | 0.462 |
| contDBP (mmHg) | 77.8 ± 14.8 | 76.8 ± 12.5 | 78.4 ± 16.1 | 0.756 |
| contmBP (mmHg) | 97.2 ± 17.7 | 97.9 ± 16.9 | 96.8 ± 18.4 | 0.801 |
| SV (ml) | 64.4 ± 14.4 | 63.6 ± 12.1 | 64.8 ± 15.7 | 0.921 |
| CO (L/min) | 4.4 ± 1.2 | 4.5 ± 0.9 | 4.4 ± 1.3 | 0.416 |
| TPR (dyne*s/cm5) | 1777 ± 501 | 1716 ± 371 | 1816 ± 570 | 0.440 |
| SI (ml/m2) | 34.8 ± 8.8 | 35.2 ± 7.8 | 34.5 ± 9.5 | 0.455 |
| CI (L/min*m2) | 2.4 ± 0.7 | 2.5 ± 0.5 | 2.4 ± 0.8 | 0.167 |
| TPRI(dyne*s*m2/cm5) | 3330 ± 1037 | 3121 ± 710 | 3464 ± 1190 | 0.154 |
| TFC (1/kΩ) | 32.9 ± 10.8 | 34.6 ± 12.1 | 31.9 ± 10 | 0.365 |
| OscSBP (mmHg) | 128.2 ± 22 | 134.4 ± 26.3 | 124.8 ± 18.7 | 0.094 |
| OscDBP (mmHg) | 81 ± 13.9 | 82.4 ± 12.8 | 80.2 ± 14.5 | 0.553 |
Abbreviations: Up-BEI up-events baroreceptor effectiveness index, Down-BEI down-events baroreceptor effectiveness index, Total-BEI total-events baroreceptor effectiveness index, BRS baroreflex sensitivity, RRI R-R interval, HR heart rate, contSBP continuous systolic blood pressure, contDBP continuous diastolic blood pressure, contmBP continuous mean blood pressure, SV stroke volume, CO cardiac output, TPR total peripheral resistance, SI stroke index, CI cardiax index, TPRI total peripheral resistance index, TFC thoracic fluid content, OscSBP oscillometric systolic blood pressure, OscDBP oscillometric diastolic blood pressure
Table 4
Haemodynamic responses to HUT-60°. Difference between the variables averaged over 5 min of HUT-60° and the variables averaged over 5 min of supine recording: results are expressed as mean ± standard deviation
| Variables | All patients (69) | Fallers (26) | Non-fallers (43) | P-value |
|---|---|---|---|---|
| RRI (ms) | −60.4 ± 66.8 | −55.9 ± 71.1 | −63 ± 65 | 0.514 |
| HR (bpm) | 6.2 ± 7.3 | 6.9 ± 9.6 | 5.8 ± 5.7 | 0.860 |
| contSBP (mmHg) | 3.9 ± 11.9 | 4.8 ± 14.9 | 3.4 ± 9.9 | 0.178 |
| contDBP (mmHg) | 6.3 ± 8.5 | 6.3 ± 10.6 | 6.3 ± 7.1 | 0.575 |
| contmBP (mmHg) | 5.3 ± 9.4 | 5.4 ± 12 | 5.2 ± 7.8 | 0.436 |
| SV (ml) | −4.1 ± 13.8 | −4.5 ± 12.7 | −3.9 ± 14.5 | 0.693 |
| CO (L/min) | 0.01 ± 1 | 0 ± 0.9 | 0.02 ± 1 | 0.734 |
| TPR (dyne*s/cm5) | 98.3 ± 374.8 | 102.8 ± 367.4 | 95.5 ± 384.1 | 0.941 |
| SI (ml/m2) | −2.3 ± 7.6 | −2.3 ± 6.9 | −2.3 ± 8 | 0.703 |
| CI (L/min*m2) | −0.01 ± 0.5 | 0.01 ± 0.5 | −0.01 ± 0.5 | 0.887 |
| TPRI(dyne*s*m2/cm5) | 173.7 ± 684 | 193.8 ± 655.3 | 161.3 ± 709.3 | 0.856 |
| TFC (1/kΩ) | −1.9 ± 1.8 | − 2 ± 1.9 | −1.8 ± 1.8 | 0.632 |
| OscSBP (mmHg) | −3.6 ± 9.8 | −5.6 ± 10.9 | −2.5 ± 9 | 0.249 |
| OscDBP (mmHg) | −0.7 ± 6.9 | −2.6 ± 7.5 | 0.3 ± 6.4 | 0.432 |
Abbreviations: RRI R-R interval, HR: heart rate, contSBP continuous systolic blood pressure, contDBP continuous diastolic blood pressure, contmBP continuous mean blood pressure, SV stroke volume, CO cardiac output, TPR total peripheral resistance, SI stroke index, CI cardiax index, TPRI total peripheral resistance index, TFC thoracic fluid content, OscSBP oscillometric systolic blood pressure, OscDBP oscillometric diastolic blood pressure
