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Article

Invasive Candidiasis in Hospitalized Patients with Major Burns

1
Division of Plastic and Reconstructive Surgery, Department of Surgery, Taichung Veterans General Hospital, Taichung 40705, Taiwan
2
Department of Critical Care Medicine, Taichung Veterans General Hospital, Taichung 40705, Taiwan
3
Institute of Medicine, School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan
4
Department of Nursing, College of Nursing, Hung Kuang University, Taichung 433304, Taiwan
5
Department of Medical Research, Taichung Veterans General Hospital, Taichung 40705, Taiwan
6
Department of Public Health, College of Medicine, Fu Jen Catholic University, New Taipei City 242062, Taiwan
7
Institute of Public Health and Community Medicine Research Center, National Yang Ming Chiao Tung University, Taipei 11221, Taiwan
8
Department of Industrial Engineering and Enterprise Information, Tunghai University, Taichung 40705, Taiwan
9
Department of Health Care Management, National Taipei University of Nursing and Health Sciences, Taipei 112303, Taiwan
10
Department of Pediatrics, Taichung Veterans General Hospital, Taichung 40705, Taiwan
*
Authors to whom correspondence should be addressed.
These authors contributed to the manuscript equally.
J. Pers. Med. 2022, 12(1), 47; https://doi.org/10.3390/jpm12010047
Submission received: 17 November 2021 / Revised: 14 December 2021 / Accepted: 21 December 2021 / Published: 4 January 2022
(This article belongs to the Special Issue Personalized Medicine in Emergency and Intensive Care)

Abstract

:
Background: Invasive candidiasis (IC) is a major cause of morbidities and mortality in patients hospitalized with major burns. This study investigated the incidence of IC in this specific population and analyzed the possible risk factors. Materials and Methods: We retrospectively analyzed data from the National Health Insurance Research Database (NHIRD) of Taiwan. We identified 3582 patients hospitalized with major burns on over 20% of their total body surface area (TBSA) during 2000–2013; we further analyzed possible risk factors. Result: IC was diagnosed in 452 hospitalized patients (12.6%) with major burns. In the multivariate analysis, patients older than 50 years (adjusted odds ratio (OR) = 1.96, 95% confidence interval (CI) 1.36–2.82), those of female sex (adjusted OR = 1.33, 95% CI 1.03–1.72), those with burns on the head (adjusted OR = 1.33, 95% CI 1.02–1.73), and those with burns over a greater TBSA had higher risks of IC. Conclusion: Treating IC is crucial in healthcare for major burns. Our study suggests that several risk factors are associated with IC in patients hospitalized with major burns, providing reliable reference value for clinical decisions.

1. Introduction

Burns are estimated to result in 180,000 deaths globally every year [1]. In developed countries, the survival rate of patients with major burns has improved in recent years because of advances in surgical treatment and intensive care [2,3], but patients still experience prolonged hospitalization, disfigurement, and disability. Infection is a major challenge during hospitalization in patients with major burns because the skin barrier is extensively compromised.
The incidence of systemic candidiasis among patients with burns has increased from 2.19% to 4.3% in the 1990s [4,5], to 6.3% in a 2008 report [6], and to 11% in a 2015 report [3]. Some literature has suggested that the increasing trend of opportunistic fungal infections is associated with the increasing early use of broad-spectrum antibacterial agents [3,6]. In patients with burns, a fungal infection may be associated with several factors, including age, burn size, and chronic comorbidities. Candida species infections have outnumbered other species of fungus in literature [7,8]. In this study, we used the Taiwan National Health Insurance Research Database (NHIRD) for a retrospective analysis, focusing on patients with severe burns who required hospitalization. This study investigated the incidence of invasive candidiasis (IC) among these patients in Taiwan and related risk factors that severe burn patients might encounter.

2. Materials and Methods

2.1. Database

Taiwan’s National Health Insurance program was established in 1995, and it currently covers 99.6% of Taiwan’s population. The NHIRD is maintained by the National Health Research Institutes of Taiwan; the NHIRD is widely used for medical research and is validated as being of high quality and as being accurate in diagnoses [9]. The identification information of every individual is encrypted before the data are publicly available for research purposes. The diagnostic codes in the NHIRD are based on the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM). Patients with major burns, defined as a burn area equal to or more than 20% of the total body surface area (TBSA) or involving the eyes or head area, are included in the list of catastrophic illnesses in the NHIRD.

