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Journal of Epidemiology logoLink to Journal of Epidemiology
. 2015 Sep 5;25(9):561–566. doi: 10.2188/jea.JE20140267

Splenectomy Correlates With Increased Risk of Pyogenic Liver Abscess: A Nationwide Cohort Study in Taiwan

Shih-Wei Lai 1,2, Hsueh-Chou Lai 3,4, Cheng-Li Lin 1,5, Kuan-Fu Liao 6,7
PMCID: PMC4549607  PMID: 26256773

Abstract

Objectives

Little is known about the risk of pyogenic liver abscess in patients with splenectomy. We explored the relationship between splenectomy and pyogenic liver abscess in Taiwan.

Methods

We conducted a nationwide cohort analysis using the hospitalization dataset of the Taiwan National Health Insurance Program. We included 17 779 subjects aged 20–84 years who underwent splenectomy in 1998 to 2010 (splenectomy group) and 70 855 randomly selected subjects without splenectomy (non-splenectomy group). Both groups were matched by sex, age, other comorbidities, and hospitalization year of receiving splenectomy. The incidence of pyogenic liver abscess at the end of 2011 was measured. The multivariable Cox proportional hazard regression model was used to estimate the hazard ratios and 95% confidence intervals for pyogenic liver abscess associated with splenectomy and other comorbidities.

Results

The overall incidence rate was 3.75-fold higher in the splenectomy group than that in the non-splenectomy group (2.15 vs 0.57 per 1000 person-years; 95% confidence interval, 3.57–3.94). After controlling for potential confounding factors, the adjusted hazard ratio of pyogenic liver abscess was 3.89 in subjects with splenectomy (95% confidence interval, 3.20–4.72) when compared with subjects without splenectomy. In further analysis, the hazard ratio markedly increased to 14.34 for those with splenectomy and having any of the assessed comorbidities, including alcoholism, biliary stone, chronic kidney disease, chronic liver diseases, and diabetes mellitus (95% confidence interval, 10.61–19.39).

Conclusions

Patients with splenectomy are at an increased risk of developing pyogenic liver abscess, particularly when they have comorbid conditions.

Key words: alcoholism, diabetes mellitus, pyogenic liver abscess, splenectomy

INTRODUCTION

The human spleen mainly serves an immune function against invading microorganisms.1,2 Patients with splenectomy are more likely than those without splenectomy to suffer severe life-threatening infections, which are recognized as overwhelming postsplenectomy infections with substantial morbidity and mortality.3,4 Recently, there is growing evidence that patients with splenectomy are at increased risk of pulmonary tuberculosis and type II diabetes mellitus,5,6 but risk of pyogenic liver abscess has not yet been examined.

Pyogenic liver abscess is an infective disease of the liver, which can be caused by numerous microorganisms. The overall mortality rate of pyogenic liver abscess ranges from 10% to 25%, depending on the population studied.7,8 An increasing amount of literature reveals that numerous risk factors, such as biliary tract disease, cirrhosis, diabetes mellitus, male sex, cancer, and renal disease, are associated with pyogenic liver abscess,812 but splenectomy has not yet been evaluated.

We rationally hypothesize an association between splenectomy and pyogenic liver abscess due to the immunocompromised condition caused by splenectomy, which can further increase the risk of microorganism invasion of the liver. However, published literature from epidemiological studies on this issue is scarce. Given that splenectomy is associated with overwhelming postsplenectomy infections and pyogenic liver abscess carries a potential fatality, exploring the risk of pyogenic liver abscess in patients with splenectomy may have significant clinical and public health implications. Therefore, to explore whether there is an association between splenectomy and pyogenic liver abscess, we conducted a nationwide cohort study using the hospitalization dataset of the Taiwan National Health Insurance Program.

METHODS

Data source

We conducted a nationwide cohort study using the National Health Insurance Research Database (NHIRD) released by the Taiwan National Health Research Institutes. In March 1995, the National Health Insurance Program was initiated in Taiwan to provide comprehensive medical care to the public. According to the annual statistic report of the National Health Insurance Program, the coverage rate was nearly 99% of the entire 23 million people living in Taiwan.13 A committee at the Bureau of National Health Insurance was responsible for randomly selecting claims and checking the accuracy of claims. The NHIRD encrypts patients’ personal information to protect privacy and provides researchers with anonymous identification numbers associated with relevant claim information, including patient’s sex, date of birth, medical services utilized, and prescriptions. We identified the investigated diseases based on the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes. This study was approved by the Institutional Review Board at China Medical University and Hospital in Taiwan (CMU-REC-101-012).

