Traditional knowledge of childhood illnesses among the Sidama nation, clinical presentation and hematological findings

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Background: Sidama possesses extensive indigenous knowledge regarding infant illnesses described as “feyancho”. Feyancho has a widespread recognition among Sidama people, though poorly documented in scientific literature. This study aimed to document the indigenous understanding of this infantile disease and examine associated clinical and biochemical profiles in the Sidama National Regional State, Ethiopia.

Methods: A household-based cross-sectional study was conducted in nine districts selected using systematic random sampling method. Data was collected through household surveys (n = 436), focus group discussions (FGDs), and clinical assessments. Clinical and biochemical evaluations were performed on children affected by” feyancho” disease.

Result: The overall prevalence of “feyancho” was 59.52%. Most respondents (66.51%) believed that maternal health influences the occurrence of “feyancho” disease. In the study group, liver function tests showed elevated levels of SGOT (AST), ALP, and direct bilirubin in more than half of the children.

Additionally, 25% presented low glucose and elevated total bilirubin. Hematological analyses revealed significant increases in LYM (+128%), EOS (+76.92%), LYM% (+79.6%), RDW-CV (+36.23%), PDW (+35.74%), and PCT (+1015.79%). Conversely, decreases were observed in NEU (−29.05%), NEU% (−36.78%), RBC (−13.26%), HGB (−28.07%), HCT (−29.36%), MCV (−20.73%), and PLT (−25.67%).

Conclusion: The Sidama people’s indigenous knowledge of infantile diseases remains an integral part of local health practices. Clinical and biochemical findings suggest conditions such as microcytic anemia, inflammation, or chronic infections. Safeguarding this traditional knowledge and validating it scientifically is crucial, requiring more comprehensive research.

Introduction Indigenous knowledge systems (IKS) play a crucial role in the understanding childhood diseases and have been used for generations to diagnose and treat illnesses [ 1 , 2 ]. The Sidama nation commonly defines infantile diseases as “ Feyancho ”. The “ feyancho ” can be either a milder form, locally called “ Sidancho ”, or a severe form, also locally known as “ Arusicho ”.

This study is the first of its kind in attempting to document this indigenous knowledge on community understanding of diseases, providing a foundation for future research in the field. The finding of the study will be used as a starting point for the integration of IKS on identifying diseases and aligning to modern medicine understanding and treatment. Indigenous communities follow a holistic approach to diagnosing and managing infantile illnesses, integrating cultural beliefs, environmental observations, and generational knowledge.

Unlike biomedical methods that focus on specific pathogens, traditional diagnosis relies on symptom-based assessments, spiritual interpretations, and behavioural changes. Infantile illnesses are often identified through signs such as appetite loss, restlessness, body temperature fluctuations, or digestive disturbances [ 3 ]. Studying traditional understanding of infantile diseases is crucial to have a clear picture of the merits and demerits.

Understanding these practices enables healthcare providers to foster trust, bridge cultural gaps, and integrate effective remedies into formal healthcare, ultimately enhancing infant health outcomes while preserving cultural heritage [ 4 ]. There has been no scientific investigation into how these diseases are understood by the local community. To fill this gap, the present study aimed to document the IKS related to “ feyancho ” among selected rural communities in the Sidama National Regional State (SNRS) and explored how people in the study area understand this infant disease.

This case study also examined the study participants clinically and biochemically. Materials and methods Study design A community-based cross-sectional mixed-methods study was conducted from January to December 2023 in the Sidama National Regional State (SNRS), Ethiopia. The study integrated quantitative household surveys, qualitative Focus Group Discussions (FGDs), and clinical, biochemical, and hematological assessments to comprehensively document indigenous knowledge related to the infantile disease locally known as “feyancho” and to examine associated clinical and laboratory findings.

The study consisted of two distinct components: A community-based cross-sectional survey involving 436 participants to document Indigenous knowledge, perceptions, and practices related to Feyancho. A clinical case series involving 13 infants diagnosed with Feyancho during the study period, in which clinical symptoms are examined and among which12 have consented for blood samples collection for hematological and biochemical analyses. The protocol of this study is supplied Supporting Information S1 File .

The study area The study was conducted in nine (9) Woredas (Districts) of the SNRS stratified based on the agro-climatic zones of the region. Two kebeles (the smallest administrative unit) were randomly selected from each woreda. Three different agro-climatic zones exist in Sidama [ 5 ].

