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Attitudes and Beliefs about HIV/AIDS and their Relationships with Sexual Practices among Senior Secondary School Students in Abakaliki, Ebonyi State, Southeast Nigeria.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj.v65i6.606
Maria-Lauretta Chito Orji, Chinwe Ifeoma Joe-Akunne, Ngozi Appolonia Ifebunandu, Ogoma Cynthia Onah, Cecilia Oluchukwu Oyim-Elechi, Miracle Anurika Nwobi, Stephnora Ezinne Agbo, Sunday Austin Otubo

Background: Attitudes and beliefs regarding HIV among adolescents and young adults (AYA) may influence practices that increase the risk of HIV transmission. The study aimed to determine the attitudes and beliefs regarding HIV among senior secondary students and their sexual practices.

Methodology: It was a cross-sectional descriptive study that involved 1,200 adolescents and young adults (AYA) aged 14-24 years in senior secondary schools in Abakaliki. Information was obtained using a two-part pre-tested questionnaire that tested attitudes and beliefs regarding HIV using a 6-item questionnaire and another part sought information on biodata and sexual practices. The p-value of < 0.05 was statistically significant.

Results: The median (IQR) age of participants was 16.0 (9.0) years, and the majority (64.4%, 773/1,200) were females with a male-to-female ratio of 1.0: 1.8. Seven hundred and thirty (60.8%) had positive attitudes and beliefs towards HIV. Although 628 (52.3%) were willing to be tested for HIV, only 25.6% (307/1,200) have ever been tested for HIV. Three hundred and fifty-five (29.6%) of them had engaged in sexual activities, of which 145 (12.1%) had multiple sexual partners. There were significant relationships between attitude, beliefs, and age ((χ2= 39.69. p = <0.001), willingness to test for HIV (χ2 = 10.20. p= 0.002), and having multiple sexual partners (χ2= 5.49, p= 0.019).

Conclusion: Positive attitudes and beliefs regarding HIV were high but were not reflected in their practices. Sustained efforts toward effective HIV-related health education in schools and improved adolescent-friendly health services where HIV screening is readily accessible are recommended.

{"title":"Attitudes and Beliefs about HIV/AIDS and their Relationships with Sexual Practices among Senior Secondary School Students in Abakaliki, Ebonyi State, Southeast Nigeria.","authors":"Maria-Lauretta Chito Orji, Chinwe Ifeoma Joe-Akunne, Ngozi Appolonia Ifebunandu, Ogoma Cynthia Onah, Cecilia Oluchukwu Oyim-Elechi, Miracle Anurika Nwobi, Stephnora Ezinne Agbo, Sunday Austin Otubo","doi":"10.60787/nmj.v65i6.606","DOIUrl":"10.60787/nmj.v65i6.606","url":null,"abstract":"<p><strong>Background: </strong>Attitudes and beliefs regarding HIV among adolescents and young adults (AYA) may influence practices that increase the risk of HIV transmission. The study aimed to determine the attitudes and beliefs regarding HIV among senior secondary students and their sexual practices.</p><p><strong>Methodology: </strong>It was a cross-sectional descriptive study that involved 1,200 adolescents and young adults (AYA) aged 14-24 years in senior secondary schools in Abakaliki. Information was obtained using a two-part pre-tested questionnaire that tested attitudes and beliefs regarding HIV using a 6-item questionnaire and another part sought information on biodata and sexual practices. The p-value of < 0.05 was statistically significant.</p><p><strong>Results: </strong>The median (IQR) age of participants was 16.0 (9.0) years, and the majority (64.4%, 773/1,200) were females with a male-to-female ratio of 1.0: 1.8. Seven hundred and thirty (60.8%) had positive attitudes and beliefs towards HIV. Although 628 (52.3%) were willing to be tested for HIV, only 25.6% (307/1,200) have ever been tested for HIV. Three hundred and fifty-five (29.6%) of them had engaged in sexual activities, of which 145 (12.1%) had multiple sexual partners. There were significant relationships between attitude, beliefs, and age ((χ<sup>2</sup>= 39.69. p = <0.001), willingness to test for HIV (χ<sup>2</sup> = 10.20. p= 0.002), and having multiple sexual partners (χ<sup>2</sup>= 5.49, p= 0.019).</p><p><strong>Conclusion: </strong>Positive attitudes and beliefs regarding HIV were high but were not reflected in their practices. Sustained efforts toward effective HIV-related health education in schools and improved adolescent-friendly health services where HIV screening is readily accessible are recommended.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"1135-1145"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770663/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061370","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Hypertriglyceridemic Waist Phenotype is Associated with an Adverse Cardiometabolic Profile in this Cohort of Nigerians.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj.v65i6.557
Ugochi Chinenye Okorafor, Chiamaka Ifeyinwa Okorafor, Casmir Ezenwa Amadi

