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Journal articles on the topic 'Viral gastroenteritis'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 March 2023

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1

Montgomery, John R., Kathleen Throckmorton, and Larry K. Pickering. "Viral Gastroenteritis." Primary Care: Clinics in Office Practice 15, no. 1 (March 1988): 43–62. http://dx.doi.org/10.1016/s0095-4543(21)01057-5.

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2

Hart, C. Anthony, and Nigel A. Cunliffe. "Viral gastroenteritis." Current Opinion in Infectious Diseases 10, no. 5 (October 1997): 408–13. http://dx.doi.org/10.1097/00001432-199710000-00016.

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3

Desselberger, Ulrich. "Viral gastroenteritis." Current Opinion in Infectious Diseases 11, no. 5 (October 1998): 565–76. http://dx.doi.org/10.1097/00001432-199810000-00008.

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4

Hart, C. Anthony, and Nigel A. Cunliffe. "Viral gastroenteritis." Current Opinion in Infectious Diseases 12, no. 5 (October 1999): 447–57. http://dx.doi.org/10.1097/00001432-199910000-00007.

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5

Desselberger, Ulrich, and Jim Gray. "Viral Gastroenteritis." Medicine 29, no. 2 (2001): 68–72. http://dx.doi.org/10.1383/medc.29.2.68.27522.

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6

Desselberger, Ulrich, and Jim Gray. "Viral gastroenteritis." Medicine 33, no. 4 (April 2005): 78–81. http://dx.doi.org/10.1383/medc.33.4.78.64361.

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7

Desselberger, Ulrich, and Jim Gray. "Viral gastroenteritis." Medicine 37, no. 11 (November 2009): 594–98. http://dx.doi.org/10.1016/j.mpmed.2009.08.005.

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8

Desselberger, Ulrich, and Jim Gray. "Viral gastroenteritis." Medicine 41, no. 12 (December 2013): 700–704. http://dx.doi.org/10.1016/j.mpmed.2013.09.009.

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9

Desselberger, Ulrich. "Viral gastroenteritis." Medicine 45, no. 11 (November 2017): 690–94. http://dx.doi.org/10.1016/j.mpmed.2017.08.005.

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10

Bányai, Krisztián, Mary K. Estes, Vito Martella, and Umesh D. Parashar. "Viral gastroenteritis." Lancet 392, no. 10142 (July 2018): 175–86. http://dx.doi.org/10.1016/s0140-6736(18)31128-0.

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11

Blacklow, Neil R., and Harry B. Greenberg. "Viral Gastroenteritis." New England Journal of Medicine 325, no. 4 (July 25, 1991): 252–64. http://dx.doi.org/10.1056/nejm199107253250406.

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12

Burns, John W., and Harry B. Greenberg. "Viral Gastroenteritis." Infectious Diseases in Clinical Practice 3, no. 6 (November 1994): 411–17. http://dx.doi.org/10.1097/00019048-199411000-00002.

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13

Desselberger, Ulrich. "Viral Gastroenteritis *." Infectious Diseases in Clinical Practice 10, no. 3 (March 2001): 149–60. http://dx.doi.org/10.1097/00019048-200103000-00007.

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14

Kapikian, A. Z. "Viral gastroenteritis." JAMA: The Journal of the American Medical Association 269, no. 5 (February 3, 1993): 627–30. http://dx.doi.org/10.1001/jama.269.5.627.

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15

Kapikian, Albert Z. "Viral Gastroenteritis." JAMA: The Journal of the American Medical Association 269, no. 5 (February 3, 1993): 627. http://dx.doi.org/10.1001/jama.1993.03500050105035.

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16

Herrmann, John E. "Viral gastroenteritis." Clinical Microbiology Newsletter 11, no. 9 (May 1989): 65–68. http://dx.doi.org/10.1016/0196-4399(89)90063-9.

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17

Torpy, Janet M., Cassio Lynm, and Robert M. Golub. "Viral Gastroenteritis." JAMA 308, no. 5 (August 1, 2012): 528. http://dx.doi.org/10.1001/jama.2012.6213.

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18

Christensen, M. L. "Human viral gastroenteritis." Clinical Microbiology Reviews 2, no. 1 (January 1989): 51–89. http://dx.doi.org/10.1128/cmr.2.1.51.