These are “ Kolla ”, “ Woina Dega ” and “ Dega ” agro-climatic zones. ‘ Kolla’ is characterized by a dry, hot tropical climate area and lies between 500 and 1500 meters above sea level. It receives an annual rainfall of 400–800 mm, with a mean annual temperature of 20–25 °C and constitutes 30% of the total area.

The ‘ Woina Dega ’ is characterized by a moist to humid, warm subtropical climate and is found between 1500–2500 meters above sea level, with an annual rainfall of 1000–1800 mm. This agro-climatic zone has a mean annual temperature of 15–20 °C and constitutes 54% of the total area of the region. The ‘Dega’ agro-climatic zone is known with its wet, cool temperate climate.

“ Dega ” has an elevation of 2500–3500 meters above sea level and receives an annual rainfall of 1200–1800 mm, and the mean annual temperature is 10–15 °C and constitutes only 16% of the total area of the region [ 6 ]. The nine woredas included in the present study were Borricha, Daraara and Hawassa Zuria woredas representing Qolla’ (dry, hot tropical climate); Haweela, Daalle, Daarra woredas from Woina Dega’ (moist to humid, warm subtropical climate) and Hula, Bursa and Arbagoona from Dega’ (wet, cool temperate climate). From each of the selected districts, two kebeles (a total of 18 kebeles) were randomly selected for the study.

The sampling units are households from the selected kebeles. The study area is presented in Fig 1 . 10.1371/journal.pone.0340246.g001 Fig 1 Map showing the woredas (districts) included in the study from Sidama National Regional State, Ethiopia.

“A” drawn using QGIS; administrative boundaries are from geoBoundaries ( https://www.geoboundaries.org/ ), used under Creative Commons Attribution 4.0 International License. “B” generated from Kobo Collect using Leaflet with OpenStreetMap base map tiles (OpenStreetMap contributors), used under the Open Data Commons Open Database License (ODbL). Study population and sample collection There is a detailed survey report based on the data collected regarding “ feyancho ” disease in SNRS, Ethiopia.

The socio-demographics, understanding of diseases and symptoms of” feyancho”, perception on disease transmission and prevention were recorded. In addition, clinical samples from children affected by the “ feyancho ” were collected for biochemical analysis. Household sample units were studied to determine the prevalence of infant diseases.

The prevalence of “ feyancho ” was based on the number of total births in the sampled households. The sample size for this study was determined based on the presence of attribute in the general population which was estimated to be at 50%. Thus, the sample size was calculated based on a single population proportion formula by taking the margin of error of 0.05 at 95% confidence level (CI), the total household unit sampled as n= (Zα/2) 2 p (1-p)/d 2 .

In addition, 10% of non-response rate was considered. Accordingly, a total of 436 study participants were included in the study. The prevalence of “feyancho”, as defined by the community, in the SNRS was determined.

During this investigation, people’s perceptions and definitions of “feyancho” disease were documented. Clinical characterization and hematological parameters were evaluated from clinical samples collected from infants claimed to be affected by “feyancho”. Household survey participants.

The study population comprised households residing in selected kebeles of the SNRS. Household heads or primary caregivers (preferably mothers or fathers) were eligible if they had at least one child and were willing to participate. Households were excluded if no responsible adult was available at the time of data collection or if consent was not provided.

Clinical and laboratory participants. Children identified by caregivers and the community as having “feyancho” (either sidancho or arusicho) were eligible for clinical examination and laboratory investigations. Written informed consent was obtained from parents or guardians prior to sample collection.

Sample collection and hematological analysis. Venous blood samples were collected from children identified with “feyancho” using aseptic techniques by trained medical laboratory professionals. Approximately 2–3 mL of blood was drawn from each child and divided into appropriate collection tubes: EDTA tubes for hematological analysis and plain or serum separator tubes for biochemical analysis.

Blood samples were gently mixed to prevent clotting and transported in cold boxes to the laboratory within 2-hour time. Samples for hematological analysis were processed promptly, while serum samples were allowed to clot, centrifuged, and stored under appropriate conditions until analysis. Hematological parameters including white blood cell count, differential counts, red blood cell indices, hemoglobin, hematocrit, platelet indices, and red cell distribution width were analyzed using a standard automated hematology analyzer following manufacturer instructions and laboratory quality control procedures.

