| Literature DB >> 25856435 |
Yung-Ming Chen1, Wen-Yi Li2, Vin-Cent Wu3, Yi-Cheng Wang3, Shang-Jyh Hwang4, Shih-Hwa Lin5, Kwan-Dun Wu3.
Abstract
Discontinuation of acute, unplanned dialysis is always an important therapeutic goal in dialysis-requiring patients with existing chronic kidney disease. Only a limited proportion of patients could be weaned off dialysis and remained dialysis-free. Here we performed a multicenter, observational study to investigate factors associated with successful weaning from acute dialysis, and to explore the potential impact of weaning itself on outcomes of patients with chronic kidney disease following urgent-start dialysis. We recruited 440 chronic kidney disease patients with a baseline estimated glomerular filtration rate <45 ml/min per 1/73 m2, and used propensity score-adjusted Cox regression analysis to measure the effect of weaning from acute dialysis on death during the index hospitalization and death or readmission after discharge. Over 2 years, 64 of 421 (15.2%) patients who survived >1 month died, and 36 (8.6%) were removed from dialysis, with 26 (6.2%) remaining alive and dialysis-free. Logistic regression analysis found that age ≧ 65 years, ischemic acute tubular necrosis, nephrotoxic exposure, urinary obstruction, and higher predialysis estimated glomerular filtration rate and serum hemoglobin were predictors of weaning off dialysis. After adjustment for propensity scores for dialysis weaning, Cox proportional hazards models showed successful weaning from dialysis (adjusted hazard ratio 0.06; 95% confidence interval 0.01 to 0.35), along with a history of hypertension and serum albumin, were independent protectors for early death. Conversely, a history of stroke, peripheral arterial disease and cancer predicted the occurrence of early mortality. In conclusion, this prospective cohort study shows that compared to patients with chronic kidney disease who became end-stage renal disease after acute dialysis, patients who could be weaned off acute dialytic therapy were associated with reduced risk of premature death over a 2-year observation period.Entities:
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Year: 2015 PMID: 25856435 PMCID: PMC4391852 DOI: 10.1371/journal.pone.0123386
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Baseline demographic characteristics and biochemical data in all participants, and between the weaner and non-weaner groups.
| All | Weaners | Non-weaners | |
|---|---|---|---|
| No. of patients | 421 | 36 | 385 |
| Men, no. (%) | 240 (57) | 18 (50) | 222 (58) |
| Mean age at entry (y) | 61.9±16.4 | 70.4±12.6 | 61.1±16.5 |
| ≧65 yr, no. (%) | 192 (46) | 26 (72) | 166 (43) |
| Primary renal disease, no. (%) | |||
| Diabetes mellitus | 185 (44) | 15 (42) | 170 (44) |
| Glomerulonephritis | 93 (22) | 5 (14) | 88 (23) |
| Others | 143 (34) | 16 (44) | 127 (33) |
| Comorbidity at entry, no. (%) | |||
| Diabetes mellitus | 213 (51) | 18 (50) | 195 (51) |
| Hypertension | 342 (81) | 28 (78) | 314 (82) |
| Dyslipidemia | 106 (25) | 14 (39) | 92 (24) |
| CAD | 69 (16) | 12 (33) | 57 (15) |
| CHF | 84 (20) | 11 (31) | 73 (19) |
| VHD | 25 (6) | 1 (3) | 24 (6) |
| Arrhythmia | 5 (1) | 0 (0) | 5 (1) |
| CVA | 39 (9) | 6 (17) | 33 (7) |
| PAOD | 30 (7) | 3 (8) | 27 (7) |
| Cancer | 40 (10) | 6 (17) | 34 (9) |