Sampled participants

Using the inpatient claim dataset of the NHIRD, all hospitalized subjects aged 20–84 who received splenectomy (ICD-9-CM procedure code 41.5) between January 1, 1998, and December 31, 2010, were identified as the splenectomy group. The date for receiving splenectomy was defined as the index date. For each subject with splenectomy, four subjects without splenectomy were randomly selected from the NHIRD as the non-splenectomy group. Both groups were matched by sex, age (every 5-year span), other comorbidities, and the hospitalization year of receiving splenectomy. Subjects with history of pyogenic liver abscess, amebic liver abscess, or liver transplantation before the index date were excluded from this study (Figure).

Figure. Flow chart depicting the selection process for study participants.

Figure.

Outcome and comorbidities

The main outcome was a new diagnosis of pyogenic liver abscess based on hospital discharge registries during the follow-up period. Each subject was monitored from the index date until being diagnosed with pyogenic liver abscess; being censored because of loss to follow-up, death, or withdrawal from insurance; or the end of December 31, 2011.

We selected the following comorbidities potentially associated with pyogenic liver abscess: alcoholism, biliary stone, chronic kidney disease, diabetes mellitus, and chronic liver diseases, which included cirrhosis, alcoholic liver damage, hepatitis B, hepatitis C, and other chronic hepatitis. All comorbidities were assessed using ICD-9-CM codes (eTable 1).

Statistical analysis

Differences in sex, age, and baseline comorbidities between the splenectomy and the non-splenectomy group were compared using the Chi-square test for categorical variables and the t test for continuous variables. Follow-up time (in person-years) was used to estimate the incidence rate and incidence rate ratio (IRR) with 95% confidence interval (CI) of splenectomy group to non-splenectomy group using Poisson regression, by sex, age, and follow-up period. The multivariable Cox proportional hazards regression model was used to estimate the hazard ratio (HR) with 95% CI of pyogenic liver abscess associated with splenectomy and other comorbidities after simultaneously controlling for variables found to be significant in the univariable Cox proportional hazard regression model. To address the concern of constant proportionality, we examined the proportional hazard model assumption using a test of scaled Schoenfeld residuals. In the model evaluating pyogenic liver abscess risk throughout the overall follow-up period, results of the test revealed a significant relationship between Schoenfeld residuals for splenectomy and follow-up time, suggesting the proportionality assumption was violated (P < 0.001). In the subsequent analyses, we stratified the follow-up duration to deal with the violation of proportional hazard assumption. All statistical analyses were performed using SAS 9.3 (SAS Institute, Cary, NC, USA). Two-tailed P < 0.05 was considered statistically significant.

RESULTS

Baseline information of the study population

Table 1 reveals the baseline information of the study population. There were 17 779 subjects with splenectomy and 70 855 subjects without splenectomy during the study period, with similar distribution in sex and age. Male subjects accounted for 62.4% of the study population. The mean (standard deviation [SD]) age of the splenectomy group was 53.6 (17.7) years, and that of the non-splenectomy group was 53.3 (17.8) years, with 42.3% of all subjects aged <40 years. The mean (SD) follow-up period was 4.48 (4.05) years in the splenectomy group and 6.46 (3.87) years in the non-splenectomy group. There was no significant difference in the prevalence of comorbidities studied between the splenectomy group and the non-splenectomy group (Chi-square test, P > 0.05 for all).

Table 1. Baseline information between splenectomy group and non-splenectomy group.

Variable Splenectomy
n = 17 779
Non-splenectomy
n = 70 855
P valuea


n (%) n (%)
Sex         0.99
 Male 11 097 (62.4) 44 219 (62.4)  
 Female 6682 (37.6) 26 636 (37.6)  
Age group, years         0.99
 20–39 7512 (42.3) 29 884 (42.2)  
 40–64 4813 (27.1) 19 180 (27.1)  
 65–84 5454 (30.7) 21 791 (30.8)  
Baseline comorbidities before index date
 Alcoholism 541 (3.04) 2058 (2.90) 0.33
 Biliary stone 1120 (6.30) 4347 (6.14) 0.42
 Chronic kidney disease 351 (1.97) 1310 (1.85) 0.27
 Chronic liver diseases 3732 (21.0) 14 672 (20.7) 0.40
 Diabetes mellitus 1967 (11.1) 7741 (10.9) 0.60

Data are presented as the number of subjects in each group, with percentages given in parentheses.

aChi-square test comparing subjects with and without splenectomy.