Background: The hypertriglyceridemic waist (HTGW) phenotype was introduced as a means of identifying individuals at risk of developing metabolic syndrome as well as cardiovascular diseases and diabetes. However, studies surrounding the prevalence of the phenotype and its relationship with established markers of cardiometabolic risk, especially in the Nigerian population, remain sparse. This study aimed to determine the prevalence of the HTGW phenotype and explore its relationship with cardiovascular risk markers, namely Castelli Risk Indices I and II (CRI-I and CRI-II), Atherogenic Index of Plasma (AIP) and serum triglyceride-HDL cholesterol ratio (TG/HDL).

Methodology: In this retrospective cross-sectional study, the records of 206 patients presenting at a cardiac hospital from November 2022 to October 2023 were analysed. The HTGW phenotype was deemed present with a waist circumference of at least 94cm in men or 80cm in women and a serum triglyceride level of 150mg/dl or more in both sexes.

Results: At-risk waist circumference was more prevalent in women (92.7% vs 77.3%; p=0.002). The prevalence of the HTWG phenotype in the patient cohort was 29.6%, with more males than females (31.8% vs 27.1%) presenting with the phenotype (p=0.004). Patients with the phenotype also had higher systolic blood pressure, waist circumference, body mass index, triglycerides, AIP, and TG/HDL (all p<0.0005). The HTWG phenotype was also associated with a lower HDL and LDL cholesterol (p<0.0005) as well as a lower CRI-II (p=0.049).

Conclusion: The HTWG phenotype correlates with an increased cardiometabolic risk among Nigerians. This finding warrants the implementation of routine anthropometric and serum triglyceride measurements in screening programmes and hospitals for the early detection of individuals at risk of developing cardiovascular diseases.

{"title":"The Hypertriglyceridemic Waist Phenotype is Associated with an Adverse Cardiometabolic Profile in this Cohort of Nigerians.","authors":"Ugochi Chinenye Okorafor, Chiamaka Ifeyinwa Okorafor, Casmir Ezenwa Amadi","doi":"10.60787/nmj.v65i6.557","DOIUrl":"10.60787/nmj.v65i6.557","url":null,"abstract":"<p><strong>Background: </strong>The hypertriglyceridemic waist (HTGW) phenotype was introduced as a means of identifying individuals at risk of developing metabolic syndrome as well as cardiovascular diseases and diabetes. However, studies surrounding the prevalence of the phenotype and its relationship with established markers of cardiometabolic risk, especially in the Nigerian population, remain sparse. This study aimed to determine the prevalence of the HTGW phenotype and explore its relationship with cardiovascular risk markers, namely Castelli Risk Indices I and II (CRI-I and CRI-II), Atherogenic Index of Plasma (AIP) and serum triglyceride-HDL cholesterol ratio (TG/HDL).</p><p><strong>Methodology: </strong>In this retrospective cross-sectional study, the records of 206 patients presenting at a cardiac hospital from November 2022 to October 2023 were analysed. The HTGW phenotype was deemed present with a waist circumference of at least 94cm in men or 80cm in women and a serum triglyceride level of 150mg/dl or more in both sexes.</p><p><strong>Results: </strong>At-risk waist circumference was more prevalent in women (92.7% vs 77.3%; p=0.002). The prevalence of the HTWG phenotype in the patient cohort was 29.6%, with more males than females (31.8% vs 27.1%) presenting with the phenotype (p=0.004). Patients with the phenotype also had higher systolic blood pressure, waist circumference, body mass index, triglycerides, AIP, and TG/HDL (all p<0.0005). The HTWG phenotype was also associated with a lower HDL and LDL cholesterol (p<0.0005) as well as a lower CRI-II (p=0.049).</p><p><strong>Conclusion: </strong>The HTWG phenotype correlates with an increased cardiometabolic risk among Nigerians. This finding warrants the implementation of routine anthropometric and serum triglyceride measurements in screening programmes and hospitals for the early detection of individuals at risk of developing cardiovascular diseases.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"1080-1088"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770662/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061645","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Factors Associated with Microalbuminuria among Children with Sickle Cell Disease in a Tertiary Centre in South-South Nigeria.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj-v65i6.493
Datonye Christopher Briggs, Chioma Okechukwu, Josiah Apollus, Ijeoma Amadi, Hannah Omunakwe, Linda Anucha Dublin-Green, Dorathy Okoh

