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Multi-Indication Carbamazepine and the Risk of Severe Cutaneous Adverse Drug Reactions in Korean Elderly Patients: A Korean Health Insurance Data-Based Study

  • Ji Young Kim,

    Affiliation Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea

  • Joongyub Lee,

    Affiliation Medical Research Collaborating Center, Seoul National University Hospital, Seoul, Republic of Korea

  • Young-Jin Ko,

    Affiliation Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea

  • Ju-Young Shin,

    Affiliation Korea Institute of Drug Safety and Risk Management, Seoul, Republic of Korea

  • Sun-Young Jung,

    Affiliation Korea Institute of Drug Safety and Risk Management, Seoul, Republic of Korea

  • Nam-Kyong Choi,

    Affiliation Medical Research Collaborating Center, Seoul National University Hospital, Seoul, Republic of Korea

  • Byung-Joo Park

    bjpark@snu.ac.kr

    Affiliations Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea, Korea Institute of Drug Safety and Risk Management, Seoul, Republic of Korea

Multi-Indication Carbamazepine and the Risk of Severe Cutaneous Adverse Drug Reactions in Korean Elderly Patients: A Korean Health Insurance Data-Based Study

  • Ji Young Kim, 
  • Joongyub Lee, 
  • Young-Jin Ko, 
  • Ju-Young Shin, 
  • Sun-Young Jung, 
  • Nam-Kyong Choi, 
  • Byung-Joo Park
PLOS
x

Abstract

Objective

To evaluate the risk of severe cutaneous adverse drug reactions (SCAR) after exposure to multi-indication antiepileptic drugs for in Korean elderly patients.

Methods

We used a nationwide database from the Korean Health Insurance Review and Assessment Service claims constructed for the monitoring of drug utilization among the entire Korean elderly population from January 2005 to June 2006. We identified cases of SCARs among inpatients aged ≥65 years and those newly diagnosed with erythema multiforme according to the International Classification of Diseases, 10th revision code (L51). Each case was matched to four controls for gender, age, and the first hospitalization date as the index date. The use of carbamazepine, gabapentin, lamotrigine, topiramate, phenobarbital, phenytoin, and valproate during a 60-day period before the index date was compared. A conditional logistic regression analysis was performed to calculate the odds ratios (OR) and 95% confidence intervals (CI) of SCARs for antiepileptic drug.

Results

We identified 286 cases of SCAR and 1,144 matched controls. Among the 25 patients who were prescribed antiepileptic drugs within 60 days of the index date. There were 11 cases (3.8%) of severe ocular manifestations, and most elderly patients were first-time or short-term users of antiepileptic drugs. Among the 10 cases of carbamazepine use, only 2 cases were prescribed carbamazepine for seizure. All antiepileptic drugs were associated with an increased SCAR risk (adjusted OR = 3.42, 95% CI: 1.75–6.63). The SCAR risk was highest in patients treated with carbamazepine (adjusted OR = 10.39, 95% CI: 2.64–40.86, for multi-indication; adjusted OR = 6.84, 95% CI: 1.55–30.10, for neuropathic pain).

Conclusion

Carbamazepine use was associated with a nearly 10-fold increase in severe cutaneous drug reactions in Korean elderly patients. This association was consistently high with SCAR patients who received carbamazepine for neuropathic pain.

Introduction

Antiepileptic drugs including carbamazepine, valproate, phenytoin, and phenobarbital consistently increase the risk of severe cutaneous adverse drug reactions (SCARs) such as Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) [1][3]. Nevertheless, the use of antiepileptic drugs has steadily increased in elderly patients. Antiepileptic drugs are prescribed for the treatment of diverse conditions including migraines, mood disorders, neuropathic pain, and epilepsy [4][6]. The use of antiepileptic drugs peaked in those aged 80–84 years in Australia [4] and according to the Norwegian Prescription Database constructed between 2004 and 2007, 24.5% of antiepileptic drugs users were elderly people (aged 60–102 years) [5]. Neuropathic pain such as post-herpes neuralgia, diabetic neuropathy, and central post-stroke pain, as well as post-stroke seizure and epilepsy are the most common reasons for antiepileptic drug use in the elderly [7], [8]. Moreover, the clearance rate of most antiepileptic drugs in the elderly has decreased by approximately 20–40% [9].

