Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Oct 11;16(10):e0010832.
doi: 10.1371/journal.pntd.0010832. eCollection 2022 Oct.

Dengue algorithms integrated into the IMCI guidelines: An updated assessment in five Southeast-Asian countries

Affiliations

Dengue algorithms integrated into the IMCI guidelines: An updated assessment in five Southeast-Asian countries

Stephanie Petzold et al. PLoS Negl Trop Dis. .

Abstract

Background: Dengue is not included explicitly in the WHO Integrated Management of Childhood Illness (IMCI) algorithm. However, the assessment, classification and management of dengue has been incorporated into several IMCI country adaptations. We aimed to evaluate the dengue algorithms incorporated into IMCI guidelines and discuss the need for harmonization, including an extension of the age range for IMCI.

Methods: This study included three steps. First, we investigated dengue algorithms incorporated into five Southeast-Asian (Myanmar, Philippines, Vietnam, Indonesia, Cambodia) country IMCI guidelines through a desk-based analysis. Second, we conducted an expert survey to elicit opinions regarding the integration of dengue and extension of the age range in IMCI. Third, we compared our findings with data from a large multicentric prospective study on acute febrile illness.

Results: We found considerable heterogeneity between the country specific IMCI guidelines in the dengue algorithms as well as classification schemes. Most guidelines did not differentiate between diagnostic algorithms for the detection of dengue versus other febrile illness, and warning signs for progression to severe dengue. Our expert survey resulted in a consensus to further integrate dengue in IMCI and extend the age range for IMCI guidelines beyond 5 years of age. Most of the interviewees responded that their country had a stand-alone clinical guideline for dengue, which was not integrated into the IMCI approach and considered laboratory testing for dengue necessary on day three of consecutive fever. Using data from a large multicentric study of children 5-15 years of age, we could confirm that the likelihood of dengue increased with consecutive fever days. However, a significant proportion of children (36%) would be missed if laboratory testing was only offered on the third consecutive day of fever.

Conclusions: This study supports the extension of the IMCI age range beyond 5 years of age as well as the inclusion of dengue relevant content in the algorithm. Because of the challenge of distinguishing dengue from other febrile illnesses, simple laboratory testing (e.g., full blood count) should be offered at an early stage during the course of the illness. Testing only children with consecutive fever over 3 days may lead to an underdiagnosis of dengue among those with acute febrile illness in children 5-15 years of age. In addition, specific laboratory testing for dengue should be made available to peripheral health facilities.

PubMed Disclaimer

Conflict of interest statement

The authors have read the journal’s policy and the authors of this manuscript have the following competing interests: MWW is a WHO staff member.

Figures

Fig 1
Fig 1. Frequency of signs and symptoms for assessment of dengue in five Southeast Asian Integrated Management of Childhood Illness (IMCI) adaptations (for children 2 month to 5 years of age).
Fig 2
Fig 2. The number of children (N = 910) in the IDAMS study with positive and negative dengue diagnosis among those with consecutive fever, by day of illness.
(The numbers of children per day of illness are overlapping, thus children with two, three, four etc. days of fever are also included in the first fever day).
Fig 3
Fig 3. The number of children (N = 910) in the IDAMS study with positive and negative dengue diagnosis among discrete non-overlapping sub-cohorts with exact number of persisting fever days.

References

    1. Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, et al.. The global distribution and burden of dengue. Nature. 2013;496(7446):504–7. doi: 10.1038/nature12060 ; PubMed Central PMCID: PMC3651993. - DOI - PMC - PubMed
    1. Wilder-Smith A, Ooi EE, Horstick O, Wills B. Dengue. Lancet. 2019;393(10169):350–63. Epub 2019/01/31. doi: 10.1016/S0140-6736(18)32560-1 . - DOI - PubMed
    1. Deen JL, Harris E, Wills B, Balmaseda A, Hammond SN, Rocha C, et al.. The WHO dengue classification and case definitions: time for a reassessment. Lancet. 2006;368(9530):170–3. Epub 2006/07/11. doi: 10.1016/S0140-6736(06)69006-5 . - DOI - PubMed
    1. Tsheten T, Clements ACA, Gray DJ, Adhikary RK, Wangdi K. Clinical features and outcomes of COVID-19 and dengue co-infection: a systematic review. BMC Infect Dis. 2021;21(1):729. Epub 20210802. doi: 10.1186/s12879-021-06409-9 ; PubMed Central PMCID: PMC8327042. - DOI - PMC - PubMed
    1. Thein S, Aung MM, Shwe TN, Aye M, Zaw A, Aye K, et al.. Risk factors in dengue shock syndrome. Am J Trop Med Hyg. 1997;56(5):566–72. Epub 1997/05/01. doi: 10.4269/ajtmh.1997.56.566 . - DOI - PubMed

Publication types