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Hyponatremia is a surrogate marker of poor outcome in peritoneal dialysis-related peritonitis
- Min-Hua Tseng1, 2,
- Chih-Jen Cheng†4,
- Chih-Chien Sung†2, 4,
- Yu-Ching Chou†3,
- Pauling Chu†4,
- Giien Shuen Chen†4 and
- Shih-Hua Lin2, 4Email author
© Tseng et al.; licensee BioMed Central Ltd. 2014
Received: 10 February 2014
Accepted: 2 July 2014
Published: 10 July 2014
Hyponatremia is known to be a marker of poor prognosis in many clinical conditions. The association between hyponatremia and clinical outcomes in peritoneal dialysis-related peritonitis (PDRP) has not been studied. We evaluated the association between hyponatremia and clinical parameters of patients with PDRP.
We conducted a retrospective analysis of medical records of patients with PDRP admitted to a medical center in the period 2004-2011. Patients with serum Na+ <130 mEq/L and ≥ 130 mEq/L at admission were divided into hyponatremic and normonatremic groups, respectively. The demographic and laboratory characteristics, pathogens of peritonitis, length of hospital stay and mortality rate were analyzed.
Hyponatremia occurred in 27% (27/99) patients with PDRP. Gram-negative bacilli were the major pathogen responsible for 78% (21/27) PDRP in hyponatremic group while gram-positive cocci were found in 75% (41/55) PDRP in normonatremic groups. There was no significant difference in age, duration of dialysis, PD catheter removal rate and technique failure between two groups. Hyponatremic group had significantly higher serum CRP (p <0.001), lower serum albumin (p < 0.001) and phosphate (p < 0.05). Of note, serum Na+ level was positively correlated with serum albumin (p < 0.001), phosphate (p < 0.04) levels, and subjective global assessment (SGA) score (p < 0.001). Moreover, the length of hospital stay was longer and in-hospital mortality rate was higher in hyponatremic group (p < 0.001). Using a multivariable logistic regression, we showed that hyponatremia at admission is an independent predictor of in-hospital mortality (OR 76.89 95% CI 3.39-1741.67, p < 0.05) and long hospital stay (OR 5.37, 95% CI 1.58- 18.19, p < 0.05).
In uremic patients with PDRP, hyponatremia at admission associated with a high frequency of gram negative bacilli infection, low serum albumin and phosphate levels, low SGA score, and poor prognosis with long hospital stay and high mortality rate.
KeywordsHyponatremia Peritoneal dialysis Peritonitis Outcome
Hyponatremia is the most common electrolyte abnormalities in clinical medicine . The estimated prevalence of hospitalized patients with serum sodium (Na+) less than 135 mEq/L was 15% [2, 3]. Based on the underlying mechanisms, hyponatremia could stem from a surplus of electrolyte-free water (EFW) or a deficit of Na+ and/or K+. The former mechanism is rarely caused by large amount of water ingestion but the effect of ADH, which impairs free-water clearance and results in water retention . Inappropriate secretion of anti-diuretic hormone (ADH) related to a variety of underlying diseases or drugs is the most common cause of euvolemic hyponatremia in patients with normal renal function. Patients with acute or chronic kidney failure are more susceptible to hypervolemic hyponatremia due to decreased renal water excretion. It has been constantly reported that hyponatremia has a significant impact on morbidity and mortality in various morbidities and also patients with chronic kidney disease, hemodialysis and peritoneal dialysis (PD) [5–7].
Continuous ambulatory peritoneal dialysis (CAPD) has been used as a popular renal replacement therapy for providing more flexibility of dialysis schedule and preserving residual kidney function. Peritoneal dialysis-related peritonitis (PDRP), the major complication of CAPD, is the leading cause of severe morbidity, technique failure and mortality in PD patients [8, 9]. Although hyponatremia is not uncommon in PD patients with reported incidence up to 14.5% , it is still unknown whether hyponatremia associates with the clinical consequences of PDRP. Here, we investigated the impact of hyponatremia on clinical parameters and outcomes in hospitalized patients with PDRP. Results to be reported indicate that hyponatremia in patients with PDRP positively correlated with the severity of underlying peritonitis, length of hospital stay and in-hospital mortality.
