Risks of Acute Cholecystitis, Acute Pancreatitis, and Acute Appendicitis in Patients with Dengue Fever: A Population-Based Cohort Study in Taiwan

Abstract

Introduction

Although cases of acute cholecystitis, acute pancreatitis, and acute appendicitis following dengue virus infections have been documented, very few large-scale studies have investigated the postdengue risk of these acute abdominal conditions.

Methods

This retrospective population-based cohort study included all patients with laboratory-confirmed dengue from 2002 to 2015 in Taiwan and 1:4 nondengue individuals matched by age, sex, area of residence, and symptom onset time. Multivariate Cox proportional hazards regression models were used to investigate the short-term (≤ 30 days), medium-term (31–365 days), and long-term (> 1 year) risks of acute cholecystitis, pancreatitis, and appendicitis after dengue infection, adjusted for age, sex, area of residence, urbanization level, monthly income level, and comorbidities. Bonferroni correction was used for multiple testing; E-values were used to assess the robustness of the results to unmeasured confounding.

Results

This study included 65,694 individuals with dengue and 262,776 individuals without dengue. Patients with dengue had a significantly increased risk of acute cholecystitis (adjusted hazard ratio (aHR) 60.21; 95% CI 29.11–124.54; P < 0.0001, E-value = 119.92) and acute pancreatitis (aHR 17.13; 95% CI 7.66–38.29; P < 0.0001, E-value = 33.75) within the first 30 days postinfection compared to those without dengue, but this increased risk was not present after that. The incidence rates of acute cholecystitis and pancreatitis in the first 30 days were 18.79 and 5.27 per 10,000, respectively. No increased risk of acute appendicitis was observed among patients with acute dengue infection.

Conclusion

This study was the first large epidemiological study to show a significantly increased risk of acute cholecystitis and pancreatitis among patients with dengue during the acute phase of dengue infection, while no such association was observed for acute appendicitis. Early identification of acute cholecystitis and pancreatitis in patients with dengue is crucial for preventing fatal complications.

Supplementary Information

The online version contains supplementary material available at 10.1007/s40121-023-00821-1.

Key Summary Points

Why carry out the study?

This population-based cohort study included 65,694 individuals with laboratory-confirmed dengue and 1:4 matched nondengue individuals to investigate the risks of acute cholecystitis, acute pancreatitis, and acute appendicitis after dengue infection.

What was learned from the study?

Patients with dengue had a significantly increased risk of acute cholecystitis (aHR 60.21; 95% CI 29.11–124.54) and acute pancreatitis (aHR 17.13; 95% CI 7.66–38.29) within the first 30 days postinfection compared to those without dengue.

No increased risk of acute appendicitis was observed among patients with acute dengue infection.

Early identification of acute cholecystitis and pancreatitis in patients with dengue is crucial for preventing fatal complications.

Introduction

For decades, arboviral diseases were thought to have minimal impact on global mortality and disability. However, the unprecedented emergence and resurgence of arboviral diseases over the past five decades, including dengue, Zika virus disease, chikungunya, and yellow fever, have changed perspectives on their influence on global mortality and disability [1]. The emergence of arboviral diseases is likely driven by the triad of the modern world: urbanization, globalization, and increased international mobility [1]. Additionally, increased urbanization facilitates the expansion and persistence of Aedes mosquitoes in endemic regions, leading to intensified endemic transmission of arboviruses [2]. Dengue is one of the most important mosquito-borne diseases in humans and is caused by four distinct but closely related dengue virus (DENV) serotypes. During the past five decades, the incidence of dengue has risen 30-fold [3]. Some 100–400 million DENV infections occur annually in 128 countries, with an estimated population at risk of up to 3.97 billion people [4, 5].

The broad spectrum of manifestations in dengue ranges from subclinical disease, classic dengue fever, to severe dengue, previously known as dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS) [6]. The initial manifestations of dengue include high fever, skin rash, headache, arthralgia, myalgia, nausea, and vomiting. Some symptoms have been identified as warning signs, which are associated with an increased risk of progression to severe dengue. These warning signs include abdominal pain, persistent vomiting, clinical fluid accumulation, mucosal bleeding, lethargy, restlessness, and hepatomegaly. Patients with warning signs require further intensive medical care [6].

