<?xml version="1.0" encoding="UTF-8"?>

<article>
<meta-data>
<journal-meta>
<journal-name>International Journal of Pediatric Research
</journal-name>
<journal-shortname>Int J Pediatr Res</journal-shortname>
<journal-doi>10.23937/2469-5769</journal-doi>
<issn>2469-5769</issn>
<publisher>
<publisher-name>ClinMed International Library</publisher-name>
<publisher-location>Wilmington, USA</publisher-location>
<publisher-doi-prefix>10.23937</publisher-doi-prefix>
</publisher>
</journal-meta>
<article-meta>
<article-title>
Management of Dengue Fever in Children: Current Situation at the Regional University Hospital of Ouahigouya (Burkina Faso)
</article-title>
<citation_author>Savadogo H Dao L</citation_author>
<article-doi>10.23937/2469-5769/1510139</article-doi>
<article-description>
Considered as re-emerging disease from the 1970s onwards, dengue fever has now become the most widespread arbovirosis in the world. The aim of our work was to provide paediatric data on the subject in our context.

</article-description>
</article-meta>
</meta-data>
<body>
<article-type>Original  Article</article-type>
<volume>11</volume>
<issue>2</issue>
<access-type>OPEN ACCESS</access-type>
<article-doi>10.23937/2469-5769/1510139</article-doi>
<article-title>
Management of Dengue Fever in Children: Current Situation at the Regional University Hospital of Ouahigouya (Burkina Faso)
 
</article-title>
<Author-Group>
<aut id="aut1">
<label>Author-1</label>
<name>Savadogo H</name>
<affiliation>
Department of Paediatrics, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
<affiliation>
Health Sciences Training and Research Unit, Lédéa-Bernard-Ouédraogo University, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut2">
<label>Author-2</label>
<name>Dao L</name>
<affiliation>
Department of Paediatrics, Tengandogo University Hospital, Ouagadougou, Burkina Faso
</affiliation>
<affiliation>
Health Sciences Training and Research Unit, Joseph Ki-Zerbo University, Ouagadougou, Burkina Faso
</affiliation>
</aut>
<aut id="aut3">
<label>Author-3</label>
<name>Kiendrébéogo L</name>
<affiliation>
Department of Paediatrics, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut4">
<label>Author-4</label>
<name>Ouermi AS</name>
<affiliation>
Department of Paediatrics, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
<affiliation>
Health Sciences Training and Research Unit, Lédéa-Bernard-Ouédraogo University, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut5">
<label>Author-5</label>
<name>Guira I</name>
<affiliation>
Department of Paediatrics, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut6">
<label>Author-6</label>
<name>Ouattara ABI</name>
<affiliation>
Department of Paediatrics, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
<affiliation>
Health Sciences Training and Research Unit, Lédéa-Bernard-Ouédraogo University, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut7">
<label>Author-7</label>
<name>Sawadogo A</name>
<affiliation>
Department of Infectious and Tropical Diseases, Regional University Hospital of Ouahigouya, Ouahigouya, Burkina Faso
</affiliation>
<affiliation>
Health Sciences Training and Research Unit, Lédéa-Bernard-Ouédraogo University, Ouahigouya, Burkina Faso
</affiliation>
</aut>
<aut id="aut8">
<label>Author-8</label>
<name> Koueta F</name>
<affiliation>
Health Sciences Training and Research Unit, Joseph Ki-Zerbo University, Ouagadougou, Burkina Faso
</affiliation>
<affiliation>
Department of Paediatrics, Yalgado-Ouédraogo University Hospital, Ouagadougou, Burkina Faso
</affiliation>
</aut>
</Author-Group>
<author-notes>
<corres-author>
<label>Corresponding-Author</label>
<name>Hamidou Savadogo</name>
<address>
 Regional University Hospital of Ouahigouya, Ouahigouya, 36, Burkina Faso, Tel: +226-610-693-05 .
</address>
</corres-author>
</author-notes>
<history>
<published-date>
<day>26</day>
<month>July  </month>
<year>2025</year>
</published-date>
</history>
<citation>
<author-names>
Savadogo H Dao L, Kiendrébéogo L
</author-names>
<published-year>2025</published-year>
<article-title>
Management of Dengue Fever in Children: Current Situation at the Regional University Hospital of Ouahigouya (Burkina Faso)
</article-title>
<journal-short-name>Int J Pediatr Res</journal-short-name>
<article-doi>10.23937/2469-5769/1510139</article-doi>
</citation>
<permissions>
<copyright>
<copyright-year>2025</copyright-year>
<copyright-holder>Savadogo H Dao L, et al. </copyright-holder>
<copyright-notes>
© This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
</copyright-notes>
</copyright>
</permissions>
<article-content>