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During the last 15 years, several different groups of fastidious viruses that are responsible for a large proportion of acute viral gastroenteritis cases have been discovered by the electron microscopic examination of stool specimens. This disease is one of the most prevalent and serious clinical syndromes seen around the world, especially in children. Rotaviruses, in the family Reoviridae, and fastidious fecal adenoviruses account for much of the viral gastroenteritis in infants and young children, whereas the small caliciviruses and unclassified astroviruses, and possibly enteric coronaviruses, are responsible for significantly fewer cases overall. In addition to electron microscopy, enzyme immunoassays and other rapid antigen detection systems have been developed to detect rotaviruses and fastidious fecal adenoviruses in the stool specimens of both nonhospitalized patients and those hospitalized for dehydration and electrolyte imbalance. Experimental rotavirus vaccines have also been developed, due to the prevalence and seriousness of rotavirus infection. The small, unclassified Norwalk virus and morphologically similar viruses are responsible for large and small outbreaks of acute gastroenteritis in older children, adolescents, and adults. Hospitalization of older patients infected with these viruses is usually not required, and their laboratory diagnoses have been limited primarily to research laboratories.

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19

Christensen, M. L. "Human viral gastroenteritis." Clinical Microbiology Reviews 2, no. 1 (1989): 51–89. http://dx.doi.org/10.1128/cmr.2.1.51-89.1989.

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20

Williams, Fred P., and Elmer W. Akin. "Waterborne Viral Gastroenteritis." Journal - American Water Works Association 78, no. 1 (January 1986): 34–39. http://dx.doi.org/10.1002/j.1551-8833.1986.tb05674.x.

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21

J. Eckardt, Alexander, and Daniel C. Baumgart. "Viral Gastroenteritis in Adults." Recent Patents on Anti-Infective Drug Discovery 6, no. 1 (January 1, 2011): 54–63. http://dx.doi.org/10.2174/157489111794407877.

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22

Dennehy, Penelope H. "Viral Gastroenteritis in Children." Pediatric Infectious Disease Journal 30, no. 1 (January 2011): 63–64. http://dx.doi.org/10.1097/inf.0b013e3182059102.

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23

Palmer, S. R. "VIRAL GASTROENTERITIS IN FOODHANDLERS." Lancet 332, no. 8622 (November 1988): 1247. http://dx.doi.org/10.1016/s0140-6736(88)90832-x.

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24

Reid, J. A. "Norwalk-like viral gastroenteritis." Biomedicine & Pharmacotherapy 43, no. 4 (January 1989): 320. http://dx.doi.org/10.1016/0753-3322(89)90018-8.

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25

Uhnoo, Ingrid, Elisabeth Olding-Stenkvist, and Goran Wadell. "Update of Viral Gastroenteritis." Digestive Diseases 6, no. 2 (1988): 102–16. http://dx.doi.org/10.1159/000171189.

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26

Uhnoo, Ungrid. "Developments in viral gastroenteritis." Clinical Biochemistry 28, no. 3 (June 1995): 348. http://dx.doi.org/10.1016/0009-9120(95)91424-2.

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27

Plata-Nazar, Katarzyna, Grazyna Luczak, Magdalena Gora-Gebka, Anna Liberek, and Barbara Kaminska. "Serum Neopterin Concentration in Children with Viral Gastroenteritis." Pteridines 21, no. 1 (February 2010): 11–16. http://dx.doi.org/10.1515/pteridines.2010.21.1.11.