Abdominal pain is a common symptom experienced by approximately 11.5–57% of patients with dengue and serves as a well-established warning sign for severe dengue [7–9]. The most frequent causes of abdominal pain in patients with dengue are acute hepatitis and nonspecific pain [10–12]. Acute abdomen, defined as the rapid onset of abdominal pain, fever, and peritoneal signs, is much less common in patients with dengue but has been documented in several case reports and case series involving individuals with dengue [13, 14]. A recent review of 9365 patients with dengue from 22 studies revealed that 1501 (16%) of patients presented with acute abdomen; the most prevalent causes were acute cholecystitis (45.4%), acute pancreatitis (7.7%), and acute appendicitis (2.7%) [13]. However, most patients included in this review were hospitalized in tertiary care hospitals, which may significantly overestimate the incidence of acute abdomen in DENV infection as a result of the selection bias of more severe cases. Another limitation of these previous studies is the lack of comparison groups to thoroughly investigate the association between dengue and acute abdomen.

Therefore, this population-based cohort study aimed to investigate the risk of acute cholecystitis, acute pancreatitis, and acute appendicitis following DENV infections by including all laboratory-confirmed patients with dengue, both inpatients and outpatients, from 2002 to 2015 in Taiwan, and comparing them to matched nondengue individuals. Failure to promptly identify these conditions in patients with dengue may result in life-threatening complications, such as gallbladder rupture and pancreatic necrosis. Understanding the risk of these three conditions among patients with dengue can increase knowledge of potential dengue complications and assist healthcare professionals in early recognition and proper management [12].

Methods

A single-payer national health insurance program was launched in Taiwan in 1995. This nationwide population-based cohort study was conducted using data from the National Health Insurance Research Database (NHIRD) in Taiwan, which comprises health insurance claims data for more than 99% of the over 23 million Taiwanese population as well as foreign nationals who possess a valid residence permit. It has become a valuable resource for health-related studies in recent years [15]. Comprehensive healthcare information for insured people, including demographic data (age, sex, area of residency, and income) and clinical data (medical diagnoses, visit dates, drugs and procedures from outpatient, inpatient, and emergency departments) is available in the NHIRD. The International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) was used in the NHIRD between 2000 and 2015, and the ICD-10-CM was introduced in 2016. To protect privacy, personal identifiers in the database were encrypted. The NHIRD can be linked to multiple national databases, including registries of birth, deaths, cancers, and reportable infectious diseases.

This study was commenced after obtaining approval from the Institutional Review Board of National Cheng Kung University Hospital (B-ER-106-184). This study was performed in accordance with the Helsinki Declaration of 1964 and its later amendments. Because the data were deidentified and analyzed for research purposes, the need for informed consent was waived.

Study Population

All cases of laboratory-confirmed dengue in Taiwan between 2002 and 2015, including hospitalized and outpatient cases, were identified from the Notifiable Disease Dataset of Confirmed Cases (NDDCC), released by the Taiwan Center for Disease Control. The criteria for laboratory confirmation included isolation of DENV, positive real-time reverse transcription polymerase chain reaction, a fourfold rise in the IgG titer in paired acute- and convalescent-phase samples, positive nonstructural protein 1 (NS1) testing, and detection of dengue-specific IgM and IgG antibodies in a single serum sample (before 2009) [16–18]. The date of symptom onset recorded in the NDDCC was set as the index date for each patient with dengue. Patients with missing or invalid data or not enrolled in the NHIRD were excluded. For each case with dengue, four nondengue controls were randomly selected from all beneficiaries of Taiwan’s National Health Insurance Program by matching on age, sex, area of residence, and the calendar year and month of the index date. The matched controls had the same index date as those for their corresponding case with dengue. Those in both the dengue and nondengue groups who had a diagnosis of cholelithiasis (ICD-9-CM code 574.x), other disorders of the gallbladder (ICD-9-CM code 575.x), diseases of the pancreas (ICD-9-CM code 577.x), and appendicitis (ICD-9-CM code 540-542) before the index date were excluded.

