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Incidence and outcome of newly-diagnosed tuberculosis in schizophrenics: a 12-year, nationwide, retrospective longitudinal study
BMC Infectious Diseasesvolume 13, Article number: 351 (2013)
To control tuberculosis (TB), it is critical to identify at risk populations. Schizophrenia is recognized as an important risk factor for TB. However, previous studies have been confounded by comorbidities, and reports of TB infection outcomes are rare. Therefore, the current nation-wide study aimed to compare the adjusted incidence and outcome of TB diseases in schizophrenics and the general population.
Using the National Health Insurance Research Database from 1998 to 2009, this retrospective longitudinal study included 60,409 schizophrenics and general population matched for age, Charlson’s score, and comorbidities. Diagnosis of TB was based on the international classification of disease, ninth revision and use of anti-TB drugs. Unfavorable outcome for TB was defined as death, loss to follow-up, or use of anti-TB treatment for more than 9 months.
The adjusted incidence of TB in schizophrenics was significantly higher than in the general population [hazard ratio, 1.52; 95% confidence interval (CI), 1.29-1.79; p < 0.001; Kaplan-Meier log-rank test, p < 0.001]. Cox regression revealed age and male gender as risk factors for newly-diagnosed TB. The outcome of TB was comparable in schizophrenics and the general population [odds ratio (OR), 0.78; 95% CI, 0.55-1.09; p =0.144]. Logistic regression revealed a statistical trend for diabetes mellitus to predict poor outcome in schizophrenics with TB (OR, 2.30; 95% CI, 0.96-5.74; p = 0.062).
Schizophrenics are at increased risk for TB, and screening may be warranted for those living in areas with high prevalence of TB.
Tuberculosis (TB) remains the most prevalent infectious disease and the major leading cause of death worldwide, accounting for more than 9 million new cases and 1.4 million deaths . The World Health Organization’s “Global Plan to Stop TB” aims to eradicate this disease by 2050. An important strategy to control TB infection is to identify high-risk groups . In addition to well-known risk factors of TB, such as diabetes mellitus (DM) and human immunodeficiency virus (HIV), many studies have demonstrated an increased incidence of TB in schizophrenics [3–8]. Schizophrenia is a debilitating mental disease affecting 1% of the general population , and it is often accompanied by physical illnesses [4, 5, 10] that may increase susceptibility to TB infection. However, previous studies have not adjusted for these confounding factors. In addition, outcomes for schizophrenics with concomitant TB have rarely been reported, though previous studies [11, 12] reported an increased risk of death due to TB in patients with mental illness. To adjust for confounding factors and determine outcomes in schizophrenics requires studies with larger sample sizes and longer follow-up than those previously conducted. Therefore, we conducted a nation-wide, retrospective longitudinal study that spanned 12 years and included 120,818 people to compare the adjusted incidence and outcome of TB diseases in schizophrenics and the general population.
Taiwan regulations stipulate mandatory registry and treatment of TB via the Directly Observed Treatment Short Course (DOTS) program, which is monitored by the Center for Disease Control (CDC, Taiwan). DOTS workers and public health nurses follow TB cases to monitor compliance and side effects, and they report directly to the local health authority. National Health Insurance (NHI) provides coverage for anti-TB treatment and monitors the cost. After its implementation by the government under the principle of mandatory and universal enrollment in 1995, the NHI program covered 99% of the population of Taiwan. Computerized claims data for inpatient and outpatient care, including demographic data, treatment, and diagnosis by international classification of disease, ninth revision (ICD-9-CM) , were collected and stored in the NHI Research Database (NHIRD), which is run by the National Health Research Institute. We retrospectively retrieved inpatient and outpatient claims data from NHIRD for the period of January 1998 to December 2009 to compare the incidence and outcome of newly-diagnosed TB in schizophrenics and controls.
As the data set used in our study consisted of de-identified secondary data released to the public for research purposes, studies of this kind were exempt from full review by the institutional review board.
We performed a nation-wide study of schizophrenics and matched controls. The schizophrenic cohort comprised all patients who were admitted with schizophrenia (ICD-9-CM code 295.x) from January 1, 1998 to December 31, 2009. Schizophrenia diagnosis was further validated if it was coded by psychiatrists. The date of admission was considered the index date. Patients who were diagnosed with TB (ICD-9-CM codes 010.x to 018.x) before the index date were excluded.