2.2. Study Design

A flowchart of patient inclusion in this study is presented in Figure 1. In this study, we retrospectively identified all patients hospitalized with burns in the NHIRD in 2000–2013 with ICD-9 CM codes 940–949. To define patients with major burns, we identified patients who had been registered as having catastrophic illness within 30 days after admission, with catastrophic illness codes 948.2–948.9 (TBSA 20–29% to >90%). Patients with no registration of catastrophic illness, those with no date of birth recorded, or those who were admitted for less than 3 days were excluded from this study. The burn site was defined according to ICD-9-CM codes. An inhalation injury was defined as ICD-9CM codes 947.0, 947.1, and 947.2 [10]. The season of a patient’s hospitalization was defined as summer (May–October) or winter (November–April), with an average outdoor temperature cutoff of 24 °C.
IC was defined as a hospitalized patient with a diagnosis of ICD-9CM codes 112.5 (disseminated candidiasis), 112.81 (Candida endocarditis), or 112.83 (Candida meningitis) [11] and a prescription for systemic antifungal agents.

2.3. Statistical Analysis

We evaluated the patients’ baseline characteristics, including age, sex, dwelling area, family income, and chronic diseases, from the NHIRD data. We assessed the risk factors for IC among the patients with major burns by using odds ratios (ORs) and accompanying 95% confidence intervals (CIs) with a chi-squared test.
Data management and statistical analyses were performed using SAS 9.4 (SAS Institute, Cary, NC, USA). Statistical significance was indicated by a two-tailed p-value of <0.05.
This study was approved by the institutional review board of Taichung Veterans General Hospital (No. CE17178A-4). For privacy protection, the identities of the patients, physicians, and institutions were deidentified in accordance with the Personal Electronic Data Protection Law.

3. Results

From the NHIRD database for 2000–2013, we identified 3582 patients hospitalized with major burns of over 20% of TBSA, with an incidence of 0.9–1.8 in every 10,000 persons/year (Table 1). IC occurred in 452 patients, accounting for 12.6% of all patients hospitalized with major burns (annual incidence ranging from 6.58 to 17.31 per 100 patients), as presented in Table 2.
The characteristics of the patients included in our study are listed in Table 3. The distribution of age was notably different between patients with burns, and with and without IC (p  <  0.001); those with IC were older. Family income distributions were different between the two groups, but sex and urbanization of dwelling areas were not.
More patients with IC had inhalation injuries than did those without IC (9.1% vs. 6.5%, p = 0.048). The seasons of patient hospitalization were not significantly different between the two groups. The head and hands were the most common burn sites in the IC group, more common than in the non-IC group. More patients in the IC group had diabetes and hypertension than those in the non-IC group.
The 30-day mortality rates were 10.4% in the IC group and 10.2% in the non-IC group (p = 0.876). The 180-day mortality rates were significantly different between IC and non-IC patients (29.7% and 12.6%, p < 0.001).
In the multivariate analysis (Table 4), patients older than 50 years were associated with a higher risk of IC compared with those younger than 30 years (adjusted OR 1.96, 95% CI 1.36–2.82, p <  0.001). Male sex was associated with less IC than female sex was (adjusted OR 0.75, 95% CI 0.58–0.97, p = 0.029). Burns occurring on the head were also associated with IC (adjusted OR 1.33, 95% CI 1.02–1.73, p =  0.036). Patients with burns covering more than 30% of TBSA were also more likely to have IC compared with those with burns covering 20–29% of TBSA.