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Abstract Increased neopterin concentrations are observed in many diseases in which cellular immunity is stimulated. Gastroenteritis is still a major cause of childhood morbidity and mortality worldwide. Over 75% of all cases are caused by viral infections. Therefore a non-specific, quick, sensitive, cheap and easy-to-perform marker of viral infection, such as neopterin concentration in serum, would be a cost-effective method of identifying patients with gastroenteritis into probable viral etiology and therefore it would optimize treatment and reduce inappropriate antibiotic treatment. This study evaluated whether serum neopterin concentration can be a reliable marker of viral etiology of gastroenteritis in children. The study group consisted of 67 children: 29 girls and 38 boys, aged from 0.1 to 16.1 years with symptoms of gastroenterits and with confirmed rotavirus or adenovirus infection; the control group consisted of 105 healthy children. Clinical examinations and laboratory test including whole blood count, serum C-reactive protein, procalcitonin, and creatinine concentration were conducted. The serum neopterin level was analyzed by Elisa. Serum neopterin concentration in the study group varied from 6.03 to 171 nmol/L (median 23.7 nmol/L) and it was significantly higher than in the control group (from 2.88 to 14.8 nmol/L; median 4.73 nmol/L) (P <0.001). Neopterin concentration was above the normal value (>11 nmol/L) in 58 children from the study group and only in 6 from the control group (86.6% sensitivity and 94.3% specificity). Serum neopterin concentration did not differ significantly between children with rotavirus and adenovirus infection (P = 0.47). The correlation between serum neopterin and C-reactive protein concentrations was of borderline significance (rs = 0.23, p = 0.06); and there was no correlation between serum concentrations of neopterin and procalcitonin, white blood count, lymphocytes count, monocytes count or the body temperature. Serum neopterin concentration is highly increased in children suffering from viral gastroenteritis, regardless of the virus type. When a cut-off of 11.0 nmol/L neopterin was applied, comparison yields 86.6% sensitivity and 94.3% specificity for the diagnosis of viral gastroenteritis in pediatric patients. Further studies are necessary for other etiological agents of gastroenteritis.

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28

Hicks, M. John, James P. Barrish, Elizabeth S. Hayes, Laurie C. Leer, Mary K. Estes, and W. D. Cubitt. "A Rapid Method for Viral Particle Detection in Viral-Induced Gastroenteritis: A TEM Study." Microscopy and Microanalysis 1, no. 5 (October 1995): 185–89. http://dx.doi.org/10.1017/s143192769511185x.

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Infectious gastroenteritis is a common cause of hospitalization in the pediatric population. The most frequent cause of gastroenteritis is viral in origin. The purpose of this study was to compare a rapid modified negative-staining TEM method with the conventional pseudoreplica technique in detection of viral particles in fecal samples from children with viral gastroenteritis. The modified negative-staining method resulted in a significantly higher (2.5 ± 0.5, p = 0.02) viral rating score than that for the conventional pseudoreplica technique (1.7 ± 0.4). In addition, the preparation time for the negative-staining method was approximately one fifth that for the conventional pseudoreplica technique. Rapid diagnosis of viral gastroenteritis may be made by ultrastructural detection of viral particles in fecal samples using the negative staining technique.

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29

Mojahed, Nooshin, Mohammad Ali Mohammadkhani, Masoumeh Pourasgari, Golnosh Gol-Jah Rad, and Ashraf Mohamadkhani. "Viral Gastroenteritis Prevalence in Iranian Pediatric Population: A Systematic Review." Avicenna Journal of Clinical Microbiology and Infection 9, no. 3 (September 29, 2022): 124–29. http://dx.doi.org/10.34172/ajcmi.2022.3389.

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Background: Viral gastroenteritis infection, a prevalent condition in adolescents and children, is still a rigid and serious problem among humans. This disease is responsible for up to three million fatalities nationwide. noroviruses, rotaviruses, astroviruses, adenoviruses, and sapoviruses are the most common and well-known pathogens associated with viral gastroenteritis agents. In this systematic review, we extracted all original articles and data on viral gastroenteritis that were performed on the Iranian pediatric population. Methods: To investigate the viral agent pathogens of gastroenteritis in Iran, 48 articles on the identification of viral gastroenteritis were gathered from the existing data. Viral gastroenteritis was detected in fourteen provinces, including the southern and northern parts of Iran. The seasonal distribution in Iran was analyzed as well. Finally, all the data from 1978-2021, along with their detailed information, were summarized, including the number of patients, the number of positive cases, applied technics, and the region of the studied cases in Iran. Results: Based on the results, most of the viral detection was associated with Rotavirus, the major pathogen responsible for gastroenteritis disease, followed by Adenovirus, Norovirus, Parechovirus, Bocavirus, Astrovirus, Aichivirus, Sapovirus, and three case reports of SARS-CoV-2 that were associated with viral gastroenteritis. Conclusion: Different studies conducted over Iran, including the northern, southern, and central regions, were obtained based on the data. Most studies had been merely dedicated to rotavirus, which had the highest prevalence of all other viral gastroenteritis. Our review clearly demonstrated that Rotavirus genotype G1P [8] is the dominating sereotype among the other studied gastroenteritis viral agents in Iran in which the most frequency rate was during the winter (44.26%), while the least frequency rate was observed during summer (8.96%).