Predictors of falls
The results from the negative binomial regression analyses are summarised in Table 5. All frailty/physical function and cardiovascular function factors reaching statistical significance in univariate analysis were adjusted in Model 1 for CRP and antidepressant use, as both of these clinical factors have been linked to an increased risk of falling in CKD-5 [1, 15]. Moreover, with concern for multi-collinearity (Additional file 1: Table S1), we only reported the baroreflex function index showing the highest correlation with number of falls (total-BEI). In fully adjusted analyses (Model 2), total-BEI, and the haemodynamic response of OscDBP to HUT-60° were associated with a higher number of falls.
Table 5
Negative binomial regression analysis: predictors of falls
| Factors | Univariate | Multivariate | ||||
|---|---|---|---|---|---|---|
| Model 1 | Model 2 | |||||
| RR (95% CI) | P-value | RR (95% CI) | P-value | RR (95% CI) | P-value | |
| Frailty & physical function | ||||||
| Frailty (yes/no) | 4.10 (1.60–10.51) | 0.003 | 2.23 (0.85–5.87) | 0.103 | 1.78 (0.70–4.51) | 0.224 |
| Daily steps (n°) | 0.99 (0.99–1.00) | 0.006 | 1.00 (0.99–1.00) | 0.137 | 1.00 (0.99–1.00) | 0.106 |
| Daily sit to stands (n°) | 0.96 (0.93–0.99) | 0.042 | 0.98 (0.94–1.02) | 0.387 | 0.99 (0.95–1.04) | 0.707 |
| Handgrip (kg) | 0.94 (0.88–0.99) | 0.034 | 0.97 (0.92–1.02) | 0.216 | 0.98 (0.93–1.04) | 0.448 |
| Gait speed (m/s) | 0.08 (0.01–0.62) | 0.016 | 0.26 (0.03–2.08) | 0.205 | 0.36 (0.04–3.32) | 0.363 |
| TUG (s) | 1.16 (1.02–1.32) | 0.021 | 1.08 (0.96–1.21) | 0.220 | 1.03 (0.91–1.17) | 0.643 |
| Cardiovascular function | ||||||
| Total-BEI (%) | 0.96 (0.93–0.98) | <0.001 | 0.96 (0.94–0.99) | 0.003 | 0.96 (0.94–0.99) | 0.004 |
| CO (L/min) | 0.51 (0.27–0.98) | 0.043 | 0.66 (0.37–1.15) | 0.143 | 0.67 (0.39–1.13) | 0.134 |
| OscDBP (mmHg) | 0.90 (0.83–0.98) | 0.010 | 0.93 (0.87–0.99) | 0.036 | 0.93 (0.87–0.99) | 0.033 |
Abbreviations: RR rate ratio, CI confidence interval, TUG timed up and go test, Total-BEI total-events baroreceptor effectiveness index, CO cardiac output response to HUT-60°, OscDBP oscillometric diastolic blood pressure response to HUT-60°, Model 1: All factors are adjusted for CRP and antidepressant use, Model 2 Frailty and physical function factors are adjusted for all variables in Model 1 and for Total-BEI. Cardiovascular function factors are adjusted for all variables in Model 1 and for frailty
Table 6 shows the goodness of fit (AIC) of the univariate regression models and its relative change following forced entry modelling of frailty and cardiovascular function (multivariate stage). The model composed of frailty and total-BEI resulted in a 19.1% decrease in AIC compared to frailty alone.