4. Discussion

Patients with burns are a high-risk group for invasive fungal infections [12], and fungal wound infection is independently associated with mortality in patients with burns [13]. Fungal wound infection also delays wound healing, causes prolonged hospitalization, and may promote scarring and contracture [7]. Indwelling medical devices, such as endotracheal tubes, mechanical devices, central venous catheters, urinary catheters, and possibly parenteral nutrition, are necessary for life support in patients with major burns, but they may be sources of IC. Antibiotics are usually prescribed for prolonged prophylaxis or treatment against bacteria and represent another risk factor for IC as an opportunistic infection [14].
In our study, the rate of IC among patients with major burns ranged from 6.58 to 17.31 per 100 hospitalized patients. According to recent reports, the incidence of IC has been increasing [15], but the rate has varied between different studies. In the study by Escrig et al. [14], the incidence of IC was between 0 and 46.3 per 1000 admissions. Zhou et al. reported an IC rate ranging from 6.06% to 17.54% in a single intensive care unit for burns [16]. Devrim et al. conducted a study of pediatric patients with burns and found an incidence of 11.5% for IC [17]. Additionally, exposure to spores at the burn scene when the patients tried to extinguish the fire increases the possibility of IC [18]. The improvement of laboratory techniques in the identification of Candida species is also related to this increasing trend [2]. The awareness and vigilance of clinicians to fungal infections could also explain a higher diagnostic rate, though this is rather difficult to measure.
The diagnosis and treatment of IC are challenging. Currently, culturing with subsequent susceptibility testing is the only diagnostic approach, but the sensitivity of this method ranges from only 21% to 71% [8,19]. Fungal infections may manifest only non-specific symptoms, and fungal cultures are time-consuming; these are some of the reasons why documenting fungal infections with cultures is difficult even when suspected [6]. Delayed antifungal administration can lead to higher mortality in hospitalization. However, prophylactic antifungal agents may lead to a higher proportion of species other than Candida albicans being present and a higher rate of reduced susceptibility [15]. The distributions of Candida species can vary with the duration of prophylaxis and the antifungal agent used for prophylaxis [19]. Other treatments including aggressive surgical debridement and catheter changes are also imperative to controlling the infection [18,20].
The risk factors vary for IC in patients with burns among different studies. Fochtmann et al. reported that female sex, gastrointestinal complications requiring surgery, non-gastrointestinal thromboembolic complications, and inhalation trauma were factors associated with proven IC [3]. According to the study by Sharma et al. [21], the incidence of fungal infection increased with age and larger TBSA involvement. In the study by Zhou et al. [16], risk factors included inhalation injury, renal dysfunction with replacement therapy, severe gastrointestinal complications, T-cell lymphopenia, and prior Candida colonization but not the percentage of TBSA. In our study, some risk factors were consistent with those of previous studies, such as female sex and larger TBSA involvement. Further studies with more patients may be necessary for more conclusive answers.
Female sex was found to be one of the risk factors for developing IC among patients with major burns in this study. Fochtmann and colleagues reported being female as one of the factors associated with candidemia (OR 5.03, 95% CI 1.25–24.9, p = 0.031) [3]. However, Zhou and colleagues reported that sex was not a significant risk factor of candidemia using multivariate logistic regression [16]. In an earlier review of patients with burns by Ha and colleagues, male sex was considered a risk factor for candidiasis (but not systemic candidiasis), with an OR of 2.4 [2]. In a report of autopsied burn patients conducted by Murray and colleagues, they found that the sex distribution was not different between patients with and without fungal infection [22].
Approximately 10–15% of asymptomatic women are colonized with Candida in their vulvovaginal areas [23]. During stress, skin and mucosa damage, urinary catheter dwelling, dysbiosis due to prolonged antibiotics use, and localized candidiasis might result in invasion candidiasis. Evidence suggested that estrogen may have an important role in Candida invasion and proliferation. Estrogens may inhibit Candida-specific human peripheral blood lymphocyte responses [24]. Estrogens also have direct effects on Candida cells with estrogen-binding proteins [25]. We propose that these could be part of the explanation for why the female sex is a risk factor for IC among patients with major burns. Nevertheless, further investigations are necessary to distinguish the role of sex differences in IC of patients with major burns.
The site of the burn injury was rarely reported or discussed in previous literature. We propose that burns involving the head indicate a more severe injury condition, which may not be reflected in TBSA. We excluded the effect of inhalation injury in the multivariate analysis; however, intubation and mechanical ventilation may be necessary in burn patients involving the head. Preexisting Candida colonization of the mucosal membranes of the nose and throat could represent a latent source of infection [26].
The mortality rate within 30 days was not significantly different between patients with burns and with and without IC; however, the mortality rate was significantly different between the two groups in 180 days. As we mentioned earlier, candidiasis acts mostly as an opportunistic infection and may not occur or be life-threatening in the early days of a burn injury. However, in long-term care, candidiasis can greatly affect patient survival. The mortality rate reported in previous literatures varied from 29% to 76% [3,11,14], but the variety could be partially explained by the different study designs (such as different definitions of major burns and exclusion criteria).
This study has some limitations. This was a retrospective database analysis study, and the patients’ physical examinations, laboratory data, Candida species, and doses of antifungal agents were unavailable in the database. We could not distinguish candidemia-related mortality from non-candidemia-related via the retrospect database. The population in this study might not have been large enough to reach significance in some of the statistical analyses.