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30

Kukkula, Marja, Pertti Arstila, Marja-Liisa Klossner, Leena Maunula, Carl-Henrik V. Bonsdorff, and Pekka Jaatinen. "Waterborne Outbreak of Viral Gastroenteritis." Scandinavian Journal of Infectious Diseases 29, no. 4 (January 1997): 415–18. http://dx.doi.org/10.3109/00365549709011840.

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31

Clark, Benjamin, and Mike McKendrick. "A review of viral gastroenteritis." Current Opinion in Infectious Diseases 17, no. 5 (October 2004): 461–69. http://dx.doi.org/10.1097/00001432-200410000-00011.

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32

Gerba, Charles P., Joan B. Rose, Shri N. Singh, and Samuel R. Farrah. "Waterborne gastroenteritis and viral hepatitis." Critical Reviews in Environmental Control 15, no. 3 (January 1985): 213–36. http://dx.doi.org/10.1080/10643388509381732.

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33

Atmar, Robert L., and Mary K. Estes. "Nonculturable agents of viral gastroenteritis." Clinical Microbiology Newsletter 19, no. 23 (December 1997): 177–82. http://dx.doi.org/10.1016/s0196-4399(00)89189-8.

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34

Beards, G. M. "Laboratory diagnosis of viral gastroenteritis." European Journal of Clinical Microbiology & Infectious Diseases 7, no. 1 (February 1988): 11–13. http://dx.doi.org/10.1007/bf01962164.

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35

Hansman, Grant Stuart, Minako Kuramitsu, Chushi Kuroiwa, Hiromu Yoshida, Kazuhiko Katayama, Naokazu Takeda, Hiroshi Ushijima, Gungaa Surenkhand, and Dugerjav Gantulga. "Viral Gastroenteritis in Mongolian Infants." Emerging Infectious Diseases 11, no. 1 (January 2005): 180–82. http://dx.doi.org/10.3201/eid1101.040337.

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36

Isolauri, Erika, Minna Kaila, Hannu Mykkänen, Wen Hua Ling, and Seppo Salminen. "Oral bacteriotherapy for viral gastroenteritis." Digestive Diseases and Sciences 39, no. 12 (December 1994): 2595–600. http://dx.doi.org/10.1007/bf02087695.

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37

Schollin Ask, Lina, Can Liu, Karl Gauffin, and Anders Hjern. "The Effect of Rotavirus Vaccine on Socioeconomic Differentials of Paediatric Care Due to Gastroenteritis in Swedish Infants." International Journal of Environmental Research and Public Health 16, no. 7 (March 27, 2019): 1095. http://dx.doi.org/10.3390/ijerph16071095.

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Background: Previous Swedish studies have shown a social gradient on paediatric care for viral gastroenteritis. Aim: To study the effect of a free rotavirus vaccine programme on hospital care for viral gastroenteritis. Method: A register-based national cohort study of paediatric in- and outpatient care for viral gastroenteritis in children <2 years old in two Swedish counties in 2014–2017, with the rest of the country as comparison. Adjusted hazard ratios were estimated by the differences-in-differences (DiD) estimator in Cox regression in the entire cohort and by social indicators. Results: Reductions of 37% and 24% for inpatient care, and 11 % and 21% for outpatient care for viral gastroenteritis were found in the Stockholm and Jönköping counties, respectively, after adjusting for time trends and social indicators. For inpatient care, the change was similar over social groups in both counties. In the larger county of Stockholm, smaller reductions in outpatient care were detected for children in socially disadvantaged families. Conclusions: A free rotavirus vaccination programme moderately reduced paediatric care for viral gastroenteritis. There were indications of an increase in socioeconomic differences in paediatric outpatient care for viral gastroenteritis, but further studies are needed to confirm this result in a broader health care perspective.

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38

Fernandez-Cassi, Xavier, Sandra Martínez-Puchol, Marcelle Silva-Sales, Thais Cornejo, Rosa Bartolome, Silvia Bofill-Mas, and Rosina Girones. "Unveiling Viruses Associated with Gastroenteritis Using a Metagenomics Approach." Viruses 12, no. 12 (December 13, 2020): 1432. http://dx.doi.org/10.3390/v12121432.