Internal quality checks were performed daily to ensure reliability and accuracy of results. Biochemical parameters such as liver enzymes, glucose, bilirubin, urea, creatinine, and lipid profile were measured using standard clinical chemistry analyzers according to established laboratory protocols. FGD design and participant selection.

Focus Group Discussions (FGDs) were conducted first to gain clearer understanding of the community, community definition of the disease’s concepts. This complemented to the household survey data and to gain in-depth insight into community perceptions, indigenous classifications, symptoms, transmission beliefs, and amelioration practices related to the infantile disease locally known as “feyancho.” Participants were selected using purposive sampling to include community members with lived experience and cultural knowledge of childhood illnesses, including parents, caregivers, elders, and individuals recognized locally for their traditional health knowledge. FGD composition and setting.

A total of eight FGD sessions were conducted across selected kebeles in the study districts. Each FGD consisted of 6–10 participants, allowing for active interaction and balanced participation. Discussions were held in familiar and neutral community settings to ensure participant comfort and openness.

Where necessary, groups were organized to minimize social or cultural power imbalances. Data collection procedure. FGDs were moderated by trained facilitators fluent in the local Sidama language, with assistance from note-takers.

Moderators encouraged inclusive participation and guided discussions using probing questions where appropriate. Each discussion lasted approximately 60–90 minutes. All sessions were audio-recorded with participants’ consent, and detailed field notes were taken to capture non-verbal cues, group dynamics, and contextual observations.

Data management. Audio recordings were transcribed verbatim and translated into English where necessary. Transcripts were checked against recordings to ensure accuracy.

All personal identifiers were removed to maintain confidentiality, and data were securely stored. Ethics approval and consent to participate. A cross-sectional household level study was conducted from January 2023 to December 2023.

Informed written assent (consent) was obtained from parents or guardians for the case study. The study was conducted in accordance with the guidelines required by the National Health Council of Ethiopia through Hawassa University Research Ethics Review Committee (Ref no: RERC 02,2022) in accordance with the Declaration of Helsinki. Data analysis.

Data entry and validation were done using STATA and every possible data quality assurance approaches were followed throughout the study period. Descriptive statistics (percentages and frequency) are used to summarize the data. FGD data analysis.

FGD data were analysed using a thematic analysis approach, following an iterative and systematic process to identify key patterns and meanings related to community understanding of “feyancho.” Data analysis was conducted manually. To ensure methodological rigor, credibility was enhanced through triangulation of FGD findings with household survey data. Dependability was supported by maintaining a clear audit trail of coding and theme development, while confirmability was strengthened through team discussions and reflexive review of interpretations.

Results Socio-demographic characteristics A total of 436 households were included from nine Woredas, with a diverse representation across the region. Each woreda was represented with about 9.86–12.16% participants from two kebeles. The respondents have varying educational backgrounds, ranging from no formal education to higher education levels.

The respondents have diverse religious affiliations, but the majority identify as Christian (Protestants). The mean age of household fathers is 45.66 (SD = 16.22) years while the median age of household mothers is 39.33 (SD = 13.50) years. The mean family size is notably larger than the mean total number of children, indicating that households also include other members beyond children, such as adults, Table 1 .

10.1371/journal.pone.0340246.t001 Table 1 Socio-demographic characteristics of the study participants (N = 436), 2023. Categorical variables Variables Category N (%) Variables Category N (%) Education Level of Household mother No formal education 188 (43.12%) Education Level of Household father No formal education 187 (42.89%) Some Primary school 184 (42.20%) Some Primary school 133 (30.50%) Some Secondary school 12 (2.75%) Some Secondary school 24 (5.50%) High school complete 22 (5.05%) High school complete 45 (10.32%) Diploma 19 (4.36%) Diploma 18 (4.13%) Bachelor’s degree 4 (0.92%) Bachelor’s degree 17 (3.90%) Master’s degree 1 (0.23%) Master’s degree 1 (0.23%) Religion of Household father Christian-protestant 352 (80.73%) Religion of Household mother Christian-protestant 346 (79.36%) Apostolic 40 (9.17%) Apostolic 44 (10.09%) Catholics 15 (3.44%) Catholics 14 (3.21%) Muslim 11 (2.52%) Muslim 11 (2.52%) Adventist 9 (2.06%) Adventist 9 (2.06%) Christian-orthodox 6 (1.38%) Christian-orthodox 7 (1.61%) Atheist 2 (0.46%) Atheist 1 (0.23%) Traditional 1 (0.23%) Traditional 1 (0.23%) Continuous variables Mean Median Mode Standard Deviation Family Size 6.03 6.0 7.0 2.19 No of Children 5.21 4 2 3.27 No of Male 2.72 2 2 2.01 No of female 2.49 2 2 1.82 Prevalence of the infant diseases (“feyancho”) “Feyancho” was widely reported, with 67.2% of households indicating mild cases and over half reporting severe cases. Most participants believed transmission occurs from mother to child (57.3%) or through breastfeeding (40.4%), while fewer mentioned contact, genetic, or airborne routes.

