Open Access

Increased risk of ischemic stroke in patients with burn injury: a nationwide cohort study in Taiwan

  • Tzu-Yao Hung1,
  • Yi-Kung Lee2, 3,
  • Ming-Yuan Huang4,
  • Chen-Yang Hsu5 and
  • Yung-Cheng Su2, 3Email author
Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine201624:44

https://doi.org/10.1186/s13049-016-0236-1

Received: 23 May 2015

Accepted: 4 April 2016

Published: 6 April 2016

Abstract

Background

Conflicting results have been obtained by studies attempting to assess the risks of ischemic stroke in patients with burn injury, while the long-term risk of stroke in survivors of burn injury remains unexplored. We evaluated whether the risk of ischemic stroke in patients hospitalized with burn injury in Taiwan is higher when compared to the general population.

Methods

The data from one million National Health Insurance (NHI) adult beneficiaries were evaluated from January 1, 2005 until December 31, 2012 to identify those who developed ischemic stroke. Each identified patient with burn injury was matched with one hundred unexposed patients based on a high-dimensional propensity score. Cox regression models were applied to compare the risks of the development of ischemic stroke in the matched cohorts.

Results

A total of 743,237 patients were enrolled. After matching, 1,763 burn injury patients and 176,300 unexposed patients were selected and compared. The adjusted hazard ratio of ischemic stroke was significantly increased in burn injury patients (1.84; 95 % CI, 1.43–2.36). A subgroup analysis based on patients who survived longer than 12 months in the matched cohort also revealed higher hazard ratio in the burn injury patients (1.54; 95 % CI, 1.11–2.13).

Conclusion

The risk of ischemic stroke is significantly higher in patients hospitalized with burn injury than in the general population, and these risks may extend longer than expected.

Keywords

BurnsIschemic strokeCohort studies

Background

Stroke remains one of the leading causes of long-term disability and mortality, with a worldwide incidence of 4.2–6.5 per 1000 person-years for people aged 55 or older, resulting in a significant societal economic burden [13]. Apart from patient management, early identification of risk factors for the development of stroke is critical to reduce morbidity and mortality. Several precipitating co-morbidity factors have been reported to be associated with stroke onset, including hypertension, diabetes, hyperlipidemia, atrial fibrillation, and a history of smoking [4]. Recently, the potential relationship between burn injury and stroke has begun to receive attention from the clinical community.

It is well known that cerebral complications are common in victims of burn injury [5, 6]. Hypovolemia, during the acute stage of burn injury, may induce poor cerebral perfusion, resulting in ischemic stroke. In addition, sepsis, a common complication in burn patients, may represent another risk factor of stroke [7], while a state of acquired hypercoagulopathy that is often encountered following burn injury may present a further risk of stroke in these patients [8, 9].

To our knowledge, few studies exist concerning the incidence of ischemic stroke after burn injury, and the results are contradictory [6, 10]. Moreover, the long-term risk of stroke in survivors of burn injury remains unexplored. In the present study, a large administrative database was used to elucidate the risks of ischemic stroke in burn injury patients in Taiwan. High-dimensional propensity score (hdPS) matching (i.e., a semi-automated statistical method) was used to address possible confounding. The results of this study may help clinicians to identify individuals at possible risk for stroke.

Methods

Ethics statement

This study was conducted in accordance to the tenets of the Helsinki Declaration. The Institutional Review Board of Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Taiwan, approved the study. The need for informed consent was waived because patient record/information was anonymous and no identifiers were employed.

Database

The Taiwanese National Health Insurance (NHI) program was initiated in 1995, and has been described in detail previously [1113]. Utilizing the Longitudinal Health Insurance Database (2005), a dataset comprising 1,000,000 individuals who were representative beneficiaries of the NHI program was randomly sampled.