Study Outcome and Follow-up

All the study participants’ medical claim data were obtained from the NHIRD; their mortality records were retrieved from the Cause of Death Database. The outcomes of this study included acute cholecystitis, acute pancreatitis, and acute appendicitis, which were defined by one hospital admission with relevant ICD-9-CM codes or ICD-10-CM codes (Supplemental Table 1). We followed all the subjects from the index date to the first date of hospital admission due to the above outcomes, death, or the end of 2018, whichever occurred first.

Covariates

In addition to age and sex, area of residence was also used as a matching variable because dengue epidemics mainly occurred in southern Taiwan, including Tainan, Kaohsiung, and Pingtung, while other places had only sporadic cases. Urbanization level and monthly income level were also considered sociodemographic variables in this study, as previously described [17, 18]. We also considered the following comorbidities as potential confounders: alcohol-related diseases, chronic obstructive pulmonary disease (COPD), dyslipidemia, diabetes mellitus (DM), and hypertension, which were defined by at least three outpatient visits or one hospital admission before the index date with ICD-9-CM codes listed in Supplementary Material Table 1.

Statistical Analysis

We used the standardized mean difference (SMD) to compare the baseline characteristics between the dengue group and the nondengue group, and an SMD > 0.1 was considered a meaningful difference [19]. The incidence rates of acute cholecystitis, acute pancreatitis, and acute appendicitis were calculated as the number of events during the follow-up period divided by the total follow-up time in person-months. We constructed multivariate Cox proportional hazards regression models to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for the abovementioned outcomes in cases with dengue compared to nondengue subjects, controlling for age, sex, area of residence, urbanization level, monthly income level, and comorbidities. Proportional hazard assumptions were examined by using log–log survival plots. Analyses stratified by the follow-up time were also performed to calculate the HRs of three outcomes at different periods (≤ 30 days, 31–365 days, and > 365 days after the index date) to investigate the short-term, medium-term, and long-term risks of acute cholecystitis, acute pancreatitis, and acute appendicitis after DENV infection. To further investigate whether the risk of acute abdomen differed between the most acute stage and the convalescent stage, we further stratified the first 30 days into ≤ 10 days and 11–30 days. To account for multiple comparisons for three different outcomes and analyses stratified by sex, age, and follow-up time, a post hoc Bonferroni correction was performed to derive an adjusted threshold for p values. Sensitivity analyses using subdistribution hazard models proposed by Fine and Gray to account for the competing risk of death were also performed [20]. In addition, we calculated E-values to evaluate how strong the unmeasured confounding would have to be to negate the observed association between DENV infection and three outcomes [21–23].

Results

A total of 65,694 individuals with laboratory-confirmed dengue and 262,776 matched individuals without dengue were included in this study. The flow diagram to identify and select study subjects is depicted in Fig. 1. The mean follow-up period was 4.95 ± 3.55 years for the dengue group and 4.95 ± 3.32 years for the nondengue group. We found that 0.53% of patients with dengue and 0.06% of individuals without dengue died in the first month, while 4.23% of patients with dengue and 4.86% of nondengue individuals died during the whole follow-up period. The baseline demographic and clinical characteristics of the two groups are tabulated in Table 1. Patients with dengue seemed to reside in more urbanized areas than nondengue subjects. Other baseline characteristics were not significantly different between the two groups.

Fig. 1.

Flow diagram of the selection of the study population

Table 1.

Demographic and clinical characteristics in dengue and nondengue groups

	Dengue cohort (n = 65,694)	Nondengue cohort (n = 262,776)	SMD
Sex
Male	33,215 (50.6)	132,860 (50.6)	–
Female	32,479 (49.4)	129,916 (49.4)	–
Age (years)	43.9 (20.3)	43.9 (20.3)	–
0–17	7775 (11.8)	31,100 (11.8)	–
18–35	16,042 (24.4)	61,468 (24.4)	–
36–50	14,416 (21.9)	57,664 (21.9)	–
51–64	16,431 (25.0)	65,724 (25.0)	–
≥ 65	11,030 (16.8)	44,120 (16.8)	–
Area of residence
Tainan	23,011 (35.0)	92,044 (35.0)	–
Kaohsiung	38,979 (59.3)	159,916 (59.3)	–
Pingtung	1645 (2.5)	6580 (2.5)	–
Others	2059 (3.1)	8236 (3.1)	–
Urbanization
1	23,623 (36.0)	61,616 (23.5)	0.284
2	26,380 (40.2)	85,442 (32.5)	0.161
3	13,075 (19.9)	70,804 (26.9)	0.161
4–7	2616 (4.0)	44,914 (17.1)	0.355
Income
Not-employed	12,094 (18.4)	45,502 (17.3)	0.029
Low	26,660 (40.6)	115,695 (44.0)	0.070
High	26,940 (41.0)	101,579 (38.7)	0.048
Comorbidity
Alcohol-related disease	226 (0.3)	1065 (0.4)	0.010
COPD	10,495 (16.0)	36,889 (14.0)	0.055
Diabetes mellitus	7694 (11.7)	28,491 (10.8)	0.028
Dyslipidemia	12,734 (19.3)	43,737 (16.6)	0.073
Hypertension	15,523 (23.6)	57,338 (21.8)	0.044

