Available online on 15.04.2026 at http://jddtonline.info
Journal of Drug Delivery and Therapeutics
Open Access to Pharmaceutical and Medical Research
Copyright © 2026 The Author(s): This is an open-access article distributed under the terms of the CC BY-NC 4.0 which permits unrestricted use, distribution, and reproduction in any medium for non-commercial use provided the original author and source are credited
Open Access Full Text Article Research Article
Ethnobotanical study of medicinal plants used in the treatment of gastroenteritis and urinary tract infections in children aged 0–5 in the city of Guelendeng and its surroundings
RONDOUBA Djetenbe ¹*, NADJIOROM Ngam-asra ¹, ATAKEWANG DJETOLOUM Martinien ¹, DJEKILAMBER Azor ², MBAIDE Yeba ³
1. Faculty of Human Health Sciences, Laboratory of Scientific Research, Diagnostics and Scientific Expertise (LaboRedDES), University of N'Djamena
2. Faculty of Exact and Applied Sciences, Laboratory of Natural Substance Research, University of N'Djamena
3. Faculty of Exact and Applied Sciences, Laboratory of Systematic Botany and Vegetation Ecology (LBSEV), University of N'Djamena.
|
Article Info: _______________________________________________ Article History: Received 10 Jan 2026 Reviewed 23 Feb 2026 Accepted 20 March 2026 Published 15 April 2026 _______________________________________________ Cite this article as: Rondouba D, Nadjiorom NA, Atakewang Djetoloum M, Djekilamber A, Mbaide Y, Ethnobotanical study of medicinal plants used in the treatment of gastroenteritis and urinary tract infections in children aged 0–5 in the city of Guelendeng and its surroundings, Journal of Drug Delivery and Therapeutics. 2026; 16(4):48-54 DOI: http://dx.doi.org/10.22270/jddt.v16i4.7644 _______________________________________________ For Correspondence: RONDOUBA Djetenbe, Faculty of Human Health Sciences, Laboratory of Scientific Research, Diagnostics and Scientific Expertise (LaboRedDES), University of N'Djamena |
Abstract _______________________________________________________________________________________________________________ In recent years, there has been growing interest in researching and developing new molecules with antimicrobial properties from various natural sources, with the aim of combating antibiotic resistance. This study was conducted with the aim of identifying medicinal plants used in the treatment of gastroenteritis and urinary tract infections in children under five in the city of Guelendeng and its surroundings. Ethnobotanical surveys were conducted using questionnaires with 33 traditional practitioners. Fieldwork allowed samples of the four most frequently cited plants for the two infections to be collected for identification and testing on bacterial strains. A total of 13 plants indicated for the treatment of gastroenteritis and 11 for the treatment of urinary tract infections were identified, distributed respectively among 7 and 6 families. The Fabaceae family is dominant (38.48% and 36.37%). Most of the respondents were women (55%), and most were not literate (48.49%) or had a primary education (39.39%). The floral diversity constitutes a natural resource for traditional medicine. Studies of this kind should encourage everyone to protect the flora. Keywords: medicinal plants, gastro-intestinal and urinary infections, children under 5.