| Acute-on-chronic precipitating factor, no. (%) | |||
| Ischemic ATN | 23 (6) | 4 (11) | 19 (5) |
| Nephrotoxic | 27 (6) | 5 (14) | 22 (6) |
| Cardiac | 157 (37) | 10 (28) | 147 (38) |
| Inflammatory/infectious | 20 (5) | 2 (6) | 18 (5) |
| Hepatic | 1 (0) | 1 (3) | 0 (0) |
| Obstructive | 12 (3) | 7 (19) | 5 (1) |
| Nil | 181 (43) | 7 (19) | 174 (45) |
| Renal sonography at entry | |||
| Kidney size, cm | 9.5±1.5 | 10.3±1.3 | 9.4±1.5 |
| Baseline CKD stage, n (%) | |||
| Stage 3b | 4 (1) | 2 (5.6) | 2 (0.5) |
| Stage 4 | 34 (8) | 12 (33.3) | 22 (5.7) |
| Stage 5 | 383 (91) | 22 (61.1) | 361 (93.8) |
| Renal function at acute dialysis | |||
| Blood urea nitrogen, mg/dL | 122.4±45.9 | 106.5±55.6 | 123.9±44.7 |
| Creatinine, mg/dL | 11.8±5.4 | 7.4±2.8 | 12.2±5.4 |
| eGFR (CKD-EPI), mL/min/1.73 m2 | 4.6±2.5 | 7.2±3.9 | 4.3±2.2 |
| Laboratory data at acute dialysis | |||
| Albumin, g/dL | 3.4±0.6 | 3.3±0.6 | 3.4±0.6 |
| Hemoglobin, g/dL | 8.6±1.8 | 9.8±2.2 | 8.5±1.7 |
| Potassium, mmol/L | 4.7±1.1 | 5.3±1.7 | 4.7±1.0 |
| Phosphorus, mg/dL | 6.9±2.3 | 6.0±2.1 | 6.9±2.3 |
| Calcium, mg/dL | 8.0±1.3 | 8.5±1.6 | 8.0±1.3 |
Abbreviations. ATN, acute tubular necrosis; CAD, coronary artery disease; CHF, congestive heart failure; CVA, cerebrovascular accident; eGFR, estimated glomerular filtration rate; PAOD, peripheral arterial occlusive disease; VHD, valvular heart disease. Values are expressed as number (percent) or mean ± standard deviation.
*<0.05;
**<0.01 vs. weaners.
+Nil denotes absence of classic acute precipitating factors, and acute dialysis was started due to unexpected occurrences of hyperkalemia, metabolic acidosis, or gastrointestinal symptoms such as nausea/vomiting.
Multivariate logistic regression analysis showing predictors for successful weaning from acute dialysis, constructed to the propensity score.
| Covariate | Estimated coefficient | Standard error | p value | Odds ratio | 95% CI | |
|---|---|---|---|---|---|---|
| Lower | Upper | |||||
| Age category (≧65 vs. <65 yr) | 1.28 | .49 | .010 | 3.59 | 1.37 | 9.44 |
| eGFR (per mL/min/1.73m2) | .20 | .08 | .010 | 1.22 | 1.05 | 1.42 |
| Hemoglobin (per g/dL) | .36 | .12 | .003 | 1.43 | 1.13 | 1.80 |
| Acute-on-chronic precipitating factor (yes vs. no) | ||||||
| Ischemic ATN | 1.71 | .77 | .026 | 5.51 | 1.23 | 24.82 |
| Nephrotoxic | 1.50 | .71 | .034 | 4.46 | 1.12 | 17.78 |
| Obstructive | 3.10 | .92 | .001 | 22.10 | 3.67 | 133.18 |
Abbreviations. ATN, acute tubular necrosis; eGFR, estimated glomerular filtration rate. The multivariate logistic regression model was conditioned on kidney size and other comorbidities including diabetes mellitus, and showed a percentage of concordant pairs = 79.3%, adjusted generalized R2 = 0.276, estimated area under the receiver operating characteristic curve = 0.841, and Hosmer and Lemeshow goodness of fit test p = 0.107>0.05. The predicted probability (propensity score) of dialysis weaning = 1/(1 + exp[-(-10.80+1.28 x (age category) + 1.71 x (ischemic ATN) + 1.50 x (nephrotoxic) + 3.10 x (obstructive) + 0.20 x eGFR + 0.36 x hemoglobin)]), where 1 for age category ≧65 years, 0 for <65 years; 1 for ischemic ATN, 0 for non-ischemic ATN; 1 for nephrotoxic, 0 for non-nephrotoxic; 1 for obstructive, 0 for non-obstructive; eGFR, and hemoglobin = observed values.