Data are number (%) or mean (standard deviation), unless otherwise stated

SMD standardized mean difference, COPD chronic obstructive pulmonary disease

The overall incidence rates of acute cholecystitis, acute pancreatitis, and acute appendicitis were 1.44, 0.63, and 0.88 per 10,000 person-months in the dengue group and 1.06, 0.50, and 0.70 per 10,000 person-months in the nondengue group, respectively. Multivariate Cox proportional hazards regression models revealed that patients with dengue had significantly higher risks of developing acute cholecystitis (adjusted HR (aHR) 1.33; 95% CI 1.20–1.46; P < 0.0001, E-value = 1.99), acute pancreatitis (aHR 1.28; 95% CI 1.11–1.48; P = 0.0009, E-value = 1.88), and acute appendicitis (aHR 1.27; 95% CI 1.12–1.43; P = 0.0002, E-value = 1.86) than nondengue subjects, after adjusting for age, sex, area of residence, urbanization level, monthly income level, and comorbidities.

To adjust for the multiple comparison problem, the Bonferroni post hoc method required a significance level of P < 0.0013 (three different outcomes and analyses stratified by sex (two groups), age (five groups), and follow-up time (five groups); total 39 tests in Tables 2 and 3). Analyses stratified by sex and age revealed that the risk of acute cholecystitis among patients with dengue remained significantly higher than that among subjects without dengue for male participants (aHR 1.25; 95% CI 1.17–1.55; P < 0.0001, E-value = 1.81), female participants (aHR 1.30; 95% CI 1.13–1.49; P = 0.0003, E-value = 1.92), and those aged 0–17 years (aHR 9.22; 95% CI 2.95–28.80; P = 0.0001, E-value = 17.93) and ≥ 65 years (aHR 1.42; 95% CI 1.21–1.67; P < 0.0001, E-value = 2.19) (Table 2). Subdistribution hazard models were used in sensitivity analyses to account for competing risks, and the results were similar to those obtained from Cox regression models (Tables 2 and 3).

Table 2.

Comparison of incidence and hazard ratio of acute abdomen between dengue and nondengue cohorts stratified by sex and age