Table 6
Further analyses: goodness of fit of negative binomial regression models
| Factors | Univariate | Multivariatea | |||||
|---|---|---|---|---|---|---|---|
| RR (95% CI) | P-value | AIC | RR (95% CI) | P-value | AIC | ΔAIC | |
| Frailty and physical function | |||||||
| Frailty (yes/no) | 4.10 (1.60–10.5) | 0.003 | 185 | 2.53 (0.96–6.70) | 0.060 | 149.6 | −19.1% |
| Daily steps (n°) | 0.99 (0.99–1.00) | 0.006 | 142.3 | 1.00 (0.99–1.00) | 0.036 | 113.2 | −20.4% |
| Daily sit to stands (n°) | 0.96 (0.93–0.99) | 0.042 | 146.7 | 0.99 (0.95–1.03) | 0.543 | 116.7 | − 20.4% |
| Handgrip (kg) | 0.94 (0.88–0.99) | 0.034 | 188.6 | 0.97 (0.91–1.03) | 0.330 | 151.8 | −19.5% |
| Gait speed (m/s) | 0.08 (0.01–0.62) | 0.016 | 176.3 | 0.14 (0.02–1.39) | 0.094 | 141.1 | −20.0% |
| TUG (s) | 1.16 (1.02–1.32) | 0.021 | 171.7 | 1.10 (0.95–1.27) | 0.226 | 138.5 | −19.3% |
| Cardiovascular function | |||||||
| Total-BEI (%) | 0.96 (0.93–0.98) | <0.001 | 150.8 | 0.96 (0.94–0.99) | 0.003 | 149.6 | −0.8% |
| CO (L/min) | 0.51 (0.27–0.98) | 0.043 | 168.6 | 0.58 (0.33–1.04) | 0.068 | 165.7 | −1.7% |
| OscDBP (mmHg) | 0.90 (0.83–0.98) | 0.010 | 144.1 | 0.92 (0.85–0.99) | 0.028 | 142.6 | −1.0% |
Abbreviations: RR rate ratio, CI confidence interval, AIC Akaike’s information criterion, TUG timed up and go test, Total-BEI total-events baroreceptor effectiveness index, CO cardiac output, OscDBP oscillometric diastolic blood pressure
aFrailty and physical function variables are adjusted by Total-BEI, cardiovascular function variables are adjusted by frailty
Sensitivity analyses
Figure 3 shows the ROC curves of frailty alone and the model composed of frailty and total-BEI. Frailty alone did not discriminate significantly fallers from non-fallers, while adding the cardiovascular variable total-BEI resulted in a significant improvement of the AUC (+ 6%). In a further sensitivity analysis (Additional file 1: Table S2), we re-ran the negative binomial regression analysis adjusting Model 1 for diabetes, a well-established risk factor for falls in HD patients [1]. In this additional analysis, only total-BEI remained significantly associated with a higher number of falls (RR: 0.97, 95%CI: 0.95–0.99, p = 0.02).
Discussion
We hypothesised that frailty and cardiovascular function would be associated with a higher number of falls in CKD-5 patients on HD. Additionally, we hypothesised that modelling the risk of falling by adding a cardiovascular function variable to frailty would improve the prediction of falls sustained over 12 months in this patient population.