Study population

The representative population sample was systematically tracked between January 1, 2003 and December 31, 2012. Individuals aged >18 years who were alive in 2005 were initially identified. Burn injury was defined by the ICD-9-CM codes 940–949. Only patients hospitalized for burn injuries were enrolled in the study, thereby excluding those sustaining mild burns. Ischemic stroke was defined by ICD-9-CM codes 433–437 [14]. To maximize the scope of our study, we included only those patients hospitalized for stroke. Patients with burn injuries and any type of stroke diagnosed before January 1, 2005 were excluded from the study to ensure all enrolled cases and events were new. We chose to focus on ischemic stroke alone to avoid any possible overlap between the ICD-9-CM codes for traumatic intracranial hemorrhage and hemorrhagic stroke. Patients diagnosed with hemorrhagic stroke during follow-up were also excluded. After excluding patients according to the aforementioned criteria, we identified 1,787 patients hospitalized with burn injuries and 741,510 without burn injuries. Each group was followed from the hospitalization date or January 1, 2005 (baseline) to December 31, 2012 (end of the study period) for verification of a diagnosis of ischemic stroke during the study period. Patients who were no longer beneficiaries of the NHI Program (due to death or transfer) or were still healthy at the end of the follow-up period were carefully monitored (Fig. 1).
Fig. 1

Flow diagram of the population-based study

Validation of exposure and outcome

We investigated the validity of the ICD-9-CM codes for the identification of burn injuries and ischemic stroke. The codes were validated by analyzing medical records randomly selected from the electronic database from 2010 to 2012 at the Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation. We then estimated the positive predictive value (PPV). A systematic chart review confirmed the diagnosis in 45 of 50 randomly selected patients with codes for burn injuries, thereby validating a PPV of 90 % (95 % CI, 78.2 %–96.7 %). In addition, the diagnosis was also confirmed in 47 of 50 randomly selected patients with codes for ischemic stroke, validating a PPV of 94 % (95 % CI, 83.5 %–98.7 %).

Pre-specified covariates

To better understand the effect of burn injury on the risk of ischemic stroke, several covariates were selected including age, sex, urbanization level (i.e., urban, suburban, and rural), and socioeconomic status (SES). Income-related insurance payment amounts were used as a proxy measure of individual SES at follow-up [15]. The prevalence of selected comorbidity factors (i.e., diabetes, hypertension, coronary artery disease, hyperlipidemia, history of alcohol intoxication, malignancies, heart failure, atrial fibrillation, history of smoking and peripheral artery disease) and the Charlson Comorbidity Index (CCI) were determined using discharge diagnoses either during outpatient clinic visits or hospitalizations before January 1, 2005. The CCI represents a scoring system with weighted factors of important concomitant diseases and is widely used in the ICD-9-CM coded administrative databases [14].

High dimensional propensity scores

The high-dimensional propensity score (hdPS), available as an SAS macro from the Brigham and Women’s Hospital [16, 17], is a multistep, empirically driven algorithm that is used to adjust for confounding bias. Candidate covariates from predefined data dimensions, such as clinical treatment received, medications administered based on the Anatomical Therapeutic Chemical (ATC) Classification System, and coded diagnoses reported in this study from January 1, 2003 to December 31, 2004, were identified using the SAS macro. It automatically assesses the repetition of the same codes, prioritizes covariates, and identifies covariates for adjustment. We selected the top 500 variables most likely to result in a bias.

In addition to these 500 variables, the pre-selected covariates were analyzed with a logistic regression model to estimate the predicted probability (propensity score) of exposure of the study subjects to burn injuries when compared with the healthy population. This exposure is conditional on all the included covariates. After using a standard greedy matching algorithm to match all burn injury patients with 100 non-burn injury patients having the closest propensity scores [18, 19], we compared the risk for the development of ischemic stroke between the two groups.