Acute abdomen	Dengue cohort		Nondengue cohort		Adjusted HRb (95% CId)	P valuee	Adjusted SHRc (95% CId)	P valuee
	No. of events	IRa	No. of events	IRa
Acute cholecystitis	564	1.44	1657	1.06	1.33 (1.20–1.46)	< 0.0001*	1.34 (1.21–1.48)	< 0.0001*
Sex
Male	291	1.48	818	1.05	1.25 (1.17–1.55)	< 0.0001*	1.37 (1.19–1.57)	< 0.0001*
Female	273	1.39	839	1.07	1.30 (1.13–1.49)	0.0003*	1.31 (1.14–1.51)	0.0002*
Age (years)
0–17	9	0.20	6	0.03	9.22 (2.95–28.80)	0.0001*	9.23 (3.42–24.91)	< 0.0001*
18–35	45	0.47	175	0.45	1.02 (0.74–1.43)	0.8873	1.03 (0.74–1.43)	0.8879
36–50	101	1.08	296	0.79	1.37 (1.09–1.73)	0.0069	1.38 (1.09–1.74)	0.0073
51–64	188	1.85	584	1.44	1.23 (1.04–1.45)	0.0180	1.24 (1.05–1.48)	0.0128
≥ 65	221	3.91	596	2.64	1.42 (1.21–1.67)	< 0.0001*	1.45 (1.23–1.71)	< 0.0001*
Acute pancreatitis	250	0.63	793	0.50	1.28 (1.11–1.48)	0.0009*	1.30 (1.12–1.50)	0.0005*
Sex
Male	131	0.67	450	0.57	1.18 (0.96–1.44)	0.1087	1.19 (0.98–1.46)	0.0852
Female	119	0.60	343	0.43	1.40 (1.13–1.74)	0.0023	1.42 (1.14–1.76)	0.0016
Age (years)
0–17	3	0.07	7	0.04	1.99 (0.47–8.49)	0.3505	2.00 (0.51–7.78)	0.3200
18–35	26	0.27	91	0.24	1.14 (0.73–1.77)	0.5738	1.14 (0.73–1.78)	0.5751
36–50	50	0.53	190	0.51	1.12 (0.82–1.54)	0.4770	1.13 (0.82–1.54)	0.4537
51–64	83	0.81	244	0.60	1.31 (1.02–1.70)	0.0373	1.34 (1.03–1.73)	0.0280
≥ 65	88	1.54	261	1.15	1.36 (1.05–1.76)	0.0191	1.38 (1.07–1.79)	0.0134
Acute appendicitis	346	0.88	1113	0.70	1.27 (1.12–1.43)	0.0002*	1.27 (1.12–1.44)	0.0002*
Sex
Male	188	0.96	604	0.77	1.30 (1.10–0.1)54	0.0020	1.31 (1.11–1.55)	0.0018
Female	158	0.80	509	0.65	1.23 (1.03–1.48)	0.0250	1.24 (1.03–1.49)	0.0235
Age (years)
0–17	52	1.17	134	0.75	1.63 (1.18–2.27)	0.0035	1.63 (1.18–2.26)	0.0032
18–35	96	1.00	312	0.81	1.25 (0.99–1.58)	0.0607	1.25 (0.99–1.58)	0.0589
36–50	75	0.80	263	0.70	1.15 (0.89–1.50)	0.2820	1.16 (0.89–1.50)	0.2764
51–64	73	0.71	248	0.61	1.14 (0.87–1.48)	0.3496	1.14 (0.88–1.49)	0.3256
≥ 65	50	0.87	156	0.69	1.40 (0.99–1.96)	0.0543	1.42 (1.00–2.00)	0.0480

^aIR = incidence rate per 10,000 person-months

^bHazard ratio adjusted for age, sex, area of residence, urbanization level, monthly income level, and comorbidities

^cSubdistribution hazard ratio adjusted for age, sex, area of residence, urbanization level, monthly income level, and comorbidities

^d95% CIs were not adjusted for multiple comparisons and thus cannot be directly used for hypothesis testing or inference

^ePost hoc adjustment for multiple comparisons by the Bonferroni method required a significance level of P < 0.0013

*Achieved statistical significance after Bonferroni correction for multiple comparisons (P < 0.0013)

Table 3.

Comparison of incidence and hazard ratio of acute abdomen between dengue and nondengue cohorts stratified by follow-up period