The univariate negative binomial regression analysis revealed that frailty and other physical function measures, such as number of daily steps and sit to stands, handgrip strength, gait speed, and TUG were associated with a higher number of falls in the study population. In addition, cardiovascular function indices such as total-BEI, CO and OscDBP responses to HUT-60°, were also associated with a higher number of falls (Table (Table5).5). However, in multivariate analysis, only total-BEI and the OscDBP response to HUT-60° were significantly predictive of a greater number of falls. In addition, modelling the risk of falling by adding a cardiovascular function index (total-BEI) to frailty resulted in a 19.1% reduction in AIC, indicating a better goodness of fit, while adding frailty to cardiovascular indices such as total-BEI, CO and OscDBP responses to HUT-60°, hardly modified the AICs (− 0.8% to − 1.7%, Table Table6).6). Moreover, the sensitivity analyses performed by means of ROC curve analysis revealed that adding total-BEI to the frailty model corresponded to a net 6% improvement of the AUC and resulted in a statistically significant prediction of falling status (Fig. 3).
The overall implications of these findings are that the addition of a baroreflex function index to an exclusively physical frailty-based model, did not only improve the prediction of falls, but it also highlighted the greater relative importance of a cardiovascular function index, implicated in the short-term regulation of BP, in predicting the occurrence of these falls. In particular, the forced entry modelling performed in Model 2 of the negative binomial regression analysis (Table (Table5),5), as well as the goodness of fit analysis (Table (Table6),6), suggest that lower baroreflex function and orthostatic decrements of BP may have an even higher impact than frailty on the prediction of falls in CKD-5 patients on HD.
The predominant role of these cardiovascular factors appeared to be also indirectly confirmed by the fall-related symptomatology reported by study participants (Fig. (Fig.2).2). The most common precipitating factors reported by fallers were dizziness/loss of consciousness (41.3% of falls), followed by loss of balance/unsteadiness of the legs (31.3% of falls), and environmental hazards (20% of falls). These symptoms seem to point out that the majority of falls were probably related to some underlying cardiovascular/haemodynamic type of mechanism. Because impairments of baroreflex function are linked to orthostatic decrements of BP [35], the dysregulation of BP during a sudden change in body position, or during prolonged standing may be one of the main mechanisms implicated in the aetiology of falls in CKD-5 patients on HD. Both of these factors predicted a higher number of falls in our study.
Another interesting finding was that BEI but not BRS was associated with a higher number of falls. The BEI is a measure that describes how often the baroreflex is activated [36], in contrast to the BRS which represents the baroreflex gain [37]. Therefore, we plausibly take the view that frequency, rather than intensity, of baroreflex activation may contribute more importantly to the increased risk of falling. Due to the fact that many spontaneous fluctuations of BP manifest suddenly throughout the day, as a result of changes in body position or more or less prolonged periods of standing [38], the baroreflex has to constantly adjust HR and peripheral resistance to maintain cardiac output. Thus, a reduced frequency of baroreflex activation (i.e. low BEI) would imply that sudden drops in BP are not coupled effectively with concomitant increases of HR, which may result in a suboptimal cerebral perfusion possibly leading to dizziness symptoms and, consequently, falls [39].
Many dialysis-specific or idiopathic risk factors may be involved in the dysregulation of BP which could possibly lead to dizziness symptoms and falls in this clinical population. First of all, the uremia-related cardiac autonomic dysfunction, characterised by alterations of the sympathetic, parasympathetic, and baroreflex components of the autonomic nervous system, is a factor that has been linked to symptomatic hypotension in CKD-5 patients [40]. Moreover, autonomic neuropathy is a common clinical complication of advanced diabetes, the most common cause of CKD [41], and it can also lead to a diminished response of BP to standing [42]. Secondly, dialysis patients are often treated with one or more antihypertensive drugs (83.8 and 51.5% of patients in our study). While this is often an unavoidable therapy for the treatment of hypertension, such antihypertensive polypharmacy has been linked to an increased risk of falling by inducing dizziness and postural hypotension [43].