Background: Microalbuminuria, an early indicator of kidney damage in Sickle Cell Disease (SCD) patients, is linked to a heightened risk of chronic kidney disease (CKD) in adulthood. This study investigates the determinants of microalbuminuria in paediatric SCD patients in South-South Nigeria.

Methodology: This cross-sectional study was conducted over six months at the Rivers State University Teaching Hospital, Nigeria, involving 60 children with [HbSS genotype, SCD] in a steady state. Data collection included demographics, past medical history, clinical measurements, and laboratory assessments of urine and blood samples. 'Steady state' was defined as SCD with a known 'steady state' haemoglobin level and stable clinical state for ≥ 3 months. Microalbuminuria was defined spot urine albumin-creatinine ratio of 30mg/g to <300 mg/g.

Results: Of the 60 children recruited, 31 children (51.7%) were males. The mean age was 9.6 ± 4.3 years. The prevalence of microalbuminuria was 16.7% (CI: 8.29 - 28.5%) and associated risk factors were hypertension (p = 0.017), use of Hydroxyurea (p = 0.008), and Ciklavit (p = 0.025), but not NSAIDs (p = 0.046). There was a significant negative correlation (ɼ = -0.28; p = 0.032) between haemoglobin level and microalbuminuria.

Conclusion: This study provides insights into the factors associated with microalbuminuria in children with SCD in our setting and highlights the need for early screening for markers of CKD among children with SCD. Further research is needed to ascertain the potential benefits of addressing anaemia and reducing haemolysis in mitigating the occurrence of microalbuminuria among children with SCD.

{"title":"Factors Associated with Microalbuminuria among Children with Sickle Cell Disease in a Tertiary Centre in South-South Nigeria.","authors":"Datonye Christopher Briggs, Chioma Okechukwu, Josiah Apollus, Ijeoma Amadi, Hannah Omunakwe, Linda Anucha Dublin-Green, Dorathy Okoh","doi":"10.60787/nmj-v65i6.493","DOIUrl":"10.60787/nmj-v65i6.493","url":null,"abstract":"<p><strong>Background: </strong>Microalbuminuria, an early indicator of kidney damage in Sickle Cell Disease (SCD) patients, is linked to a heightened risk of chronic kidney disease (CKD) in adulthood. This study investigates the determinants of microalbuminuria in paediatric SCD patients in South-South Nigeria.</p><p><strong>Methodology: </strong>This cross-sectional study was conducted over six months at the Rivers State University Teaching Hospital, Nigeria, involving 60 children with [HbSS genotype, SCD] in a steady state. Data collection included demographics, past medical history, clinical measurements, and laboratory assessments of urine and blood samples. 'Steady state' was defined as SCD with a known 'steady state' haemoglobin level and stable clinical state for ≥ 3 months. Microalbuminuria was defined spot urine albumin-creatinine ratio of 30mg/g to <300 mg/g.</p><p><strong>Results: </strong>Of the 60 children recruited, 31 children (51.7%) were males. The mean age was 9.6 ± 4.3 years. The prevalence of microalbuminuria was 16.7% (CI: 8.29 - 28.5%) and associated risk factors were hypertension (p = 0.017), use of Hydroxyurea (p = 0.008), and Ciklavit (p = 0.025), but not NSAIDs (p = 0.046). There was a significant negative correlation (ɼ = -0.28; p = 0.032) between haemoglobin level and microalbuminuria.</p><p><strong>Conclusion: </strong>This study provides insights into the factors associated with microalbuminuria in children with SCD in our setting and highlights the need for early screening for markers of CKD among children with SCD. Further research is needed to ascertain the potential benefits of addressing anaemia and reducing haemolysis in mitigating the occurrence of microalbuminuria among children with SCD.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"885-898"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770667/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sero-prevalence of hepatitis B and C and HIV among students at the Federal University of Health Sciences, Azare.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj.v65i6.596
Musa A Garbati, Alkali Mohammed, Mairo Kadaura, Uchenna S Ezenkwa, Bala M Audu

Background: Infection with the human immunodeficiency virus and hepatitis viruses B and C have been reported to be endemic in some Nigeria's institutions of higher learning. Several studies have reported varying prevalence rates for hepatitis B and C viruses and HIV among undergraduate students in Nigerian universities.