The condition was most commonly reported in infants under one year of age (50%), Table 2 . 10.1371/journal.pone.0340246.t002 Table 2 Prevalence of “ feyancho ” as defined by the community among study participants (N = 436), 2023. Variable Category Frequency (%) Households have children with a mild “feyancho” (Sidancho) Yes 275 (67.24%) No 134 (32.76%) Households have children with a severe “feyancho” (Arusicho) Yes 124 (58.22%) No 89 (20.41%) Household belief on route of transmission of “feyancho” Mother to child (MTC) 250 (57.34%) Breastfeeding 176 (40.37%) Contact 63 (14.45%) Genetic 41 (9.4%) Airborne 2 (0.46%) Age of infants affected by “feyancho” Up to 1 year 218 (50%) Up to 5 months 73 (16.74%) Up to 3 months 62 (14.22%) According to the participants, sidancho or arusicho primarily affects very young children, with the highest prevalence observed in infants up to one year old, as reported by 218 respondents (50%).

Within this age range, 19 respondents (4.36%) specifically identified children up to 8–10 months, while 73 respondents (16.74%) noted cases in infants between 3–5 months. Additionally, 62 respondents (14.22%) indicated that children up to 3 months were affected ( Table 2 ). The data highlights that early infancy is the most vulnerable period for these diseases, emphasizing the need for targeted health interventions during this stage.

Study participants’ belief on the mechanisms of transmission of the diseases Most participants (N = 290; 66.51%) believed that a mother affected by “ feyancho ” increases the likelihood of her children being affected. In contrast, 73 respondents (16.74%) did not share this belief. These findings suggest that most participants recognize a potential hereditary or environmental link between a mother’s condition and her children’s susceptibility to “ feyancho ”.

The participants identified several possible ways through which “ feyancho ” may be transmitted. The most believed mode of transmission was direct transmission from mother to child, with 250 respondents (57.34%) supporting this view. Similarly, a significant portion of respondents (176 cases, 40.37%) believed that transmission occurs through breastfeeding, indicating concerns about the role of maternal feeding practices in the spread of the disease.

Overall, the findings indicate that most participants believe maternal transmission, particularly through direct contact and breastfeeding, is the primary way “ feyancho ” spreads among children, Table 2 . Community’s perception about the symptoms and amelioration of “ feyancho ” Focused group discussions (FDGs) were conducted with community participants to complement the data obtained from structured interviews. A total of eight interview sessions were carried out to explore people’s understanding of the disease condition known as ”feyancho” .

The summaries of these interviews provide insights into participants’ perceptions and statements and are complementary with the interview findings. Sidama nation categorizes “ feyancho ” into two types: arusicho (a severe form) and sidancho (a milder form). “ Feyancho” is characterized by a range of symptoms and conditions.

Severe cases are characterized by skin peeling, sunken fontanels, emaciation, and stomach issues. Milder conditions involve symptoms such as stomach-aches, diarrhoea, restlessness, and minor skin rashes. The amelioration of the conditions is characterized by purging of green diarrhoea, disappearance of rushes, good sleeping, and fontanels normalized, resumes normal breastfeeding, physical betterment and fattening, the stiffened belly begins to soften and so on.

Symptoms and characteristics of the diseases as defined by the community The symptoms vary in frequency, with skin rashes being the most common and hair loss the least common among those believed to be affected by the milder form of “ feyancho ” ( Sidancho ). Significant portion of individuals report abdominal pain as one of major symptoms, Fig 2 . 10.1371/journal.pone.0340246.g002 Fig 2 Frequency of common symptom of the mild “ feyancho ” ( Sidancho ) as described by the community.