Statistical analysis

We used an SAS statistical package (Version 9.4, SAS Institute, Inc., Cary, NC, USA), and STATA (Version 11.2, StataCorp, College Station, TX, USA) for all data analyses. All covariates except age and propensity scores were included as categorical variables (age and propensity scores were considered continuous variables). Categorical variables and continuous variables were compared using Pearson’s chi-square test and a t test, respectively, to determine the baseline heterogeneity within the two groups. The cumulative risks of ischemic stroke were first determined by plotting the Nelson–Aalen curves. The hazard ratios (HRs) for ischemic stroke in patients with burn injury in the matched group were calculated using the Cox proportional hazard regression models after adjustment for age, gender, urbanization level, SES, diabetes, hypertension, coronary artery disease, hyperlipidemia, malignancies, heart failure, atrial fibrillation, peripheral artery disease, history of alcohol use and smoking, and CCI. Adjusted HRs were analyzed on the basis of the following parameters: (1) Hospitalization periods for subjects with or without burn injuries from baseline through the end of the study and (2) 12-month periods after hospitalization for burn injury and non-burn injury subjects from baseline through the end of the study to evaluate the long-term impact of burn injuries on the risk of ischemic stroke onset.

To further validate the accuracy of our results, we also performed sensitivity analyses to evaluate the extent of the effect of an unmeasured confounder on the results [20]. A two-tailed p-value of 0.05 was considered significant.

Results

The distribution of demographic characteristics and selected morbidities in both study groups is shown in Table 1. There were 1,787 patients in the burn injury group and 741,510 in the unexposed group. The total follow-up time was 6,564 and 5,581,503 person-years, and the mean follow-up period was 3.67 and 7.53 years, respectively. Patients with burn injury were mostly male, older, and more likely to have diabetes, hypertension, coronary artery disease, a history of alcohol intoxication, heart failure, and higher CCI. By the end of the follow-up period, 20,562 patients had been admitted for ischemic stroke (66 patients in the burn injury group and 20,496 in the unexposed group). The crude hazard ratio (HR) of ischemic stroke for the burn injury group was 2.64 (95 % confidence interval [CI], 2.07–3.36), and the Nelson-Aalen plot showed a higher cumulative risk in the burn injury group (Fig. 2).
Table 1

Baseline characteristics of the burn injury group and the unexposed group

Variables, n (%)

Burn injury group

Unexposed group

P-value

n = 1787

n = 741510

Male

1042

58.3

362518

48.9

<0.001

Mean age (SD)

46.6

17.4

42.6

16.4

<0.001

Socioeconomic status

    

<0.001

 Low

867

48.5

312208

42.1

 

 Moderate

740

41.4

292075

39.4

 

 High

180

10.1

137167

18.5

 

Urbanization level

    

<0.001

 Urban

867

48.5

221749

29.9

 

 Suburban

740

41.4

341946

46.1

 

 Rural

180

10.1

177755

24.0

 

Charlson Comorbidity Index

    

<0.001

 0

1099

61.5

501427

67.6

 

 1

412

23.1

147724

19.9

 

 ≥2

276

15.4

92299

12.4

 

Diabetes

191

10.7

50273

6.8

<0.001

Hypertension

298

16.7

106683

14.4

0.006

Coronary artery disease

140

7.8

42221

5.7

<0.001

Hyperlipidemia

176

9.9

64947

8.8

0.104

History of alcohol intoxication

40

2.2

5288

0.7

<0.001

Malignancies

23

1.3

11861

1.6

0.293

heart failure

20

1.1

4402

0.6

0.004

Atrial fibrillation

6

0.3

2430

0.3

0.953

Smoking

1

0.1

318

0.04

0.790

Peripheral artery disease

13

0.7

3898

0.5

0.239

Stroke

66

3.7

20496

2.8

0.017

Mean Propensity score (SD)

0.0069

0.0219

0.0024

0.0031

<0.001

p-Values less than 0.05 are presented as bold type

Fig. 2

Nelson-Aalen curves showing a higher cumulative risk of ischemic stroke in the burn injury group