<Abstract>
<p>
	
	
	Introduction: Considered as re-emerging disease from the 1970s onwards, dengue fever has now become the most widespread arbovirosis in the world. The aim of our work was to provide paediatric data on the subject in our context.
</p>
<p>
	Patients and method: This was a retrospective study covering the period from January 1st to 31st December 2023. Children aged 29 days to 14 years hospitalised in the paediatric department of the Regional University Hospital of Ouahigouya, were included.
</p>
<p>
	Results: One hundred and five patients were included in the study. The mean age of these patients was 4.9 &#38;plusmn; 2.6 years, with extremes of 08 months and 14 years. The sex ratio was 1.4. Children under five years of age accounted for 54.3% of cases. The main reasons for consultation were fever, headache, vomiting and epistaxis. The main complications were haemorrhage (37.1%), severe thrombocytopenia (18.1%) and hepatic cytolysis (10.5%). More than half the patients (51.4%) were AgNS1 positive. The average hospital stay was 3.9 &#38;plusmn; 2.2 days, with extremes of 2 and 11 days. The case fatality rate was 4.8%. Severe malaria (p = 0.012) and shock (p = 0.001) were statistically associated with death.
</p>
<p>
	Conclusion: Dengue fever has become a public health problem in our context. Preventing and managing it requires raising public awareness, ongoing training for healthcare professionals and epidemiological surveillance.
</p></Abstract>
<Keywords>
<p>
	
	
	Dengue fever, Child, Ouahigouya, Burkina Faso, Africa
</p></Keywords>
<Introduction>
<p>
	
	
	Dengue fever, or tropical flu, is currently considered a neglected tropical disease. It is a viral disease transmitted by the bite of a female mosquito, mainly Aedes aegypti , but also Aedes albopictus . The dengue virus belongs to the Flaviviridae family. There are four serotypes of the virus responsible for dengue fever, namely DENV-1, DENV-2, DENV-3 and DENV-4, and severe forms can be observed with all serotypes [1-3]. Dengue is currently the most widespread arbovirus disease in the world. It is particularly prevalent in tropical and subtropical regions, making this infection a public health problem [4,5]. In recent years, there has been an increase in the global incidence of the disease. The World Health Organisation estimates that there are more than 390 million cases of dengue fever worldwide each year, with approximately 20,000 to 25,000 deaths per year (mainly children in developing countries). We are therefore witnessing an unprecedented peak, with the disease spreading to other regions of the world [3,6]. Africa is one of the regions most affected by dengue fever, with 171,991 cases of dengue fever and 753 deaths in 2023. Burkina Faso was the most affected country in the region. As of 18 December 2023, the country had recorded a total of 68,346 probable cases and 688 deaths [6,7]. The clinical manifestations of dengue fever are polymorphic and no clinical signs are specific [8]. Reinfection with other serotypes increases the risk of developing severe dengue fever [3]. There is currently no specific treatment for the disease. Management is therefore symptomatic [9].
</p>
<p>
	The northern region of Burkina Faso was not spared by the dengue epidemic that occurred in the country in 2023. Several patients, both adults and children, were treated at the Regional University Hospital of Ouahigouya, the major city in the north of the country. We faced an influx of dengue cases in paediatrics, some of which were severe. However, data on dengue in children in our context is scarce. That is why we decided to conduct this study with a view to providing data on the subject and contributing to better management of dengue in paediatrics at the Regional University Hospital of Ouahigouya.
</p></Introduction>
<Patients-and-Method>
<p>
	
