1. Introduction
End-stage renal disease is characterized by a number of abnormalities that disrupt the body’s homeostasis. Overhydration is a particularly important problem, especially in patients on dialysis. In less advanced stages of chronic kidney disease (CKD), overhydration accelerates the loss of renal function and the time to start renal replacement therapy [
1]. Overhydration also increases arterial stiffness and left ventricular hypertrophy, leading to the development of hypertension and heart failure [
2]. In addition, the condition is associated with an increase in total and cardiovascular mortality in both hemodialysis (HD) and peritoneal dialysis (PD) patients [
3,
4,
5,
6]. Therefore, the clinical consequences of overhydration justify considering water as a uremic toxin [
7]. On the other hand, hypovolemia is a risk factor for increased mortality [
8]. Hypovolemic episodes are one of the basic mechanisms responsible for the decrease in residual renal function in HD patients [
9,
10] Therefore, optimizing hydration status remains a key therapeutic goal in nephrology patients.
Achieving and maintaining proper hydration in a dialysis patient is a serious challenge. Decisions on the volume of ultrafiltration are made during HD, or after prior analysis of weight gain between HD procedures. Significant interdialytic weight gain, defined as a weight gain > 4.8%, increases the overall mortality of HD patients [
11]. However, the risk of death associated with high interdialytic weight gain is much lower than the risk associated with chronic overhydration [
12]. Patients without signs of hypovolemia or advanced hypervolemia after uncomplicated HD can reach their target body mass (“dry mass”). Dry mass is assumed to correspond to the optimal hydration status [
13]. However, studies have shown that approximately 20% of patients do not achieve this therapeutic goal [
14].
According to some researchers, overhydration occurs with a similar frequency in HD and PD patients and is associated with negative clinical consequences in both groups [
15]. However, most data on the occurrence and clinical significance of overhydration concern HD patients. Reports on PD patients are scarce and inconclusive. For example, in the European Body Composition Monitoring (EuroBCM) study concerning patients with PD, severe overhydration was found in only 25.2% of patients based on bioelectrical impedance analysis (BIA) [
16]. However, the results of the EuroBCM study do not correspond to the prevailing opinion that PD promotes overhydration. Studies comparing the hydration status of patients based on the method of dialysis are few, especially those taking into account diagnostic methods other than clinical assessment and body composition monitoring (BCM).
Accurately assessing the hydration status of dialysis patients is one of the main problems. Conclusions based on symptoms and signs, such as high arterial pressure, shortness of breath, auscultatory changes over the lung fields, peripheral edema, jugular vein widening, hepatomegaly, or weight gain are characterized by low sensitivity and specificity, though it remains the basic diagnostic tool [
2,
17]. Diagnostic tools that can clarify the data on the patient’s hydration status obtained from the clinical assessment are still needed. The ideal method should be accurate and repeatable, with simple and quick implementation, and potential for bedside use. Additional tests that we usually use to assess the state of hydration are X-ray, electrical bioimpedance, assessment of the concentration of natriuretic peptides (brain natriuretic peptide (BNP) and N-terminal pro-brain natriuretic peptide (NT-proBNP)), impedance cardiography (ICG) and other methods of segmental bioimpedance, and ultrasound methods (inferior vena cava (IVC) assessment, echocardiography, and the increasingly popular lung ultrasound (LUS)). Notably, none of the tests determine the state of hydration in an ideal way, and the overall assessment may be the conclusions drawn from results obtained with each of the methods.
The aim of the present study was to compare the results of a comprehensive hydration assessment of chronically dialyzed HD and PD patients carried out by clinical assessment and select additional methods.
4. Discussion
To the best of our knowledge, this study is the first to compare the hydration status of PD and HD patients using a number of complementary diagnostic methods: clinical examination; assessment of fluid content in the chest by two methods (LUS and ICG); and intravascular volemia including myocardial overload (ECHO), IVCDi, IVCCi, NT-pro-BNP, and BCM. This is the basis for saying that PD patients do not differ significantly from HD patients in terms of hydration status in both clinical assessment and objective results of additional tests. Furthermore, the additional content of dialysis fluid in the peritoneal cavity and significantly higher daily diuresis in the PD group did not affect the clinical significance of the presented results.
The ability to control hydration in HD and PD patients varies significantly and may influence clinical decisions. The planning of dehydration, i.e., ultrafiltration immediately before each dialysis procedure, and the possibility of changing this parameter during its duration allows the removal of excess water accumulated between treatments and quick achievement of the controlled target weight within a few hours. In contrast, in PD patients, the volume of ultrafiltration depends on hydration status, peritoneal properties, and the type of dialysis fluid. Intervention efficiency can be achieved more slowly in PD patients than HD patients. In addition, PD patients report for medical check-ups every 2–6 weeks, which is an advantage of this method, but also increases the risk of worse control of hydration status. The presence of fluid in the peritoneal cavity in PD is due to the dialysis method, but can also affect the results of additional tests assessing overhydration.