Acute abdomen	Dengue cohort		Non-dengue cohort		Adjusted HRb (95% CI)d	P valuee	Adjusted SHRc (95% CI)d	P valuee
	No. of events	IRa	No. of events	IRa
Acute cholecystitis
≤ 30 days	121	18.79	8	0.31	60.21 (29.11–124.54)	< 0.0001*	60.01 (28.24–127.53)	< 0.0001*
≤ 10 days	110	51.13	4	0.46	111.67 (40.80–305.65)	< 0.0001*	111.44 (39.76–312.31)	< 0.0001*
11–30 days	11	2.56	4	0.23	9.25 (2.79–30.65)	0.0003*	9.23 (2.57–33.18)	0.0007*
31–365 days	68	0.95	212	0.74	1.32 (0.99–1.74)	0.0579	1.32 (0.99–1.75)	0.0576
> 365 days	375	1.19	1437	1.14	1.01 (0.90–1.13)	0.9293	1.03 (0.91–1.16)	0.6488
Acute pancreatitis
≤ 30 days	34	5.27	8	0.31	17.13 (7.66–38.29)	< 0.0001*	17.02 (7.95–36.46)	< 0.0001*
≤ 10 days	e	e	e	e	45.65 (10.64–195.93)	< 0.0001*	45.51 (11.77–176.01)	< 0.0001*
11–30 days	e	e	e	e	5.54 (1.66–18.44)	0.0053	5.53 (1.54–19.90)	0.0088
31–365 days	33	0.46	119	0.41	1.15 (0.77–1.71)	0.4986	1.15 (0.78–1.71)	0.4885
> 365 days	183	0.58	666	0.53	1.11 (0.94–1.32)	0.2127	1.14 (0.96–1.35)	0.1374
Acute appendicitis
≤ 30 days	10	1.55	23	0.89	1.65 (0.78–3.49)	0.1952	1.64 (0.76–3.55)	0.2086
≤ 10 days	e	e	e	e	3.74 (1.39–10.09)	0.0091	3.74 (1.29–10.83)	0.0150
11–30 days	e	e	e	e	0.51 (0.11–2.25)	0.3720	0.51 (0.12–2.15)	0.3560
31–365 days	51	0.71	208	0.72	1.01 (0.74–1.38)	0.9591	1.01 (0.74–1.38)	0.9558
> 365 days	285	0.90	882	0.70	1.32 (1.15–1.51)	< 0.0001*	1.33 (1.12–1.52)	< 0.0001*

^aIR = incidence rate per 10,000 person-months

^bHazard ratio adjusted for age, sex, area of residence, urbanization level, monthly income level, and comorbidities

^cSubdistribution hazard ratio adjusted for age, sex, area of residence, urbanization level, monthly income level, and comorbidities

^d95% CIs were not adjusted for multiple comparisons and thus cannot be directly used for hypothesis testing or inference

^eThe cells left blank indicated that the numbers of events in some cells was too small and were therefore not allowed to be exported under the regulations of the Health and Welfare Data Science Center of Taiwan to prevent re-identification

^fPost hoc adjustment for multiple comparisons by the Bonferroni method required a significance level of P < 0.0013

*Achieved statistical significance after Bonferroni correction for multiple comparisons (P < 0.0013)

We further analyzed the time trend for the risks of the three outcomes after DENV infection (Table 3). Patients with dengue had a significantly increased risk of developing acute cholecystitis in the first 30 days after symptom onset (incidence rate 18.79 per 10,000 person-months; aHR 60.21; 95% CI 29.11–124.54; P < 0.0001, E-value = 119.92), but no increased risk was observed after 30 days. A significantly higher risk of developing acute pancreatitis was also observed in the first 30 days (incidence rate 5.27 per 10,000 person-months; aHR 17.13; 95% CI 7.66–38.29; P < 0.0001, E-value = 33.75) but not thereafter. For acute appendicitis, the results showed no increased risk in the first year but an increased risk after 1 year of DENV infection (aHR 1.32; 95% CI 1.15–1.51; P < 0.0001, E-value = 1.97).

To further investigate the differences in acute abdomen risk between the most acute phase and the convalescent phase, we subdivided the initial 30 days into two periods: the first 10 days and the subsequent 11–30 days (Table 3). In accordance with the regulations of the Health and Welfare Data Science Center of Taiwan, the number of events was too small to allow data to be reported in certain instances in order to prevent re-identification; therefore, the case numbers and incidence rates of acute pancreatitis and appendicitis were not shown. The results showed that the risk of acute cholecystitis was highest during the first 10 days after symptom onset in patients with dengue (aHR 111.67; 95% CI 40.80–305.65; P < 0.0001, E-value = 222.84), and the risk dropped but remained significantly higher compared to nondengue subjects between 11 and 30 days after infection (aHR 9.25; 95% CI 2.79–30.65; P = 0.0003, E-value = 17.99). The risk of acute pancreatitis among patients with dengue was also highest during the first 10 days (aHR 45.65; 95% CI 10.64–195.93; P < 0.0001, E-value = 90.8), but the aHR became statistically non-significant in the convalescent stage after considering multiple comparisons (aHR 5.54; 95% CI (1.66–18.44); P = 0.0053).