Next, we matched 1,763 patients in the burn injury group with 176,300 in the unexposed group. In the subcohort, 6,860 patients were admitted for ischemic stroke, (62 in the burn injury group and 6,798 in the unexposed group. The distribution of all pre-specified covariates within the two subgroups was found to be similar and summarized in Table 2. A multivariate Cox regression model based on the pre-specified covariates was used to evaluate the adjusted HRs of ischemic stroke, which after controlling for age, gender, urbanization level, SES, diabetes, hypertension, coronary artery disease, hyperlipidemia, history of alcohol use, malignancies, heart failure, atrial fibrillation, history of smoking, peripheral artery disease and CCI, remained significantly higher in patients with burn injury (1.84; 95 % CI, 1.43–2.36; p < 0.001). All statistical results are summarized in Table 3.
Table 2

Baseline characteristics of the propensity matched cohort

Variables, n(%)

Burn injury group

Unexposed group

P-value

n = 1763

n = 176300

Male

1028

58.3

101561

57.6

0.552

Mean age (SD)

46.6

17.4

46.0

17.3

0.155

Socioeconomic status

    

0.410

 Low

847

48.0

82936

47.0

 

 Moderate

736

41.8

73690

41.8

 

 High

180

10.2

19674

11.2

 

Urbanization level

    

0.546

 Urban

365

20.7

38300

21.7

 

 Suburban

834

47.3

82999

47.1

 

 Rural

564

32.0

55001

31.2

 

Charlson Comorbidity Index

    

0.441

 0

1096

62.2

111944

63.5

 

 1

402

22.8

39449

22.4

 

 ≥2

265

15.0

24907

14.1

 

Diabetes

181

10.3

16578

9.4

0.217

Hypertension

291

16.5

28058

15.9

0.500

Coronary artery disease

135

7.7

12299

7.0

0.264

Hyperlipidemia

173

9.8

16819

9.5

0.698

History of alcohol intoxication

34

1.9

2653

1.5

0.147

Malignancies

23

1.3

2300

1.3

1.000

heart failure

20

1.1

1630

0.9

0.360

Atrial fibrillation

6

0.3

555

0.3

0.849

Smoking

1

0.1

81

0.1

0.834

Peripheral artery disease

13

0.7

1169

0.7

0.702

Stroke

62

3.5

6798

3.9

0.462

Mean Propensity score (SD)

0.0051

0.0063

0.0041

0.0043

<0.001

p-Values less than 0.05 are presented as bold type

Table 3

Adjusted HRs for patients with burn injury in the propensity score matched cohort

Variables

Hazard ratio

95 % confidence interval

P-value

Burn injury

1.84

1.43–2.36

<0.001

Male

1.39

1.32–1.46

<0.001

Patient age

1.07

1.06–1.07

<0.001

Socioeconomic status

   

 Low

1

--

--

 Moderate

0.68

0.65–0.72

<0.001

 High

0.42

0.35–0.50

<0.001

Urbanization level

   

 Urban

1

--

--

 Suburban

1.12

1.05–1.20

<0.001

 Rural

1.38

1.28–1.48

<0.001

Charlson Comorbidity Index

   

 0

1

--

--

 1

1.31

1.23–1.41

<0.001

 ≥2

1.65

1.54–1.77

<0.001

Diabetes

1.76

1.66–1.87

<0.001

Hypertension

1.72

1.62–1.81

<0.001

Coronary artery disease

0.99

0.94–1.06

0.946

Hyperlipidemia

0.94

0.88–0.99

0.043

History of alcohol intoxication

1.49

1.25–1.79

<0.001

Malignancies

0.86

0.74–0.99

0.045

Heart failure

1.15

1.02–1.30

0.028

Atrial fibrillation

1.27

1.04–1.54

0.017

Smoking

0.98

0.37–2.61

0.963

Peripheral artery disease

1.07

0.91–1.26

0.417

p-Values less than 0.05 are presented as bold type

A subgroup analysis based on subjects who were followed longer than 12 months in the matched cohort was performed (1,461 patients in the burn injury group and 172,543 in the unexposed group). The adjusted HR for ischemic stroke remained statistically significant. (1.54; 95 % CI, 1.11—2.13) (Table 4).
Table 4