	
	This was a retrospective, single-center, descriptive and analytical study conducted in the paediatric department of the Regional University Hospital of Ouahigouya covering the period from January 1st to 31 st December 2023. The study included children aged 29 days to 14 years who were hospitalised in the department for dengue fever during the study period and who tested positive in a rapid dengue diagnostic test (NS1 antigen or immunoglobulin M and/or immunoglobulin G positive).
</p>
<p>
	We used the following operational definitions:
</p>
<p>
	&#38;bull; Thrombocytopenia: platelet count below 150,000 cells/mm 3
</p>
<p>
	&#38;bull; Severe thrombocytopenia: platelet count &#38;lt; 50,000 cells/mm 3
</p>
<p>
	&#38;bull; Complications: the following situations were considered complications of dengue fever:
</p>
<p>
	&#38;nbsp;
</p>
<p>
	- Shock syndrome: systolic blood pressure &#38;lt; 90 mm Hg with signs of peripheral hypoperfusion
</p>
<p>
	- Presence of visible or occult bleeding.
</p>
<p>
	The data were extracted from hospitalisation and consultation medical records using an individual form, then collectively integrated anonymously into an Excel file to enable statistical analysis. The variables concerned socio-demographic information, clinical data and biological data. Information on the progression of the disease was also collected. These data were analysed using Stata 16 software. The mean and standard deviation were used to estimate quantitative variables and proportions for qualitative variables. The Chi-square statistical test was used to compare proportions with a significance threshold of 5%. We obtained authorisation from the General Director of the University Hospital of Ouahigouya and the head of the Paediatrics Department to conduct the study. The confidentiality of the information collected was respected for each patient included.
</p></Patients-and-Method>
<Results>
<p>
	
	
	Sample characteristics
	
	During the study period, 2,916 patients were admitted to the paediatric department of the Ouahigouya Regional University Hospital Centre. Among them, 105 cases of dengue fever were recorded, representing a frequency of 3.6%.
</p>
<p>
	Age and gender
	
	The mean age of patients was 4.9 &#38;plusmn; 2.6 years, ranging from 8 months to 14 years. The sex ratio was 1.4. The distribution of patients by age group and sex is shown in table 1.
</p>
<p>
	Table 1: Distribution of patients by age group and gender (n = 105). View Table 1
</p>
<p>
	Place of residence
	
	In our series, 76 children resided in urban areas, representing 72.4% of cases, and 29 patients, representing 27.6% of cases, lived in rural areas.
</p>
<p>
	Clinical aspects
	
	Reasons for consultation
	
	The various reasons for consultation are shown in table 2.
</p>
<p>
	Table 2: Distribution of patients by reason for consultation. View Table 2
</p>
<p>
	Clinical signs at admission to the pediatric emergency
	
	The main clinical signs found on physical examination at admission were crackles (4.8% of cases), respiratory distress and hepatomegaly in 3.8% of cases respectively.
</p>
<p>
	Biological signs
	
	Immunologically, the NS1 antigen was positive in 51.4% of cases (Table 3). The average haemoglobin level was 9.9 &#38;plusmn; 3.2 g/dL, with extremes of 2.3 and 16.1 g/dL. Haematocrit was elevated in four patients (3.8% of cases) and decreased in 70 patients (66.7% of cases). Sixty-nine patients (65.7% of cases) had thrombocytopenia, and 37.7% of these had severe thrombocytopenia. Leukopenia was present in 19% of cases. In these patients, the mean leukocyte count was 2,874.4 &#38;plusmn; 802.2 cells/mm 3 , with extremes of 1,144 and 3,890 cells/mm 3 . Hepatic cytolysis was recorded with elevated alanine aminotransferase (ALT) in 10.5% of cases. The mean ALT in these patients was 233.8 &#38;plusmn; 94.9 IU/L, with extremes of 111 and 341 IU/L.
</p>
<p>
	Table 3: Distribution of patients according to immunological profile (n = 105). View Table 3
</p>
<p>
	Complications and comorbidities
	