Elderly patients are more vulnerable to adverse drug reactions than younger patients, because of multi-morbidity and polypharmacy [10], [11]. These factors are important cause of hospital admissions in the elderly [12], [13]. One study found that inpatients with adverse drug reactions (ADRs) were significantly older (median age, 76 years) than patients without ADRs (median age, 66 years) [13]. Most of the cutaneous ADRs are not life threatening, but they can be a major cause of poor quality of life among the elderly [14]. SJS and TEN have a high mortality rate of 20%–25%, and long-lasting sequelae including corneal ulcerations represent a considerable disease burden [15]. Additionally, the mortality in SJS and TEN patients increased with age [16]. Recently, a 1-year follow-up study of patients with SCARs reported that high in-hospital mortality and after-discharge deaths were associated with older age [17].

There are few recent data on the epidemiology of SCARs in the elderly. Previous studies on SCAR were conducted across all age groups in the West, but did not specifically focus on the elderly. A recent SCAR study using the National Health Insurance database in Taiwan focused on bipolar disorders in middle-aged patients (mean age, 41 years) [18].

To our knowledge, there are no previous large-scale epidemiological studies of antiepileptic drug-related SCARs on the Korean elderly. In 2007, a nationwide database was constructed for monitoring drug utilization among the elderly in Korea. The aim of this study was to evaluate the risk of SCARs after exposure to multi-indication antiepileptic drugs in Korean patients aged ≥65 years. We conducted a case-control study based on the Korean Health Insurance Review and Assessment Service (HIRA) database constructed from January 1, 2005, to June 30, 2006.

Materials and Methods

Data Source

We used the Korean HIRA database of elderly patients aged ≥65 years, which was constructed between January 1, 2005, and June 30, 2006. The database contained information on 4,159,305 elderly patients aged ≥65 years and 100,838,744 prescriptions. The HIRA database contained information on the patients' de-identified number, age, gender, institutional region, diagnosis as per the International Classification of Diseases 10th Revision code (ICD-10 code), prescribed drug names, formulas, doses, prescription duration, and expenses [19]. The Korean National Health Insurance (KNHI) program was initiated in 1977 and achieved universal coverage for the entire Korean population of approximately 50 million individuals by 1989 [20]. The HIRA provided de-identified patient claim data for the purpose of public health research. In the HIRA database, the positive predictive value (PPV) for the diagnosis of inpatients was 81.8% [21].

Ethics Statement

This study was approved by the Institutional Review Board of Seoul National University College of Medicine/Seoul National University Hospital (E-1305-036-487).

Definition of Case and Control Patients

Cases were defined as inpatients aged ≥65 years who newly diagnosed with erythema multiforme (ICD-10 code: L51) between April 1, 2005, and June 30, 2006 [18], [22][24]. The first hospitalization due to erythema multiforme was defined as the index date for the case. To identify incident cases of SCAR, we excluded patients with pre-existing erythema multiforme during the preceding 3 months, from January 1, 2005, to March 31, 2005. Among them, patients diagnosed prior to the index date with epidermolysis bullosa (Q81), Kawasaki's disease (Q81), pemphigus (L10), pemphigoid (L12), psoriasis (L40), staphylococcal scalded skin syndrome (L00), toxic shock syndrome (A48.3), vasculitis (L95), or graft-versus-host disease (T86.0), according to the exclusion criteria of the European Registry of Severe Cutaneous Adverse Reactions (RegiSCAR) study, were also excluded in order to increase the validity of SCAR diagnosis [17], [25]. Potential controls were selected among inpatients with no diagnosis of skin and subcutaneous tissue disease (L00–L99) during the study periods. The exclusion criteria in controls were also based on the same as the criteria used in the cases. The index date of control patients were defined as the date of hospital admission for treatment. For each incident case, four controls were matched by gender, age (±5 years), and index date (±5 days).