|
Introduction
According to the World Health Organization, infectious diseases are the leading cause of mortality and morbidity in developing countries¹,². Gastro-enteritis and urinary tract infections are among the most common of these diseases and cause significant human and economic losses. Children and the elderly are most at risk. Infectious gastroenteritis in children is a public health concern, undoubtedly due to the presence of certain pathogenic bacteria, particularly Escherichia coli, Salmonella non typhi and Shigella 3,4,5. These bacteria are normally present in the digestive flora of humans and warm-blooded animals. Certain Escherichia. coli strains are pathogenic because they have acquired virulence factors6. They are associated with a high risk of morbidity and mortality in children under 5, particularly in developing countries7.S
Urinary tract infections are among the most common bacterial infections in paediatrics8. In children, it is a significant daily issue in clinical practice: its prevalence varies according to the study, reaching up to 7.8% of girls and 1.6% of boys. In developed countries, it accounts for around 5% of hospitalisations in general paediatric wards. In Africa, studies indicate frequencies ranging from 8.3% to 30% in paediatric hospitals⁹. In Ouagadougou (Burkina Faso), it is 18.67%, compared to 25% in children in Côte d'Ivoire. At the Centre Hospitalier Universitaire de Yopougon in Côte d'Ivoire, the prevalence of this condition is 53.6% in girls¹. Urinary tract infection is a concern for paediatricians, regardless of the country in which they practise⁸. It is a severe condition in children due to the possibility of cortical renal involvement with a risk of renal insufficiency or hypertension in the long term. Furthermore, in recurrent forms, it often indicates an underlying uropathy or condition such as haemoglobinopathy, diabetes or immunodeficiency⁹. The most frequently implicated germs are Escherichia coli and Klebsiella pneumoniae, which belong to the Enterobacteriaceae family, as well as Staphylococcus aureus¹⁰. Diagnosis of urinary tract infection is based on cytobacteriological examination of urine (ECBU)⁹. Factors that favour the persistence and propagation of the strains responsible for these infections include the consumption of food and water of poor hygienic quality, a lack of environmental sanitation and contact with animals, which is favoured by their transhumance in certain cities, as well as urban and peri-urban farming11.
In recent years, there has been growing interest in researching and developing new molecules with antimicrobial properties from various natural sources, with the aim of combating antibiotic resistance. Consequently, great attention has been given to medicinal and aromatic plants and their secondary metabolites, such as terpenes, alkaloids and phenolic compounds12.
In Chad, certain institutions such as the University of N'Djamena have conducted pharmacological research on medicinal plants with anti-radical and antibacterial properties, such as Anogeissus leiocarpus¹³. Acacia amythestophilla has been used in urinary tract treatment in Chad¹⁴.
In order to promote our plants and, above all, to propose a traditional alternative to the management of these infections, this study was conducted to compile a list of medicinal plants and traditional therapeutic knowledge related to their use in the management of gastroenteritis and urinary tract infections in children under five.
1. Materials and methods
1.1. Description of the study area
The ethnobotanical survey of gastroenteritis and urinary tract infections was conducted in the Republic of Chad, specifically in the city and villages of the Mayo-Lémié Department, Mayo-Kebbi Est Province. The town of Guelendeng is the administrative centre of the Mayo-Lémié department. Its geographical coordinates are: Latitude North: 10° 9' 45.8", Longitude East: 15° 55' 0.3", Altitude: 321 metres. Its population is estimated at 31,578 according to recent data from the ADREM-Tchad.
Figure 1: the study area map
1-2. Methods
1-2-1. Types and period of study
This is a prospective, cross-sectional and descriptive study taking place from 16 to 23 November 2025.
1-2-2. Study population
The study population consisted of traditional practitioners and herbalists in the city of Guelendeng and its surroundings.
1-2-3. Inclusion criteria
The study included tradipraticians and herbalists of both sexes, aged over 20, from the Mayo-Lémié department and surrounding areas.
1-2-4. Sociodemographic characteristics of master traditional practitioners
The variables studied are: sex, age category, experience and level of education.
1-2-5. Sampling
A total of thirty-three (33) traditional practitioners and herbalists were included in the study.
1-2-6. Survey
The study was conducted using a series of ethnobotanical surveys involving direct interviews based on a pre-established questionnaire in the various districts of the city of Guelendeng and its surroundings.
1-2-7. Sampling and herbarium preparation
After collecting information from traditional practitioners and herbalists on medicinal plants, a field trip was made to the habitats of the four most commonly cited medicinal plants for these two infections. Samples of each plant were collected and taken to N'Djamena for botanical identification. The herbariums were identified or confirmed using reference specimens by a botanist at the Faculty of Exact and Applied Sciences.
1.2.8. Data analysis
The graphs were created using Excel and the results were presented as percentages in the form of graphs and tables.