Adjusted HRs for patients followed longer than 12 months in the matched cohort

Variables

Hazard ratio

95 % confidence interval

P-value

Burn injury

1.54

1.11–2.13

0.009

Male

1.39

1.31–1.46

<0.001

Patient age

1.07

1.06–1.07

<0.001

Socioeconomic status

   

 Low

1

--

--

 Moderate

0.71

0.67–0.76

<0.001

 High

0.42

0.35–0.51

<0.001

Urbanization level

   

 Urban

1

--

--

 Suburban

1.12

1.04–1.21

0.003

 Rural

1.37

1.27–1.48

<0.001

Charlson Comorbidity Index

   

 0

1

--

--

 1

1.31

1.22–1.41

<0.001

 ≥2

1.57

1.45–1.69

<0.001

Diabetes

1.76

1.65–1.87

<0.001

Hypertension

1.65

1.55–1.75

<0.001

Coronary artery disease

0.97

0.91–1.04

0.394

Hyperlipidemia

0.97

0.91–1.04

0.420

History of alcohol intoxication

1.41

1.15–1.73

0.001

Malignancies

0.84

0.71–1.00

0.054

Heart failure

1.18

1.03–1.36

0.018

Atrial fibrillation

1.28

1.03–1.60

0.027

Smoking

1.16

0.43–3.09

0.769

Peripheral artery disease

1.09

0.91–1.31

0.331

p-Values less than 0.05 are presented as bold type

Sensitivity analyses showed that an unmeasured confounder present in 10 % of the matched cohort would be required to elevate the risk of ischemic stroke by a factor of 3.8 and would also be required to have a prevalence amongst burn injury patients of 3.8 times that observed amongst the unexposed group to explain a lower 95 % confidence limit HR of 1.43 (Fig. 3).
Fig. 3

Sensitivity analyses of an unmeasured confounding

Discussion

To our knowledge, this study represents the first systematic evaluation of the long-term risk between burn injury and ischemic stroke. We evaluated the risk of ischemic stroke onset in burn injury patients, utilizing the largest cohort to date. In our patient population, the risk of ischemic stroke was increased in patients with burn injury (HR 1.84; 95 % CI, 1.43–2.36) and still significant in those survived more than 12 months. (HR 1.54; 95 % CI, 1.11–2.13). These results reveal that burn injury patients have a higher risk of ischemic stroke that persists for more than one year post-injury. Burn injury prevention may therefore not only reduce the incidence of acute complications, but also ameliorate associated long-term morbidities.

Several hypotheses may be proposed to explain the higher risk of ischemic stroke in burn injury patients when compared to the general population. First, it is known that watershed stroke may occur in patients with compromised hemodynamic status [21, 22], and hypovolemia associated with the acute stage of burn injury patients may therefore account for the increased risk of stroke. Secondly, acute infection, a common complication in patients hospitalized with burn injury, may result in endothelial dysfunction, coagulopathy or direct platelet activation that may trigger or promote the cellular cascades associated with the onset of ischemic stroke [23, 24]. Finally, a hypercoagulable state known to occur during the post-burn recovery phase [25] may also elevate the risk for the development of stroke in patients with burn injury [26].

