10.17843/rpmesp.2020.373.4744
BRIEF REPORT

Peritonitis in peritoneal dialysis patients from a hospital in Lima, Peru

Vanessa Pineda-Borja , Medical Doctor
Carolina Andrade-Santiváñez , Medical Doctor
Gustavo Arce-Gomez , Medical Doctor
Cristian León Rabanal , Nephrologist

ABSTRACT

In order to determine the rate and factors related to peritonitis in peritoneal dialysis (PD) patients treated at a hospital in Lima, Peru; a retrospective single-cohort study was conducted during the period 2014-2016. All patients diagnosed with chronic renal disease from the PD program at the Cayetano Heredia Hospital were included. The incidence rate of peritonitis was estimated and a bivariate analysis was performed to assess related factors. A total of 73 patients were included. The incidence rate of peritonitis was 0.60 episodes per patient per year; 46.7% of the cultures were positive and the most common isolated germ was S. aureus. Lower albumin and hematocrit values were found to be related to peritonitis. In this study, the incidence rate of peritonitis and negative cultures were found to be higher than the internationally estimated rate.

Keywords: Peritonitis, Peritoneal Dialysis, Risk Factors (Source: MeSH NLM).

INTRODUCTION

In Peru, the frequency of patients on renal replacement therapy (RRT) is 415 patients per million population, 88% of whom are on chronic hemodialysis (CHD), and 12% on peritoneal dialysis (PD) ⁽¹⁾. PD is a type of RRT as effective as CHD in terms of survival and, it shows a better health-related quality of life during the initial period of the illness compared to CHD, even adjusted for clinical and socioeconomic variables ⁽²⁾.

The first cause of PD failure is peritonitis; this complication causes the removal of the peritoneal catheter and the transition to CDH ⁽³⁾. The possible factors related to the development of peritonitis in PD patients reported include obesity, hypo-albuminemia, depression, greater geographical distance between the patient’s residence and dialysis unit, dialysis technique (lack of training, limited biosecurity), invasive interventions (colonoscopies, hysteroscopies), peritoneal catheter exit-site infections, nasopharyngeal colonization of S. aureus, etc. ⁽³⁾

In terms of the survival rate and health status, automated PD has not been shown to be superior to continuous ambulatory PD ^(4,5); however, in terms of the relative risk of PD-associated peritonitis, the results are contradictory ^(3,4,6). For a PD program, the frequency of infectious complications, local frequencies of peritonitis, microbiological profile, and resistance pattern need to be determined to guide clinical practice regarding treatment and prognosis ⁽⁷⁾. Currently, there is little public information about the procedures or complications in PD programs Peru.

Thus, the aim of this study is to determine the incidence rate of peritonitis and related risk factors in adult patients in a PD program in Lima, Peru between 2014 and 2016.

THE STUDY

This is a single-cohort retrospective longitudinal study. All patients over 18 years of age, diagnosed with chronic kidney disease (CKD) and in the PD program at the Hospital Cayetano Heredia in Lima, Peru, between January 2014 and December 2016 were included. We excluded patients who began treatment at another PD center or who did not have the necessary information, i.e., laboratory values from the last three months. Three patients were excluded for the latter reason.

An episode of peritonitis was considered when patients presented at least two of the following criteria recommended by the International Society for Peritoneal Dialysis (ISPD) ⁽³⁾: a) clinical characteristics related to peritonitis (abdominal pain or cloudy peritoneal effluent); b) leukocytes in peritoneal effluent >100/μL, with >50% polymorphonuclears (PMN); c) positive culture of peritoneal effluent. The peritonitis episode was classified according to the terminology established by ISPD as “recurrent”, “relapsing”, “repeat”, and “isolated” ⁽³⁾.

Demographic, clinical, and laboratory information recorded by the PD program and medical records were collected. Regarding patient variables, data were recorded on age, sex, origin, educational attainment, employment, admissions, etiology of CKD, comorbidity, body mass index (BMI), type of PD, person performing dialysis, time on PD, number of hospitalizations for any reason, months since the last hospitalization, serum albumin value, hematocrit value, and patient destination after the episode of peritonitis.

For the peritonitis episodes, we recorded the time in PD, the cellularity of the peritoneal fluid (leukocytes and polymorphonuclear cells), the culture result, the type of peritonitis, the isolated microorganisms, the antibiotic sensitivity, the antibiotic treatment, the infection of the exit hole of the peritoneal catheter, the serum albumin value and the hematocrit nearest to the moment of diagnosis, BMI and destination. We used the values obtained at the time when the peritonitis diagnosis was made.