Discussion

This study demonstrated that patients with dengue had a significantly higher risk of acute cholecystitis and pancreatitis compared to nondengue subjects, specifically in the first month after symptom onset. The aHRs (60.21 and 17.13, respectively) and corresponding E-values (119.92 and 33.75, respectively) were very large, suggesting that the results were robust and unlikely to be caused by unmeasured confounding. The risk of acute cholecystitis and pancreatitis was highest during the most acute stage (first 10 days), which is consistent with existing literature that indicates most case reports of acute cholecystitis and pancreatitis in patients with dengue occur during the first week [24–28]. However, we reported a novel finding that patients with dengue still had an increased risk of acute cholecystitis between 11 and 30 days after symptom onset. This might be because some patients with more severe diseases had a prolonged clinical course and thus still had an increased risk of acute cholecystitis after 10 days.

Despite observing high aHRs for the correlation between dengue and acute cholecystitis and pancreatitis, we found that the incidence rates of acute cholecystitis, acute pancreatitis, and acute appendicitis in the first month of DENV infection were only 18.79, 5.27, and 1.55 per 10,000, respectively. This is consistent with a large multicenter prospective study of 1165 hospitalized patients, which found that 11.5% of patients with dengue fever and 21.9% of patients with DHF had abdominal pain; however, acute cholecystitis, acute pancreatitis, and acute appendicitis were not identified in this study [9]. Therefore, although abdominal pain is prevalent in patients with dengue and is considered an important warning sign of progression to severe dengue [29], cases presenting with acute abdomen are rare. However, the reported risks of acute cholecystitis and acute pancreatitis during acute DENV infection in other literature vary widely, with ranges of 0.15–57.0% and 0.03–15.0%, respectively [13, 30–49]. This wide range of reported risks probably results from different selection criteria in previous studies. For example, although most of the studies included hospitalized patients, some selected only cases with DHF [50], cases with abdominal pain [31], or cases admitted to surgical units [14]. In addition, previous studies did not include nondengue subjects for comparison to investigate the association between dengue and acute abdomen. Our study was a population-based study including all cases of laboratory-confirmed dengue in Taiwan from 2002 to 2015, providing an accurate estimated risk of the three diseases after DENV infection and unraveling the association between DENV infection and three acute abdominal conditions.

Acute acalculous cholecystitis and pancreatitis were previously reported after DENV infection, especially in patients with DHF [24, 25, 27, 51–54]. Detailed mechanisms of acute cholecystitis and pancreatitis remain unknown in the acute phase of DENV infection. One proposed hypothesis is that direct virus invasion triggers a cascade of events, including local inflammation, tissue swelling, and destruction of gall bladder and pancreatic acinar cells, leading to biliary stasis and obstruction of pancreatic fluid outflow [12, 54]. Other possible contributing factors for developing acute cholecystitis include systemic inflammatory responses, endotoxemia, secondary bacterial translocation, spasms of the ampulla of Vater, microangiopathic changes, and ischemia–reperfusion injury [13, 30]. An autoimmune response to pancreatic islet cells triggered by DENV infection may play a role in the development of acute pancreatitis [12]. Gallbladder wall thickening and ascites usually resolve entirely with the recovery of acute dengue. Surgical treatment is generally not recommended in dengue-associated acute cholecystitis in the absence of complications such as gallbladder perforation [13, 54]. Identifying acute cholecystitis and pancreatitis in patients with dengue, particularly in critical cases, can be challenging. However, it is crucial to detect these conditions early in patients with dengue and closely monitor potentially fatal complications, such as gallbladder rupture and pancreatic necrosis, to reduce mortality. Deteriorating biochemical indicators and clinical decline with abdominal guarding and stiffness can aid in diagnosis [13].

Our study investigated the risk of acute abdomen among patients diagnosed with dengue. On the other hand, there have been reports of cases initially presenting with acute abdomen in surgical units but later diagnosed with dengue [14]. In a separate instance, a patient in Germany who had contracted dengue abroad developed acute acalculous cholecystitis, underwent cholecystectomy, and unfortunately died from massive bleeding due to the initial failure to diagnose dengue [55]. Given the strong association between dengue and acute cholecystitis and pancreatitis found in our study, healthcare providers should exercise caution and consider dengue as a potential diagnosis when evaluating patients with acute abdomen during dengue epidemics or when encountering patients with relevant travel histories. Misdiagnosis and unnecessary surgical intervention can lead to poor outcomes, as DENV infection can cause microvascular changes and coagulopathy, making surgical intervention highly risky [14].