Methodology: A cross-sectional descriptive prevalence study of hepatitis B and C viruses and HIV among students at Federal University of Health Sciences, Azare conducted on the 2nd of December 2023. Screening for hepatitis B and C viruses and HIV was done using standard procedures. Ethical approval was obtained in addition to individual consent from all participants.

Results: Three hundred students with the mean age of 19.43±2.352 years were studied. 96.7% were aged 24 years or younger; females being the majority [185, 61.7%]. The majority of the participants were in their 200 level (190, 63.3%). Ten health-related programmes were represented in the survey. Twelve participants (4%) were positive for HBsAg; nine (75%) being males. One participant was positive for HBeAg, while only three (1%) of the participants had evidence of prior HBV vaccination, thus giving us a window of opportunity for vaccination. None of the participants had evidence of infection with HCV or HIV.

Conclusion: Screening students of health-related courses should be routinely done to ascertain their status to prevent occupational exposures and transmission in the healthcare setting. Results from this survey will inform formulation of policies that will protect our future healthcare force and safeguard the lives of patients.

{"title":"Sero-prevalence of hepatitis B and C and HIV among students at the Federal University of Health Sciences, Azare.","authors":"Musa A Garbati, Alkali Mohammed, Mairo Kadaura, Uchenna S Ezenkwa, Bala M Audu","doi":"10.60787/nmj.v65i6.596","DOIUrl":"10.60787/nmj.v65i6.596","url":null,"abstract":"<p><strong>Background: </strong>Infection with the human immunodeficiency virus and hepatitis viruses B and C have been reported to be endemic in some Nigeria's institutions of higher learning. Several studies have reported varying prevalence rates for hepatitis B and C viruses and HIV among undergraduate students in Nigerian universities.</p><p><strong>Methodology: </strong>A cross-sectional descriptive prevalence study of hepatitis B and C viruses and HIV among students at Federal University of Health Sciences, Azare conducted on the 2nd of December 2023. Screening for hepatitis B and C viruses and HIV was done using standard procedures. Ethical approval was obtained in addition to individual consent from all participants.</p><p><strong>Results: </strong>Three hundred students with the mean age of 19.43±2.352 years were studied. 96.7% were aged 24 years or younger; females being the majority [185, 61.7%]. The majority of the participants were in their 200 level (190, 63.3%). Ten health-related programmes were represented in the survey. Twelve participants (4%) were positive for HBsAg; nine (75%) being males. One participant was positive for HBeAg, while only three (1%) of the participants had evidence of prior HBV vaccination, thus giving us a window of opportunity for vaccination. None of the participants had evidence of infection with HCV or HIV.</p><p><strong>Conclusion: </strong>Screening students of health-related courses should be routinely done to ascertain their status to prevent occupational exposures and transmission in the healthcare setting. Results from this survey will inform formulation of policies that will protect our future healthcare force and safeguard the lives of patients.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"1112-1123"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770648/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143060994","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Undesirable occupants of bone marrow creating a menace: A 4.5-year audit from a tertiary care centre in Eastern India.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj.v65i6.574
Iffat Jamal, Shuchi Smita, Ravi Bhushan Raman, Vijayanand Choudhary, Kshiti Atreya, Manoj Kumar Choudhary, Alok Ranjan

Background: Bone marrow (BM) in addition to being the origin of primary hematological malignancies is also commonly involved in metastatic solid tumors. Bone marrow examination includes aspiration and biopsy, and it is a well-known procedure not only to diagnose hematological malignancies but also for staging and prognosis of various solid tumors. The presence of metastasis in the bone marrow is of grave prognostic significance and it is imperative to rule out marrow involvement in any malignancy where curative treatment is considered. The study's objectives were to evaluate the clinical, hematological, and biochemical characteristics of patients with BM metastases of solid tumors diagnosed by bone marrow (BM) aspiration and trephine biopsy and to find out the accuracy rate of diagnosing metastatic infiltration between bone marrow aspiration, trephine imprints, and trephine biopsy procedures.