	Complications were noted in 40 patients, representing 38.1% of cases. The distribution of patients according to the different types of complications is shown in table 4. Epistaxis accounted for 37.1% of haemorrhagic complications. Severe malaria accounted for 88% of comorbidities.
</p>
<p>
	Table 4: Distribution of patients according to the frequency of complications (n = 105). View Table 4
</p>
<p>
	Outcome of patients
	
	The average length of hospital stay was 3.9 days, ranging from 2 to 11 days. The outcome was favourable in 93.3% of patients. Five patients (4.8% of cases) died. A statistically significant association was found in univariate analysis between the occurrence of complications and residence in an urban area (p = 0.00; odds ratio = 2.6), age under 5 years (p = 0.03; odds ratio = 0.4) and the presence of comorbidities (p = 0.03; odds ratio = 2.4). Multivariate analysis of factors associated with death showed a statistically significant association between death and shock syndrome (p = 0.01; odds ratio = 0.8), severe dengue (p = 0.04; odds ratio = 0.7) and co-infection with dengue and severe malaria (p = 0.01; odds ratio = 0.1).
</p></Results>
<Discussion>
<p>
	
	
	Characteristics of the sample
	
	The average age of our patients was 4.9 &#38;plusmn; 2.6 years, ranging from 8 months to 14 years. Pothapregada, et al. [10] in India reported an average age of 6.9 &#38;plusmn; 3.3 years. Bonsi, et al. [11] in Cameroon found an average age of 7.1 &#38;plusmn; 2.9 years. In our series, children under 5 years of age (54.3%) were the most affected by dengue fever. Other authors have also reported this predominance, notably Soudr&#38;eacute;, et al. (58.09%) [7] and Ilboudo [12] in Ouagadougou. This predominance could be explained by the vulnerability of this age group. Indeed, protection by maternal antibodies is effective during the first months of life and then gradually decreases from 6 months onwards. Added to this is the immaturity of the immune system of children in this age group [13,14].
</p>
<p>
	The male predominance (sex ratio = 1.4) found in our study has also been reported by other authors, notably Mistry, et al. in India (male predominance in 57.9% of cases) [15], as well as Traor&#38;eacute; in Bamako (male predominance in 55.8% of cases) [16]. This could be explained by the fact that boys are more mobile and may frequent damp areas that are breeding grounds for mosquitoes.
</p>
<p>
	Clinical data
	
	The clinical signs were dominated by fever (100% of cases). This result is comparable to that of Doho [17] and Monnin, et al. [18], who reported fever as the main reason for consultation in 86.24% and 100% of cases, respectively. Fever during dengue fever is thought to be linked to the release of pro-inflammatory mediators in response to infection [19]. The physical signs found in our study (respiratory distress and hepatomegaly in 3.8% of cases respectively, lace sign in 2.9% of cases) were reported by Pothapregada, et al. [10] in India, but with different frequencies (hepatomegaly, the lace sign and respiratory distress were observed in 59.8%, 12.6% and 1.5% of cases, respectively). This difference could be explained by the retrospective nature of our study, with medical records that were not always complete. Furthermore, the lace sign is difficult to assess on black skin.
</p>
<p>
	Biological signs
	
	Biologically, thrombocytopenia was found in 65.7% of patients, and among them, 37.7% had severe thrombocytopenia. These results are comparable to those of Sondo et al. [20], Ilboudo [12] in Ouagadougou, and Prasad, et al. [21] in India, who found thrombocytopenia in 89%, 69.2%, and 73.5% of cases, respectively. Sondo et al. and Ilboudo noted severe thrombocytopenia in 16% and 53.8% of cases, respectively. These results prove that thrombocytopenia is the main haematological disorder in dengue fever. It is generally caused by the action of the virus.
</p>
<p>
	Complications and comorbidities
	