In our study, we evaluated the risk of ischemic stroke onset in burn injury patients, utilizing the largest cohort to date. The database was representative of the whole population of the country of Taiwan, and loss to follow-up or selection bias is, therefore, not a relevant concern. In a study by Cho et al. [10], stroke was reported to be a rare complication in patients admitted with burn injury. We advocate three possible reasons that could explain the discrepant results between their study and ours. First, the younger age of the patients in the Cho et al. [10] study than those comprising our study cohort may have been associated with reduced pre-existing vascular lesions such as atherosclerosis of brain vessels. Secondly, the patient population reported by Cho et al. [10] was enrolled from a single burn center, and the possibility exists that improved care (when compared to our patients from the general population) may have reduced the onset of medical complications. Finally, the severity of injury in patients evaluated by Cho et al., [10] may have been more severe, resulting in a reduced detection of stroke onset.

Another strength of the present study is that we extensively adjusted for possible confounding factors by applying hdPS analysis. In an administrative database, possible risk factors for ischemic stroke (such as functional status or dietary habits) cannot be assessed. However, a set of proxies may indirectly describe the overall status of patients. This status is viewed through the lenses of the health care system that provides the interventions [26]. A battery of proxies is a good overall proxy to account for the effect of unobserved confounding factors. The use of a large number of proxy covariates for propensity score estimation is known to effectively control for confounding factors in epidemiologic studies [22]. In our study, as many as 500 covariates were generated for analysis from the procedure codes, medication records and diagnostic codes recorded up to 2 years before entry of the follow-up data. In this way, we believe our study methods are more robust compared to traditional adjustment methods.

Limitations

Our study was associated with several limitations. We used administrative data to generate our findings and ICD-9-CM codes for defining burn injury and ischemic stroke. These codes are often not as useful for precise operative definitions, since they are primarily used for insurance reimbursement. Thus, it is impossible to accurately determine the sensitivity, specificity, and clinical accuracy of the diagnoses when employing such data. To mitigate the number of false-positive cases, the inclusion criteria for burn injury and ischemic stroke patients were restricted to only those patients who had been hospitalized. The high PPVs that we observed validated the selection process, despite the size of our study and the use of a local database.

In the present study, the relationship between the affected body region(s) and risk of ischemic stroke in burn injury patients was not evaluated because we were able to obtain only limited information from the administrative database. Individual studies will be required to determine whether HRs differ significantly among different body regions (e.g., head versus torso).

In our study, subgroup analyses in patients with severe burn injuries to evaluate the severity-response effects were not performed. As mentioned previously, severe burn patients may have more comorbid risk factors (e.g., restricted mobility and higher mortality), possibly precluding ischemic stroke diagnosis.

Finally evaluation of other possible risk factors of burn injuries and ischemic stroke by the matched cohort method was complicated by the use of propensity score analyses to adjust for possible confounders. Although extensive adjustments for many possible covariates were made, the possibility of the presence of unmeasured confounders and overmatching bias remain. However, the adjusted HR for ischemic stroke in burn injury was sufficiently significant to indicate that the residual confounders may be unable to completely account for the results.

Conclusion

The risk of ischemic stroke is significantly higher in patients hospitalized with burn injury than in the general population, and these risks may extend longer than expected.

Declarations

Acknowledgements

The abstract of the manuscript can be cited in the link below: http://ccforum.com/content/19/S1/P470/.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Emergency Department, Zhongxing Branch of Taipei City Hospital
(2)
School of Medicine, Tzu Chi University
(3)
Emergency Department, Dalin Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
(4)
Department of Emergency Medicine, Mackay Memorial Hospital
(5)
Department of Public Heath, National Taiwan University