Table 1: Distribution of traditional practitioners and herbalists surveyed
|
Localities |
Number of traditional practitioners and herbalists surveyed |
|
Guelendeng |
1 |
|
Kakalé campement |
3 |
|
Kakalé Gama |
14 |
|
Kakalé Mbeuri |
12 |
|
Boudanassa |
3 |
2. Results
2.1. Characteristics of the traditional practitioners and herbalists surveyed
The survey was conducted with thirty-three people, comprising two ethnic groups: thirty-two (32) Ngambaye and one (1) Massa.
2.1.1 Distribution of respondents by sex
The traditional practitioners and herbalists surveyed are made up of men and women, the distribution of which is as follows:
Figure 2: Distribution of respondents by sex
It was observed in this figure a slight dominance of women, at 54.55%, compared to men, at 45.45%.
2.1.2. Distribution of respondents by age group
The distribution was made over 10-year intervals and is presented as follows:
Table 2: Distribution of respondents by age group
|
Age groups (AN) |
Number of respondents |
Percentage (%) |
|
20-30 |
5 |
15,15 |
|
31-40 |
4 |
12,12 |
|
41-50 |
10 |
30, 30 |
|
51-60 |
5 |
15,15 |
|
More than 60 |
9 |
27,28 |
|
Total |
33 |
100 |
High frequencies were observed in the age groups 41–50 (30.3%) and over 60 (27.28%). The 20–30 and 51–60 age groups had an equal frequency. The 31-40 age group had the lowest frequency.
Their years of experience range from 3 to 20 years.
2.1.3. Distribution of respondents by level of education
Respondents did not have a high level of education. Their level is between primary and secondary; the rest are not educated.
Table 3: Distribution of respondents by level of education.
|
Level of education |
Number(s) |
Percentages |
|
Out-of-school |
16 |
48,49% |
|
Primary |
13 |
39,39% |
|
Secondary |
4 |
12,12% |
|
Total |
33 |
100% |
The majority of respondents had no formal education (48.49%); 39.39% had completed primary education, whilst those who had completed secondary education were in the minority (12.12%).
2.2. Diversity of plants used in the treatment of gastroenteritis
The survey identified 13 plant species, belonging to 7 botanical families, used in the traditional treatment of gastroenteritis. The Fabaceae family is the most common, with 5 species (38.48%). The Combretaceae family is represented by 2 species (15.38%). The Rhamnaceae family is represented by 2 species (15.38%). The Malvaceae, Anacardiaceae, Annonaceae and Moraceae families are each represented by 1 species (7.69%).
Figure 3: Distribution of plant families identified in the treatment of gastroenteritis. With regard to growth habit, 8 out of 13 (61.63%) of the species identified are trees; 5 (38.37%) are shrubs; With regard to citation rates, the most frequently cited plants for the treatment of gastroenteritis are: Terminalia avicennioides Guill. et Per. (57.58%) and Detarium microcarpum (51.52%) (Table 4). The list of species, the parts used, the methods of preparation and administration, and their citation frequencies (CF) are summarised in Table 4.