Methodology: It was a 4.5-year retrospective hospital-based observational study where relevant clinical, biochemical, and hematological parameters including bone marrow aspirate and biopsy were analyzed and compiled from hospital medical records.

Results: The total number of BMA and trephine biopsies that came during the duration of 4.5 years were 3850 and 2980 respectively. Out of the 3850-bone marrow aspiration and 2980 trephine biopsies received in the dept of Hematology, 305 cases were referred to look for metastatic bone marrow infiltration. Out of these 305 cases, 69 cases showed the presence of metastatic deposits (12.6%). 45 patients (65.2%) were males, and 24 patients (34.7%) were females with M:F ratio of 1.8:1. Most common age group was 51-60 years (31.8%). The most common complaints were fever, body aches, weight loss, and weakness. Clinical examination revealed pallor in 38 out of 69 cases (55%) and organomegaly in 14 cases (20.2%). Microcytic hypochromic anemia (26%) was the most common finding on peripheral blood smear examination followed by pancytopenia (18.8%). The biochemical findings most commonly observed were raised LDH (60.8%), serum PSA (36.3%), and alkaline phosphatase (21.7%).

Conclusion: Trephine biopsy is a sensitive method for detecting marrow metastasis and should be done in all cases being investigated for this purpose. BMA alone may miss marrow metastases in almost half of cases. Trephine imprint cytology is more sensitive than BMA and can provide rapid diagnoses while waiting for trephine biopsy results.

{"title":"Undesirable occupants of bone marrow creating a menace: A 4.5-year audit from a tertiary care centre in Eastern India.","authors":"Iffat Jamal, Shuchi Smita, Ravi Bhushan Raman, Vijayanand Choudhary, Kshiti Atreya, Manoj Kumar Choudhary, Alok Ranjan","doi":"10.60787/nmj.v65i6.574","DOIUrl":"10.60787/nmj.v65i6.574","url":null,"abstract":"<p><strong>Background: </strong>Bone marrow (BM) in addition to being the origin of primary hematological malignancies is also commonly involved in metastatic solid tumors. Bone marrow examination includes aspiration and biopsy, and it is a well-known procedure not only to diagnose hematological malignancies but also for staging and prognosis of various solid tumors. The presence of metastasis in the bone marrow is of grave prognostic significance and it is imperative to rule out marrow involvement in any malignancy where curative treatment is considered. The study's objectives were to evaluate the clinical, hematological, and biochemical characteristics of patients with BM metastases of solid tumors diagnosed by bone marrow (BM) aspiration and trephine biopsy and to find out the accuracy rate of diagnosing metastatic infiltration between bone marrow aspiration, trephine imprints, and trephine biopsy procedures.</p><p><strong>Methodology: </strong>It was a 4.5-year retrospective hospital-based observational study where relevant clinical, biochemical, and hematological parameters including bone marrow aspirate and biopsy were analyzed and compiled from hospital medical records.</p><p><strong>Results: </strong>The total number of BMA and trephine biopsies that came during the duration of 4.5 years were 3850 and 2980 respectively. Out of the 3850-bone marrow aspiration and 2980 trephine biopsies received in the dept of Hematology, 305 cases were referred to look for metastatic bone marrow infiltration. Out of these 305 cases, 69 cases showed the presence of metastatic deposits (12.6%). 45 patients (65.2%) were males, and 24 patients (34.7%) were females with M:F ratio of 1.8:1. Most common age group was 51-60 years (31.8%). The most common complaints were fever, body aches, weight loss, and weakness. Clinical examination revealed pallor in 38 out of 69 cases (55%) and organomegaly in 14 cases (20.2%). Microcytic hypochromic anemia (26%) was the most common finding on peripheral blood smear examination followed by pancytopenia (18.8%). The biochemical findings most commonly observed were raised LDH (60.8%), serum PSA (36.3%), and alkaline phosphatase (21.7%).</p><p><strong>Conclusion: </strong>Trephine biopsy is a sensitive method for detecting marrow metastasis and should be done in all cases being investigated for this purpose. BMA alone may miss marrow metastases in almost half of cases. Trephine imprint cytology is more sensitive than BMA and can provide rapid diagnoses while waiting for trephine biopsy results.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"1101-1111"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770638/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Genetic Modifiers in Sickle Cell Disease Leg Ulcers: Unveiling the Pathways associated with the development and, or progression of Leg Ulcers - A Scoping Review Protocol.
Pub Date : 2025-01-10 eCollection Date: 2024-11-01 DOI: 10.60787/nmj.v65i6.628
Livingstone Gayus Dogara, Sani Awwalu, Doyinsade Awodele