	In our study, the overall frequency of complications was 38.1%. This frequency is higher than those reported by Gnamou [22] in Burkina Faso and Monin, et al. [18] in Martinique (5%). The high frequency of complications in our study could be explained by the fact that 2023 saw an unprecedented dengue epidemic in the sub-region in general and in Burkina Faso in particular, which recorded the highest number of cases [23]. Complications in our study were dominated by haemorrhages in 37.1% of patients. Gnamou, [22] also found a predominance of haemorrhagic complications (38.55% of cases) in his series. Haemorrhagic complications are therefore common during dengue and may be aggravated in cases of severe thrombocytopenia. Co-infections were dominated by malaria. This could be explained by the fact that Burkina Faso is located in a malaria-endemic area.
</p>
<p>
	Evolution and prognosis
	
	The average length of hospital stay was 3.9 days in our study. This duration is comparable to that reported by Ly, [24] and lower than that reported by Badianne, et al. [25], who found 4.18 days and 6 days, respectively. The outcome was favorable in 93.3% of patients. There was a low mortality rate of 4.8%. Badianne, et al. [25] reported similar results, with a favorable outcome in 88.6% of cases and a mortality rate of 6.8%. These results could be explained by the existence of national guidelines for the management of dengue fever in Burkina Faso [26,27]. In our study, there was a statistically significant link between comorbidities and the risk of complications. Marois, et al. [28] reported that comorbidities were significantly associated with severe forms of the disease.
</p>
<p>
	In our study, there was a statistically significant link between dengue fever combined with severe malaria and death. Badianne, et al. [25] made the same observation in Senegal. The concomitant diagnosis of both diseases is made difficult by their clinical similarity. The comorbidity of dengue fever and malaria therefore results in a poor prognosis, hence the need to investigate and treat any possible association in order to prevent complications.
</p></Discussion>
<Conclusion>
<p>
	
	
	Dengue fever is a real public health issue in our context. A prospective multicenter study will enable us to better assess the subject in a pediatric setting in our context.
</p></Conclusion>
<p>
	&#38;nbsp;
</p>



<figures-and-tables>
	<text>All Figures and Tables link given in below</text>
	<link>https://clinmedjournals.org/articles/ijpr/international-journal-of-pediatric-research-ijpr-11-139.php?jid=ijpr</link>
</figures-and-tables>