Table 4: Species used, parts used, methods of preparation and routes of administration in cases of gastroenteritis
|
N° |
Scientific names |
Local name |
Plant type |
Family |
Parts used |
Form of the drug |
Methods of preparation |
Methods of administration |
Dosage |
Total citations |
Fréquency (%) |
|
1 |
Piliostigma reticulatum (DC.) Hochst. |
Karoum (arabe) |
shrub |
Fabaceae |
bark |
fresh or dried |
decoction or infusion |
Oral |
1 glass 3 times a day |
2 |
6,06 |
|
2 |
Detarium microcarpum Guill. & Perr. |
Gasta (massa) |
shrub |
Fabaceae |
bark |
fresh or dried |
decoction or infusion |
Oral |
1 glass 3 times a day |
17 |
51,52 |
|
3 |
Ficus platyphylla Delile |
Kob (ngambaye) |
tree |
Moraceae |
leaf |
fresh or dried |
decoction |
Oral |
variable |
4 |
12,12 |
|
4 |
Anogeissus leiocarpa (DC.) Guill. & Perr. |
Ida (ngambaye) |
tree |
Combretaceae |
bark |
fresh or dried |
decoction |
Oral |
variable |
8 |
24,24 |
|
5 |
Ziziphus mauritiana Lam. |
Ngogro (Ngambaye) |
shrub |
Rhamnaceae |
bark |
fresh or dried |
decoction |
Oral |
variable |
10 |
30,3 |
|
6 |
Faidherbia albida (Delile) A. Chev. |
Diri (Ngambaye) |
tree |
Fabaceae |
bark |
fresh or dried |
decoction |
Oral |
variable |
2 |
6,06 |
|
7 |
Ziziphus mucronata Willd. |
Ngogro-bichi (Ngambaye) |
shrub |
Rhamnaceae |
Bark, roots |
fresh or dried |
decoction |
Oral |
variable |
15 |
45,45 |
|
8 |
Terminalia avicennioides Guill. et Perr. |
Rho (Ngambaye) |
tree |
Combretaceae |
bark |
fresh or dried |
decoction |
Oral |
variable |
19 |
57,58 |
|
9 |
Acacia nilotica (L.) Willd. ex Delile |
Garat (arabe), Madjirang (Ngambaye) |
tree |
Fabaceae |
bark |
fresh |
decoction |
Oral |
variable |
3 |
9,09 |
|
10 |
Prosopis juliflora (Sw.) DC. |
soussoubane (arabe) |
tree |
Fabaceae |
leaf |
fresh |
decoction |
Oral |
variable |
2 |
6,06 |
|
11 |
Annona senegalensis Pers. |
Mboro (ngambaye) |
shrub |
Annonaceae |
bark |
fresh |
decoction |
Oral |
variable |
1 |
3,03 |
|
12 |
Sclerocarya birrea (A. Rich.) Hochst. |
Ngolobe (ngambaye) |
tree |
Anacardiaceae |
bark |
fresh |
decoction |
Oral |
variable |
1 |
3,03 |
|
13 |
Sterculia setigera Delile |
Da(ngambaye) |
tree |
Malvaceae |
bark |
fresh |
decoction |
oral |
variable |
3 |
9,09 |
2.3. Diversity of plants used in the treatment of urinary tract infections
During this study, 11 plant species, belonging to 6 botanical families, used in the traditional treatment of urinary tract infections were identified. The Fabaceae family is the most widely represented, with 4 species (36.36%). The Euphorbiaceae and Rhamnaceae families are each represented by 2 species (18.18%). The Moraceae, Olaceae and Poaceae families are each represented by one species (9.09%)
Figure 4: Distribution of plant families recorded
In terms of growth habit, 7 out of 11 (63.63%) of the species recorded are shrubs; 2 out of 11 (18.19%) are shrubs; 1 out of 11 (9.09%) is a herb; and 1 out of 11 (9.09%) is a subshrub.
With regard to citation rates, the most frequently cited plants for the treatment of urinary tract infections are: Cassia sieberiana DC, with 18 citations (57.58%), and Bridelia ferrugineana Mull et arg, with 17 citations (51.52%) (Table 5).
The list of species, the parts used, the methods of preparation and administration, and their citation frequencies (CF) are summarised in Table 5.
