Examination of Socio-demographic, Clinical and Laboratory Findings of Patients Hospitalized in Our Clinic with the Diagnosis of Rotavirus Gastroenteritis
PDF
Cite
Share
Request
Original Research
P: 80-86
June 2024

Examination of Socio-demographic, Clinical and Laboratory Findings of Patients Hospitalized in Our Clinic with the Diagnosis of Rotavirus Gastroenteritis

Bagcilar Med Bull 2024;9(2):80-86
1. University of Health Sciences Turkey Kartal Dr. Lütfi Kırdar City Hospital, Clinic of Pediatrics, İstanbul, Turkey
2. İstanbul Yeni Yüzyıl University Faculty of Medicine Department of Pediatrics, İstanbul, Turkey
3. University of Health Sciences Turkey Prof. Dr. Cemil Taşcıoğlu City Hospital, Clinic of Pediatrics, İstanbul, Turkey
No information available.
No information available
Received Date: 06.11.2023
Accepted Date: 11.03.2024
PDF
Cite
Share
Request

Abstract

Objective

Nowadays, viruses are the leading cause of acute gastroenteritis, while Rotavirus (RV) is the most common cause of acute viral gastroenteritis. In this study, the RV antigen positive diagnosis of gastroenteritis patients hospitalized in the pediatric service of the socio-demographic, clinical and laboratory features was aimed to be interpreted by comparison with literature data.

Method

Socio-demographic data of patients hospitalized with the diagnosis of RV gastroenteritis, clinical and laboratory findings were retrospectively evaluated the hospital’s file was obtained from the records.

Results

The study of children hospitalized with acute gastroenteritis caused a mean age of 17.68 months from 740 patients who were enrolled, and 270 patients who were positive for RV and RV ratio was found to be 36%. Although the cases were most frequently seen in the spring, the most common months were February, March and April. The most frequent application causes were diarrhea and vomiting and the most common age group was the age group of 6 months-2 years of age. Five patients developed complications were detected. Laboratory findings in 101 patients with C-reactive protein positive (37.4%), 213 patients (78.8%) serum aspartate aminotransferase levels were high, in 94 patients (34.8%) had elevated alanine aminotransferase levels.

Conclusion

Most cases of gastroenteritis were admitted to the service accounted for RV diarrhea and especially important cause of diarrhea is seen in winter and spring seasons. Therefore, the RV detection in cases of gastroenteritis is important to predict patient’s clinic and prevent unnecessary use of antibiotics.

Keywords:
Child, gastroenteritis, Rotavirus

Introduction

Rotavirus (RV) continues to be a significant viral pathogen, constituting a serious global health issue and leading to child deaths worldwide (1, 2). Among viral agents causing acute gastroenteritis, RV is the most prevalent, with adenovirus being the second (3). Epidemiological data indicates that RV infections are the second leading cause of child deaths. In 2013, approximately 215,000 children worldwide died from RV-related diarrhea, with the majority of these deaths occurring in low-income countries (4). Epidemiological studies reveal that RV infections exhibit seasonal variations worldwide, often peaking during the winter months (5, 6).

RV infections, particularly in developing countries, prominently contribute to acute diarrhea in children under the age of 2 and are recognized as a leading cause of dehydration due to acute diarrhea (7, 8). A notable characteristic of RV diarrhea is the high rate of hospitalization associated with it (9). Globally, 40% of hospitalizations for severe diarrhea in young children are attributed to RV infections (10). While it is known to be associated with high mortality rates in developing countries, in developed nations, it is linked to high disease rates and economic burden (3).

This study aims to retrospectively analyze the socio-demographic, clinical, and laboratory characteristics of patients diagnosed with RV antigen-positive gastroenteritis who were admitted to the pediatric department over a 2-year period. The goal is to compare the results with existing literature and previous studies.