Summary and dispersion measures were used according to the distribution of the data obtained and compared between the groups of patients with peritonitis and without peritonitis. The incidence rate of peritonitis per patient per year, the incidence rate per patient per month, and the proportion of positive and negative cultures were determined. The analysis of factors related to peritonitis associated with peritoneal dialysis was evaluated per episode of peritonitis, rather than per participant; therefore, in some cases, patient-specific variable measures are repeated because some episodes occur in the same patient. The groups of patients with peritonitis and without peritonitis were compared by means of a bivariate analysis: chi-square for the qualitative variables, Student’s t test for the quantitative variables with parametric distribution and the Wilcoxon rank-sum test for the quantitative variables with non-parametric distribution.

The study project was previously approved by the Ethics Committee of the Universidad Peruana Cayetano Heredia. The information was analyzed without personal identifiers to preserve patient confidentiality.

FINDINGS

A total of 73 patients were included: their median age was 39.0 years (IQR 22-59), 58.9% of them were women, 67.6% lived in Lima, 38.2% had complete secondary education, and 27.8% had chronic glomerulonephritis as the most frequent etiology for CKD. The most frequent comorbidity was arterial hypertension with 56.0%, the most frequent modality of dialysis was manual (72.2%), performed in most cases (58.6%) by the same patient.

Serum albumin means and standard deviation (SD) in patients who developed peritonitis (3.19 mg/dL; SD 0.74) and in patients who did not develop peritonitis (3.58 mg/dL; SD 0.44) had a significant difference (p = 0.041). Similarly, the mean hematocrit in patients who developed (30.39%; SD 7.02) and those who did not develop peritonitis (34.39%; SD 6.35) had a significant difference (p = 0.032) (Table 1).

Table 1. Characteristics of patients in the dialysis program at the Hospital Cayetano Heredia (2014-2016).

IQR: inter quartile range; SD: standard deviation; MLW: minimum vital wage; PD: peritoneal dialysis.

The average time on dialysis was 52.8 months (SD 32.9). Patients had an average of 1.1 hospitalizations (SD 1.1) (Table 1). At the end of the study period, 63.0% of the patients continued peritoneal dialysis.

A total of 114 episodes of peritonitis was recorded; 50 patients (68.5%) developed at least one episode of peritonitis during the study period. The incidence rate of peritonitis was 0.60 episodes per patient per year and 0.05 episodes per patient per month (1 episode every 20 patient-months). Other characteristics of peritonitis episodes according to patient, infection, and treatment are presented in Table 2. 

Table 2. Characteristics according to peritonitis episodes in patients of the dialysis program of the Hospital Cayetano Heredia (2014-2016).

Culture data were obtained for 107 of the peritonitis episodes, 50 of which (46.7%) were positive cultures. Staphylococcus aureus was reported in 14 (28%) episodes, coagulase-negative Staphylococcus in 12 (24%) cultures and Candida sp. in 8 (16%) cultures. No polymicrobial cultures were reported, the antibiotic resistance in isolated germs are presented in the supplementary material (Annex 1).

DISCUSSION

The obtained incidence rate of peritonitis (0.60 episodes per patient-year) exceeds the ISPD recommendation of less than 0.50 episodes per patient-year ⁽³⁾. This finding is similar to that reported in the same PD program for the pediatric population (0.61 episodes per patient-year) ⁽⁸⁾, and is comparable to the incidence rates of peritonitis in other Latin American countries, which report between 0.35 and 0.80 episodes per patient-year ^(9-12). Considerably low rates have been reported in the United States with 0.37 episodes per patient-year ⁽¹³⁾, and in China with 0.17 episodes per patient-year ⁽¹⁴⁾. This heterogeneity can be explained by the difference between countries in the percentage of RRT patients treated with PD, particularly in Mexico, the United States, and China where government policies favor PD.

In this study, the most frequent etiology for CKD was chronic glomerulonephritis (27.8%), a finding similar to that reported by studies conducted at a single PD center ^(8,10,15), which differs from multiple studies that show that diabetic nephropathy is the main cause of CKD ^(1,2). This could be explained by the small sample size, and the fact that only PD patients were analyzed.

A high rate of episodes with negative culture was found (53.3%), which could be related to the non-standardized method of processing peritoneal fluid samples or to the initiation of antibiotic therapy prior to sampling. This demonstrates the need to establish protocols for collecting and analyzing peritoneal fluid samples throughout the country. The same laboratory evaluated the peritoneal fluid samples, but not necessarily with the same machine, which can introduce measurement bias; however, it is likely that this bias is not different in natural settings.