Table 5: Species used, parts used, methods of preparation and routes of administration for urinary tract infections
|
N° |
Scientific names |
Local name |
Plant type |
Family |
Parts used |
Form of the drug |
Methods of preparation |
Methods of administration |
Dosage |
Number of citations |
Frequency |
|
1 |
Ficus platyphylla Delile |
Kob (ngambaye) |
Tree |
Moraceae |
Leaves |
Fresh or dried |
Decotion |
Oral route |
Variable |
1 |
3,03 |
|
2 |
Faidherbia albida (Delile) A. Chev. |
Diri (Ngambaye) |
Tree |
Fabaceae |
Bark |
Fresh or dried |
Decotion |
Oral route |
Variable |
1 |
3,03 |
|
3 |
Ziziphus mucronata Willd. |
Ngogro-bichi (Ngambaye) |
Shrub |
Rhamnaceae |
Root or bark |
Fresh or dried |
Decotion |
Oral route |
Variable |
11 |
33,33 |
|
4 |
Eleusine indica (L.) Gaertn. |
Tchoumdaita (Massa) |
Crass |
Poaceae |
Whote plant |
Fresh or dried |
Decotion |
Oral route |
1 glass 3 times a day |
1 |
3,03 |
|
5 |
Cassia sieberiana DC. |
Alala (Ngambaye) |
Shrub |
Fabaceae |
Root |
Fresh |
Decotion |
Oral route |
unchanged |
18 |
54,55 |
|
6 |
Bauhinia rufescens Lam. |
Koulkoul (arabe) |
Shrub |
Fabaceae |
Leaves |
Fresh |
Decotion |
Oral route |
unchanged |
1 |
3,03 |
|
7 |
Senna occidentalis (L.) Link |
Kinkéliba |
Semi-woody |
Fabaceae |
Root |
Fresh or dried |
Decotion |
Oral route |
unchanged |
1 |
3,03 |
|
8 |
Ziziphus mauritiana Lam. |
Ngogro (Ngambaye) |
Shrub |
Rhamnaceae |
Bark |
Fresh or dried |
Decotion |
Oral route |
unchanged |
1 |
3,03 |
|
9 |
Ximenia americana L. |
Tidi (Ngambaye) |
Shrub |
Olacaceae |
Root |
Fresh or dried |
Decotion |
Oral route |
unchanged |
1 |
3,03 |
|
10 |
Flueggea virosa (Roxb. ex Willd.) Voigt |
Kassi (Ngambaye) |
Shrub |
Euphorbiaceae |
Root |
Fresh or dried |
Decotion |
Oral route |
unchanged |
1 |
3,03 |
|
11 |
Bridelia ferrugenea Müll. Arg. |
Sibian (Ngambaye) |
Shrub |
Euphorbiaceae |
Bark |
Fresh or dried |
Decotion |
Oral route |
unchanged |
17 |
51,52 |
Discussion
This ethnobotanical field survey involved interviewing 33 people, 55% of whom were female and 45% male. Both sexes are interested in traditional medicine. However, women use medicinal plants much more than men. As the study focused heavily on children, this high percentage among women can be explained by the fact that, as women have more contact with children, they develop greater knowledge of plants in order to care for them. These findings confirm the results of other ethnobotanical studies conducted in Morocco¹⁵, which found 56.70% women and 43.30% men; Nguinambaye et al., in Chad, found 54% women and 46% men¹⁶. However, they differ from those of Goumou et al., in Guinea, who found a higher proportion among men (58%) than among women (42%)¹⁷.
the field, it was found that practitioners range in age from 21 to 90 years old. The most represented age group is 41–50 years old (30.30%), followed by those aged over 60 (27.28%). The 21–30 and 51–60 age groups are equally represented (15.15%). The 31–40 age group brings up the rear with 12.12%. These results effectively explain why older people are more familiar with traditional herbal medicine compared to other age groups. This trend can be explained by the fact that traditional knowledge has been accumulated over generations. These results are similar to those of Nguinambaye et al., in Chad¹⁶. The overexploitation of plant resources and the growing reliance on modern medicines among younger generations may lead to a loss of knowledge about medicinal plants. These findings are consistent with those of Elhassan et al.,¹⁵ and Goumou et al.,¹⁷. The study showed that traditional practitioners have between 3 and 20 years’ experience. Years of experience provide some assurance of knowledge of plants, as the more one uses them, the more one’s knowledge increases. These findings are also reported by Goumou et al.,¹⁷ and Mbaihougadobé et al.,¹⁸
The study found that the profession is practised by people who do not have a very high level of education. Those with no formal education accounted for the largest proportion (48.49%), followed by those with primary education (39.39%), whilst those with secondary education were under-represented. This high proportion of those with no schooling explains why knowledge of medicinal plants is passed down from parents to children and from master to apprentice. Certain ancestral and cultural practices occupy children from a young age and prevent them from attending school or progressing far in their studies. This was the case for the traditional practitioners in this study. These findings are reported by Nguinambaye et al.,¹⁶, Mbaihougadobé et al.,¹⁸ and Goumou et al.¹⁷. These data show that throughout Chad, the profession is practised much more by people with no schooling or very little schooling.