Materials and Methods

At the University of Health Sciences Turkey, Prof. Dr. Cemil Taşcıoğlu City Hospital, the medical records of 270 patients who were hospitalized for RV gastroenteritis diagnosis during a 2 year period (01.01.2012-31.12.2013) were retrospectively analyzed. The diagnosis of RV gastroenteritis was established using the qualitative immunochromatographic method (Simple/Stick Rota Adeno Operon, Spain) on fecal samples. Furthermore, bacterial agents such as Vibrio cholerae, Salmonella, Shigella, Campylobacter, Yersinia enterocolitica, etc., and parasitic agents were examined using standard microbiological methods. The patients who exhibited bloody findings in the macroscopic examination of fecal samples, showed the presence of parasites in laboratory analysis, and had bacterial growth detected in fecal cultures were excluded from the study. The patients were categorized into three groups based on their age: 0-6 months, 6-24 months, and over 24 months. The socio-demographic characteristics, clinical features, and laboratory findings of the patients were compared. The study was conducted in accordance with the principles of the Helsinki Declaration and received approval from the Ethics Committee of University of Health Sciences Turkey, Prof. Dr. Cemil Taşcıoğlu City Hospital with decision number 177 on February 25, 2014. The study was derived from the thesis titled “inpatients to our clinic with the diagnosis of RV gastroenteritis and socio-demographic, clinical and laboratory findings investigation”.

Statistical Analysis

In the evaluation of data obtained in the study, statistical analysis was performed using SPSS (Statistical Package for Social Sciences) version 15.0 and Graph Pad InStat demo version. In addition to descriptive statistical methods (such as mean, standard deviation, minimum, maximum), in the analyses comparing groups, categorical variables were assessed using the chi-square test and Fisher’s Exact test. For comparisons between two groups, Student’s t-test and Mann-Whitney U test were employed, while One-Way ANOVA (Analysis of Variance) was used for comparisons among three groups, followed by post-hoc Tukey test for pairwise comparisons and Kruskal-Wallis test followed by Dunn’s test. Pearson correlation test was used for assessing correlations. Results were evaluated at a significance level of p<0.05 with a confidence interval of 95% (*p<0.05, p<0.01, *p<0.001).

Results

In the study, 270 out of 740 patients who were admitted to the Pediatric Clinic of University of Health Sciences Turkey, Prof. Dr. Cemil Taşcıoğlu City Hospital, with complaints of acute diarrhea were included, and they were diagnosed with RV gastroenteritis (36.5%). The ages of the patients ranged from 1 month to 116 months, with 58.9% (n=159) being male and 41.1% (n=111) female. Regarding the presenting complaints, 64.8% (n=175) had diarrhea and vomiting, 18.1% (n=49) had diarrhea, vomiting, and fever, 9.6% (n=26) had only diarrhea, 7% (n=19) had diarrhea and fever, and 0.4% (n=1) had only vomiting. During the follow-up of hospitalized patients, 48.5% (n=131) had a temperature below 37.5 °C, 25.9% (n=70) had a temperature between 38-39 °C, 22.6% (n=61) had a temperature between 37.5-38 °C, and 3% (n=8) had a temperature above 39 °C (Table 1).

When examining the seasonal distribution of cases, 35.9% (n=97) were observed in spring, 31.1% (n=84) in winter, 18.1% (n=49) in autumn, and 14.8% (n=40) in summer (Figure 1). By monthly distribution, cases were as follows: 13.3% (n=36) in February-March-April, 12.2% (n=33) in January, 9.3% (n=25) in May-October, 8.1% (n=22) in June, 5.6% (n=15) in December, 4.8% (n=13) in November, 4.1% (n=11) in September, and 3.3% (n=9) in July-August (Figure 2). Among the patients, 62.6% (n=169) had negative C-reactive protein (CRP), while 37.4% (n=101) had positive CRP.

Regarding the biochemical values of the patients, the average urea level was 27.66±13.86 mg/dL (ranging from 3 to 92, median: 26), the average creatinine level was 0.30±0.13 mg/dL (ranging from 0.05 to 0.86, median: 0.28), the average sodium level was 136.14±4.11 mmol/L (ranging from 125 to 154, median: 136), the average potassium level was 4.29±0.57 mmol/L (ranging from 2.60 to 6.10, median: 4.20), the average aspartate aminotransferase (AST) level was 55.46±30.40 IU/L (ranging from 20 to 323, median: 48), and the average alanine aminotransferase (ALT) level was 35.84±30.93 IU/L (ranging from 6 to 366, median: 29). Among the patients, 78.8% (n=213) had elevated serum AST levels, and 34.8% (n=94) had ALT levels above the upper limit of normal (Table 2).

In those aged below 6 months, the complaint of vomiting was significantly lower compared to those aged 6-24 months and those above 24 months (p<0.001). Among those aged over 24 months, the rate of having a fever below 37.5 °C was significantly lower compared to the other two age groups (p=0.034, p<0.05). Among those aged over 24 months, the length of hospital stay was significantly shorter compared to the other two age groups (p=0.003).

