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Global Coinfections with Bacteria, Fungi, and Respiratory Viruses in Children with SARS-CoV-2: A Systematic Review and Meta-Analysis.
Alhumaid, Saad; Alabdulqader, Muneera; Al Dossary, Nourah; Al Alawi, Zainab; Alnaim, Abdulrahman A; Al Mutared, Koblan M; Al Noaim, Khalid; Al Ghamdi, Mohammed A; Albahrani, Suha Jafar; Alahmari, Abdulaziz A; Al Hajji Mohammed, Sarah Mahmoud; Almatawah, Yameen Ali; Bayameen, Omar Musa; Alismaeel, Ahmed Abdulwhab; Alzamil, Sherifah Khaled; Alturki, Samiah Ahmad; Albrahim, Zahra'a Radi; Al Bagshi, Nasreen Ahmad; Alshawareb, Hesham Yousef; Alhudar, Jaafar Abdullah; Algurairy, Qassim Abdulatif; Alghadeer, Samirah Mansour; Alhadab, Hassan Ali; Aljubran, Taleb Nasser; Alabdulaly, Yousif Ahmad; Al Mutair, Abbas; Rabaan, Ali A.
  • Alhumaid S; Administration of Pharmaceutical Care, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 31982, Saudi Arabia.
  • Alabdulqader M; Pediatric Nephrology Specialty, Pediatric Department, Medical College, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
  • Al Dossary N; General Surgery Department, Alomran General Hospital, Ministry of Health, Al-Ahsa 36358, Saudi Arabia.
  • Al Alawi Z; Division of Allergy and Immunology, College of Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
  • Alnaim AA; Department of Pediatrics, College of Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
  • Al Mutared KM; Administration of Pharmaceutical Care, Ministry of Health, Najran 66255, Saudi Arabia.
  • Al Noaim K; Department of Pediatrics, College of Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
  • Al Ghamdi MA; Department of Pediatrics, King Fahad Hospital of the University, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam 34212, Saudi Arabia.
  • Albahrani SJ; Division of Diabetology, Family Medicine Department, College of Medicine, King Faisal University, Al-Ahsa 36364, Saudi Arabia.
  • Alahmari AA; Department of Pediatrics, King Fahad Hospital of the University, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam 34212, Saudi Arabia.
  • Al Hajji Mohammed SM; Pharmacy Department, Prince Saud Bin Jalawi Hospital, Al-Ahsa 36424, Saudi Arabia.
  • Almatawah YA; Division of Infectious Diseases and Infection Control, Pediatric Department, Maternity and Children Hospital, Ministry of Health, Al-Ahsa 36422, Saudi Arabia.
  • Bayameen OM; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Alismaeel AA; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Alzamil SK; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Alturki SA; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Albrahim ZR; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Al Bagshi NA; Public Health Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Alshawareb HY; Southern Sector, Primary Care Medicine, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 36421, Saudi Arabia.
  • Alhudar JA; Regional Medical Supply, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 36361, Saudi Arabia.
  • Algurairy QA; Nutrition Department, King Fahad Hofuf Hospital, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Alghadeer SM; Infection Prevention and Control Administration, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 36421, Saudi Arabia.
  • Alhadab HA; Ambulatory Transportation Administration, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa 36421, Saudi Arabia.
  • Aljubran TN; Pharmacy Department, Prince Saud Bin Jalawi Hospital, Al-Ahsa 36424, Saudi Arabia.
  • Alabdulaly YA; Quality Assurance and Patient Safety Administration, Directorate of Health Affairs, Ministry of Health, Al-Ahsa 36441, Saudi Arabia.
  • Al Mutair A; Research Center, Almoosa Specialist Hospital, Al-Ahsa 36342, Saudi Arabia.
  • Rabaan AA; College of Nursing, Princess Norah Bint Abdulrahman University, Riyadh 11564, Saudi Arabia.
Trop Med Infect Dis ; 7(11)2022 Nov 15.
Article in English | MEDLINE | ID: covidwho-2115938
ABSTRACT

BACKGROUND:

Coinfection with bacteria, fungi, and respiratory viruses has been described as a factor associated with more severe clinical outcomes in children with COVID-19. Such coinfections in children with COVID-19 have been reported to increase morbidity and mortality.

OBJECTIVES:

To identify the type and proportion of coinfections with SARS-CoV-2 and bacteria, fungi, and/or respiratory viruses, and investigate the severity of COVID-19 in children.

METHODS:

For this systematic review and meta-analysis, we searched ProQuest, Medline, Embase, PubMed, CINAHL, Wiley online library, Scopus, and Nature through the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines for studies on the incidence of COVID-19 in children with bacterial, fungal, and/or respiratory coinfections, published from 1 December 2019 to 1 October 2022, with English language restriction.

RESULTS:

Of the 169 papers that were identified, 130 articles were included in the systematic review (57 cohort, 52 case report, and 21 case series studies) and 34 articles (23 cohort, eight case series, and three case report studies) were included in the meta-analysis. Of the 17,588 COVID-19 children who were tested for co-pathogens, bacterial, fungal, and/or respiratory viral coinfections were reported (n = 1633, 9.3%). The median patient age ranged from 1.4 months to 144 months across studies. There was an increased male predominance in pediatric COVID-19 patients diagnosed with bacterial, fungal, and/or viral coinfections in most of the studies (male gender n = 204, 59.1% compared to female gender n = 141, 40.9%). The majority of the cases belonged to White (Caucasian) (n = 441, 53.3%), Asian (n = 205, 24.8%), Indian (n = 71, 8.6%), and Black (n = 51, 6.2%) ethnicities. The overall pooled proportions of children with laboratory-confirmed COVID-19 who had bacterial, fungal, and respiratory viral coinfections were 4.73% (95% CI 3.86 to 5.60, n = 445, 34 studies, I2 85%, p < 0.01), 0.98% (95% CI 0.13 to 1.83, n = 17, six studies, I2 49%, p < 0.08), and 5.41% (95% CI 4.48 to 6.34, n = 441, 32 studies, I2 87%, p < 0.01), respectively. Children with COVID-19 in the ICU had higher coinfections compared to ICU and non-ICU patients, as follows respiratory viral (6.61%, 95% CI 5.06-8.17, I2 = 0% versus 5.31%, 95% CI 4.31-6.30, I2 = 88%) and fungal (1.72%, 95% CI 0.45-2.99, I2 = 0% versus 0.62%, 95% CI 0.00-1.55, I2 = 54%); however, COVID-19 children admitted to the ICU had a lower bacterial coinfection compared to the COVID-19 children in the ICU and non-ICU group (3.02%, 95% CI 1.70-4.34, I2 = 0% versus 4.91%, 95% CI 3.97-5.84, I2 = 87%). The most common identified virus and bacterium in children with COVID-19 were RSV (n = 342, 31.4%) and Mycoplasma pneumonia (n = 120, 23.1%).

CONCLUSION:

Children with COVID-19 seem to have distinctly lower rates of bacterial, fungal, and/or respiratory viral coinfections than adults. RSV and Mycoplasma pneumonia were the most common identified virus and bacterium in children infected with SARS-CoV-2. Knowledge of bacterial, fungal, and/or respiratory viral confections has potential diagnostic and treatment implications in COVID-19 children.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Reviews / Systematic review/Meta Analysis Language: English Year: 2022 Document Type: Article Affiliation country: Tropicalmed7110380

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Reviews / Systematic review/Meta Analysis Language: English Year: 2022 Document Type: Article Affiliation country: Tropicalmed7110380