The severe form of “ feyancho ” ( Arusicho ) is associated with several symptoms, which may include physical symptoms, psychological symptoms and cultural or spiritual implications: in some contexts, the symptoms might be interpreted as being linked to cultural or spiritual beliefs, potentially influencing the perception and treatment of the symptoms. Most reported symptom during the severe form of “ feyancho ” ( arusicho ) is that of sunken fontanelle, Fig 3 . 10.1371/journal.pone.0340246.g003 Fig 3 Frequency of common symptom of the severe form of “ feyancho ” ( arusicho ) as described by the community.

Clinical characteristics of children claimed to have “ feyancho” Examinations were conducted by physicians to clinically define the “ feyancho” (arusicho/sidancho) . It included data on the place of birth, previous episodes, symptom resolution, and gender distribution. The table also covered medical evaluation and hospitalization history, maternal employment, respiratory and environmental exposures, and immunization status.

Various symptoms and conditions were detailed, such as fever, sweating, chills, cough, wheezing, shortness of breath, chest pain, runny nose, throat issues, difficulty swallowing, ear pain, red draining eye, muscle ache, joint pain, swollen glands, rash, stiffened neck, seizures, vomiting, diarrhea, bloody urine, yellow skin/eyes, weight loss, irritability, skin rashes, and hair loss, Table 3 . 10.1371/journal.pone.0340246.t003 Table 3 Clinical characteristics of “feyancho” (sidancho/ arusicho) in SNRS, (N = 13), 2023. Characteristics Options Frequency (%) Characteristics Options Frequency (%) Place of birth Facility-based 11(84.62) Muscle ache Yes 0 No 8(61.54) Home delivery 2(15.38) UK 5(38.46) Ever have similar episode Yes 3(23.08) Joint pain/ swelling Yes 0 No 10(76.92) No 13(100) Similar case in the vicinity Yes 3(23.08) Enlarged/swollen glands Yes 1(7.69) No 10(76.92) No 12(92.31) Symptom-resolved without intervention Yes 3(23.08) Rash Yes 9(69.23) No 10(76.92) No 4(30.77) Sex Male 9(69.23) Red draining eye Yes 1(7.69) Female 4(30.77) No 12(92.31) Ever evaluated by physician before Yes 1(7.69) Bloody urea Yes 0 No 12(92.31) No 13(100) Ever hospitalized Yes 1(7.69) Yellow skin/eye Yes 0 No 12(92.31) No 13(100) Mother works outside home Yes 3(23.08) T 0 c raised Yes 0 No 10(76.92) No 3(23.08) Ever have respiratory distress Yes 0 Wheezing bronchi UK 10(76.92) No 13(100) Yes 0 Ever exposed to soil Yes 4(30.77) Mucosal lesions No 2(15.38) No 9(69.23) UK 11(84.62) Have pets in the same house Yes 5(38.46) Altered mental status Yes 2(15.38) No 8(61.54) No 11(84.62) Ever have contacts with pets Yes 2(15.38) Neurological abnormalities Yes 0 No 11(84.62) No 13(100) Ever have contacts with rodents Yes 4(30.77) Hepatosplenomegaly Yes 0 No 9(69.23) No 13(100) Immunized Yes 13(100) Jaundice Yes 0 No 0 No 4(30.77) Ever used medication including OTC Yes 7(53.85) Excessive crying UK 9(69.23) No 6(46.15) Yes 0 Ever have depressed fontanelle Yes 0 Constipation No 13(100) No 6(46.15) Yes 9(69.23) Unknown 7(53.85) No 4(30.77) Current fever Yes 7(53.85) Failure to thrive Yes 1(7.69) No 6(46.15) No 12(92.31) Current sweet Yes 10(76.92) Reduced breast Feeding Yes 5(38.46) No 3(23.08) No 8(61.54) Current chills Yes 2(15.38) Abdominal pain Yes 4(30.77) No 11(84.62) No 9(69.23) Current cough Yes 7(53.85) Watery diarrhea Yes 0 No 6(46.15) No 5(38.46) Current cough with sputum Yes 0 Weight loss UK 8(61.54) No 13(100) Yes 10(76.92) Wheezing Yes 0 Irritability No 3(23.08) No 12(92.31) Yes 11(84.62) Unknown 1(7.69) No 2(15.38) Shortness of breath Yes 0 Skin rashes Yes 10(76.92) No 12(92.31) No 3(23.08) Chest pain Yes Hair loss Yes 10(76.92) No 7(53.85) No 3(23.08) Unknown 6(46.15) Yes 2(15.38) Runny nose Yes 0 Stiff neck No 11(84.62) No 13(100) Yes 1(7.69) Nose throat Yes 2(15.38) Seizures No 12(92.31) No 11(84.62) Yes 2(15.38) Difficulty swallowing Yes 1(7.69) Vomiting No 11(84.62) No 12(92.31) Yes 7(53.85) Ear pain Yes 1(7.69) Vomiting with blood No 6(46.15) No 8(61.54) Yes 0 Unknown 4(30.77) No 13(100) Clinical manifestations of the “ feyancho ” disease A total of 12 clinical cases were investigated.