Discussion

RV infection is a leading cause of diarrhea-related morbidity and mortality globally among children under the age of 5 (11). Each year, RV gastroenteritis leads to the hospitalization of 2 million children and causes an average of 440,000 child deaths (12). Research related to etiology is of importance for diagnosis, treatment, and prognosis, as identifying viral agents can help prevent unnecessary antibiotic use.

In our study, the prevalence of RV among patients hospitalized for gastroenteritis was 36.5%. When looking at studies abroad, a study in Spain from 2001 to 2005 found a prevalence of 17.1% in children under 5 years of age hospitalized with gastroenteritis (13). In India, a study of children under 5 years hospitalized from 2009 to 2011 found a RV frequency of 35.9% (14). When we look at our country, in a study conducted by Ilktac et al. (15) in Istanbul between 2006-2010, 11711 cases of acute gastroenteritis were examined, and the prevalence of RV was found to be 15.5%. In a study conducted by Konca et al. (16) between March 2012 and February 2013, they determined the prevalence of RV to be 16.5%. In Turkey, studies in different cities and periods, predominantly focusing on the age group of 0-5 years, have reported significantly different RV positivity rates. In our study, which included only hospitalized children, the RV positivity rate was higher at 36.5%.

Although the cause is not known, the seasonal nature of RV diarrhea is well established (2). In temperate climates, RV peaks during the winter months (17). In our study, the seasonal distribution showed that RV gastroenteritis cases were observed in 35.9% in spring, 14.8% in summer, 18.1% in autumn, and 31.1% in winter. The months with the highest incidence of RV diarrhea were February (13.3%), March (13.3%), and April (13.3%), followed by January (12.2%) and May (9.3%), October (9.3%). A multicenter prospective study in Europe conducted in 2004-2005 similarly found that diarrheal cases occurred most frequently between October and May, with a peak in January to March (18). Studies in Spain also found a higher incidence during the winter months (13). Carneiro et al. (19) conducted a study involving 218 cases of children aged 0-19 years who were hospitalized in Brazil due to severe RV infections. In their research, they examined the clinical and epidemiological findings of these cases. They found that RV-positive cases were most commonly observed in the months of June and July (19). In contrast to many other studies, the reason for the high prevalence of RV gastroenteritis during the summer months in this study was attributed to the unique tropical climate in Brazil. Unlike in other countries where RV is more frequently detected during rainy seasons in winter, in Brazil, it is observed during the summer months due to the specific characteristics of the climate (19).

When examining the clinical features of RV diarrheas, fever, diarrhea, and vomiting are the most common symptoms, either alone or in combination (20). In our study, the most common complaint was diarrhea-vomiting (73.4%), followed by diarrhea-vomiting-fever (16.6%). Only 7.4% of patients presented with diarrhea alone. This may indicate that families are more concerned about vomiting. Additionally, patients under 6 months of age had a significantly lower rate of vomiting as their presenting complaint compared to those aged 6-24 months and over 24 months (p<0.001). This observation is consistent with the literature, which suggests that milder infections in the first 6 months are related to transplacental transfer of maternal antibodies and breastfeeding (21). In our study, it was found that the hospital stay was significantly shorter in individuals aged over 24 months compared to the other age groups of 0-6 and 6-24 months. The shorter hospital stay after 24 months of age can be attributed to the natural course of previously experienced infections, which reduces the incidence and severity of subsequent episodes.

After RV infections, viremia can lead to extraintestinal involvement (22). In Taiwan, a study conducted by Wu et al. (23) comparing the clinical characteristics of RV and norovirus gastroenteritis found that AST and ALT levels were higher in cases of RV gastroenteritis. Similarly, in studies by Akelma et al. (24), which covered the years 2005 to 2012 and included 272 patients with confirmed RV infection, it was reported that 42% (15.4%) of the patients had elevated ALT levels, and 69% (25.4%) had elevated AST levels. In our study, 78.8% of the 270 patients had elevated serum AST levels, with an average AST level of 55 IU/L (range: 20-323 IU/L). Serum ALT levels were elevated in 34.8% of the cases, with an average ALT level of 36 IU/L (range: 6-366 IU/L).