Exposure Assessment

Patients who were prescribed at least one antiepileptic drug before the index date were defined as the antiepileptic drugs prescription group. Seven antiepileptic drugs – carbamazepine, gabapentin, lamotrigine, topiramate, phenobarbital, phenytoin, and valproate – were selected as the exposure agents. Patients who were simultaneously prescribed different antiepileptic drugs during the research period were classified into the combination-therapy group, and those who were prescribed only one medication were classified into the mono-therapy group. The exposure period was defined as the prescription of antiepileptic drugs within 60 days before the index date. Previous studies reported that the risk of SCARs increases within 8 weeks following the first use of such drugs [3], [18], [26]. To estimate the time delay between the beginning of antiepileptic drug use and the occurrence of SCARs, the latent period was defined as the duration between the date of the antiepileptic drug prescription and the index date. To evaluate the effect of short- or long-term use, the prescription duration was defined as the total period for which antiepileptic drugs were prescribed before the index date.

Confounding Factors

Information on confounding factors was collected using ICD-10 codes for diagnoses and drug prescriptions in the HIRA database. Cancer (C00-C97), connective tissue/rheumatic diseases (M05, M06, M32-M 34, M31.5, M35.1, M35.3, M36.0), herpes virus infection (B00), Human immunodeficiency virus (HIV) infection (B20–B24), influenza (J11), histoplasmosis (B39), and mycoplasma pneumonia (J15.7), which are non-medication risk factors for SJS or TEN, were included [3], [26]. To adjust for the severity of accompanying diseases, Charlson Comorbidity Index scores were calculated [27]. In addition, bipolar disorder (F31), diseases of the spinal cord (G95), neuropathy (G56–G64, G99), trigeminal neuralgia (G50, G53), seizures (G40, G41, R56), cerebrovascular diseases (G45, G46, I60–I69, H34.0), diabetes mellitus (E10–E14), and renal diseases (N18, N19, N05.2–N05.7, N03.2–N03.7, Z49.0–Z49.2) were included as underlying diseases before the index date. Other concomitant medications such as acetate derivative non-steroidal anti-inflammatory drugs (NSAIDs), allopurinol, aminopenicillins, cephalosporin, imidazole, macrolide, oxicam NSAIDs, quinolones, sulfonamide, and tetracyclines, which are related to the risk of SCARs, were considered as confounding factors [28].

Statistical Analysis

The general characteristics of patients, including age, gender, prescription of antiepileptic drugs, comorbidities, and Charlson Comorbidity Index scores, were analyzed. Categorical variables are presented as numbers and percentages and continuous variables are presented as means and standard deviations (SD). For the continuous variables, we used the Wilcoxon signed-ranks test to compare means. Comorbidities of cases and controls were compared using the McNemar test. For each incident case, four controls were matched by gender, age (±5 years) and index date (±5 days) using the Greedy method. Because controls were matched individually, conditional logistic regression was used to assess the risk of SCARs after use of antiepileptic drugs. If exposure rate of the antiepileptic drug in the controls is assumed to be 2% and the odds ratios (OR), 3.0 based on results of previous studies, then on taking into account the 1∶4 matched case-control study design, the appropriate number of study subjects was calculated to be 284 in the case group, which would yield a 80% statistical power and 5% significance. Univariate and multivariate conditional logistic regression analyses were performed to calculate the ORs and 95% confidence intervals (CI) of SCARs for each antiepileptic drug. For some antiepileptic drugs taken by few or no patients, we used the exact method for estimating ORs. Among comorbidities and co-medications previously established as risk factors, variables with p-values <0.2 in the univariate analysis were selected as potential confounders for the final multivariate model. Subgroup analyses were performed only for SJS (L51.1) or TEN (L51.2) with the four-digit ICD-10 codes to assess the validated patients with SCAR. Latent periods and prescription durations were calculated using both medians (range) and means (SD). All p-values of <0.05 were considered statistically significant, and all tests were two-tailed. All data were analyzed using SAS 9.3 (SAS Institute Inc., Cary, NC, USA).

Results

A flowchart of the inclusion and exclusion criteria is shown in Figure 1. Our study identified 286 cases and 1,144 matched controls. Table 1 shows the demographic characteristics and use of antiepileptic drugs for both groups before the onset of SCARs. There were 286 cases (121 men and 165 women), with a mean age ± SD of 73.6±6.6 years. Sixty-two (21.7%) cases and 105 (9.2%) controls received at least one antiepileptic drug before the index date. The proportion of antiepileptic drug prescriptions in the cases was significantly higher than that in the controls. The mean Charlson Comorbidity Index score was 2.0 ± 1.5 for cases and 1.4±1.3 for controls, and this difference was statistically significant. Underlying diseases such as cerebrovascular diseases, diabetes mellitus, seizures, and renal diseases were frequent among the cases (p<0.001). Similarly, the proportion of patients with connective tissue/rheumatic diseases and herpes virus infection was higher among the cases than the controls. Recent herpes viral infection within 3 months before the index date was reported in only 7 cases and 4 controls. No patients had HIV infection, histoplasmosis, mycoplasma pneumonia, or mumps. There were no statistically significant differences between the two groups in terms of the incidence of other diseases. Eleven (3.8%) cases were diagnosed with severe ocular complications: 2 with corneal ulcer, 2 with corneal ulcers and entropion, 2 with corneal scars and opacities, 2 with entropion, and 3 with visual impairment (table not shown).