References

  1. Ingall T. Stroke--incidence, mortality, morbidity and risk. J Insur Med. 2004;36(2):143–52. Epub 2004/08/11.PubMedGoogle Scholar
  2. Feigin VL, Lawes CM, Bennett DA, Anderson CS. Stroke epidemiology: a review of population-based studies of incidence, prevalence, and case-fatality in the late 20th century. Lancet Neurol. 2003;2(1):43–53. Epub 2003/07/10.View ArticlePubMedGoogle Scholar
  3. Ma VY, Chan L, Carruthers KJ. Incidence, prevalence, costs, and impact on disability of common conditions requiring rehabilitation in the United States: stroke, spinal cord injury, traumatic brain injury, multiple sclerosis, osteoarthritis, rheumatoid arthritis, limb loss, and back pain. Arch Phys Med Rehabil. 2014;95(5):986–95.e1. Epub 2014/01/28. doi: 10.1016/j.apmr.2013.10.032. PubMed PMID: 24462839; PubMed Central PMCID: PMCPmc4180670.View ArticlePubMedPubMed CentralGoogle Scholar
  4. Hsieh FI, Chiou HY. Stroke: morbidity, risk factors, and care in taiwan. J Stroke. 2014;16(2):59–64. doi:10.5853/jos.2014.16.2.59. PubMed PMID: 24949310, PubMed Central PMCID: PMC4060269.View ArticlePubMedPubMed CentralGoogle Scholar
  5. Brusselaers N, Monstrey S, Vogelaers D, Hoste E, Blot S. Severe burn injury in Europe: a systematic review of the incidence, etiology, morbidity, and mortality. Crit Care. 2010;14(5):R188. doi:10.1186/cc9300. PubMed PMID: 20958968, PubMed Central PMCID: PMC3219295.View ArticlePubMedPubMed CentralGoogle Scholar
  6. Winkelman MD, Galloway PG. Central nervous system complications of thermal burns. A postmortem study of 139 patients. Medicine. 1992;71(5):271–83. Epub 1992/09/01.View ArticlePubMedGoogle Scholar
  7. Syrjanen J. Infection as a risk factor for cerebral infarction. Eur Heart J. 1993;14(Suppl K):17–9. Epub 1993/12/01.PubMedGoogle Scholar
  8. Sebastian R, Ghanem O, DiRoma F, Milner SM, Price LA. Pulmonary embolism in burns, is there an evidence based prophylactic recommendation? Case report and review of literature. Burns. 2014. Epub 2014/08/15. doi: 10.1016/j.burns.2014.06.018.
  9. Bang OY, Seok JM, Kim SG, Hong JM, Kim HY, Lee J, et al. Ischemic stroke and cancer: stroke severely impacts cancer patients, while cancer increases the number of strokes. J Clin Neurol (Seoul, Korea). 2011;7(2):53–9. Epub 2011/07/23. doi: 10.3988/jcn.2011.7.2.53. PubMed PMID: 21779292; PubMed Central PMCID: PMCPmc3131539.View ArticleGoogle Scholar
  10. Cho SJ, Minn YK, Kwon KH. Stroke after burn. Cerebrovasc Dis (Basel, Switzerland). 2007;24(2–3):261–3. doi:10.1159/000104488. Epub 2007/07/17.View ArticleGoogle Scholar
  11. National Health Insurance Database 2014 [cited 2014 April 9]. Available from: http://w3.nhri.org.tw/nhird/en/ind.
  12. Lee YK, Lee CC, Chen CC, Wong CH, Su YC. High risk of 'failure' among emergency physicians compared with other specialists: a nationwide cohort study. Emerg Med J. 2013. doi:10.1136/emermed-2012-201440. Epub 2013/04/27.Google Scholar
  13. Hou SW, Lee YK, Hsu CY, Lee CC, Su YC. Increased risk of acute pancreatitis in patients with chronic hemodialysis: a 4-year follow-up study. PLoS ONE. 2013;8(8):e71801. doi:10.1371/journal.pone.0071801. Epub 2013/08/27.View ArticlePubMedPubMed CentralGoogle Scholar