Kang et al. (25) retrospectively examined 755 patients with RV infections between 1999 and 2011 and identified 17 patients (2.2%) with febrile seizures and 42 patients (5.5%) with afebrile seizures. In a retrospective study by Hung et al. (26) covering a 10-year period and including 1937 patients with RV gastroenteritis, 40 patients (2.06%) were observed to have afebrile seizures. In our study, convulsions were observed in 2 patients, constituting 0.7% of all patients. In a study conducted by Scheier and Aviner (27) which included 632 patients hospitalized for RV gastroenteritis between May 1999 and May 2010, sepsis was detected in 2 patients (0.32%). In a study by Gözmen et al. (28), among 376 cases of RV gastroenteritis, bacteremia was found in 5 patients (1.3%). In our study, sepsis was observed in 2 patients, constituting 0.7% of all patients.

Study Limitations

The single-center and retrospective nature of our study are limitations. Additionally, the fact that the vaccination status of patients regarding RV was not queried constitutes another limitation of our study. We believe that conducting multi-center, prospective studies would contribute significantly to the understanding of the topic.

Conclusion

The detection of RV, the most common cause of diarrhea in children, is crucial not only for understanding the causative agent but also for predicting the patient’s clinical condition and determining the appropriate treatment approach. Additionally, it plays a significant role in contributing to epidemiological knowledge. Identifying the causative agent can help prevent unnecessary antibiotic use and promote the expansion of vaccination programs that have been reintroduced.

Providing the appropriate approach to childhood diarrhea and evaluating the potential benefits of RV vaccines require each country to have its own data. Therefore, in Turkey as well, there is a need to determine the estimated rates of RV diarrhea and the clinical and epidemiological characteristics of the disease. This information is vital for healthcare decision-makers and public health officials to make informed choices regarding prevention and control strategies.