Incidence of pyogenic liver abscess stratified by sex, age, and follow-up period

Table 2 reveals the incidence rates of pyogenic liver abscess. At the end of the cohort study, the overall incidence rate was 3.75-fold higher in the splenectomy group than in the non-splenectomy group (2.15 vs 0.57 per 1000 person-years; 95% CI, 3.57–3.94). The incidence rates of pyogenic liver abscess, as stratified by sex, age, and follow-up period, were all higher in the splenectomy group than in the non-splenectomy group. The incidence rates of pyogenic liver abscess increased with age in both groups, with the highest incidence rates in the splenectomy group aged 65–84 years. Stratified analysis by follow-up period revealed that the incidence rate of pyogenic liver abscess decreased with follow-up time in the splenectomy group. The IRR of pyogenic liver abscess was significantly increased in the first year of follow-up (IRR 8.40; 95% CI, 7.97–8.85) and subsequently decreased with increasingly longer follow-up, to 2.40 for 5 years of follow-up. The risk remained for more than 5 years of follow-up. In the analysis on the entire follow-up period, the proportional hazard assumption was not met. These observations consistently suggested a time-varying association between splenectomy and pyogenic liver abscess, particularly within the first year after splenectomy.

Table 2. Incidence density of pyogenic liver abscess stratified by sex, age and follow-up period between splenectomy group and non-splenectomy group.

Variable Splenectomy Non-splenectomy IRR
(95% CI)


n Event Person-years Incidencea n Event Person-years Incidencea
All 17 779 171 79 669 2.15 70 855 262 457 798 0.57 3.75 (3.57–3.94)
Sex                  
 Male 11 097 106 48 677 2.18 44 219 164 284 391 0.58 3.78 (3.55–4.01)
 Female 6682 65 30 993 2.10 26 636 98 173 407 0.57 3.71 (3.43–4.01)
Age group, years                  
 20–39 7512 59 43 809 1.35 29 884 69 211 477 0.33 4.13 (3.83–4.45)
 40–64 4813 59 19 769 2.98 19 180 91 121 908 0.75 4.00 (3.65–4.38)
 65–84 5454 53 16 092 3.29 21 791 102 124 414 0.82 4.02 (3.68–4.38)
Follow-up period                  
 ≤1 year 17 779 82 14 697 5.58 70 855 46 69 252 0.66 8.40 (7.97–8.85)
 2–3 years 13 254 35 22 004 1.59 67 766 70 120 702 0.58 2.74 (2.59–2.90)
 4–5 years 9217 34 27 430 1.24 53 353 86 166 703 0.52 2.40 (2.25–2.57)
 >5 years 4864 20 15 538 1.29 30 696 60 101 141 0.59 2.17 (1.99–2.37)

CI, confidence interval; IRR, incidence rate ratio (splenectomy vs non-splenectomy).

aIncidence: per 1000 person-years.

Hazard ratio of pyogenic liver abscess associated with splenectomy

Table 3 reveals the HR of pyogenic liver abscess associated with splenectomy and other comorbidities. Only those found to be significant in the univariable analysis were further examined in the multivariable analysis. After controlling for age, alcoholism, biliary stone, chronic liver diseases, chronic kidney disease, and diabetes mellitus, the multivariable Cox proportional hazards regression model revealed that the adjusted HR of pyogenic liver abscess was 3.89 (95% CI, 3.20–4.72) for the splenectomy group when compared with the non-splenectomy group. Alcoholism (adjusted HR 1.77; 95% CI, 1.17–2.67), biliary stone (adjusted HR 2.19; 95% CI, 1.69–2.84), chronic kidney disease (adjusted HR 1.93; 95% CI, 1.18–3.15), chronic liver diseases (adjusted HR 2.50; 95% CI, 2.02–3.09) and diabetes mellitus (adjusted HR 1.74; 95% CI, 1.37–2.22) were also associated with pyogenic liver abscess. Every 1-year increase in age was associated with a 1.03-fold increased risk of developing pyogenic liver abscess (95% CI, 1.02–1.03).