Staphylococcus aureus was the most frequently isolated germ, which is consistent with a previous study conducted in Peru in 2007 ⁽¹⁶⁾. This microorganism has been associated with episodes of greater severity, increased risk of hospitalization, catheter removal, and even death ⁽¹⁷⁾.

In addition, we found a relationship between lower hematocrit values and the occurrence of peritonitis. In the few studies that have evaluated this variable, no statistically significant relationship has been found with the occurrence of peritonitis ^(18,19).

Despite being a recognized risk factor ⁽³⁾, the variable of previous or concomitant nasopharyngeal colonization was not considered as a variable because not all the patients had such a record.

No relationship was found between the dialysis method and the occurrence of peritonitis. Some studies suggest that the relative risk would be lower in the automated modality ^(4,6); however, most studies report conflicting results.

In this study, no relationship was found between low income or low educational attainment and the occurrence of peritonitis, which differs from what was found in Australia ⁽²⁰⁾, the United States ⁽¹³⁾, and Taiwan ⁽¹⁵⁾. It should be noted that two-thirds of the population observed in this study live in poverty, which may have influenced the outcome.

In the evaluated PD program, training sessions of no more than 2 hours per session are carried out for a period of 15 days, for a total of 30 hours. Likewise, retraining sessions are carried out every 6 months, or when the patient presented an episode of peritonitis. Evaluations are performed, in addition to follow-up visits after the placement of the peritoneal catheter, or for reported complications (peritonitis). Even though the results of the written assessment and home visits are recorded, these instruments have not been validated to assess the efficiency of the training, and therefore were not included in the analysis.

Given the nature of the study, it is possible that there are intervening variables not considered in our analysis or not captured by the program. Another limitation could have been introduced by the exclusion of patients with incomplete analysis records, thus generating a selection bias. The small number of patients who did not develop peritonitis limited the possibility of an analytical design. It is suggested to carry out further studies of the longitudinal analytical type, with a larger population and a longer follow-up time to determine association and temporality between the mentioned factors and the occurrence of peritonitis in the study population.

In conclusion, the incidence rate of peritonitis and the amount of positive cultures found in the peritoneal dialysis program evaluated in a hospital in Lima, Peru, were found to be above internationally suggested limits. Lower hematocrit and lower serum albumin values were found to be related to the occurrence of peritonitis.

REFERENCES

1. Ministerio de Salud, Análisis de la situación de la enfermedad renal crónica en el Perú, 2015. [Internet]. Lima: Dirección General de Epidemiología, MINSA; 2015 [citado el 14 de agosto del 2019]. Disponible en: https://www.dge.gob.pe/portal/index.php?option=com_content&view=article&id=598&Itemid=353 .

2. Jung H, Jeon Y, Park Y, Kim YS, Kang SW, Yang CW, et al. Better Quality of Life of Peritoneal Dialysis compared to Hemodialysis over a Two-year Period after Dialysis Initiation. Sci Rep. 2019;9(1):10266. doi: 10.1038/s41598-019-46744-1.

3. Li PK, Szeto CC, Piraino B, de Arteaga J, Fan S, Figuereido AE, et al. International Society Peritoneal Dialysis peritonitis recommendations: 2016 update on prevention and treatment. Perit Dial Int. 2016;36(5):481-508. doi: 10.3747/pdi.2016.00078.

4. Balasubramanian G, McKitty K, Fan SL. Comparing automated peritoneal dialysis with continuous ambulatory peritoneal dialysis: survival and quality of life differences?. Nephrol Dial Transplant. 2011;26(5):1702-8. doi: 10.1093/ndt/gfq607.

5. Michels WM, Verduijn M, Boeschoten EW, Dekker FW, Krediet RT, NECOSAD Study Group. Similar Survival on Automated Peritoneal Dialysis and Continuous Ambulatory Peritoneal Dialysis in a Large Prospective Cohort. Clin J Am Soc Nephrol. 2009;4(5):943-9. doi: 10.2215/CJN.04440908.

6. Li X, Xu H, Chen N, Ni Z, Chen M, Chen L, et al. The Effect of Automated Versus Continuous Ambulatory Peritoneal Dialysis on Mortality Risk In China. Perit Dial Int. 2018;38(Suppl 2):S25-S35. doi: 10.3747/pdi.2017.00235.

7. Ghali JR, Bannister KM, Brown FG, Rosman JB, Wiggins KJ, Johnson DW, et al. Microbiology and outcomes of peritonitis in Australian peritoneal dialysis patients. Perit Dial Int. 2011;31(6):651-62. doi: 10.3747/pdi.2010.00131.

8. Bernuy J, Cieza J. Tipos de membrana peritoneal y su sobrevida en función al test de equilibrio peritoneal en pacientes en DPCA. Rev Med Hered. 2010;21(1):11-17.