Control subjects were selected from the Longitudinal Health Insurance Database dataset, which contains complete data of 1,000,000 randomly sampled beneficiaries from the original NHIRD. There were no significant differences in age or gender distribution in this sample of 1,000,000 beneficiaries and the original NHIRD. We excluded those patients who were diagnosed with schizophrenia and antecedent TB (ICD-9-CM codes 010.x to 018.x). However, there were significant differences in age, gender, and comorbid disease between schizophrenics and controls. Thus, we further refined our control cohort criteria by randomly selecting subjects to match schizophrenic patients on age (±2 years), gender, index date, Charlson’s score , chronic pulmonary disease, diabetes, and rheumatoid disease. To determine the incidence of TB, subjects were tracked from the index date until December 31, 2009, death, or diagnosis of TB. The diagnosis of new TB required the presence of ICD-9-CM code 010.x-018.x plus prescription of at least two anti-TB drugs (e.g., isoniazid, ethambutol, rifampin, pyrazinamide) for two months. Unfavorable outcomes included death, loss to follow-up, and prolonged treatment, which was defined as presence of ICD-9-CM code of TB for more than 9 months. Other comorbid diseases were retrieved by ICD-9-CM codes from the NHI database inpatient and outpatient datasets .
Pearson chi-square tests were used for categorical variables, while independent t-tests and Mann–Whitney U tests were used for parametric and nonparametric continuous variables, respectively. The incidence of TB diseases was compared by Poisson distribution method, and the cumulative incidence of TB diseases was compared by the Kaplan-Meier method (log-rank test). Risk factors with p values of < 0.1 in univariate analysis were entered into the multivariate analysis. Multivariate Cox proportional hazard regression was performed using backward elimination to analyze independent risk factors for TB diseases. A p value of < 0.05 was considered significant.
Baseline characteristics of schizophrenics
A total of 60,409 schizophrenics were included. The median follow-up period was 2,368 days (range, 1,449-3,295 days). Table 1 shows the clinical characteristics of this group. They were predominantly male (33,271, 55.1%), and the majority (93.4%) did not have any severe comorbidities (Charlson’s score < 3). The most prevalent underlying diseases were peptic ulcer diseases (11,549, 19.1%), chronic pulmonary diseases (10,096, 16.7%), and liver disease (7,796, 12.9%). A total of 60,409 controls were matched for gender, Charlson’s score, chronic pulmonary disease, DM, and rheumatoid disease (All p > 0.99).
Higher incidence and risk factors of newly diagnosed TB cases in schizophrenics
There were 366 new TB cases among schizophrenics and 241 among controls during the total follow-up period of 771,657 person-years, as shown in Table 2. The crude hazard ratio (HR) of TB diseases in schizophrenics was 1.48 [95% confidence interval (CI), 1.26-1.74; p < 0.001]. After adjusting for all variables in Table 1, the HR of TB in schizophrenics was 1.52 (95% CI, 1.29-1.79; p < 0.001) compared with general population. As shown in Figure 1, Kaplan-Meier analysis also revealed a higher rate of newly-diagnosed TB in schizophrenics (log-rank test, p < 0.001). Most of the diseases were pulmonary in origin, occurring in 321 (87.7%) schizophrenics and 206 (85.5%) controls, as shown in Table 3 (p = 0.50). Compared with schizophrenics without TB (Table 4), those with TB tended to have advanced age, male gender, higher Charlson’s score, DM, myocardial infarction, and hypertension. Cox regression showed independent risks for newly-diagnosed TB to be age and male gender, while patients with hypertension were less likely to have new TB diseases.
Comparable outcome of newly-diagnosed TB cases in schizophrenics and controls
Unfavorable outcomes occurred in 138 (37.7%) of 366 schizophrenics and in 105 (43.6%) of 241 controls with new TB diseases [crude odds ratio (OR), 0.78; 95% CI, 0.56-1.09; p =0.149]. During anti-TB therapy, 26 (7.1%) schizophrenics were lost to follow-up, 4 (1.1%) died, and 108 (29.5%) underwent treatment for more than 9 months. In the control group, 19 (7.9%) were lost to follow-up, one died (0.4%), and 85 (35.3%) underwent treatment for more than 9 months (All p > 0.05). After adjusting for comorbidities, schizophrenics and controls with new TB diseases had comparable outcomes (OR, 0.78; 95% CI, 0.55-1.09; p = 0.144). Multivariate analysis revealed a statistical trend for DM to predict poor outcome in schizophrenics (OR, 2.30; 95% CI, 0.96-5.74; p = 0.062, Additional file 1: Table S1).