Taking all of the above into consideration, there is a widespread belief that PD patients may be expected to have worse hydration status and a higher frequency of overhydration than HD patients. The research results available in the medical literature regarding this issue are ambiguous. Plum et al. compared BIA parameters and atrial natriuretic peptide levels obtained in 39 HD and 43 PD patients, and found that PD patients have higher total body water (TBW) and extracellular body fluid (ECF) values assessed by BIA compared to HD patients, both before and after dialysis [
25]. However, in the discussion, the authors emphasized that the assessment of extracellular compartments in BIA does not allow differentiation of intravascular and extravascular volumes. They intended to resolve these doubts by examining the concentration of ANP as a reflection of the increase in intravascular volume, but found comparable average values in both groups. The results of the hydration assessment in the present study turned out to be more consistent; PD and HD patients did not differ in NT-proBNP concentration or BCM-OH results. However, the use of other natriuretic peptides (ANP vs. NT-proBNP) and bioimpedance parameters (TBW, ECF vs. BCM-OH estimation) may be relevant. Moreover, in the Plum et al. study, the HD and PD groups did not differ by daily diuresis (<1.0 L), whereas in our study, the mean daily diuresis was significantly higher in the PD group (~1.4 L) than the HD group (~0.7 L). This may explain the better hydration control of PD patients in our study. Aguiar et al. concluded that this method does not have to be associated with chronic overhydration after observing 30 PD patients for 2 years. At the beginning of their observations, BIA indicated significant overhydration in less than 7% of respondents, and this percentage did not change significantly during the 2-year follow-up. At the end of the observation period, not only the BIA results, but also the NT-proBNP concentrations of the examined patients, were comparable [
26].
Similar results as in the present study were reported by Oe et al., who did not find significant differences in BIA results or ultrasound assessments of the IVC between PD and HD when comparing the degree of overhydration in much smaller groups (11 PD and 20 HD tested before dialysis) using only two methods [
27]. Notably, similar to the present study, PD patients had much higher residual diuresis than HD patients. Yao et al. also used BIA, but assessed a much larger population: 95 PD patients and 75 HD patients before middle HD per week [
28]. In this study, the mean BIA-OH values in both groups were comparable. The authors also did not observe significant echocardiographic differences, including LVMI, between the groups. Interestingly, in their conclusion, Yoa et al. supported the statement that PD patients are more overhydrated than HD patients, likely based on the assumption adopted in the regression analysis. The average values of BIA parameters determined before and after HD were used in calculations for HD patients [
28]. The aim of our study was to verify clinical assessment before HD; in this regard, our observations are consistent with the results reported by Yao et al. Our results are also consistent with the observations of Papakrivopoulou et al., who compared the hydration status of 72 HD patients and 115 PD patients [
29]. PD patients had significantly higher residual diuresis. All parameters assessed by BIA were comparable in both groups if pre-dialysis results were taken into account for HD patients [
29]. The mean NT-proBNP concentrations in both groups were also comparable. Finally, Papakrivopoulou et al. did not find significant differences in the echocardiography results. The studied group was characterized as asymptomatic in regards to overhydration, but the ECW/TBW ratio exceeded the normal range in >30% of patients [
29]. This finding confirms the need to verify subclinical overhydration using objective results from additional studies.
The use of comprehensive volemic assessment in our study was intended to increase the strength of scientific evidence for a planned comparison of hydration status in both groups of patients. The position of BIA in the assessment of nephrology patients is well established. Moissl et al. compared parameters obtained during bioimpedance of the whole body with the results of determinations made using isotope tests, showing high compliance of these methods [
30]. Modification of the ultrafiltration size during HD based on BIA has also been shown to improve the control of hypertension, reduce vascular stiffness, and reduce left ventricular mass [
31]. On the other hand, the whole body’s electrical bioimpedance assumes that the human body is a cylinder with uniform conductivity. Thus, the total impedance in the BIA test depends as much as 90% on the impedance of the limbs, which is a frequently raised limitation of this method. Therefore, segmental bioimpedance analysis (SBIA) has been suggested to better reflect hydration status [
32]. In an earlier study of 40 HD patients, we showed that the only element of clinical assessment independently affecting the determination of overhydration in the whole body bioimpedance test is the severity of edema (R
2 = 0.44;
p <0.0001) [
33]. Therefore, BIA likely underestimates overhydration in non-edema patients with fluid redistribution mainly within the chest compartment. This justifies the use in everyday practice of diagnostic tools assessing the water content of the chest, such as LUS and ICG.