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Figure 1. Sampling procedures of cases and controls.

Abbreviations; EM, Erythema multiforme; SCARs, Severe cutaneous adverse drug reactions a Index date: The first SCAR (EM, ICD-10: L51) hospitalization date for the cases. b The sum of the numbers for the three exclusion criteria is greater than the total number because some patients met more than one exclusion criterion.

https://doi.org/10.1371/journal.pone.0083849.g001

Table 2 shows the risk estimates of SCARs associated with antiepileptic drugs, calculated by multiple conditional logistic regression analysis. We excluded the antiepileptic drug combination-therapy group, and the final analysis was based on 269 cases matched with 1,076 controls with prescriptions within 60 days of the index date. All antiepileptic drugs showed an increased risk of SCARs (adjusted OR = 3.42; 95% CI: 1.75–6.63). Among the antiepileptic drugs, carbamazepine was associated with the highest risk of SCARs (adjusted OR = 10.39; 95% CI: 2.64–40.86). For gabapentin, phenobarbital, and valproate, the adjusted ORs were 1.10, 2.10, and 8.89, respectively, but no significant association was observed. The risk estimate was consistent when analysis was restricted to patients without recent herpes viral infection. The adjusted OR was 3.69 (95% CI: 1.89–7.23) for all antiepileptic drugs (table not shown).

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Table 2. Estimates of SCAR risk from antiepileptic drugs within 60 days of index date (N = 1,345).

https://doi.org/10.1371/journal.pone.0083849.t002

Figure 2 shows the distribution of the latent period in the 25 cases exposed to antiepileptic drugs within 60 days before the index date. Nineteen cases (76%) initiated their treatment less than 30 days before the index date. The median duration of latency (range) for all antiepileptic drugs was 16.0 (range, 3–56) days. The mean duration of prescription for all antiepileptic drugs was 19.3±14.0 days (Table 3). All 25 cases were short-term users (less than 60 days of antiepileptic drugs treatment), and 12 cases (48%) were new users with the first prescription of antiepileptic drugs given during the study period (table not shown).

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Table 3. Duration of prescription and latent period before onset of SCARs in 25 cases. a

https://doi.org/10.1371/journal.pone.0083849.t003

A subgroup analysis was conducted for 134 cases with SJS or TEN selected using the four-digit ICD-10 codes. Among the 134 cases, 80.6% (n = 108) were classified as having SJS, 17.2% (n = 23) as having TEN, and 2.2% (n = 3) as having both SJS/TEN. The adjusted OR was 10.22 (95% CI: 1.64–63.60) for carbamazepine. The SCAR risk was consistently high in patients treated with carbamazepine for neuropathic pain (adjusted OR = 6.84, 95% CI: 1.55–30.10) (Table 4). Among the 10 cases of carbamazepine use, 8 patients were women; additionally, only 2 of the 10 cases were prescribed carbamazepine for seizure (Table 5).

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Table 5. Clinical features of 10 cases who prescribed carbamazepine within 60 days of SCARs.

https://doi.org/10.1371/journal.pone.0083849.t005

Discussion

In elderly Korean patients, the use of antiepileptic drugs increased the risk of SCARs about three-fold as compared to patients who had not used antiepileptic drugs, and the use of carbamazepine was associated with the greatest increase in the risk of SCARs (adjusted OR = 10.69, 95% CI: 2.75–41.57). Among individual antiepileptic drugs, gabapentin, phenobarbital, and valproate increased the risk of SCARs, but this increase was not statistically significant.

