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Severe Recurrent Bacterial Pneumonia Among Children Living With HIV.
Boettiger, David C; An, Vu Thien; Lumbiganon, Pagakrong; Wittawatmongkol, Orasri; Huu Truong, Khanh; Chau Do, Viet; Van Nguyen, Lam; Sun Ly, Penh; Kinikar, Aarti; Ounchanum, Pradthana; Puthanakit, Thanyawee; Kurniati, Nia; Kumarasamy, Nagalingeswaran; Kumara Wati, Dewi; Chokephaibulkit, Kulkanya; Jamal Mohamed, Thahira A; Sudjaritruk, Tavitiya; Nik Yusoff, Nik Khairulddin; Siew Fong, Moy; Nallusamy, Revathy A; Kariminia, Azar.
  • Boettiger DC; From the The Kirby Institute, UNSW Sydney, Australia.
  • An VT; Institute for Health and Aging, University of California, San Francisco, USA.
  • Lumbiganon P; Biostatistics Excellence Centre, Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Wittawatmongkol O; Children Hospital 2, Ho Chi Minh City, Vietnam.
  • Huu Truong K; ¶Division of Infectious Disease, Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
  • Chau Do V; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Van Nguyen L; Children's Hospital 1, Ho Chi Minh City, Vietnam.
  • Sun Ly P; Children Hospital 2, Ho Chi Minh City, Vietnam.
  • Kinikar A; National Hospital of Pediatrics, Hanoi, Vietnam.
  • Ounchanum P; National Centre for HIV/AIDS, Dermatology and STDs, Phnom Penh, Cambodia.
  • Puthanakit T; BJ Medical College and Sassoon General Hospitals, Maharashtra, India.
  • Kurniati N; ¶¶Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.
  • Kumarasamy N; Department of Pediatrics and Center of Excellence for Pediatric Infectious Diseases and Vaccines, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Kumara Wati D; Cipto Mangunkusumo - Faculty of Medicine Universitas Indonesia, Jakarta, Indonesia.
  • Chokephaibulkit K; Chennai Antiviral Research and Treatment Clinical Research Site (CART CRS), VHS-Infectious Diseases Medical Centre, VHS, Chennai, India.
  • Jamal Mohamed TA; Sanglah Hospital, Udayana University, Bali, Indonesia.
  • Sudjaritruk T; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Nik Yusoff NK; Department of Pediatrics, Women and Children Hospital Kuala Lumpur (WCHKL), Kuala Lumpur, Malaysia.
  • Siew Fong M; Department of Pediatrics, Faculty of Medicine, and Research Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
  • Nallusamy RA; Hospital Raja Perempuan Zainab II, Kelantan, Malaysia.
  • Kariminia A; Hospital Likas, Kota Kinabalu, Malaysia.
Pediatr Infect Dis J ; 41(5): e208-e215, 2022 05 01.
Article in English | MEDLINE | ID: covidwho-1831448
ABSTRACT

BACKGROUND:

Bacterial pneumonia imparts a major morbidity and mortality burden on children living with HIV, yet effective prevention and treatment options are underutilized. We explored clinical factors associated with severe recurrent bacterial pneumonia among children living with HIV.

METHODS:

Children enrolled in the TREAT Asia Pediatric HIV Observational Database were included if they started antiretroviral therapy (ART) on or after January 1st, 2008. Factors associated with severe recurrent bacterial pneumonia were assessed using competing-risk regression.

RESULTS:

A total of 3,944 children were included in the analysis; 136 cases of severe recurrent bacterial pneumonia were reported at a rate of 6.5 [95% confidence interval (CI) 5.5-7.7] events per 1,000 patient-years. Clinical factors associated with severe recurrent bacterial pneumonia were younger age [adjusted subdistribution hazard ratio (aHR) 4.4 for <5 years versus ≥10 years, 95% CI 2.2-8.4, P < 0.001], lower weight-for-age z-score (aHR 1.5 for <-3.0 versus >-2.0, 95% CI 1.1-2.3, P = 0.024), pre-ART diagnosis of severe recurrent bacterial pneumonia (aHR 4.0 versus no pre-ART diagnosis, 95% CI 2.7-5.8, P < 0.001), past diagnosis of symptomatic lymphoid interstitial pneumonitis or chronic HIV-associated lung disease, including bronchiectasis (aHR 4.8 versus no past diagnosis, 95% CI 2.8-8.4, P < 0.001), low CD4% (aHR 3.5 for <10% versus ≥25%, 95% CI 1.9-6.4, P < 0.001) and detectable HIV viral load (aHR 2.6 versus undetectable, 95% CI 1.2-5.9, P = 0.018).

CONCLUSIONS:

Children <10-years-old and those with low weight-for-age, a history of respiratory illness, low CD4% or poorly controlled HIV are likely to gain the greatest benefit from targeted prevention and treatment programs to reduce the burden of bacterial pneumonia in children living with HIV.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / Pneumonia, Bacterial / Anti-HIV Agents Type of study: Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2022 Document Type: Article Affiliation country: INF.0000000000003494

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Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / Pneumonia, Bacterial / Anti-HIV Agents Type of study: Experimental Studies / Observational study / Prognostic study Topics: Long Covid Limits: Child / Humans Language: English Journal: Pediatr Infect Dis J Journal subject: Communicable Diseases / Pediatrics Year: 2022 Document Type: Article Affiliation country: INF.0000000000003494