Of the two diseases covered by this study, it was found that many plants are used in their treatment. For the management of diarrhoea in children, thirteen (13) plants from seven (7) families are used; this figure demonstrates that floral diversity is also a valuable asset in the field of healthcare in Chad. The most represented families are: Fabaceae (38.48%), followed by Combretaceae and Rhamnaceae (15.38%). The species with the highest frequency of mention are: Terminalia avicennioides Guill. et Per. (57.58%) and Detarium microcarpum (51.52%). The study found, through these citations, that knowledge in this field is passed down from one generation to the next and through the sharing of experiences among practitioners in the locality covered by this study. These plants were cited by Lawaly et al. in Niger¹⁹ and Foutse et al. in Cameroon²⁰ in their ethnobotanical studies on plants used to treat gastrointestinal infections.
In the management of urinary tract infections in children, the survey identified eleven medicinal plants belonging to six families. The most common families were the Fabaceae (36.36%), the Euphorbiaceae and the Rhamnaceae (18.18%) each. The most frequently cited species are: Cassia sieberiana DC (54.55%) and Bridelia ferrugenea Mull. et Arg. (51.52%). Whether for gastrointestinal infections or urinary tract infections, the Fabaceae family is dominant; this family contains species with significant antibacterial activity. Studies evaluating the antioxidant and antibacterial activities of all these plants in countries such as Burkina Faso by Ali et al.,²¹ Cameroon by Foutse et al.,²⁰, Côte d’Ivoire by Ambe et al.,²² Nigeria by Mubo et al.,²³ and Senegal by Elhadji et al.,²⁴ have demonstrated high efficacy and are used as alternatives in the treatment of certain bacterial infections.
The Chadian population as a whole is predominantly poor and relies heavily on medicinal plants for primary healthcare. This has enabled them to acquire a good knowledge of medicinal plants. The study involved interviewing a total of 33 traditional healers in the town of Guelendeng and the surrounding area. The respondents were predominantly women (55%), the majority of whom had no formal education or had only completed primary school. Thirteen plants from seven families were identified for the treatment of gastroenteritis, and 11 plants for the treatment of urinary tract infections. Terminalia avicennioides Guill & Perr (57.58%) and Detarium microcarpum Guill & Perr (51.52%) were the most frequently cited for gastroenteric infections. For the treatment of urinary tract infections, Cassia sieberiana DC (54.55%) and Bridelia ferrugenea Müll. Arg. (51.52%) were frequently cited. Further surveys on the same conditions should be conducted in other towns across Chad to gain a comprehensive understanding of the plants used in the treatment of these infections.
Conflicts of Interest: For this article, the authors declare that they have no conflict of interest.
Authors' Contributions: RD contributed to the literature search, field data collection, data analysis and first draft. MAD, MY and DA contributed to the first draft and data analysis. NN contributed to the correction, scientific orientation of the draft and coordinated all the work.
Acknowledgements: The authors would like to thank the staff of the Biology Department of the Faculty of Exact and Applied Sciences, N'Djaména/Chad. The staff of the Faculty of Human Health Sciences, Laboratory for Research, Diagnostics and Scientific Expertise (LaboRedDES), University of N’Djamena.
Références
1- Bredou J. B., Boua B., Konan K. F., Guessennd-K. N., Mamyrbekova-B. Janat A, Bekro Y.-A., Phytochemical and antibacterial investigations of medicinal plants used in the traditional treatment of urinary tract infections in Côte d'Ivoire: the case of Lannea barteri Engl. (Anarcadiaceae), J. Soc. Ouest-Afr. Chim. 2019;047; 8-15
2- WHO. World Health Report: Reducing risks, promoting healthy lives. WHO, 2002 edition, Geneva.