5. Conclusions

In conclusion, our study suggests that IC in patients hospitalized with major burns is associated with risk factors including an age older than 50 years, female sex, burns on the head, and larger TBSA involvement. Identifying high-risk patients with proper antifungal prophylaxis is paramount, and our study may provide more information for clinical decision-making.

Author Contributions

Conceptualization, Y.-L.L., I.-C.C., and Y.-C.H.; methodology, W.-S.L., Y.-C.H., and C.-H.L.; software and validation, W.-S.L. and C.-H.L.; formal analysis, Y.-L.L., W.-S.L., Y.-C.H., and C.-H.L.; writing—original draft preparation, Y.-L.L. and Y.-C.H.; writing—review and editing, Y.-L.L., I.-C.C., J.-H.Y., C.-S.L., Y.-C.T., C.-T.L., and C.-Y.W.; supervision, I.-C.C. and C.-H.L.; funding acquisition, Y.-C.H. and C.-H.L. All authors have read and agreed to the published version of the manuscript.

Funding

This study was supported in part by grants from Taichung Veterans General Hospital, Taiwan (TCVGH-NHRI10703 and TCVGH-1106501A).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the institutional review board of Taichung Veterans General Hospital (No. CE17178A-4).

Informed Consent Statement

This study is based in part on data from the National Health Insurance Research Database provided by the National Health Insurance Administration, and individual patient consent was waived.

Data Availability Statement

Raw data for this work were obtained by application from the National Health Insurance Research Database, Taiwan (http://nhird.nhri.org.tw/en/index.html, accessed on 19 July 2020), and may not be shared according to the database’s rules governing use. Access to the data used in this study may be obtained by citizens of Taiwan who fulfill the requirements of conducting research projects.