This scoping review aims to assess the literature on genetic modifiers of leg ulcers in sickle cell disease, evaluating available evidence, methodologies, and research gaps. A major morbidity in sickle cell disease is the development of leg ulcers. This clinical syndrome of SCD leg ulcers (SLU) has continued to be an enigma due to its multifactorial evolution, dearth of promising guidelines on treatment, and generally unsatisfactory response to treatment. Underlying genetic susceptibilities for SLU may impact counselling, prognostication, risk of development, severity as well as response to interventions. Hence the need for this scoping review. This scoping review will collate and assess studies in English on genetic markers of SLU among all SCD age groups, genders, races, and regions. Genetic or molecular markers to be assessed among patients with sickle cell leg ulcers included, genetic markers of Inflammation, vasculopathy, tissue damage, oxidative stress, coagulopathy as well as genetic predispositions that have been studied in relation to SLUs across all countries. This includes most common biomarkers that promote development of SLU, the single nucleotide polymorphic markers (SNPs) that work through the MAPK and SMAD signaling pathway. A PubMed search of all fields for literature published in English using the strategy (sickle cell) AND (leg ulcer), and (sickle cell) AND (leg ulcer genetics) from 1998 to 2023 (last 25 years) will be undertaken. This will be modified, according to the inclusion criteria, as appropriate across other databases. The other databases will include Google Scholar, web of Knowledge, Scopus, New Zealand Science, Silver chair, Taylor and Francis+NEJM, and journals.lww.com.

{"title":"Genetic Modifiers in Sickle Cell Disease Leg Ulcers: Unveiling the Pathways associated with the development and, or progression of Leg Ulcers - A Scoping Review Protocol.","authors":"Livingstone Gayus Dogara, Sani Awwalu, Doyinsade Awodele","doi":"10.60787/nmj.v65i6.628","DOIUrl":"10.60787/nmj.v65i6.628","url":null,"abstract":"<p><p>This scoping review aims to assess the literature on genetic modifiers of leg ulcers in sickle cell disease, evaluating available evidence, methodologies, and research gaps. A major morbidity in sickle cell disease is the development of leg ulcers. This clinical syndrome of SCD leg ulcers (SLU) has continued to be an enigma due to its multifactorial evolution, dearth of promising guidelines on treatment, and generally unsatisfactory response to treatment. Underlying genetic susceptibilities for SLU may impact counselling, prognostication, risk of development, severity as well as response to interventions. Hence the need for this scoping review. This scoping review will collate and assess studies in English on genetic markers of SLU among all SCD age groups, genders, races, and regions. Genetic or molecular markers to be assessed among patients with sickle cell leg ulcers included, genetic markers of Inflammation, vasculopathy, tissue damage, oxidative stress, coagulopathy as well as genetic predispositions that have been studied in relation to SLUs across all countries. This includes most common biomarkers that promote development of SLU, the single nucleotide polymorphic markers (SNPs) that work through the MAPK and SMAD signaling pathway. A PubMed search of all fields for literature published in English using the strategy (sickle cell) AND (leg ulcer), and (sickle cell) AND (leg ulcer genetics) from 1998 to 2023 (last 25 years) will be undertaken. This will be modified, according to the inclusion criteria, as appropriate across other databases. The other databases will include Google Scholar, web of Knowledge, Scopus, New Zealand Science, Silver chair, Taylor and Francis+NEJM, and journals.lww.com.</p>","PeriodicalId":94346,"journal":{"name":"Nigerian medical journal : journal of the Nigeria Medical Association","volume":"65 6","pages":"844-850"},"PeriodicalIF":0.0,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770651/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143061790","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Growing Trend of Surrogacy in Nigeria: Implications for Quality Newborn Care: A Case Report. 尼日利亚代孕的增长趋势:对新生儿护理质量的影响:一个案例报告。
Pub Date : 2024-11-06 eCollection Date: 2024-09-01 DOI: 10.60787/nmj-v65i3.515
Beatrice Nkolika Ezenwa, Usman Olaitan Ibrahim, Olaolu Aziza Moronkola, Iretiola Bamikeolu Fajolu, Lilian Ndukwu, Khadijah Omobusola Oleolo-Ayodeji, Adaku Akunna Ibe, Veronica Chinyere Ezeaka