3- Dewa B., Mitan P., Amaht M. A., Bessimbaye N. and Brahim B. O. Escherichia coli Gastroenteritis in Children Aged 0 to 5 in Three Hospitals in Chad. Int. J. Curr. Microbiol. Appl. Sci. 2023;12(12): 152-159. https://doi.org/10.20546/ijcmas.2023.1212.019
4- Lanata CF, Fischer-Walker CL, Olascoaga AC, Torres CX, Aryee MJ, Black RE, on behalf of the Child Health Epidemiology Reference Group of the World Health Organization and UNICEF. Global Causes of Diarrhoeal Disease Mortality in Children <5 Years of Age: A Systematic Review. Sestak K, editor. PLoS ONE. 2013;8(9):72788. https://doi.org/10.1371/journal.pone.0072788 PMid:24023773 PMCid:PMC3762858
5- Titilawo Y, Obi L, Okoh A. Occurrence of virulence gene signatures associated with diarrhoeagenic and non-diarrhoeagenic pathovars of Escherichia coli isolates from selected rivers in south-western Nigeria. BMC Microbiology. 2015; 15(204):1-14 https://doi.org/10.1186/s12866-015-0540-3 PMid:26449767 PMCid:PMC4599032
6- Bruyère, F., Cariou, G., Boiteux, J.-P., Hoznek, A., Mignard, J.-P., Escaravage, L., Bernard, L., Sotto, A., Soussy, C.-J., & Coloby, P. Generalities. Progrès En Urologie, 2008;18 :4-8. https://doi.org/10.1016/S1166-7087(08)70505-0 PMid:18455075
7- Liu L, Oza S, Hogan D, Perin J, Rudan I, Lawn JE, Cousens S, Mathers C, Black RE. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities: an updated systematic analysis. The Lancet. 2015;385(9966):430-40. https://doi.org/10.1016/S0140-6736(14)61698-6 PMid:25280870
8- Savadogoa H., Lassina D, Issa T., Laure Tamini/Toguyenia, Arzouma Idrissa Oue'draogoa, Alain S. O., Sonia K., Aïssata K., Fla Koue'tad, Diarra Ye'a, Urinary tract infections in paediatric patients: bacterial ecology and antibiotic susceptibility at the Charles-de-Gaulle Paediatric University Hospital in Ouagadougou (Burkina Faso); https://doi.org/10.1016/j.nephro.2021.04.003 1769-7255/C 2021 Francophone Society of Nephrology, Dialysis and Transplantation.
9- Kahindo K. C., Kambale M. R, Maganya K. C., epidemiological, clinical, bacteriological and progression profile of urinary tract infection in children aged 0 to 5 years at the North Kivu Provincial Hospital, Journal of the ISTM-Goma./ Rev. Hig. Inst. Med. Techn-Goma June 2019;1(1): 40-49
10- Zafindrasoa Domoina R-R., Fidiniaina Mamy R., Saïda R. et al: Resistance phenotypes of Escherichia coli strains responsible for urinary tract infections at the laboratory of the Befelatanana University Hospital Centre, Antananarivo. Pan African Medical Journal 2017;26:166.
11- M.Ali Mahamata,∗,O. Ngaringuemb, A.D. Mahamat-Nour Abakarb, M. Jallohc, I. Hamata, L. Niangc, S. M. Gueye; Lower urinary tract lithiasis: Diagnostic and therapeutic aspects at the Mother and Child Hospital (HME) in N'Djamena (Chad); African Journal of Urology 2017;23:295-299
12- NABTI L. Z., Thesis: Antibiotic and essential oil sensitivity of Origanum glandulosum Desf. in Escherichia coli strains isolated from urinary tract infections at the University Hospital of Sétif. Defended publicly on 17 November 2020.