The increased risk of SCARs associated with the use of antiepileptic drugs in the general population has been a consistent finding in several studies [18], [26], [28], [29]. In 2008, one study using the database from Taiwan National Health Insurance showed that the use of carbamazepine and valproate as mood stabilizers increased the risk of SCARs (carbamazepine: adjusted OR = 3.10, 95% CI: 1.51–6.35; valproate: adjusted OR = 5.17, 95% CI: 1.26–5.92). In Taiwan, Gau et al. investigated patients with bipolar disorder only, and the mean age of the subjects was 41 years [18]. Therefore, we cannot make a direct comparison between the results of the study by Gau et al. and our results which focused on elderly patients. In France, the incidence of TEN was 2.7-fold higher among patients aged above 65 years than in those aged below 65 years. This study was performed 20 years ago with a relatively small sample size of only 77 patients [30]. In the pooled analysis of children aged <15 years, Levi et al. found that the crude OR was 91 (95% CI: 14–∞) for all antiepileptic drugs as a group and 15 (95% CI: 1.8–∞) for carbamazepine. However, Levi at al. reported 24 cases and only one control exposed to antiepileptic drugs (total, 80 cases and 216 controls), and therefore, they did not conduct multivariate analysis after adjusting for confounders [29]. According to the SCAR and EuroSCAR studies conducted in European countries, the multivariate relative risk (mRR) of carbamazepine was 12 (95% CI 3.5–38) [26] and 72 (95% CI: 23–225) [28], respectively.

Herpes infection has previously been reported to increase the risk of SCAR in the general population [31], [32]. Our results show significant differences between cases and controls with recent herpes infection. Therefore, we conducted analysis after exclusion of patients with recent herpes infection and the risk of SCAR consistently increased. However, in children, recent herpes infection had no significant association with SCARs [29].

Our results did not find an association between SCARs and lamotrigine, topiramate, phenobarbital, phenytoin, and valproate in the elderly. Because of the small number of patients by each antiepileptic drug, our study did not have enough statistical power to identify certain SCAR risks. However, in the general population, these antiepileptic drugs have frequently been reported to increase the risk of SJS or TEN [1][3]. Our study did not show a significantly increased SCARs risk with the use of gabapentin. Gabapentin is usually considered a safe medication for patients with a genetic risk factor of carbamazepine-induced SJS [22] and only a few studies have reported an association between SJS or TEN risk and gabapentin use [33][35]. However, in 2011, the US FDA cautioned that potentially serious, multi-organ hypersensitivity, known as drug reaction with eosinophilia and systemic symptoms, has been reported following gabapentin use.

Patients with SJS or TEN frequently had ocular manifestations ranging from conjunctivitis to corneal ulceration [1], which significantly impaired their overall quality of life [36]. Yip et al. reported that 81 (69%) patients with SJS or TEN had ocular complications and 4% had severe ocular involvement during a median follow-up period of 2 months [37]. In our study, only 11 (3.8%) cases diagnosed with severe ocular complications.

Among 25 cases in our study, 13 (52%) patients were prescribed antiepileptic drugs for the first time during the study period. This finding is consistent with previous reports showing an increased risk of antiepileptic drug-induced SCARs, which was mostly observed in short-term or recent-start drug users in the general population [3], [28]. In our study, the mean prescription duration for carbamazepine use was 20.5±14.3 days, which was similar to that for carbamazepine (27.4±14.3 days) in Taiwan [18]. Recently in Korea, Kim et al. reported that the mean treatment duration of carbamazepine was 25.9±15.1 days in 24 carbamazepine-induced SCAR patients [38]. The latent period in our study was defined as the time from the intake of antiepileptic drugs to the first hospitalization due to SCARs, and thus, the mean latent period was 19.1 days for all antiepileptic drug users and 17.3 days for carbamazepine users. The latent period in elderly patients with SCARs was not prolonged as compared to the results of studies in the general population. In the EuroSCAR study, the distribution of the latent period for carbamazepine was similar, ranging from 4 days to 28 days [28]. Yang et al. reported that among 154 SCARs patients, the latent period was 12.32±5.07 days for carbamazepine users and ≤27 days for antiepileptic drug users (lamotrigine, oxcarbazepine, phenobarbital, and phenytoin) [1]. In a recent study based on the EuroSCAR and RegiSCAR databases, Lee et al. showed that prior exposure to corticosteroids prolonged the period of latency before the onset of SJS and TEN [19]. In our analysis, there were only two cases of antecedent corticosteroid users (gabapentin exposure) as per the criteria of Lee et al., and therefore, the result of the latent period was minimally affected. In reality, a mean lag time of 3–3.9 days exists between the date of skin lesion occurrence and the date of hospitalization in children [29]. Therefore, it is reasonable to assume that skin reactions occur 3–4 days before the latent period, and this period can be important for prognosis improvement.