</article-content>

<article-references>
<title>References</title>

		 
<ref id="ref1">
    <label>Reference-1</label>
    <mixed-citation>
				Laversanne J, Donutil G, Hamiche K, Guegueniat P, Djossou F, et al. (2007) Dengue fever, a reemerging disease. Ann Fr Med Urg 2: 413-425.
				    #
    </mixed-citation>
</ref>
<ref id="ref2">
    <label>Reference-2</label>
    <mixed-citation>
					(2017) Integrating neglected tropical diseases into global health and development: Fourth WHO report on neglected tropical diseases. World Heath Organization, Geneva.
				    https://reliefweb.int/report/world/integrating-neglected-tropical-diseases-global-health-and-development-fourth-who-report
    </mixed-citation>
</ref>
<ref id="ref3">
    <label>Reference-3</label>
    <mixed-citation>
				Musso D, Cao-Lormeau VM (2012) Biological diagnosis of dengue fever. Rev Franc Lab 12: 53-62.
				    #
    </mixed-citation>
</ref>
<ref id="ref4">
    <label>Reference-4</label>
    <mixed-citation>
				Flamand M, Despr&#38;egrave;s P (2014) Dengue fever. Med Sci 18: 816-818.
				    #
    </mixed-citation>
</ref>
<ref id="ref5">
    <label>Reference-5</label>
    <mixed-citation>
				Daud&#38;eacute; E, Vaguet A, Paul R (2015) Dengue fever, a complex disease. Nat Sci Soc 23: 331-342.
				    #
    </mixed-citation>
</ref>
<ref id="ref6">
    <label>Reference-6</label>
    <mixed-citation>
					Diallo I, Sondo KA, Tieno H, Tamelokpo EY, Zoungrana J, et al (2017) About 98 cases of dengue fever hospitalized in a private clinic in Ouagadougou: Epidemiological, diagnostic, and evolution. Bull Soc Pathol Exot 110: 291-296.
				    https://pubmed.ncbi.nlm.nih.gov/29299882/
    </mixed-citation>
</ref>
<ref id="ref7">
    <label>Reference-7</label>
    <mixed-citation>
				Soudre F, Kiba A, Karfo R, Kane C, Kouraogo A, et al (2020) Biochemical parameter disturbances during dengue fever at the Charles de Gaulle pediatric University Hospital in Ouagadougou (Burkina Faso). Sci Tec 39: 97-109.
				    #
    </mixed-citation>
</ref>
<ref id="ref8">
    <label>Reference-8</label>
    <mixed-citation>
				Hober D, Roulin G, Deubel V, Wattre P (2014) Dengue fever: A rapidly spreading viral disease. M&#38;eacute;decine Mal Infect 25: 888-895.
				    #
    </mixed-citation>
</ref>
<ref id="ref9">
    <label>Reference-9</label>
    <mixed-citation>
					Heilman JM, De Wolff J, Beards GM, Basden BJ (2014) Dengue fever: A Wikipedia clinical review. Open Med 8: e105-115.
				    https://pubmed.ncbi.nlm.nih.gov/25426178/
    </mixed-citation>
</ref>
<ref id="ref10">
    <label>Reference-10</label>
    <mixed-citation>
					Pothapregada S, Kamalakannan B, Thulasingham M, Sampath S (2016) Clinically profiling pediatric patients with dengue. J Glob Infect Dis 8: 115-120.
				    https://pubmed.ncbi.nlm.nih.gov/27621562/
    </mixed-citation>
</ref>
<ref id="ref11">
    <label>Reference-11</label>
    <mixed-citation>
					Tchuandom SB, Tchadji JC, Tchouangueu TF, Biloa MZ, Atabonkeng EP, et al (2019). A cross-sectional study of acute dengue infection in paediatric clinics in Cameroon. BMC Public Health 19: 958.
				    https://pubmed.ncbi.nlm.nih.gov/31319834/
    </mixed-citation>
</ref>
<ref id="ref12">
    <label>Reference-12</label>
    <mixed-citation>
				Ilboudo S (2019) The complications of dengue fever in children at the Charles De Gaulle pediatric University Hospital in Ouagadougou.
				    #
    </mixed-citation>
</ref>
<ref id="ref13">
    <label>Reference-13</label>
    <mixed-citation>
					Jain A, Chaturvedi UC (2010) Dengue in infants: An overview. FEMS Immunol Med Microbiol 59: 119-130.
				    https://pubmed.ncbi.nlm.nih.gov/20402771/
    </mixed-citation>
</ref>
<ref id="ref14">
    <label>Reference-14</label>
    <mixed-citation>
					(2012) Handbook for clinical management of dengue. World Heath Organization, Geneva.
				    https://www.who.int/publications/i/item/9789241504713
    </mixed-citation>
</ref>
<ref id="ref15">
    <label>Reference-15</label>
    <mixed-citation>
					Mistry M, Chudasama RK, Goswami Y (2019) Profile of dengue fever in hospitalized children in Saurashtra, Gujarat, 2013-2017. Indian Pediatr 56: 123-125.