Although case reports of acute appendicitis during acute DENV infection have been documented [13, 39, 56, 57], our study found no significant increase in the risk of acute appendicitis in the first month or first year following DENV infection. However, we found a slightly increased risk of acute appendicitis after 1 year of DENV infection (aHR 1.32; P < 0.0001); the results remained statistically significant after adjusting for multiple comparisons, suggesting that the results were unlikely due to type 1 error. It is difficult to explain why patients with dengue had a long-term increased risk of developing appendicitis in our study. Our previous study found a significantly higher risk of leukemia after DENV infection [17]. The appendix contains abundant lymphoid tissue, and recent evidence suggests that it may be an essential part of the immune system [58]. Therefore, it is possible that DENV infection has a long-term effect on the hematolymphoid system through certain currently unknown mechanisms. However, the E-value in our study was only 1.97, suggesting that unmeasured and uncontrolled confounding might explain away this observed association. Acute appendicitis has also been reported after coxsackievirus, measles virus, and cytomegalovirus infection [59–63]. A previous study suggests that viral infections are unlikely to be the immediate cause of appendicitis; however, there may be common etiological determinants, pathogenic mechanisms, or environmental factors that impact the incidence of both viral infections and appendicitis [59].

The strengths of our study included the following. First, this study has a large number of patients diagnosed with dengue in Taiwan, comprising both hospitalized and outpatient patients, which provides better generalizability compared to many studies that only included hospitalized patients. In addition, the outcomes were retrieved from the national health insurance database with a coverage rate of greater than 99%. Therefore, selection bias due to different enrollment criteria or loss to follow-up was unlikely. Second, corrections for multiple testing by the Bonferroni method were performed, reducing the chance of false-positive findings. Third, sensitivity analyses using the Fine and Gray methods to adjust for competing risk of death showed similar results to the original analyses. Finally, we calculated E-values to evaluate the robustness of study findings with respect to potential uncontrolled and unmeasured confounding.

This study also has some limitations. First, the NHIRD did not contain information on some potential confounders, such as family history, body weight, diet, and self-paid hormone use, such as oral contraceptives. Second, although all the patients were laboratory-confirmed, some nondengue subjects might have been misclassified because DENV infection might be subclinical and underreported. Although this misclassification may occur, it is not expected to significantly impact our results because dengue is currently not endemic in Taiwan, with a relatively low overall incidence and seroprevalence [64, 65]. Third, the criteria for laboratory confirmation of dengue before 2009 involved detecting DENV IgM or IgG in a single serum sample, which might have led to some misclassification due to cross-reactivity with other similar flaviviruses. However, since dengue is not endemic in Taiwan and the seroprevalence was low before 2009, the misclassification bias should not pose a significant issue. Fourth, the NHIRD used in this study is a claims database used for insurance reimbursements, which includes records of diagnoses, drugs, and procedures received by all beneficiaries of Taiwan’s National Health Insurance. However, detailed medical records, such as test results and clinical symptoms, are not available. Therefore, we could not classify the severity of dengue on the basis of the 1997 or 2009 World Health Organization (WHO) classification criteria. In addition, for patients with acute cholecystitis, acute pancreatitis, or acute appendicitis, we only know that they had been hospitalized during the specified period with a discharge diagnosis of these three diseases; the exact dates of the occurrence of the diseases were unknown. Finally, further analyses stratified by both follow-up and age groups were not performed because the results of fewer than three persons could not be reported to prevent re-identification under the privacy regulation of the Health and Welfare Data Science Center in Taiwan.

Conclusion

This study revealed that patients with dengue had a significantly increased risk of developing acute cholecystitis and acute pancreatitis during the initial month compared to those without dengue but no increased risk of acute appendicitis. Early detection of acute cholecystitis and pancreatitis in patients with dengue is crucial to prevent fatal complications.

Supplementary Information

Below is the link to the electronic supplementary material.