Acknowledgments

This study is based in part on data from the National Health Insurance Research Database provided by the National Health Insurance Administration, Ministry of Health and Welfare and managed by National Health Research Institutes (Registered numbers 101095, 102148, and 102253). The interpretations and conclusions contained herein do not represent those of the National Health Insurance Administration, Ministry of Health and Welfare, or National Health Research Institutes. The authors thank the Healthcare Service Research Center of Taichung Veterans General Hospital for statistical support.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Flowchart of patient inclusion in this study. NHIRD, National Health Insurance Research Database; ICD-9-CM, International Classification of Diseases, Ninth Revision, Clinical Modification.
Figure 1. Flowchart of patient inclusion in this study. NHIRD, National Health Insurance Research Database; ICD-9-CM, International Classification of Diseases, Ninth Revision, Clinical Modification.
Jpm 12 00047 g001
Table 1. Annual incidence of patients hospitalized with major burns (over 20% of TBSA involved).
Table 1. Annual incidence of patients hospitalized with major burns (over 20% of TBSA involved).
YearIncidenceTotal Population at RiskAnnual Incidence
per 105/Year
FemaleMaleTotalFemaleMaleTotalFemaleMaleTotal
200046 150 196 14,109,224 14,085,347 28,194,571 0.33 1.06 0.70
200139 127 166 13,981,319 13,896,934 27,878,253 0.28 0.91 0.60
200264 191 255 13,823,504 13,711,521 27,535,025 0.46 1.39 0.93
200394 231 325 13,651,279 13,523,811 27,175,090 0.69 1.71 1.20
200486 236 322 13,526,372 13,378,291 26,904,663 0.64 1.76 1.20
200598 241 339 13,406,980 13,244,026 26,651,006 0.73 1.82 1.27
200672 228 300 13,276,737 13,103,229 26,379,966 0.54 1.74 1.14
200782 196 278 13,154,033 12,959,788 26,113,821 0.62 1.51 1.06
200872 225 297 13,034,087 12,820,600 25,854,687 0.55 1.75 1.15
200971 187 258 12,903,363 12,664,408 25,567,771 0.55 1.48 1.01
201064 165 229 12,769,325 12,510,816 25,280,141 0.50 1.32 0.91
201152 174 226 12,666,864 12,388,276 25,055,140 0.41 1.40 0.90
201256 176 232 12,558,021 12,258,413 24,816,434 0.45 1.44 0.93
201349 110 159 12,444,261 12,125,619 24,569,880 0.39 0.91 0.65
Table 2. Number and annual incidence of invasive candidiasis in patients.
Table 2. Number and annual incidence of invasive candidiasis in patients.
YearInvasive CandidiasisTotal Number of PatientsAnnual Incidence
per 100/Year
FemaleMaleTotalFemaleMaleTotalFemaleMaleTotal
20003 10 13 46 150 196 6.52 6.67 6.63
20018 10 18 39 127 166 20.51 7.87 10.84
20029 15 24 64 191 255 14.06 7.85 9.41
200316 27 43 94 231 325 17.02 11.69 13.23
200412 26 38 86 236 322 13.95 11.02 11.80
20054 27 31 98 241 339 4.08 11.20 9.14
200611 26 37 72 228 300 15.28 11.40 12.33
200712 38 50 82 196 278 14.63 19.39 17.99
200810 20 30 72 225 297 13.89 8.89 10.10
200912 28 40 71 187 258 16.90 14.97 15.50
20108 22 30 64 165 229 12.50 13.33 13.10
20119 26 35 52 174 226 17.31 14.94 15.49
20126 33 39 56 176 232 10.71 18.75 16.81
20137 17 24 49 110 159 14.29 15.45 15.09
Table 3. Characteristics of patients with major burns and with and without invasive candidiasis.
Table 3. Characteristics of patients with major burns and with and without invasive candidiasis.
CharacteristicsWithout Invasive Candidiasis (n = 3130)With Invasive Candidiasis (n = 452)Total
(n = 3582)
p-Value
n (%)n (%)n (%)
Age, mean ± SD <0.001
 <301146 (36.6)99 (21.9)1245
 30–491202 (38.4)195 (43.1)1397
 ≥50782 (25.0)158 (35)940
Sex 0.376
 Female818 (26.1)127 (28.1)945
 Male2312 (73.9)325 (71.9)2637
Urbanization 0.301
 Urban1569 (53.7)226 (56.5)1795
 Suburban432 (14.8)48 (12.0)480
 Rural919 (31.5)126 (31.5)1045
Family income (NTD) 0.002
 ≤15,840 1839 (58.8)223 (49.3)2062
 15,841–28,800 977 (31.2)173 (38.3)1150
 28,801–45,800 211 (6.7)36 (8.0)247
 >45,800 103 (3.3)20 (4.4)123
Diabetes <0.001
 No2973 (95.0)410 (90.7)3383
 Yes157 (5.0)42 (9.3)199
Hypertension 0.001
 No2812 (89.8)382 (84.5)3194
 Yes318 (10.2)70 (15.5)388
Hyperlipidemia 0.536
 No2991 (95.6)429 (94.9)3420
 Yes139 (4.4)23 (5.1)162
Burn sites
 Head1664 (53.2)292 (64.6)1956 <0.001
 Trunk2196 (70.2)326 (72.1)2522 0.393
 Upper limbs1951 (62.3)268 (59.3)2219 0.213
 Hands621 (19.8)68 (15.0)689 0.016
 Lower limbs1726 (55.1)233 (51.5)1959 0.151
 Internal organs269 (8.6)49 (10.8)318 0.117
TBSA of burn <0.001
 20–29%1423 (45.5)64 (14.2)1487
 30–39%676 (21.6)66 (14.6)742
 40–49%398 (12.7)82 (18.1)480
 50–59%187 (6.0)62 (13.7)249
 60–69%125 (4.0)57 (12.6)182
 70–79%106 (3.4)50 (11.1)156
 80–89%94 (3.0)37 (8.2)131
 90% or more121 (3.9)34 (7.5)155
Inhalation injury 0.048
 No2925 (93.5)411 (90.9)3336
 Yes205 (6.5)41 (9.1)246
Season 0.675
 Winter 1449 (46.3)214 (47.3)1663
 Summer 1681 (53.7)238 (52.7)1919
Mortality
 In 30 days318 (10.2)47 (10.4)3650.876
 In 180 days404 (12.6)134 (29.7)538<0.001
Table 4. Multivariate analysis of factors associated with invasive candidiasis.
Table 4. Multivariate analysis of factors associated with invasive candidiasis.
VariablesMultivariatep-Value
Adjusted OR (95%CI)
Age, mean ± SD
 <301.00 (ref)
 30–491.34 (0.97–1.84)0.074
 ≥501.96 (1.36–2.82)<0.001
Gender
 Female1.00 (ref)
 Male0.75 (0.58–0.97)0.029
Urbanization
 Urban1.00 (ref)
 Suburban0.89 (0.63–1.27)0.517
 Rural1.03 (0.80–1.32)0.838
Family income (NTD)
 ≤15,840 TWD1.00 (ref)
 15,841–28,800 TWD0.98 (0.74–1.29)0.865
 28,801–45,800 TWD1.19 (0.76–1.85)0.446
 >45,800 TWD1.13 (0.64–2.01)0.674
Diabetes 1.59 (0.99–2.54)0.053
Hypertension1.17 (0.80–1.71)0.421
Hyperlipidemia0.81 (0.47–1.41)0.456
Burn sites
 Head1.33 (1.02–1.73)0.036
 Trunk0.79 (0.60–1.05)0.103
 Upper limbs0.83 (0.64–1.07)0.149
 Hands0.80 (0.59–1.09)0.154
 Lower limbs0.88 (0.69–1.12)0.301
 Internal organs0.89 (0.40–1.98)0.776
TBSA of burn
 TBSA 20–29%1.00 (ref)
 TBSA 30–39%2.41 (1.63–3.57)<0.001
 TBSA 40–49%4.81 (3.28–7.05)<0.001
 TBSA 50–59%8.51 (5.63–12.84)<0.001
 TBSA 60–69%11.59 (7.45–18.05)<0.001
 TBSA 70–79%14.02 (8.83–22.25)<0.001
 TBSA 80–89%12.06 (7.28–19.97)<0.001
 TBSA 90% or more6.91 (4.04–11.82)<0.001
Inhalation injury
 No1.00 (ref)
 Yes1.16 (0.48–2.76)0.744
Season
 Winter 1.00 (ref)
 Summer 0.83 (0.66–1.04)0.111
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MDPI and ACS Style