				    https://pubmed.ncbi.nlm.nih.gov/30819991/
    </mixed-citation>
</ref>
<ref id="ref16">
    <label>Reference-16</label>
    <mixed-citation>
				Traor&#38;eacute; S (2019) Epidemiological surveillance of dengue fever at the Charles Merieux Infectious Diseases Center from January to December 2019: University of Science, Technology, and Engineering of Bamako.
				    #
    </mixed-citation>
</ref>
<ref id="ref17">
    <label>Reference-17</label>
    <mixed-citation>
				Doho U (2019). Prevalence of dengue fever at the Charles de Gaulle Pediatric University Hospital among children aged 0 to 5 years from 2016 to 2019.
				    #
    </mixed-citation>
</ref>
<ref id="ref18">
    <label>Reference-18</label>
    <mixed-citation>
					Monnin M, M&#38;rsquo;bou F (2005) n epidemic of dengue fever in a department of paediatrics: Report on 58 cases in Lamentin. Arch Pediatr 12: 144-150.
				    https://pubmed.ncbi.nlm.nih.gov/15694537/
    </mixed-citation>
</ref>
<ref id="ref19">
    <label>Reference-19</label>
    <mixed-citation>
					(2009) Dengue: Guidelines for diagnosis, treatment, prevention and control. World Heath Organization, Geneva.
				    https://www.who.int/publications/i/item/9789241547871
    </mixed-citation>
</ref>
<ref id="ref20">
    <label>Reference-20</label>
    <mixed-citation>
				Sondo KA, Gnamou A, Diallo I, Ka D, Zoungrana J (2022) Descriptive study of dengue complications during the 2016 outbreak in Ouagadougou, Burkina Faso. PAMJ-OH 27: 1-13.
				    #
    </mixed-citation>
</ref>
<ref id="ref21">
    <label>Reference-21</label>
    <mixed-citation>
					Prasad D, Bhriguvanshi A (2020) Clinical profile, liver dysfunction and outcome of dengue infection in children: A prospective observational study. Pediatr Infect Dis J 39: 97-101.
				    https://pubmed.ncbi.nlm.nih.gov/31815826/
    </mixed-citation>
</ref>
<ref id="ref22">
    <label>Reference-22</label>
    <mixed-citation>
				Gnamou A (2017) Complications of dengue fever in the city of Ouagadougou (Burkina Faso) from November 2015 to October 2016. University of Ouaga 1 Prof. Josph Ki-Zerbo.
				    #
    </mixed-citation>
</ref>
<ref id="ref23">
    <label>Reference-23</label>
    <mixed-citation>
				Ouattara CA, Traore S, Traore TI, Sangare I, M&#38;eacute;da CZ, et al. (2022) Epidemiological trends and strategies for controlling dengue fever in Burkina Faso from 2013 to 2020: A systematic review. Sci Sant&#38;eacute; 45: 1371-51.
				    #
    </mixed-citation>
</ref>
<ref id="ref24">
    <label>Reference-24</label>
    <mixed-citation>
				LY D (2016) Co-infection of dengue fever and malaria in the city of Ouagadougou: Epidemiological, clinical, biological, and evolutionary aspects. University of Ouaga 1 Prof. Josph Ki-Zerbo.
				    #
    </mixed-citation>
</ref>
<ref id="ref25">
    <label>Reference-25</label>
    <mixed-citation>
				Badianne A, Sarr N, Sarr N, Thioub D, Wembula B, et al (2024) Epidemiological, clinical, biological, and evolutionary profile of arboviruses and factors associated with death in an infectious disease department in an urban area of Senegal from 2020 to 2022. Rev Mali Infect Microbiol 19: 70-79.
				    #
    </mixed-citation>
</ref>
<ref id="ref26">
    <label>Reference-26</label>
    <mixed-citation>
				(2017) Guide to the diagnosis and treatment of dengue fever in Burkina Faso. (1
				<sup>
					st
				</sup>
					edn), Ministry of Health Ouagadougou, Burkina Faso.
				    #
    </mixed-citation>
</ref>
<ref id="ref27">
    <label>Reference-27</label>
    <mixed-citation>
				(2024) National guidelines for the management of dengue cases in Burkina Faso. (3rd edn), Ouagadougou, Burkina Faso.
				    #
    </mixed-citation>
</ref>
<ref id="ref28">
    <label>Reference-28</label>
    <mixed-citation>
				Marois I, Forfait C, Valiame A, Aubert D, Gourinat A, et al. (2018) Factors contributing to the severity of dengue fever in an overseas territory. M&#38;eacute;decine Mal Infect 48: 17-18.
				    #
    </mixed-citation>
</ref>

</article-references>
</body>
</article>