Our nationwide study included a total of 60,409 schizophrenics and controls with a median follow-up duration of 6 years. After adjusting for underlying diseases, schizophrenics had a higher incidence of newly-diagnosed TB, but comparable outcomes to the general population. Independent risk factors for TB in schizophrenics were age and male gender. A statistical trend was found for DM as an independent risk factor for unfavorable prognosis in schizophrenics with TB.
The increased prevalence of TB in schizophrenics [3–8] may be related to different incidences of physical comorbidities , which could influence the likelihood of TB diseases. The relative risk of DM and colon cancer in schizophrenics has been reported as 1.5-2.0  and 2.9 , respectively, compared with the general population, while infection rate of HIV in mentally ill patients was 4-23% compared with 0.3% for the general population in an area with high prevalence . To our knowledge, this study has the largest number of schizophrenic subjects and is the first matched retrospective longitudinal study of its kind, which enabled adjusting for comorbidities. After adjustment, the incidence of newly-diagnosed TB was 1.5 times higher in schizophrenics compared to the general population, lower than previously reported [3–8]. The reason for the higher risk of TB in schizophrenics is unknown. Development of TB has been associated with several biological and social factors [1, 17]. By adjusting biological factors, our study may indicate behavior and socioeconomic factors play an important role [17, 18]. First, overcrowding and close contact is an established risk factor for TB . Josoph et al. recently reported an outbreak within an assisted living facility for adults with mental illness , concluding that elevated risk for TB disease among this population was due to sustained transmission in crowded settings. Second, mentally ill patients have higher levels of substance abuse, such as smoking or alcohol use , which has been associated with active TB diseases . Third, the low socioeconomic status of this vulnerable population [22, 23] may predispose them to TB diseases . Fourth, poor communication skills in this group may prevent or delay diagnosis and management of physical diseases . Unfortunately, the anonymous and hospital-based nature of the NHI database precluded collection of data related to socioeconomic status and whether subjects lived in community-based facilities. Further studies are needed to evaluate the influence of these behavioral and socioeconomic factors on incidence of newly-diagnosed TB cases in schizophrenics.
The relative risk of death due to TB in patients with mental illness has been decreasing from 7.0 in the 1930s to 5.5 in the 1970s [11, 12]. This has been attributed to improvements in treatment . In our study, the rates of unfavorable outcomes for TB (mortality, loss to follow-up, and prolonged treatment) were comparable between schizophrenics and the general population after adjusting for comorbidities. This may be explained by coverage of 99% of the population by Taiwan NHI, as well as policies by the Taiwan CDC for enhancing diagnosis, follow-up, and treatment [26, 27].
In conclusion, schizophrenics had a higher incidence of newly-diagnosed TB than the general population. Fortunately, with advances in treatment and support from the national health care system, outcomes from TB were comparable in schizophrenics and the general population.
As the data set used in our study consisted of de-identified secondary data released to the public for research purposes, the study was exempt from full review by the institutional review board.
Center for disease control
Directly observed treatment short course
Human immunodeficiency virus
International classification of disease, ninth revision
National health insurance
NHI Research database
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The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/13/351/prepub
The authors would like to thank the National Health Research Institute making their database available. This work was supported by grants from the National Health Research Institute (IV-101-PP-12), Taipei Veterans General Hospital (V101E4-003 and V101A-017), and the National Science Council (98-2314-B-010-010-MY3).
The authors declare that they have no competing interests.
SCK, SYL, YTL, and ACY managed the literature searches, designed the study, and completed the draft of the manuscript. YTC, CJL, and TJC collected the data, organized the database, undertook data analysis, and interpreted the data. TLC, IJS, and CPF monitored this program and contributed to manuscript revisions and approved the final version. All authors contributed to and have approved the final manuscript.
Shu-Chen Kuo, Yung-Tai Chen contributed equally to this work.
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