The study found that creatinine and serum glutamic-pyruvic transaminase (SGPT) / alanine aminotransferase (ALT) levels were within normal ranges for all participants. However, blood urea levels were elevated in one participant (8.33%). A significant percentage of participants exhibited elevated levels of Serum Glutamic-Oxaloacetic Transaminase (SGOT) aspartate aminotransferase (AST) (58.33%), Alkaline Phosphatase (ALP) (91.66%), and Direct Bilirubin (DB) (58.33%).

Cholesterol levels were within a healthy range across the participants, bilirubin findings (both total and direct) pointed to mild jaundice in some cases. Overall, this study highlights that while most participants exhibit healthy biochemical profiles, a subset presented with abnormal liver enzyme levels and elevated bilirubin, Table 4 . 10.1371/journal.pone.0340246.t004 Table 4 Clinical chemistry of samples collected from children with Feyancho disease, (N = 12) 2023.

Variable Range in study Mean Range less than 1year %below normal %above normal Laboratory range Creatinine (mg/dl) 0.21-0.39 0.31 0.2-0.4 0 0 0.9-1.3 Urea (mg/dl) 6.3-18.2 12.21 5–18 0 8.33 16.6-48.5 SGPT U/L 11.3-50.9 24.72 7-56 0 0 0-41 SGOT U/L 5-40 52.69 5-40 0 58.33 0-40 ALP U/L 244.8 −1237.9 701.9 81.9 - 350.3 0 91.66 120-460 TC (mg/dl) 70.9 −147.9 121.92 ± 29.19 <170 0 0 0-200 Glucose (mg/dl) 56.0–108.8 74.83 ± 13.97 60-200 8.33 0 74-109 Albumin (g/l) 3.52-4.66 4.35 ± 38.84 3.4–5.2 0 3.5-5.2 TB (mg/dl) 0.2- 3.28 1.15 ± 1.01 <2.0 0 25 0.2-1.0 DB (mg/dl) 0.23 −4.15 1.40 ± 1.36 <0.3 0 58.33 0-0.2 TP (mg/dl) 6.6 −8.6 7.83 ± 0.58 4.5 −7.0 6.6-8.7 Hematological parameters of the “ feyancho ” disease The haematological profile of children with Feyancho disease demonstrated abnormalities across all major blood cell lineages. Mild leukocytosis was observed, characterized by marked lymphocytosis with concurrent neutropenia and increased eosinophil counts, while monocyte and basophil counts were reduced. Red blood cell indices indicated microcytic, hypochromic anaemia, evidenced by reduced RBC count, haemoglobin, haematocrit, MCV, and MCH, with normal MCHC and elevated RDW, suggesting significant anisocytosis.

Platelet analysis showed a moderately reduced platelet count with increased PDW, whereas MPV, PCT, and P-LCR remained within normal limits, indicating altered platelet morphology despite preserved platelet size indices. Overall, the findings suggest that Feyancho disease is associated with abnormalities in erythrocyte, leukocyte, and platelet parameters, Table 5 . 10.1371/journal.pone.0340246.t005 Table 5 Investigation of the hematological parameters of the samples collected from children with Feyancho disease, (N = 12), 2023.