Table 3. Adjusted hazard ratio and 95% confidence interval of pyogenic liver abscess associated with splenectomy and other comorbidities.

Variable Crude Adjusteda


HR (95% CI) HR (95% CI)
Age, per year 1.02 (1.02–1.03) 1.03 (1.02–1.03)
Baseline comorbidities before index date, yes vs no
 Splenectomy 3.60 (2.97–4.37) 3.89 (3.20–4.72)
 Alcoholism 2.68 (1.82–3.96) 1.77 (1.17–2.67)
 Biliary stone 3.80 (2.96–4.87) 2.19 (1.69–2.84)
 Chronic kidney disease 3.14 (1.93–5.10) 1.93 (1.18–3.15)
 Chronic liver diseases 3.35 (2.86–4.06) 2.50 (2.02–3.09)
 Diabetes mellitus 3.00 (2.38–3.77) 1.74 (1.37–2.22)

aAdjusted for age, alcoholism, biliary stone, chronic kidney disease, chronic liver diseases and diabetes mellitus.

Interaction effect on risk of pyogenic liver abscess between splenectomy and comorbidities

Table 4 reveals the interaction effect on risk of pyogenic liver abscess between splenectomy and other comorbidities, including alcoholism, biliary stone, chronic kidney disease, chronic liver diseases, and diabetes mellitus. Compared to subjects without splenectomy or comorbidity, the adjusted HR of pyogenic liver abscess was 5.84 (95% CI, 4.37–7.81) for subjects with splenectomy alone but without comorbidity. The HR was 5.01 (95% CI, 3.89–6.47) for subjects with any comorbidity but without splenectomy. The HR markedly increased to 14.34 (95% CI, 10.61–19.39) for those with splenectomy and any comorbidity (P value for interaction <0.001).

Table 4. Interaction effect on pyogenic liver abscess between splenectomy and other comorbidities.

Variable n Event Person-years Incidencea Adjusted HRb
(95% CI)
Splenectomy Comorbidityc          
No No 49 400 93 345 670 0.27 1 (Reference)
No Yes 21 455 169 112 128 1.51 5.01 (3.89–6.47)
Yes No 12 350 91 61 082 1.49 5.84 (4.37–7.81)
Yes Yes 5429 80 18 587 4.30 14.34 (10.61–19.39)

CI, confidence interval; HR, hazard ratio.

aIncidence: per 1000 person-years.

bAdjusted for age.

cPatients with any examined comorbidities, including alcoholism, biliary stone, chronic kidney disease, chronic liver diseases and diabetes mellitus, were classified as the comorbidity group.

The interaction between splenectomy and comorbidities was significant (P value for interaction <0.001).

DISCUSSION

In this nationwide cohort study, we found that the incidence rate of pyogenic liver abscess among patients with splenectomy was slightly higher than that reported in Tsai et al’s study among patients in Taiwan with end-stage renal disease (21.5 vs 18.2 per 10 000 person-years)11 but was significantly higher than that reported in Molle et al’s study among patients in Denmark with cirrhosis (215 vs 23.3 per 100 000 person-years).9 Whether this is due to differences in patient-finding strategy or because patients with splenectomy have a substantially higher risk of developing pyogenic liver abscess needs further research to clarify.

In our study, after controlling for potential confounding factors, we also observed that patients with splenectomy were at increased risk of pyogenic liver abscess (adjusted HR 3.89). The HR seems to be higher than that observed for other comorbidities. The HR was not confounded by other studied comorbidities because there was no significant difference in the prevalence of comorbidities between the splenectomy group and the non-splenectomy group, so the increased risk of pyogenic liver abscess in patients with splenectomy cannot be totally attributable to the effect of comorbidities. In further analysis, even in the absence of any comorbidity, patients with splenectomy still had a higher risk of pyogenic liver abscess than those without splenectomy (adjusted HR 5.84). This indicates splenectomy may have a unique role on risk of pyogenic liver abscess independent of other comorbidities. These findings are compatible with the literature showing that patients with splenectomy are not only more prone than those without splenectomy to suffer severe life-threatening infection due to the immunocompromised condition caused by splenectomy3,4 but are also at an increased risk of developing pyogenic liver abscess.