In the present study, a patient admitted to hospital and diagnosed with SJS or TEN with the four-digit ICD-10 codes was considered more valid and severe case, because recording of diagnosis with the four-digit ICD-10 code was not compulsory in Korean clinics during the study period. We applied subgroup analysis for 134 cases with SJS or TEN selected using the four-digit ICD-10 codes, and the results were as follows: for carbamazepine, adjusted OR = 10.22 (95% CI: 1.64–63.60). This result was similar to the result of the initial analysis. Among the 10 cases of carbamazepine use, only 2 patients were prescribed carbamazepine for seizure. Treating pain of neurologic origin was the most common indication of carbamazepine in our study. In Taiwan, peripheral neuropathy was the most frequent underlying disease in antiepileptic drugs-induced SCAR patients [1]. When sensitivity analysis was conducted after selecting cases of carbamazepine use for neuropathic pain, the adjusted OR was 6.84 (95% CI 1.55–30.10). As therapeutic indications have extended, antiepileptic drugs have been used more frequently in pain management [39]. In addition to its use in epilepsy, carbamazepine is also effective in many patients with chronic neuropathic pain [40]. However, carbamazepine is the most common causative agent for SJS or TEN in Southeast Asia, accounting for 26% of cases in Taiwan and 35.7% in Malaysia [41]. Our finding showed that patients who received carbamazepine for pain were consistently associated with risk of SCAR. Physicians should consider medications other than carbamazepine, especially when initiating therapy for pain in elderly patients.

The present study has several limitations. First, lifestyle factors of individual patients, such as smoking, alcohol drinking, family history, and past medical history before the study period were not available. However, the severity of comorbidities was adjusted in the analysis using the Charlson Comorbidity Index score. Moreover, other lifestyle factors are less affected because most SCARs are caused by medication or medical conditions. Second, we used a case-control design in our study. To avoid misclassification bias, the controls were selected from patients who were not hospitalized previously for skin diseases. Lastly, hospital inpatients were selected as controls for each case. Hospital-based controls are unlikely to be representative of the general population and may result in a selection bias because of different hospital admission rates. We compared the admission diagnosis and rate of our study subjects and that of the general population during the study period. The distributions of the admission diagnosis and rate for the controls were consistent with that of the national annual report on elderly patients in Korea.

Conclusions

In conclusion, the use of carbamazepine increased the risk of severe cutaneous adverse drug reactions by almost 10-fold in Korean elderly patients aged ≥65 years. This association was consistently high with SCAR patients of carbamazepine use for neuropathic pain. When prescribing carbamazepine for the first time to elderly patients, prodromal symptoms that may occur before the skin lesions should be assessed, and special care should be taken to achieve earlier diagnosis and referral in order to improve prognosis.

Author Contributions

Conceived and designed the experiments: JYK SYJ BJP. Performed the experiments: JYK JL YJK. Analyzed the data: JYK YJK JYS. Contributed reagents/materials/analysis tools: NKC BJP. Wrote the paper: JYK JL.