Multivariate Cox proportional hazard models of independent predictors of all-cause mortality.
| All-cause mortality | Model 1 | Model 2 | Model 3 | Model 4 |
|---|---|---|---|---|
| Predicted probability | - | - | - | 42.52 (4.77–379.25) p = 0.001 |
| Weaners vs. non-weaners | 0.85 (0.34–2.12) p = 0.732 | - | 0.20 (0.06–0.64) p = 0.007 | 0.06 (0.01–0.35) p = 0.002 |
| Age category (≧65 vs. <65 yr) | - | 3.35 (1.80–6.22) p<0.001 | 3.75 (2.01–7.00) p<0.001 | - |
| Hypertension (yes vs. no) | - | 0.66 (0.35–1.27) p = 0.214 | 0.74 (0.37–1.46) p = 0.383 | 0.47 (0.23–0.98) p = 0.045 |
| CVA (yes vs. no) | - | 1.24 (0.57–2.67) p = 0.585 | 1.44 (0.66–3.12) p = 0.358 | 3.00 (1.34–6.74) p = 0.008 |
| PAOD (yes vs. no) | - | 2.41 (1.11–5.26) p = 0.027 | 2.39 (1.10–5.19) p = 0.028 | 3.88 (1.70–8.83) p = 0.001 |
| Cancer (yes vs. no) | - | 3.37 (1.79–6.31) p<0.001 | 1.68 (1.06–2.67) p = 0.028 | 4.61 (2.19–9.69) p<0.001 |
| eGFR (per mL/min/1.73 m2) | - | 1.10 (1.02–1.19) p = 0.010 | 1.16 (1.07–1.26) p<0.001 | - |
| Albumin (per g/dL) | - | 0.61 (0.38–0.97) p = 0.037 | 0.56 (0.35–0.91) p = 0.018 | 0.55 (0.32–0.94) p = 0.030 |
Values are shown as hazard ratio (95% confidence interval). Abbreviations. CVA, cerebrovascular accident; eGFR, estimated glomerular filtration rate; PAOD, peripheral arterial occlusive disease.
* Adjusted for hemoglobin, and other comorbidities (diabetes mellitus, dyslipidemia, coronary artery disease, and congestive heart failure).
**Adjusted for dyslipidemia, coronary artery disease, and congestive heart failure.
Fig 1Cox proportional plots showing cumulative rates of overall surviva (adjusted hazard ratio 0.06; 95% confidence interval 0.01 to 0.35, p = 0.002) between the weaner and non-weaner groups.
Multivariate Cox proportional hazard models of independent predictors of overall rehospitalization.
| Overall readmission | Model 1 | Model 2 | Model 3 | Model 4 |
|---|---|---|---|---|
| Predicted probability | - | - | - | 1.41 (0.44–4.59) p = 0.563 |
| Weaners vs. non-weaners | 0.79 (0.50–1.27) p = 0.331 | - | 0.57 (0.33–0.96) p = 0.036 | 0.59 (0.31–1.10) p = 0.095 |
| Hypertension (yes vs. no) | - | 0.67 (0.47–0.96) p = 0.027 | 0.67 (0.47–0.96) p = 0.028 | 0.59 (0.40–0.86) p = 0.006 |
| Coronary artery disease (yes vs. no) | - | 1.48 (1.05–2.09) p = 0.024 | 1.53 (1.09–2.16) p = 0.014 | 1.62 (1.11–2.36) p = 0.012 |
Values are shown as hazard ratio (95% confidence interval).
#Adjusted for age category, eGFR, albumin, hemoglobin, and other comorbidities (diabetes mellitus, dyslipidemia, congestive heart failure, cerebrovascular accident, PAOD, and cancer).
##Adjusted for albumin and other comorbidities (dyslipidemia, congestive heart failure, cerebrovascular accident, PAOD, and cancer).
Fig 2Cox proportional plots showing cumulative rates of overall rehospitalization (adjusted hazard ratio 0.59; 95% confidence interval 0.31 to 1.10, p = 0.095) between the weaner and non-weaner groups.