9. Nieto-Ríos JF, Díaz-Betancur JS, Arbeláez-Gómez M, García-García Á, Rodelo-Ceballos J, Reino-Buelvas A, et al. Peritoneal dialysis-related peritonitis: twenty-seven years of experience in a Colombian medical center. Nefrologia. 2014;34(1):88-95. doi: 10.3265/Nefrologia.pre2013.Nov.12002.

10. Figuereido AE, Poli-de-Figuereido CE, Meneghetti F, Pachecho GA, Costa C, Silva LB. Peritonitis in patients on peritoneal dialysis: analysis of a single Brazilian center based on the International Society for Peritoneal Dialysis. J Bras Nefrol 2013;35(3):214-219. doi: 10.5935/0101-2800.20130034.

11. Gadola L, Gomez T, Saez L, Perez D, Orihuela L, et al. Diez años del Registro Uruguayo de Peritonitis en Diálisis peritoneal. Rev Med Urug. 2016; 32(3):166-177.

12. Ramos A, Madonia C, Rascon-Pacheco RA. Improved patient/technique survival and peritonitis rates in patients treated with automated peritoneal dialysis when compared to continuous ambulatory peritoneal dialysis in a Mexican PD center. Kidney Int Suppl. 2008; (108):S76-80. doi: 10.1038/sj.ki.5002606.

13. Kumar VA, Sidell MA, Yang WT, Jones JP. Predictors of peritonitis, hospital days, and technique survival for peritoneal dialysis patients in a managed care setting. Perit Dial Int. 2014;34(2):171-8. doi: 10.3747/pdi.2012.00165.

14. Tian Y, Xie X, Xiang S, Yang X, Zhang X, Shou Z, et al. Risk factors and outcomes of high peritonitis rate in continuous ambulatory peritoneal dialysis patients: A retrospective study. Medicine (Baltimore). 2016;95(49):e5569. doi: 10.1097/MD.0000000000005569.

15. Chern YB, Ho PS, Kuo LC, Chen JB. Lower education level is a major risk factor for peritonitis incidence in chronic peritoneal dialysis patients: a retrospective cohort study with 12-year follow-up. Perit Dial Int. 2013;33(5):55-2. doi: 10.3747/pdi.2012.00065.

16. Pecoits-Filho R, Abensur H, Cueto-Manzano AM, Dominguez J, Divino Filho JC, Fernandez-Cean J, et al. Overview of peritoneal dialysis in Latin America. Perit Dial Int. 2007;27(3):316-21. doi: 10.1177/089686080702700321.

17. Barretti P, Moraes T, Camargo C, Caramori J, Mondelli A, Montelli AC, et al. Peritoneal dialysis-related peritonitis due to Staphylococcus aureus: a single-center experience over 15 years. PloS One. 2012;7(2):e31780. doi: 10.1371/journal.pone.0031780.

18. Fan X, Huang R, Wang J, Ye H, Guo Q, Yi C et al. Risk factors for the first episode of peritonitis in Southern Chinese continuous ambulatory peritoneal dialysis patients. PloS One. 2014 ;9(9):e107485. doi: 10.1371/journal.pone.0107485.

19. Hsieh Y, Chang C, Wen Y, Chiu P, Yang Y. Predictors of peritonitis and the impact of peritonitis on clinical outcomes of continuous ambulatory peritoneal dialysis patients in Taiwan—10 years’ experience in a single center. Perit Dial Int. 2014;34(1):85-94. doi: 10.3747/pdi.2012.00075.

20. Tang W, Grace B, McDonald S, Hawley C, Badve S, Boudville NC, et al. Socio-Economic Status and Peritonitis in Australian Non-Indigenous Peritoneal Dialysis Patients. Perit Dial Int. 2015 ;35(4):450-9. doi: 10.3747/pdi.2013.00004.

Correspondence to: Carolina Andrade Santiváñez, carolina.andrade@upch.pe.

Authors’ contribution: VPB, CAS, GAG and CLR conceived, designed and wrote the manuscript; collected, analyzed and interpreted the results; made the critical review and approved the final version.

Conflicts of interest: The authors deny having any conflict of interest that could affect the objectivity of this work.

Funding sources: Self-funded.

Supplementary material: Available in the electronic version of the RPMESP.

Cite as: Pineda-Borja V, Andrade-Santiváñez C, Arce-Gomez G, León-Rabanal C. Peritonitis in peritoneal dialysis patients from a hospital in Lima, Peru. Rev Peru Med Exp Salud Publica. 2020;37(3):521-6. Doi: https://doi.org/10.17843/rpmesp.2020.373.4744