Importantly, a systematic review with meta-analysis has recently concluded that exercise training can ameliorate autonomic regulation in CKD patients [44]. In particular, Petraki et al. [20] have shown that a seven-month intradialytic exercise programme led to improvements amounting to 27–35% in number of baroreceptor events and BEI in CKD-5 patients on HD. Since such measures were predictive of a higher number of falls in our study (Table (Table5),5), this raises the question as to whether an exercise training intervention may reduce the risk of falling by improving indices of autonomic function in people affected by CKD-5. Further research is warranted to explore this hypothesis as well as the cost-effectiveness of this potential intervention strategy.
The estimates of association between frailty and number of falls experienced emerging from this study are similar to those observed by previous research [4, 12]. In particular, McAdams-DeMarco et al. [4] explored the association between the Fried’s frailty phenotype and number of falls sustained over 6 months. The authors found that frailty was associated with a roughly 3.5 times higher number of falls in univariate Poisson regression analysis, an estimate that echoes the results from the univariate negative binomial regression analysis in our study (Table (Table5).5). Therefore, we conclude that our findings on the relationship between frailty and falls exhibit good external validity and may be generalised to the wider population of CKD-5 patients receiving HD.
Interestingly, the exploratory independent comparisons of fallers and non-fallers revealed that those who fell were more likely to use antidepressants (50% vs 23.8%) and had higher CRP levels (37.6 ± 59.2 mg/L vs 18.3 ± 32.7 mg/L). Because both antidepressant use and high CRP levels have been linked to a higher risk of falling by previous research conducted on HD patients [1, 15], we adjusted the analysis for these possible clinical confounders (Model 1). In this first model of multivariate analysis, neither frailty nor the additional physical function measures were significantly associated with a higher number of falls (Table (Table5).5). This finding further reinforces the observation that total-BEI and the OscDBP response to HUT-60° had a greater relative importance than frailty in predicting the number of falls experienced by study participants during the 12-month follow up.
It should be acknowledged that because the sample size was relatively small, we could not apply a more exhaustive multivariate negative binomial regression analysis to more robustly test the interrelationships between frailty/physical function, cardiovascular function, and falls. In addition, we should also acknowledge that, while orthostatic decrements of OscDBP were significantly associated with falls (Table (Table5),5), orthostatic decrements of OscSBP were not. However, in univariate negative binomial regression analysis, OscSBP decrements also exhibited a potential trend of association with falls (RR: 0.95, 95%CI: 0.89–1.01, p = 0.084), and it is possible that a larger sample size may have also resulted into better chances of detecting a significant association between OscSBP decrements and falls, by decreasing the chances of committing a type II error. The lack of relationship between contBP and falls may also be explained in light of the orthostatic challenge used in our study, as previous research has shown that the initial response of contBP to passive tilting is less pronounced or even absent compared to active stand procedures [45, 46]. Additionally, the relatively short duration of HUT-60° may be partially responsible for the apparent lack of difference in BP response during the orthostatic challenge in fallers compared with non-fallers (Table (Table4).4). Particularly, the five-minute HUT-60° protocol employed in this study was designed to investigate only the short-lived haemodynamic adjustments to orthostasis [18, 47]. Previous research has shown that, during a 15-min passive orthostatic challenge, elderly people with a history of falls tend to exhibit a larger drop of BP compared with non-fallers [39]. Therefore, it is plausible that a longer HUT-60° protocol may have revealed a larger decrement of both contBP and OscBP in fallers [46].
Conclusions
This prospective cohort study indicates that by adding a cardiovascular index, implicated in the short-term regulation of BP, to a frailty-only model it was possible to improve significantly the prediction of falls in CKD-5 patients on HD. Baroreflex function, as assessed by means of BEI, and orthostatic decrements of BP showed a higher impact, and thus greater relative importance, than frailty in predicting number of falls in the study population. The clinical implications of these findings indicate that a simple non-invasive, time-efficient, assessment consisting of a continuous and simultaneous recording of BP and HR may be more useful than frailty assessment alone when predicting falls in HD patients. A high number of falls appear to be mediated by a degree of cardiovascular dysregulation, evidenced by the predominance of self-reported dizziness symptoms. We therefore recommend that interventions designed to improve baroreflex function/short-term regulation of BP should be considered when implementing falls prevention programmes in this patient population.