13- Bakarnga-Via, I.; Potaisso D., Bessimbaye N., Issa R. A., Brahim B. O., Abdoullahi H. O., Mbaigolmem B. V., and Abdelsalam T. Antiradical and antibacterial activities of the athanolic extract bark of Anogeissus leiocarpus (Guill. Et Perr) from Chad. Journal of Medical Plants Studies 2022;10-6):127-132. https://doi.org/10.22271/plants.2022.v10.i6b.1499
14- Bessimbaye N, Haoua A. B., Ali S.M., Bakarnga V.I. and Mbayngone E., Phytochemical study and evaluation of the antibacterial activity of extracts from Acacia amythethophylla Steud. ex A. Rich. (Fabaceae) against bacteria responsible for urinary tract infections. American Journal of Science and Education Research: AJSER, 2024;165.
15- Elhassan I., Fouad M., and Khalil C., Ethnobotanical survey of medicinal plants used in treatment of kidney stones in Tarfaya province (Morocco), International Journal of Innovation and Applied Studies, 2019;26(3):711-719
16- Nguinambaye M. M. , Christophe D., Eugène E., Brahim B. O., Béchir A. S. and Mahamat B. A., Survey of traditional healers and inventory of medicinal plants in selected ecosystems of the Mao Department in Chad; Afrique SCIENCE 18(1) 2021;56-68 56 ISSN 1813-548X, http://www.afriquescience.net
17- GOUMOU K., HABA N. L., TRAORE M. S., BAH F., BALDE M. A., An ethnobotanical study on the use of medicinal plants in the traditional treatment of skin conditions in Guinea, RAMReS Journal - African Traditional Medicine and Pharmacy Series, 2022;21(1):50-65. ISSN 2630-1296
18- Mbaihougadobe S., Nguinambaye M. M., Mbaiogaou A., Mbaissidara R., Mbayngone E., Yaya M., Ethnobotanical and phytochemical study of eleusine coracana (l.) gaertner), plants used in various ways in Chad, World Journal of Pharmaceutical Volume 4, Issue 1, 2025 ISSN: 2583-6579 Science and Research, 2025;4(1) :1-16
19- Lawaly M. M., Idrissa M., Khalid I., Medicinal plants used in the treatment of diarrhoea in Niger. An ethnobotanical study, Algerian Journal of Natural Products 2017;5(2):475-482, Online ISSN: 2353-0391, www.univ-bejaia.dz/ajnp
20- FOUTSE Y., thesis: ethnobotanical survey of medicinal plants used in western cameroon: phytochemical and pharmacological study of afzelia africana J.E. Smith ex Pers. Presented on 8 December 2017 in Marseille
21- Ali BM, Youssouf AG, Djamalladine MD, Brahim A.A., Zongo C., Sanon S. and Savadogo A., study of the pharmacological properties of the three plants used in medicine, ejbps, 2022;9(9):400-407.
22- AMBE A. Serge A., ODOH A. E., Yao K., KOUASSI R. H. and Z. Guédé N., Antioxidant activity and determination of total polyphenol and flavonoid content in Bridelia ferruginea Benth. and Enantia polycarpa (DC) Engl. and Diels, two plants used in the traditional treatment of diarrhoea in Abidjan (Ivory Coast), RAMReS Journal - African Traditional Medicine and Pharmacy Series, 2022;21(2):46-53.
23- Mubo A. S., Caleb O. O, Akingbolabo D. O., Opeyemi J. A., Samuel A. A., Pharmacognostic Standardisation and Antioxidant Activity of Cassia sieberiana DC. (Fabaceae) , JOPAT, 2024;23(2):1398- 1410. https://doi.org/10.4314/jopat.v23i2.1
24- Elhadji O. F., Rokhaya G., Abdoulaye D., Idrissa W. F., Pape I. D., Harouna T., Thierno M. W., Kady D. B., Mbaye D., Assane D., Amadou D., Khadidiatou T., Serigne O.S., Amadou D., Bara N., Cheikh S. B. B. and Yérim D., Phytochemical characterisation and study of the antimicrobial activity of leaf extracts from three plants of the Senegalese flora: Detarium senegalense, Detarium microcarpum and Piliostigma reticulatum Int. J. Biol. Chem. Sci. 2022;16(1):286-299. https://doi.org/10.4314/ijbcs.v16i1.24