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Acute infectious gastroenteritis is an important illness worldwide, especially on children, with viruses accounting for approximately 70% of the acute cases. A high number of these cases have an unknown etiological agent and the rise of next generation sequencing technologies has opened new opportunities for viral pathogen detection and discovery. Viral metagenomics in routine clinical settings has the potential to identify unexpected or novel variants of viral pathogens that cause gastroenteritis. In this study, 124 samples from acute gastroenteritis patients from 2012–2014 previously tested negative for common gastroenteritis pathogens were pooled by age and analyzed by next generation sequencing (NGS) to elucidate unidentified viral infections. The most abundant sequences detected potentially associated to acute gastroenteritis were from Astroviridae and Caliciviridae families, with the detection of norovirus GIV and sapoviruses. Lower number of contigs associated to rotaviruses were detected. As expected, other viruses that may be associated to gastroenteritis but also produce persistent infections in the gut were identified including several Picornaviridae members (EV, parechoviruses, cardioviruses) and adenoviruses. According to the sequencing data, astroviruses, sapoviruses and NoV GIV should be added to the list of viral pathogens screened in routine clinical analysis.

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39

Leung, Alexander KC, and Kam Lun Hon. "Paediatrics: how to manage viral gastroenteritis." Drugs in Context 10 (March 26, 2021): 1–11. http://dx.doi.org/10.7573/dic.2020-11-7.

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40

Millichap, J. Gordon. "Mild Viral Gastroenteritis and Afebrile Seizures." Pediatric Neurology Briefs 21, no. 2 (February 1, 2007): 12. http://dx.doi.org/10.15844/pedneurbriefs-21-2-4.

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41

Hart, C. Anthony, and Nigel A. Cunliffe. "Diagnosis and causes of viral gastroenteritis." Current Opinion in Infectious Diseases 9, no. 5 (October 1996): 333–39. http://dx.doi.org/10.1097/00001432-199610000-00009.

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42

KOHASHI, Shigechika, HomeHisashi INUTSUKA, and Hideo KIMURA. "Kampo Therapy for Acute Viral Gastroenteritis." Kampo Medicine 60, no. 1 (2009): 1–23. http://dx.doi.org/10.3937/kampomed.60.1.

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43

Shoja, Zabihollah, Somayeh Jalilvand, Yaghoub Mollaei-Kandelous, and Majid Validi. "Epidemiology of Viral Gastroenteritis in Iran." Pediatric Infectious Disease Journal 33, no. 2 (February 2014): 218–20. http://dx.doi.org/10.1097/inf.0000000000000028.

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44

HO, M. "VIRAL GASTROENTERITIS ABOARD A CRUISE SHIP." Lancet 334, no. 8669 (October 1989): 961–65. http://dx.doi.org/10.1016/s0140-6736(89)90964-1.

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45

Krenzer, Maureen E. "Viral Gastroenteritis in the Adult Population." Critical Care Nursing Clinics of North America 24, no. 4 (December 2012): 541–53. http://dx.doi.org/10.1016/j.ccell.2012.07.003.

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46

Rose, Markus A. "Mucosal Immunity and acute viral gastroenteritis." Human Vaccines & Immunotherapeutics 10, no. 7 (July 7, 2014): 2112–14. http://dx.doi.org/10.4161/hv.29605.

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47

Oldak, Elzbieta. "Vaccination in acute childhood viral gastroenteritis." Pediatric Health 2, no. 5 (October 2008): 595–603. http://dx.doi.org/10.2217/17455111.2.5.595.

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48

Bresee, Joseph S., Marc‐Alain Widdowson, Stephan S. Monroe, and Roger I. Glass. "Foodborne Viral Gastroenteritis: Challenges and Opportunities." Clinical Infectious Diseases 35, no. 6 (September 15, 2002): 748–53. http://dx.doi.org/10.1086/342386.

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49

Beckett, Gail, and Janice Bright. "Prevention and control of viral gastroenteritis." Nursing and Residential Care 15, no. 6 (June 2013): 426–30. http://dx.doi.org/10.12968/nrec.2013.15.6.426.

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50

Rhoads, F. A. "Oral rehydration therapy for viral gastroenteritis." JAMA: The Journal of the American Medical Association 270, no. 5 (August 4, 1993): 578–79. http://dx.doi.org/10.1001/jama.270.5.578.

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