Extensive evidence has revealed that the human spleen mainly serves a protective role against invading microorganisms on the basis of bactericidal capacity of lymphoid cells and macrophages and the humoral immune response.1417 Upon removal of the spleen, normal immune functions, such as phagocytic activities and the humoral immune response, may be significantly changed. Therefore, impaired immune functions after splenectomy may increase the risk of life-threatening infection and pyogenic liver abscess.

Some important caveats in this present study deserve discussion. First, the underlying causes for splenectomy in this present study were not recorded due to the inherent limitation of this insurance database. For example, hematological malignant diseases may require splenectomy in some patients. Cancer is also associated with pyogenic liver abscess.8,10 In fact, we observed that cancer was the most common diagnosis accompanying splenectomy at the time of discharge in the present study. In further analysis, compared to patients without splenectomy, the adjusted HR of pyogenic liver abscess was 5.42 (95% CI, 4.14–7.10) for patients with splenectomy and with cancer (data not shown in table). Therefore, whether the risk of pyogenic liver abscess can be attributable to splenectomy alone or is confounded by the underlying causes for splenectomy is a critical point meriting further clarification. Second, due to the same limitation, the exact causes of pyogenic liver abscess in the present study were not recorded. According to our data, alcoholism, biliary stone, chronic kidney disease, chronic liver diseases, and diabetes mellitus may be other factors related to pyogenic liver abscess. Third, the adjusted HR of pyogenic liver abscess was 5.84 for patients with splenectomy alone, and the adjusted HR markedly increased to 14.34 for patients with splenectomy and any of the comorbidities, including alcoholism, biliary stone, chronic kidney disease, chronic liver diseases, and diabetes mellitus. Fourth, the highest risk of pyogenic liver abscess was noted within the first year after splenectomy. Although the risk gradually decreased over time, the risk remained for more than 5 years after splenectomy. These findings are compatible with previous studies showing that the majority of severe infections occur within the first 3 years after splenectomy, and, although the risk declines over time, the risk might last for more than 5 years after splenectomy.1820 We think that the impaired immune functions might be more significant within the first year after splenectomy, which more likely precipitates development of pyogenic liver abscess and other severe infections. Therefore, when patients present with typical features of pyogenic liver abscess, including fever, right upper abdominal pain, and body weight loss,12 clinicians should strongly suspect the probability of pyogenic liver abscess among patients within the first year after splenectomy, particularly when they have other comorbidities.

The strength of this study is that we used a hospitalization dataset with a large sample size and great statistical power. The diagnosis codes of included comorbidities have been documented in previous studies.21,22 In addition, the topic is novel and the results are fascinating, and the study design, statistical methods, and limitations are described in detail. The results suggest some clinical importance and contribute to understanding of pyogenic liver abscess. Our results were relatively convincing because the splenectomy group and the non-splenectomy group had similar distributions of studied comorbidities. Therefore, the confounding effects of these comorbidities on risk of pyogenic liver abscess should be minimal.

In conclusion, patients with splenectomy are at an increased risk of developing pyogenic liver abscess compared to those without splenectomy, particularly when splenectomy patients also have other comorbid conditions, including alcoholism, biliary stone, chronic kidney disease, chronic liver diseases, and diabetes mellitus.

ONLINE ONLY MATERIAL

eTable 1. Comorbidities examined in the study.
je-25-561-s001.pdf (26.6KB, pdf)

ACKNOWLEDGEMENT

This study was supported in part by Taiwan Ministry of Health and Welfare Clinical Trial and Research Center of Excellence (MOHW104-TDU-B-212-113002), China Medical University Hospital, Academia Sinica Taiwan Biobank, Stroke Biosignature Project (BM104010092), NRPB Stroke Clinical Trial Consortium (MOST 103-2325-B-039-006), Tseng-Lien Lin Foundation in Taichung in Taiwan, Taiwan Brain Disease Foundation in Taipei in Taiwan, and Katsuzo and Kiyo Aoshima Memorial Funds in Japan. These funding agencies did not influence the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Conflicts of interest: None declared.

Specific author contributions

Shih-Wei Lai substantially contributed to the conception of this article. He planned and conducted this study. He initiated the draft of the article and critically revised the article. Hsueh-Chou Lai planned and conducted this study and critically revised the article. Cheng-Li Lin conducted the data analysis and critically revised the article. Kuan-Fu Liao planned and conducted this study, participated in the data interpretation, and critically revised the article.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

eTable 1. Comorbidities examined in the study.
je-25-561-s001.pdf (26.6KB, pdf)

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