References

1
Tavakoli Nick S, Mohebbi SR, Ghaemi A, Hosseini SM. Human rotavirus in Iran; molecular epidemiology, genetic diversity and recent updates on vaccine advances. Gastroenterol Hepatol Bed Bench 2019;12(2):98-109.
2
Omatola CA, Olaniran AO. Rotaviruses: From Pathogenesis to Disease Control-A Critical Review. Viruses 2022;14(5):875.
3
Şay Coşkun US, Kasap T. Frequency of rotavirus and adenovirus in pediatric patients with acute gastroenteritis. J Contemp Med 2019;9(1):85-88.
4
Girish Kumar CP, Giri S, Chawla-Sarkar M, Gopalkrishna V, Chitambar SD, Ray P, et al. Epidemiology of rotavirus diarrhea among children less than 5 years hospitalized with acute gastroenteritis prior to rotavirus vaccine introduction in India. Vaccine 2020;38(51):8154-8160.
5
Asare EO, Al-Mamun MA, Sarmin M, Faruque ASG, Ahmed T, Pitzer VE. The influence of demographic and meteorological factors on temporal patterns of rotavirus infection in Dhaka, Bangladesh. Proc Biol Sci 2022;289(1976):20212727.
6
Wang LP, Zhou SX, Wang X, Lu QB, Shi LS, Ren X, et al. Etiological, epidemiological, and clinical features of acute diarrhea in China. Nat Commun 2021;12(1):2464.
7
Steele AD, Victor JC, Carey ME, Tate JE, Atherly DE, Pecenka C, et al. Experiences with rotavirus vaccines: can we improve rotavirus vaccine impact in developing countries?. Hum Vaccin Immunother 2019;15(6):1215-1227.
8
Ardura-Garcia C, Kreis C, Rakic M, Jaboyedoff M, Mallet MC, Low N, et al. Rotavirus disease and health care utilisation among children under 5 years of age in highly developed countries: A systematic review and meta-analysis. Vaccine 2021;39(22):2917-2928.
9
Zaraket R, Salami A, Bahmad M, Roz AE, Khalaf B, Ghssein G, et al. Prevalence, risk factors, and clinical characteristics of rotavirus and adenovirus among Lebanese hospitalized children with acute gastroenteritis. Heliyon 2020;6(6):e04248.
10
Burnett E, Parashar UD, Tate JE. Global Impact of Rotavirus Vaccination on Diarrhea Hospitalizations and Deaths Among Children <5 Years Old: 2006-2019. J Infect Dis 2020;222(10):1731-1739.
11
Troeger C, Khalil IA, Rao PC, Cao S, Blacker BF, Ahmed T, et al. Rotavirus Vaccination and the Global Burden of Rotavirus Diarrhea Among Children Younger Than 5 Years. JAMA Pediatr 2018;172(10):958-965. Erratum in: JAMA Pediatr 2022;176(2):208.
12
Parashar UD, Gibson CJ, Bresee JS, Glass RI. Rotavirus and severe childhood diarrhea. Emerg Infect Dis 2006;12(2):304-306.
13
López-de-Andrés A, Jiménez-García R, Carrasco-Garrido P, Alvaro-Meca A, Galarza PG, de Miguel AG. Hospitalizations associated with rotavirus gastroenteritis in Spain, 2001-2005. BMC Public Health 2008;8:109.
14
Mathew MA, Paulose A, Chitralekha S, Nair MK, Kang G, Kilgore P. Prevalence of rotavirus diarrhea among hospitalized under-five children. Indian Pediatr 2014;51(1):27-31.
15
Ilktac M, Sahin A, Nazik H, Ongen B. Investigation of Rotavirus Frequency and Following up the Rotavirus Season among Children with Acute Gastroenteritis: Evaluation of Five-year Results. ANKEM Dergisi 2012;26(1):25-29.
16
Konca Ç, Tekin M, Akgün S, Bülbül M, Çoban M, Kahramaner Z, et al. Prevalence of rotavirus in children with acute gastroenteritis, seasonal distribution, and laboratory findings in the southeast of Turkey. J. Pediatr Inf 2014;8:7-11.
17
17. Ureña-Castro K, Ávila S, Gutierrez M, Naumova EN, Ulloa-Gutierrez R, Mora-Guevara A. Seasonality of Rotavirus Hospitalizations at Costa Rica's National Children's Hospital in 2010-2015. Int J Environ Res Public Health 2019;16(13):2321.
18
Van Damme P, Giaquinto C, Huet F, Gothefors L, Maxwell M, Van der Wielen M, et al. Multicenter prospective study of the burden of rotavirus acute gastroenteritis in Europe, 2004-2005: the REVEAL study. J Infect Dis 2007;195(Suppl 1):S4-S16.
19
Carneiro NB, Diniz-Santos DR, Fagundes SQ, Neves LL, Reges RMB, Lima EKP, et al. Clinical and epidemiological aspects of children hospitalized with severe rotavirus-associated gastroenteritis in Salvador, BA, Brazil. Braz J Infect Dis 2005;9(6):525-528.
20
Staat MA, Azimi PH, Berke T, Roberts N, Bernstein DI, Ward RL, et al. Clinical presentations of rotavirus infection among hospitalized children. Pediatr Infect Dis J 2002;21(3):221-227.
21
Clark HF, Offit PA, Glass RI, Ward RL. Rotavirus. In: Plotkin SA, Orenstein WA Eds. Vaccines. 4th edition. Elsevier, Philadelphia. 2004:1327-1345.
22
Chiappini E, Azzari C, Moriondo M, Galli L, de Martino M. Viraemia is a common finding in immunocompetent children with rotavirus infection. J Med Virol 2005;76(2):265-267.
23
Wu TC, Liu HH, Chen YJ, Tang RB, Hwang BT, Yuan HC. Comparison of clinical features of childhood norovirus and rotavirus gastroenteritis in Taiwan. J Chin Med Assoc 2008;71(11):566-570.
24
Akelma AZ, Kütükoğlu I, Köksal T, Cizmeci MN, Kanburoğlu MK, Catal F, et al. Serum transaminase elevation in children with rotavirus gastroenteritis: seven years' experience. Scand J Infect Dis 2013;45(5):362-367.
25
Kang B, Kim DH, Hong YJ, Son BK, Kim DW, Kwon YS. Comparison between febrile and afebrile seizures associated with mild rotavirus gastroenteritis. Seizure 2013;22(7):560-564.
26
Hung JJ, Wen HY, Yen MH, Chen HW, Yan DC, Lin KL, et al. Rotavirus gastroenteritis associated with afebrile convulsion in children: clinical analysis of 40 cases. Chang Gung Med J 2003;26(9):654-659.
27
Scheier E, Aviner S. Septicemia following rotavirus gastroenteritis. Isr Med Assoc J 2013;15(3):166-169.
28
Gözmen S, Sükran Gözmen K, Apa H, Aktürk H, Sorguç Y, Bayram N, et al. Secondary bacteremia in rotavirus gastroenteritis. Pediatr Infect Dis J 2014;33(7):775-777.