The study protocol was approved by the Ethics Committee on Human Studies at Tri-Service General Hospital, National Defense Medical Center, in Taiwan, R.O.C. All patients provided written informed consent prior to participation. We retrospectively reviewed the medical records of unselected PD patients who admitted to a single medical center (Tri-Service General Hospital) due to PDRP from January 2004 to December 2011. These patients received CAPD with standard glucose solution for more than 3 months and were followed up monthly at CAPD clinic. All patients were on disconnect system and used 1.5 or 2 L bags of Baxter dialysate containing 1.5%, 2.5% or 4.25% glucose, which were exchanged 3-5 times per day. Dialysate sodium concentration is 132 mmol/L. A diagnosis of PDRP was made if the patient had at least two of the following criteria: (A) clinical features of peritonitis such as abdominal pain or cloudy peritoneal dialysis effluent, (B) total leukocyte count ≧ 100 cells/mm3, with more than 50% polymorphonuclear cells in the differential count, (C) positive gram stain or culture of peritoneal dialysis effluent. All patients with PDRP were treated with empiric antibiotics administered by the intraperitoneal route. All patients did not have hemodialysis while they underwent serum Na determination. We excluded patients who had chronic hyponatermia or hyponatremia before the event of PDRP, patients with pseudohyponatremia due to extracellular hyperosmolality secondary to hyperglycemia, hyperlipidemia or the use of icodextrin-based peritoneal dialysis or mannitol, and patients without enough clinical parameters for analysis. In addition, patients with other cormobid diseases, including hypothyroidism, adrenal insufficiency, liver cirrhosis and nephrotic syndrome, which might have impact on serum Na during hospitalization, were also excluded.
The following data were retrieved from the medical records of all eligible subjects: age, gender, primary renal disease, residual renal function, peritoneal membrane characteristics, dialysis adequacy, nutrition status, co-morbidity and medication. The residual renal function was measured using mean urea and creatinine clearance. The membrane transport status was evaluated by standard peritoneal equilibration test (PET) a month after initiation of CAPD and then repeated every 6 month as suggested . Dialysis adequacy evaluated by dialysate volume and averaged glucose concentration and small-solute clearance determined by total Kt/V urea (the sum of peritoneal Kt/V and renal Kt/V) prior to peritonitis were recorded. We collected the laboratory data on admission, including C-reactive protein (CRP), Na+, K+, Cl-, creatinine, urea, total cholesterol, triglyceride, total calcium, inorganic phosphate, albumin, total protein and fasting glucose measured by standard laboratory techniques with automatic analyzer (AU 5000 chemistry analyzer; Olympus, Tokyo, Japan). The nutrition status measured as normalized protein nitrogen appearance and 7-point subjective global assessment (SGA) score was also recorded . Co-morbidities, including congestive heart failure, hypertension, diabetes mellitus, liver cirrhosis, malignancy, systemic lupus erythematosus, were obtained from previous history. Anti-hypertensive agents including calcium channel blocker, α-adrenergic blocker, β-adrenergic blocker, angiotensin-converting enzyme inhibitor, angiotensin-II blocker, thiazide, spironolactone and furosemide were recorded. Microorganisms responsible for each PDRP were collected. Clinical outcomes of PDRP, including length of hospital stay, subsequent peritonitis, removal of PD catheter, failure of peritoneal dialysis and hospital mortality were evaluated.
Definition of hyponatremia
Hyponatremia was defined as serum Na+ concentration <130 mEq/L for 2 consecutive measures on the first two days of admission. The patients were then divided into hyponatremic group with serum Na+ <130 mEq/L and normonatremic group with serum Na+ ≧130 mEq/L. To accurately analyze the association between serum Na+ and serum albumin and phosphate, the effect of hyperglycemia on serum Na+ concentration was adjusted by the formula as previously described .
Spectrum of microorganisms
All microorganisms responsible to PDRP were recorded. To determine the influence of microbial spectrum on clinical outcome, patients with polymicrobial PDRP were excluded.
The clinical events and consequences including hospital mortality, length of hospital stay, removal of PD catheter, peritonitis episodes, and technique failure, were examined. Hospital mortality was defined as any death occurred during the same hospitalization or within one week after discharge. Length of hospital stay in the patients who died during hospitalization was calculated as the period from the date of admission to that of death. Peritonitis episodes were defined as any occurrence of recurrent, relapsed, and repeated peritonitis. Technique failure was defined as any failure of continued peritoneal dialysis after PDRP. To understand if hyponatremia is an independent predictor of outcomes in PDRP patients, we adjusted the effects of multiple confounders of outcome of interest including age, gender, spectrum of microorganisms and comorbidities, which was quantitatively scored by the Deyo modification of Charlson comorbidity index (Deyo-CCI) [14–16].