References

  1. 1. Yang CY, Dao RL, Lee TJ, Lu CW, Yang CH, et al. (2011) Severe cutaneous adverse reactions to antiepileptic drugs in Asians. Neurology 77: 2025–2033.
  2. 2. Mockenhaupt M, Messenheimer J, Tennis P, Schlingmann J (2005) Risk of Stevens-Johnson syndrome and toxic epidermal necrolysis in new users of antiepileptics. Neurology 64: 1134–1138.
  3. 3. Rzany B, Correia O, Kelly JP, Naldi L, Auquier A, et al. (1999) Risk of Stevens-Johnson syndrome and toxic epidermal necrolysis during first weeks of antiepileptic therapy: a case-control study. Study Group of the International Case Control Study on Severe Cutaneous Adverse Reactions. Lancet 353: 2190–2194.
  4. 4. Hollingworth SA, Eadie MJ (2010) Antiepileptic drugs in Australia: 2002–2007. Pharmacoepidemiol Drug Saf 19: 82–89.
  5. 5. Johannessen Landmark C, Larsson PG, Rytter E, Johannessen SI (2009) Antiepileptic drugs in epilepsy and other disorders-a population-based study of prescriptions. Epilepsy Res 87: 31–39.
  6. 6. Tsiropoulos I, Gichangi A, Andersen M, Bjerrum L, Gaist D, et al. (2006) Trends in utilization of antiepileptic drugs in Denmark. Acta Neurol Scand 113: 405–411.
  7. 7. Sheorajpanday RV, De Deyn PP (2007) Epileptic fits and epilepsy in the elderly: general reflections, specific issues and therapeutic implications. Clin Neurol Neurosurg 109: 727–743.
  8. 8. Ahmad M, Goucke CR (2002) Management strategies for the treatment of neuropathic pain in the elderly. Drugs Aging 19: 929–945.
  9. 9. Italiano D, Perucca E (2013) Clinical pharmacokinetics of new-generation antiepileptic drugs at the extremes of age: an update. Clin Pharmacokinet 52: 627–645.
  10. 10. Field TS, Gurwitz JH, Harrold LR, Rothschild J, DeBellis KR, et al. (2004) Risk factors for adverse drug events among older adults in the ambulatory setting. J Am Geriatr Soc 52: 1349–1354.
  11. 11. Green JL, Hawley JN, Rask KJ (2007) Is the number of prescribing physicians an independent risk factor for adverse drug events in an elderly outpatient population? Am J Geriatr Pharmacother 5: 31–39.
  12. 12. Shamliyan T (2010) Adverse drug effects in hospitalized elderly: data from the healthcare cost and utilization project. Clin Pharmacol 2: 41–63.
  13. 13. Pirmohamed M, James S, Meakin S, Green C, Scott AK, et al. (2004) Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ 329: 15–19.
  14. 14. Carneiro SC, Azevedo-e-Silva MC, Ramos-e-Silva M (2011) Drug eruptions in the elderly. Clin Dermatol 29: 43–48.
  15. 15. Rzany B, Mockenhaupt M, Baur S, Schroder W, Stocker U, et al. (1996) Epidemiology of erythema exsudativum multiforme majus, Stevens-Johnson syndrome, and toxic epidermal necrolysis in Germany (1990–1992): structure and results of a population-based registry. J Clin Epidemiol 49: 769–773.
  16. 16. Bastuji-Garin S, Fouchard N, Bertocchi M, Roujeau JC, Revuz J, et al. (2000) SCORTEN: a severity-of-illness score for toxic epidermal necrolysis. J Invest Dermatol 115: 149–153.
  17. 17. Sekula P, Dunant A, Mockenhaupt M, Naldi L, Bouwes Bavinck JN, et al. (2013) Comprehensive survival analysis of a cohort of patients with Stevens-Johnson syndrome and toxic epidermal necrolysis. J Invest Dermatol 133: 1197–1204.
  18. 18. Gau SS, Chao PF, Lin YJ, Chang CJ, Gau CS (2008) The association between carbamazepine and valproate and adverse cutaneous drug reactions in patients with bipolar disorder: a nested matched case-control study. J Clin Psychopharmacol 28: 509–517.
  19. 19. Lee J, Youn K, Choi NK, Lee JH, Kang D, et al. (2013) A population-based case-control study: proton pump inhibition and risk of hip fracture by use of bisphosphonate. J Gastroenterol 48: 1016–1022.
  20. 20. Choi NK, Chang Y, Jung SY, Choi YK, Lee J, et al. (2011) A population-based case-crossover study of polyethylene glycol use and acute renal failure risk in the elderly. World J Gastroenterol 17: 651–656.