Surrogacy involves a woman (surrogate) who consents to carry a pregnancy on behalf of an individual or a couple who cannot conceive for medical reasons. Surrogacy is gaining popularity in Nigeria among infertile couples, partly because surrogacy provides an easier means to having children than adoption. Surrogacy can be either gestational or traditional. Though surrogacy gives hope to infertile individuals, it also comes with peculiar challenges that affect the newborn with medical, ethical, and legal dimensions that caregivers need to be aware of. We present three sets of preterm triplets conceived by Invitro fertilization (IVF), carried by gestational surrogacy, and managed in our facility. This case report highlights challenges encountered while managing these neonates to create awareness and suggest solutions and guidance to neonatal practitioners. Topmost challenges include the unsustainability of feeding with the mother's own milk, lack of kangaroo mother care, abandonment of care by commissioning parents, delay in getting consent for treatment/procedures, determining the legal status of the child vis-à-vis simple issues such as changing the name of the child from that of the surrogate to that of the commissioning parents. The hospital's legal and welfare departments were key resource units and were involved early in managing these neonates. One baby from each set of triplets was successfully discharged home to the commissioning parents. In conclusion, surrogacy is becoming increasingly common as a means of becoming parents for infertile individuals. There is an urgent need for proper regulation and legal framework for surrogacy and assisted reproduction in Nigeria.

代孕是指一名妇女(代孕母亲)代表因医疗原因不能怀孕的个人或夫妇同意怀孕。代孕在尼日利亚不孕夫妇中越来越受欢迎,部分原因是代孕比收养孩子更容易。代孕可以是妊娠代孕,也可以是传统代孕。虽然代孕给不孕不育的人带来了希望,但它也带来了特殊的挑战,这些挑战会影响到新生儿,包括医疗、伦理和法律方面,护理人员需要意识到这一点。我们提出了三组早产三胞胎通过体外受精(IVF),妊娠代孕,并在我们的设施管理。本病例报告强调了在管理这些新生儿时遇到的挑战,以提高认识,并为新生儿从业人员提出解决方案和指导。最主要的挑战包括母乳喂养的不可持续性,缺乏袋鼠式的母亲护理,委托父母放弃照顾,延迟获得治疗/程序的同意,确定孩子的法律地位,如将孩子的名字从代孕母亲改为委托父母等简单问题-à-vis。医院的法律和福利部门是关键的资源单位,很早就参与了对这些新生儿的管理。每组三胞胎中有一名婴儿成功出院回家。总之,代孕作为不育个体成为父母的一种手段正变得越来越普遍。尼日利亚迫切需要为代孕和辅助生殖制定适当的法规和法律框架。
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引用次数: 0
Prevalence and Factors Associated with Zero-Dose Children amongst Nomadic and Non-Nomadic Fulani in Yobe State, North-East Nigeria. 尼日利亚东北部约贝州游牧和非游牧富拉尼人中零剂量儿童的患病率及相关因素。
Pub Date : 2024-11-06 eCollection Date: 2024-09-01 DOI: 10.60787/nmj-v65i3.545
Usman Muhammad Ibrahim, Dauda Abdulhamid, Boateng Kofi, Mahdi Musa Wade, Abba Ahmed Danzomo, Sunday Audu, Nuruddeen Muhammad, Faruk Abdullahi Namadi, Usman Lawal Shehu, Rabiu Ibrahim Jalo, Fatimah Ismail Tsiga-Ahmed, Serawit Lisanework, Murtala Jibril, Awwal Umar Gajida, Abubakar Mohammed Jibo

Background: Immunization is a very cost-effective and readily available intervention capable of preventing Vaccines Preventable Diseases (VPDs). This study aimed to identify and compare the prevalence and factors associated with zero-dose immunization status among children of nomadic and non-nomadic Fulani in Yobe State, North-East Nigeria.