Variable Min value Max value Observed Mean Normal Mean Difference % Difference Deviation WBC (×10³/µL) 4.560 18.21 8.84 7.5 +1.34 +17.87% Elevated NEU (×10³/µL) 1.300 6.86 3.37 4.75 -1.38 -29.05% Decreased LYM (×10³/µL) 2.760 7.33 4.56 2.0 +2.56 +128.00% Elevated MON (×10³/µL) 0.200 0.93 0.42 0.6 -0.18 -30.00% Decreased EOS (×10³/µL) 0.050 3.24 0.46 0.26 +0.20 +76.92% Elevated BAS (×10³/µL) 0.020 0.02 0.02 0.1 -0.08 -80.00% Decreased NEU % 21.400 50.80 37.93 60.0 -22.07 -36.78% Decreased LYM % 36.000 70.60 53.88 30.0 +23.88 +79.60% Elevated MON % 2.400 7.00 4.78 5.0 -0.22 -4.40% Normal EOS % 0.700 17.80 3.52 3.5 +0.02 +0.57% Normal BAS % 0.100 0.50 0.29 0.5 -0.21 -42.00% Decreased RBC (×10⁶/µL) 2.510 4.98 4.12 4.75 -0.63 -13.26% Decreased HGB (g/dL) 4.600 14.00 10.07 14.0 -3.93 -28.07% Decreased HCT (%) 15.400 40.60 29.67 42.0 -12.33 -29.36% Decreased MCV (fL) 54.500 81.80 71.34 90.0 -18.66 -20.73% Decreased MCH (pg) 16.200 28.20 24.24 29.5 -5.26 -17.83% Decreased MCHC (g/dL) 29.800 37.20 33.86 34.0 -0.14 -0.41% Normal RDW-CV (%) 13.300 25.90 17.71 13.0 +4.71 +36.23% Elevated RDW-SD (fL) 39.700 55.70 47.12 42.5 +4.62 +10.87% Elevated PLT (×10³/µL) 17.000 501.00 223.0 300 -77.0 -25.67% Decreased MPV (fL) 7.100 12.40 9.34 9.5 -0.16 -1.68% Normal PDW (fL) 14.300 16.40 15.61 11.5 +4.11 +35.74% Elevated PCT (%) 0.120 4.55 0.214 0.23 -0.016 -6.96% Normal PLCR 0.172 0.44 0.25 0.28 -0.03 -10.71% Normal Discussion Illnesses in newborns typically range from mild skin rashes and common colds to more severe infections and genetic defects. While some are easily managed at home, others may require prompt medical attention. “ Feyancho ” among Sidama nation is characterized symptomatically and almost exclusively managed at home.

Yet, its western equivalence has not yet been established. To establish the etiological manifestations, communities’ description of the diseases, signs and symptoms, clinical samples were analyzed. This study, the first in its kind, has found out that the overall prevalence of “ feyancho ” was 59.52%.

The disease is higher among females (63.93%) than males (55.48%). Clinical evaluations of “ feyancho ” cases revealed the possibility of microcytic anemia, high lymphocytes, low neutrophils, increased RDW (Red Cell Distribution Width) , and anisocytosis, suggest iron deficiency, inflammation, or chronic infection. Slightly higher prevalence among female might indicate that females are either more susceptible to “ feyancho ” disease possibly due to biological or environmental factors.

A previous study conducted in the region found that all children tested were positive for fungal elements (dermatophytosis) in microscopy with 97.6% exhibited growth in culture [ 7 ]. The skin manifestations observed in the current study participants may agree with the report. Regarding disease classification, participants categorized “ feyancho ” into two types: sidancho (a milder form) and arusicho (a severe form).

Arusicho is associated with more severe clinical manifestations mainly manifested as sunken fontanelles and ultimately leads to death if left untreated with traditional treatments. A sunken fontanel can be caused by dehydration, kwashiorkor (severe protein deficiency), failure to thrive (poor growth in children), and serious medical conditions like toxic megacolon and diabetes insipidus. The understanding of this condition as well as prevention and treatment have corresponded to the specific cultural setting and is a culturally interpreted symptom [ 8 ].