Data are expressed as mean ± standard deviations for continuous variables, and percentages for categorical variables. Chi-square test was used for categorical variables and Pearson correlation coefficients for linear correlation. All of the covariates were examined in univariate analyses. Logistic regression analysis was performed to estimate the risk of increased length of hospital stay, peritonitis episodes, Technique failure, removal of PD catheter and hospital mortality. All statistical analyses were performed using SPSS for window software version 18.0 (SPSS Inc., Chicago, IL, USA). For all analyses, statistical significance was reached when a two-tailed p-value was less than 0.05.
Clinical characteristics on admission of patients with PDRP
Hyponatremic group (n = 27)
Normonatremic group (n = 72)
49.1 ± 9.9
52.6 ± 11.7
Duration of dialysis (years)
4.0 ± 1.5
3.4 ± 1.8
Primary renal disease
Systemic lupus erythematosus
Polycystic kidney disease
Oral Hypoglycemic agent
Calcium channel blocker
ACEI or ARB+
Number of 4.25% Dialysate (bags/day)
1.2 ± 0.8
1.0 ± 0.7
Duration before antibiotics delivery (day)
1.1 ± 0.5
1.1 ± 0.8
3.6 ± 1.2
3.7 ± 1.5
Subjective global assessment score
4.6 ± 1.2
5.7 ± 0.6
Nutritional status: mean nPNA*
1.1 ± 0.3
1.2 ± 0.4
RRF** (mL/min/1.73 m2)
1.2 ± 1.4
1.5 ± 1.5
Laboratory studies and hyponatremia
Laboratory characteristics on admission of patients with PDRP
Hyponatremic group (n = 27)
Normonatremic group (n = 72)
126.8 ± 2.4*
135 ± 3.4
3.3 ± 0.7
3.7 ± 0.8
91.0 ± 2.6*
98.1 ± 4.2
Total calcium (mg/dl)
9.0 ± 1.0
9.0 ± 0.9
3.9 ± 1.3*
5.3 ± 2.8
C-reactive protein (mg/dl)
10.9 ± 2.9**
4.5 ± 1.6
2.6 ± 0.7**
3.3 ± 0.5
163.9 ± 19.6
164.0 ± 24.0
191.3 ± 34.4
197.8 ± 20.4
Blood urea nitrogen (mg/dl)
64.3 ± 22.7
64.3 ± 21.0
Uric acid (mg/dl)
5.6 ± 1.5
6.1 ± 1.5
109.9 ± 18.5
119.7 ± 32.4
Membrane transport (U/P Cr)
0.7 0 ± 0.1
0.64 ± 0.1
WCC+ (L/week/1.73 m2)
62.6 ± 10.3
68.9 ± 16.7
1.1 ± 0.3
1.2 ± 0.4
1.9 ± 0.4
2.1 ± 0.4
Spectrum of microorganisms and hyponatremia
The relationship between spectrum of microorganisms and clinical outcomes
Length of stay
Removal of PD catheter
8.4 ± 3.2*
11.0 ± 4.0*
9.1 ± 3.6***
P. A.+++ (10)
11.3 ± 4.3***
Clinical outcomes and hyponatremia
Hospital outcomes of hyponatremia and normonatremic PDRP +
Hyponatremic group (n = 27)
Normonatremic group (n = 72)
Length of hospital stay
11.9 ± 4.3*
8.3 ± 2.9
Removal of PD++ catheter
Logistic regression analysis of risk factors of hospital mortality and length of hospital stay
Length of hospital stay+
The current study represented the first to demonstrate the prognostic significance of hyponatremia in uremic patients with PDRP. Hyponatremia exerted a negative influence on length of hospital stay and in-hospital mortality independently, even after the adjustment for age, gender, spectrum of pathogens and co-morbidity. Our results suggested that hyponatremia per se is a surrogate marker of poor clinical outcome in uremic patients with PDRP.