The interstitial syndrome found in LUS is an expression of the presence of water in the extravascular lung space (EVLW) [
34]. Agricola et al. observed a correlation between the number of B lines and EVLW measured by thermodilution (r = 0.42,
p = 0.001; PICCO System), EVLW assessment in chest radiology based on the Extravascular Lung Water Score (r = 0.60,
p = 0.0001), and wedge pressure in pulmonary capillaries (r = 0.48,
p = 0.01) [
34]. A significant relationship between the presence of the B line and pulmonary interstitial edema was confirmed by computed tomography [
35]. In many studies, a significant relationship has also been observed between the number of B lines and the declared degree of dyspnea according to NYHA classification in both HD and PD patients [
18,
36,
37,
38]. Much evidence possibly confirms lung congestion on LUS in asymptomatic, and even optimally hydrated, patients according to other studies, regardless of the method of dialysis [
36,
37,
38]. The lack of differences in the mean B-line scores in the PD and HD groups in this study is consistent with the results of the clinical assessment.
Impedance cardiography is a noninvasive method for hemodynamically monitoring a patient, allowing estimation of thoracic fluid content, reflecting the amount of both intracellular and extracellular fluid [
39]. This indicator is useful both in differentiating causes of dyspnea [
40,
41,
42] and in optimizing diuretic treatment [
39,
43]. However, the number of studies conducted to date regarding the use of ICG in dialysis patients is limited. In one publication, Wynne et al. observed a reduction in thoracic fluid content during HD. They also found a correlation between thoracic fluid content reduction and ultrafiltration (r = 0.58,
p < 0.001) [
44]. In another study of PD patients, no significant relationship was found in the logistic regression analysis between the assessment of hydration status based on a subjective and physical examination, and BNP and TFC levels [
45]. In our group, no significant differences in TFC were observed between HD and PD patients, which is consistent with the results of other studies. This complementarity suggests the possibility of broader use of ICG in nephrology.
Ultrasound assessment of the IVC allowed evaluation of vascular filling [
46]. In one study performed on patients prior to HD in dry weight or above, IVC assessment was useful for identifying hypovolemia [
47]. The features of reduced intravascular volume, despite seemingly optimal volemia, were demonstrated in 39% of subjects, confirming the individual variability in intravascular and extravascular fluid distribution. In our study, this method also revealed no differences between HD and PD patients. Ultrasound of the IVC has not yet found wider application in assessing the hydration status of patients on PD. Therefore, as in the case of ICG, the results of our study are an important contribution to current knowledge about the potential applications of this method in dialysis patients.
In summary, a comprehensive assessment of hydration status using complementary methods did not show significant differences between HD and PD patients. Our observations regarding BIA results, average NT-proBNP values, and analyzed echocardiographic parameters are consistent with the observations of other authors. In a recently published review of studies on hydration status in PD patients, Alexandrou et al. point to BIA and LUS as potentially complementary methods [
48]. The usefulness of BIA in assessing the hydration status of PD patients was analyzed in studies on groups of patients larger than ours. Though, to the best of knowledge, comparable results from LUS, ICG, and IVC ultrasound in HD and PD patients are unique. Compliance of the LUS, ICG, and IVC ultrasound results with the clinical assessment and BIA increases their clinical value and encourages further research using these methods in renal replacement patients. Whether these methods have independent diagnostic value or increase the discriminatory power of hydration assessment algorithms in select patients is unclear.
Despite the promising conclusions, the present study has several limitations. First, the HD group was larger than the PD group, which could affect the results of the comparisons. On the other hand, the results reported by Papakrivopoulou et al. (BIA, ECHO, and NT-proBNP) for the inverse distribution of the study groups (PD > HD) were consistent with ours [
25]. Doubts may also be raised by comparing the hydration status of HD patients prior to HD (potentially overhydrated) with PD patients, who remain in a relatively constant euvolemic state. Based on this assumption, the lack of differences between the compared groups suggests a relatively greater overhydration of PD patients, as suggested by other researchers [
24]. Therefore, solving the issue of greater overhydration of PD patients compared to HD patients would require supplementing the HD group assessment with post-dialysis measurements. In the end, in our study, groups did not differ in the quantity of overhydrated patients. However, this lack of differences in the results of additional methods could be related to the rather small sample size of PD group and should be interpreted with caution. On the other hand, based on our results, to show a significant difference in BCM-OH between PD and HD groups, with the power of the test of 80%, the estimated sample size should overcome 455 patients. Nevertheless, presented sample size of PD group relates to the one dialysis center (mean 22.5 patients/center) [
16]. Thus, our results, showing no differences between PD and HD patients, appear to be adequate in everyday clinical practice. In conclusion, the use of different methods of assessing hydration status does not differentiate dialysis patients in terms of the dialysis technique used. In the absence of differences in the hydration status of patients on chronic HD and PD in both the clinical assessment and the results of additional methods, it seems reasonable to use common algorithms to objectify the results of clinical assessment of hydration status.