The study of Tswana-speaking urbanites’ cultural perceptions of diarrhoeal disease in infants is often linked to sorcery, with concepts like “phogwane” (sunken fontanelle) and “kokwana” (intestinal snake) used to explain its origins [ 9 ]. This concept of a sunken fontanelle overrides among several communities and is attributed to various understandings and treatment aspects, and culturally informed and plausible approaches are important to such conditions [ 10 ]. A significant majority (66.51%) of respondents believed that mothers affected by “ feyancho ” increased the likelihood of their children contracting the disease.

Maternal-to-child transmission was considered the primary route (57.34%), followed by transmission through breastfeeding (40.37%) and direct contact among children (14.45%). Genetic and airborne transmissions were believed to play a minimal role. This indicates that cultural beliefs about transmission heavily influence local health perceptions and may impact preventive health behaviors.

Medical evaluations provided additional insights into the disease’s presentation. Notably, symptoms such as excessive crying, weight loss, and irritability were commonly observed in affected children. Despite the widespread community belief in maternal transmission, clinical examinations did not find strong correlations with maternal health conditions.

Furthermore, hospitalization rates among affected children were low, suggesting either underreporting of severe cases or limited access to healthcare facilities. Laboratory analysis revealed that a significant portion of participants exhibited elevated SGOT, ALP, and direct bilirubin (DB) levels, suggesting potential liver dysfunction or stress, possibly linked to the underlying conditions affecting liver function or even possible toxicity of herbal medicine use. In contrast, creatinine and urea levels remained mostly within normal ranges, indicating no major kidney issues.

However, the slight elevation in urea observed in some participants warrants further assessment of hydration status or early signs of kidney function impairment. While cholesterol levels were within a healthy range across participants, bilirubin findings (both total and direct) pointed to mild jaundice in some cases—an expected condition in infants but one that requires close monitoring. Overall, this study highlights that while most participants exhibit healthy biochemical profiles, a subset presents with abnormal liver enzyme levels and elevated bilirubin, warranting further investigation to rule out any underlying health concerns.

The haematological analysis revealed several key findings. Red blood cell (RBC) parameters suggest a prevalence of anaemia among participants, as evidenced by low RBC count, haemoglobin, and haematocrit levels. The reduced mean corpuscular volume (MCV) and mean corpuscular haemoglobin (MCH) indicate microcytic anaemia, commonly associated with iron deficiency [ 11 , 12 ].

Despite these findings, the mean corpuscular haemoglobin concentration (MCHC) remained within normal limits, suggesting that while red blood cells were smaller; their haemoglobin concentration was not significantly altered. An elevated red cell distribution width (RDW) further supports the presence of anisocytosis, a condition characterized by varying RBC sizes, often seen in nutritional deficiencies [ 13 ]. Platelet counts were within the normal range, indicating no major clotting disorders, though platelet distribution width (PDW) were slightly reduced, suggesting variations in platelet size and potential changes in platelet production.

Additionally, elevated lymphocyte levels may point to underlying viral infections or chronic inflammatory conditions [ 14 ]. Despite slight increases in PDW, platelet function appears normal, as overall platelet counts remain within the expected range. Lastly, eosinophil levels show mild elevations in some cases, which could indicate allergic reactions or parasitic infections among certain participants [ 15 ].

The lower-than-normal neutrophil percentage likely correlates with the relatively higher lymphocyte count, reinforcing the possibility of underlying viral infections. Overall, these hematological abnormalities suggest that children with Feyancho disease experience multisystem hematological disturbances, dominated by microcytic iron-deficiency anemia, lymphocyte-predominant leukocyte responses, relative neutropenia, eosinophilia, and anisocytosis. Conclusion This study provided valuable insights into the characteristics and health conditions associated with “ feyancho ”.

The findings underscore the need for targeted interventions to address both healthcare access and community health education to mitigate the impact of “ feyancho ”. Given the high prevalence of “ feyancho ” and the strong cultural beliefs surrounding its transmission, community-based health education programs should be implemented. These programs should focus on improving awareness of evidence-based disease transmission and preventive measures.

Currently, cases are managed through traditional methods. Strengthening collaboration between healthcare providers and local communities will be very crucial in improving child health outcomes in the region. Further epidemiological studies that integrate medical diagnostics with community perceptions could help bridge the knowledge gap and inform public health interventions.

The findings also support the need for comprehensive clinical evaluation, including assessment of iron status (serum ferritin, transferrin saturation), inflammatory markers (CRP), stool examination for intestinal parasites, and evaluation for concurrent viral infections.

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