Acknowledgements
We would like to express our gratitude to the Renal Staff at Monklands Hospital, Airdrie, and Victoria Hospital, Kirkcaldy, for their continuous support and courtesy. In particular, we would like to thank Mr. Raymond Donnelly and Mr. Tom McCafferty for the extremely helpful IT support provided throughout the study. We would also like to thank Dr. Hadi Oun and Dr. Jonathan Price for facilitating the data collection process at Monklands Hospital.
Abbreviations
| ACE | Angiotensin-converting enzyme |
| AIC | Akaike’s Information criterion |
| AngII | Angiotensin II |
| AUC | Area under the curve |
| BEI | Baroreceptor effectiveness index |
| BMI | Body mass index |
| BP | Blood pressure |
| BRS | Baroreflex sensitivity |
| Ca | Calcium |
| CCI | Charlson comorbidity index |
| CI | Cardiac index |
| CI | Confidence interval |
| CKD-5 | Stage 5 chronic kidney disease |
| CO | Cardiac output |
| ContDBP | Continuous diastolic blood pressure |
| ContmBP | Continuous mean blood pressure |
| ContSBP | Continuous systolic blood pressure |
| CRP | C-reactive protein |
| CSTS-5 | 5 repetitions chair sit to stand test |
| CVD | Cardiovascular disease |
| Down-BEI | Down-events baroreceptor effectiveness index |
| ECG | Electrocardiography |
| Hb | Hemoglobin |
| HD | Haemodialysis |
| HR | Heart rate |
| HUT-60° | Head-up tilt test at 60° |
| ICG | Impedance cardiography |
| IPAQ-SF | Short-form international physical activity |
| K | Potassium |
| K-S | Kolmogorov-Smirnov test |
| Na | Sodium |
| NHS | National Health Service |
| OscDBP | Oscillometric diastolic blood pressure |
| OscSBP | Oscillometric systolic blood pressure |
| PA | Physical activity |
| PTH | Parathyroid hormone |
| ROC | Receiver operating characteristic |
| RR | Rate ratio |
| RRI | R-R interval |
| SF-36 | Short form health survey |
| SI | Stroke index |
| SV | Stroke volume |
| TFC | Thoracic fluid content |
| Total-BEI | Total-events baroreceptor effectiveness index |
| TPR | Total peripheral resistance |
| TPRI | Total peripheral resistance index |
| TUG | 3-m timed up and go test |
| Up-BEI | Up-events baroreceptor effectiveness index |
| URR | Urea reduction ratio |
Authors’ contributions
PK, TM, TZ and MvdL conceived and designed the study; TZ, PK, KC, NA, IS and AD participated in data acquisition, curation and interpretation; TZ, PK, TM, MvdL, RR, JT, and CP participated in data analysis and interpretation of findings; TZ and RR performed the statistical analysis; PK, TM, MvdL, JT, CP, AD and IS provided supervision or mentorship. TZ drafted the manuscript. All authors reviewed and approved the final version of the manuscript and accept accountability for the overall work.
Funding
This work was supported by a British Kidney Patient Association – British Renal Society joint grant (BKPA-BRS grant number: 16–003). The funders of this study had no role in study design; collection, analysis, and interpretation of data; writing the report; or the decision to submit the report for publication.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
This research project abided by the ethical principles for medical research involving human participants, as set out by the world medical association declaration of Helsinki, and received ethical approval by the West of Scotland NHS and Queen Margaret University Research Ethics Committees (NHS REC reference number: 15/WS/0079). All patients who agreed to take part in the study provided written informed consent.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
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Supplementary information
Supplementary information accompanies this paper at 10.1186/s12882-020-01759-z.