Lin, Y.-L.; Chen, I.-C.; Yen, J.-H.; Lai, C.-S.; Tsai, Y.-C.; Lu, C.-T.; Wu, C.-Y.; Lin, W.-S.; Lin, C.-H.; Huang, Y.-C. Invasive Candidiasis in Hospitalized Patients with Major Burns. J. Pers. Med. 2022, 12, 47. https://doi.org/10.3390/jpm12010047

AMA Style

Lin Y-L, Chen I-C, Yen J-H, Lai C-S, Tsai Y-C, Lu C-T, Wu C-Y, Lin W-S, Lin C-H, Huang Y-C. Invasive Candidiasis in Hospitalized Patients with Major Burns. Journal of Personalized Medicine. 2022; 12(1):47. https://doi.org/10.3390/jpm12010047

Chicago/Turabian Style

Lin, Yi-Ling, I-Chen Chen, Jung-Hsing Yen, Chih-Sheng Lai, Yueh-Chi Tsai, Chun-Te Lu, Cheng-Yeu Wu, Wei-Szu Lin, Ching-Heng Lin, and Yung-Chieh Huang. 2022. "Invasive Candidiasis in Hospitalized Patients with Major Burns" Journal of Personalized Medicine 12, no. 1: 47. https://doi.org/10.3390/jpm12010047

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