  21. 21. Park BJ, Sung JH, Park KD (2003) Report of the evaluation for validity of discharged diagnoses in Korean Health Insurance database [ in Korean]. Seoul: Seoul National University.
  22. 22. Chen P, Lin JJ, Lu CS, Ong CT, Hsieh PF, et al. (2011) Carbamazepine-induced toxic effects and HLA-B*1502 screening in Taiwan. N Engl J Med 364: 1126–1133.
  23. 23. Lin MS, Dai YS, Pwu RF, Chen YH, Chang NC (2005) Risk estimates for drugs suspected of being associated with Stevens-Johnson syndrome and toxic epidermal necrolysis: a case-control study. Intern Med J 35: 188–190.
  24. 24. Strom BL, Carson JL, Halpern AC, Schinnar R, Snyder ES, et al. (1991) A population-based study of Stevens-Johnson syndrome. Incidence and antecedent drug exposures. Arch Dermatol 127: 831–838.
  25. 25. Genin E, Schumacher M, Roujeau JC, Naldi L, Liss Y, et al. (2011) Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. Orphanet J Rare Dis 6: 52.
  26. 26. Roujeau JC, Kelly JP, Naldi L, Rzany B, Stern RS, et al. (1995) Medication use and the risk of Stevens-Johnson syndrome or toxic epidermal necrolysis. N Engl J Med 333: 1600–1607.
  27. 27. Quan H, Sundararajan V, Halfon P, Fong A, Burnand B, et al. (2005) Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Medical Care 43: 1130–1139.
  28. 28. Mockenhaupt M, Viboud C, Dunant A, Naldi L, Halevy S, et al. (2008) Stevens-Johnson syndrome and toxic epidermal necrolysis: assessment of medication risks with emphasis on recently marketed drugs. The EuroSCAR-study. J Invest Dermatol 128: 35–44.
  29. 29. Levi N, Bastuji-Garin S, Mockenhaupt M, Roujeau JC, Flahault A, et al. (2009) Medications as risk factors of Stevens-Johnson syndrome and toxic epidermal necrolysis in children: a pooled analysis. Pediatrics 123: e297–304.
  30. 30. Bastuji-Garin S, Zahedi M, Guillaume JC, Roujeau JC (1993) Toxic epidermal necrolysis (Lyell syndrome) in 77 elderly patients. Age Ageing 22: 450–456.
  31. 31. Golden HE (1993) Stevens-Johnson syndrome associated with herpes simplex virus. Arch Intern Med 153: 1396.
  32. 32. Rzany B, Hering O, Mockenhaupt M, Schroder W, Goerttler E, et al. (1996) Histopathological and epidemiological characteristics of patients with erythema exudativum multiforme major, Stevens-Johnson syndrome and toxic epidermal necrolysis. Br J Dermatol 135: 6–11.
  33. 33. Gonzalez-Sicilia L, Cano A, Serrano M, Hernandez J (1998) Stevens-Johnson syndrome associated with gabapentin. Am J Med 105: 455.
  34. 34. DeToledo JC, Minagar A, Lowe MR, Ramsay RE (1999) Skin eruption with gabapentin in a patient with repeated AED-induced Stevens-Johnson's syndrome. Ther Drug Monit 21: 137–138.
  35. 35. Ma JE, Kim HS, Park DJ, Kim HC, Lee JD, et al. (2007) A Case of Stevens-Johnson Syndrome Induced by Gabapentin [ in Korean]. Korean J Asthma Allergy Clin Immunol 27: 283–286.
  36. 36. Paquet P, Pierard GE (2010) New insights in toxic epidermal necrolysis (Lyell's syndrome): clinical considerations, pathobiology and targeted treatments revisited. Drug Saf 33: 189–212.
  37. 37. Yip LW, Thong BY, Lim J, Tan AW, Wong HB, et al. (2007) Ocular manifestations and complications of Stevens-Johnson syndrome and toxic epidermal necrolysis: an Asian series. Allergy 62: 527–531.
  38. 38. Kim SH, Lee KW, Song WJ, Jee YK, Lee SM, et al. (2011) Carbamazepine-induced severe cutaneous adverse reactions and HLA genotypes in Koreans. Epilepsy Res 97: 190–197.
  39. 39. Hall GC, Carroll D, McQuay HJ (2008) Primary care incidence and treatment of four neuropathic pain conditions: a descriptive study, 2002–2005. BMC Fam Pract 9: 26.
  40. 40. Wiffen PJ, Derry S, Moore RA, McQuay HJ (2011) Carbamazepine for acute and chronic pain in adults. Cochrane Database Syst Rev: CD005451.
  41. 41. Chung WH, Hung SI, Chen YT (2010) Genetic predisposition of life-threatening antiepileptic-induced skin reactions. Expert Opin Drug Saf 9: 15–21.