  14. Lee Y-K, Lee C-W, Huang M-Y, Hsu C-Y, Su Y-C. Increased risk of ischemic stroke in patients with mild traumatic brain injury: a nationwide cohort study. Scand J Trauma Resusc Emerg Med. 2014;22(1):66. doi:10.1186/s13049-014-0066-y. PubMed PMID.View ArticlePubMedPubMed CentralGoogle Scholar
  15. Cheng PL, Lin HY, Lee YK, Hsu CY, Lee CC, Su YC. Higher mortality rates among the elderly with mild traumatic brain injury: a nationwide cohort study. Scand J Trauma Resusc Emerg Med. 2014;22(1):7. doi:10.1186/1757-7241-22-7. Epub 2014/01/29.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Schneeweiss S, Rassen JA, Glynn RJ, Avorn J, Mogun H, Brookhart MA. High-dimensional propensity score adjustment in studies of treatment effects using health care claims data. Epidemiology. 2009;20(4):512–22. doi:10.1097/EDE.0b013e3181a663cc. PubMed PMID: 19487948, PubMed Central PMCID: PMC3077219.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Ng KJ, Lee YK, Huang MY, Hsu CY, Su YC. Risks of Venous Thromboembolism in Patients with Liver Cirrhosis: A Nationwide Cohort Study in Taiwan. J Thromb Haemost. 2014. doi:10.1111/jth.12805. Epub 2014/12/05.Google Scholar
  18. Guan H-L, Lin H-Y, Lee Y-K, Hsu C-Y, Su Y-C. Early Endoscopy Can Shorten the Duration of Hospitalization in Suspected Variceal Hemorrhage. ISRN Emergency Medicine. 2013;2013:1–6. doi:10.1155/2013/839126.View ArticleGoogle Scholar
  19. Lee YK, Chen CC, Lin HY, Hsu CY, Su YC. Propofol for sedation can shorten the duration of ED stay in joints reduction. Am J Emerg Med. 2011. Epub 2011/12/16. doi: 10.1016/j.ajem.2011.09.024.
  20. Lee YK, Hou SW, Lee CC, Hsu CY, Huang YS, Su YC. Increased risk of dementia in patients with mild traumatic brain injury: a nationwide cohort study. PLoS ONE. 2013;8(5), e62422. doi:10.1371/journal.pone.0062422. Epub 2013/05/10.View ArticlePubMedPubMed CentralGoogle Scholar
  21. Bijker JB, Persoon S, Peelen LM, Moons KG, Kalkman CJ, Kappelle LJ, et al. Intraoperative hypotension and perioperative ischemic stroke after general surgery: a nested case–control study. Anesthesiology. 2012;116(3):658–64. doi:10.1097/ALN.0b013e3182472320. Epub 2012/01/27.View ArticlePubMedGoogle Scholar
  22. Momjian-Mayor I, Baron JC. The pathophysiology of watershed infarction in internal carotid artery disease: review of cerebral perfusion studies. Stroke. 2005;36(3):567–77. doi:10.1161/01.STR.0000155727.82242.e1. Epub 2005/02/05.View ArticlePubMedGoogle Scholar
  23. Dalager-Pedersen M, Sogaard M, Schonheyder HC, Nielsen H, Thomsen RW. Risk for myocardial infarction and stroke after community-acquired bacteremia: a 20-year population-based cohort study. Circulation. 2014;129(13):1387–96. doi:10.1161/circulationaha.113.006699. Epub 2014/02/14.View ArticlePubMedGoogle Scholar
  24. Grau AJ, Urbanek C, Palm F. Common infections and the risk of stroke. Nat Rev Neurol. 2010;6(12):681–94. doi:10.1038/nrneurol.2010.163. Epub 2010/11/10.View ArticlePubMedGoogle Scholar
  25. Van Haren RM, Thorson CM, Valle EJ, Busko AM, Guarch GA, Andrews DM, et al. Hypercoagulability after burn injury. J Trauma and Acute Care Surgery. 2013;75(1):37–43. doi:10.1097/TA.0b013e3182984911. discussion Epub 2013/06/20.View ArticleGoogle Scholar
  26. Levine SR. Hypercoagulable states and stroke: a selective review. CNS Spectr. 2005;10(7):567–78. Epub 2005/09/13.PubMedGoogle Scholar

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© Hung et al. 2016

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