The cutoff value of serum Na+ 130 mEq/L has been popularly used to define hyponatremia in many studies [17–19]. In this study, the incidence of hyponatremia in PDRP patients was approximately 27%, much higher than 2.4% in general hospitalization and 4.1% in patients with community-acquired pneumonia [18, 19]. The reported incidences of hyponatremia in PD population varied greatly from 2.4% to 14.5% [10, 17]. It seems likely that PDRP patients are more susceptible to hyponatremia than general PD patients. People have proposed several mechanisms to explain the development of hyponatremia in PD, including  net water gain due to excessive water intake or low ultrafiltration rate of free-water , negative Na+/K+ balance caused by low Na+/K+ intake or high Na+/K+ removal, and  shift of intracellular water to extracellular space induced by the use of icodextrin or hypercatabolism and malnutrition [17, 20]. It is still unknown why PDRP patients have higher incidence of hyponatremia than other PD patients. Our speculation is that peritonitis may disrupt aquaporin-mediated water removal, reduce Na+ intake due to poor appetite, and, probably most important, lead to a hypercatabolic state, in which intracellular osmoles, such as protein, nucleic acids, phosphates, are degraded and thus move intracellular water into extracellular space. Compatible with this concept, we showed that the Na+ concentration in PDRP was positively correlated with serum albumin and phosphate levels, and SGA, indicating the relationship between serum Na+ and nutritional status in PDRP patients.
By analyzing the microbial spectrum of PDRP, we found that patients with hyponatremia had higher percentage of gram-negative peritonitis than those without hyponatremia. It is known that gram-negative microorganisms enter peritoneum mainly through direct transmural migration from gut . The underlying pathogenesis of this phenomenon is still unclear. It is possible that the hypoalbuminemia and malnutrition (lower nPNA) cause swelling of the intestinal mucosa and loss of intestinal barrier integrity, and thus allow the normal gut flora penetrate into peritoneum . Furthermore, our results demonstrated that gram-negative peritonitis, especially Pseudomonas aeruginosa, had poorer clinical outcome than those with gram-positive peritonitis, compatible with previous findings [23–25]. Gram-negative microorganisms have adapted to many antibiotics, especially the first-line β-lactams antibiotic treatment, and may therefore exaggerate the severity of peritonitis . Similarly, Szeto et al. reviewed the gram-negative PDRP and suggested that Pseudomonas species were the most important cause of serious peritonitis in PD patients . Although higher risk of catheter removal and technique failure were reported in patients with Pseudomonas aeruginosa peritonitis, we did not observe this phenomenon, probably due to small number of Pseudomonas aeruginosa peritonitis in this study. Culture-negative peritonitis accounted for 15.2% of all PD peritonitis in the study, similar to most of the reported series [28–30].
It seems plausible that the trend of gram-negative microorganism infection per se can lead to overall poorer clinical outcomes in PDRP patient with hyponatremia. However, the fact that hyponatremia associates with poor prognosis in various clinical situations implies the potential effect of hyponatremia on clinical course of PDRP. Indeed, we confirmed that hyponatremia at admission was independently associated with hospital length of stay and hospital mortality rate in PDRP patients. The underlying mechanisms of hyponatremia-induced poor clinical outcomes are mostly unknown. Therefore, it is difficult to confirm the direct causal relationship between hyponatremia and outcomes of clinical diseases at present . A recent study performed microarray analysis in cells maintained in low sodium (90-127 mEq/L), and found that genes involved in cell death and survival are mostly altered . These detrimental effects of hyponatremia are independent of osmolality and cause neural toxicity in vitro. In humans, hyponatremia was usually mild and may not generate the similar in vitro effects. Konstam et al had demonstrated that correction of hyponatremia by using vasopressin antagonist in patients with congestive heart failure does not improve prognosis . Furthermore, Kin et al. showed that the effect of hyponatremia on mortality diminished as the severity of end-stage liver disease increased . These studies support the notion that severe underlying disease worsens hyponatremia and clinical outcome and hyponatremia itself may be a surrogate marker for the severity of underlying disease . Several studies have shown the association between hyponatremia and severe inflammation in clinical infectious diseases .
There were some limitations in this study. First, we were unable to evaluate the effect of correction of serum Na+ level on clinical outcome owing to the retrospective fashion of analysis. Second, although there were crude associations between hyponatremia and outcomes, we acknowledged the possibility of existence of residual confounders despite multivariable analysis. Third, this study was limited to relatively small sample size in PDRP patients with hyponatremia.
Hyponatremia on admission is common in uremic patients with PDRP. It is independently associated with poor clinical outcomes including increased length of hospital stay and hospital mortality. The association of hyponatremia and poor prognosis may be a reflection of initial severity of illness. Patients with PDRP who developed hyponatremia at admission may need more aggressive therapy and more intensive monitoring during hospitalization.
Min-Hua Tseng first author.
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