Methodology: A comparative cross-sectional design was used to study 348 nomadic, and 345 non-nomadic under-five children, selected using a multi-staged sampling technique. Data were collected using interviewer administered questionnaire, observation of child immunization card, and recall by the caregivers, and were analysed using IBM SPSS version 22.0 with a statistical significance set at P ≤5%.

Results: The maximum age of the nomadic caregivers was 60 and the minimum was 17 years with a mean ±SD of 28.2±7.7 years. The maximum age of the non-nomadic caregivers was 78 and the minimum was 17 years with a mean ±SD of 33.0±10.0 years. The prevalence of zero dose children among nomadic and non-nomadic Fulani were (70.1%, 242), (61.8%, 63) respectively. The zero-dose children were significantly higher among nomads (87.2%, p<0.001) and non-nomad (54.4%, p<0.001) with no available child immunization card.The children of vaccines hesitant caregivers of nomads and non-nomads were 10 or more times more likely to be zero dose than non-hesitant caregivers (adjusted odds ratio [aOR] =477, 95% CI = [177-13031]), and (Adjusted odds ratio [aOR] =9.7, 95% CI = [2.1-44.3]) respectively.

Conclusion: The burden of zero-dose was alarmingly high among nomads compared to non-nomad Fulani despite widespread immunization outreach services in the study area. The government and relevant stakeholders should intensify Context-specific health promotion activities and outreach services targeting these underserved populations.

背景:免疫是一种非常具有成本效益和容易获得的干预措施,能够预防疫苗可预防疾病(VPDs)。本研究旨在确定和比较尼日利亚东北部约贝州游牧和非游牧富拉尼儿童中零剂量免疫状况的流行情况和相关因素。方法:采用比较横断面设计,采用多阶段抽样技术对348名游牧和345名非游牧五岁以下儿童进行了研究。采用访谈者问卷、儿童免疫卡观察、照顾者回忆等方式收集数据,采用IBM SPSS 22.0进行分析,P≤5%。结果:游牧照顾者年龄最大为60岁,最小为17岁,平均±SD为28.2±7.7岁。非游牧照顾者年龄最大为78岁,最小为17岁,平均±SD为33.0±10.0岁。富拉尼游牧民和非游牧民的零剂量儿童患病率分别为(70.1%,242人)和(61.8%,63人)。结论:尽管在研究地区广泛开展免疫外展服务,但与非游牧民族的富拉尼人相比,游牧民族的零剂量负担高得惊人。政府和相关利益攸关方应针对这些服务不足的人群,加强针对具体情况的健康促进活动和外展服务。
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引用次数: 0
Neonatal Hyperbilirubinemia: A Case of Complex Management Involving ABO Incompatibility, Sepsis, and Suspected G6PD Deficiency treated with Methyl Prednisolone. 新生儿高胆红素血症:一例复杂的管理涉及ABO不相容,败血症,并怀疑G6PD缺乏症与甲基强的松龙治疗。
Pub Date : 2024-11-06 eCollection Date: 2024-09-01 DOI: 10.60787/nmj-v65i3.498
Aishatu ZaiduMusa, Samaha Saleh Mustapha, Bawa Ibrahim Abubakar, Nurat Oluwabunmi Lawal, Mustapha Falmata Grema, Auwal Ahmed Muhammed Bashir

Newborn jaundice (NNJ), especially due to ABO incompatibility, is a major global health concern. Phototherapy is standard treatment, with exchange transfusions reserved for severe cases. However, in some babies these therapies may be ineffective, requiring additional immunomodulatory treatments. Limited access to these treatments in developing countries creates a critical gap, worsening jaundice severity. A 22-hour old term neonate presented with rapidly progressive severe neonatal hyperbilirubinemia (NNJ) within 15 hours of life, consistent with ABO incompatibility based on discordant maternal and infant's blood types (mother: O, baby: B-positive). Despite aggressive initial management with phototherapy and exchange transfusions, the NNJ exhibited limited improvement. Sepsis and G6PD deficiency were considered as potential contributing factors, although confirmatory testing for G6PD deficiency was deferred due to unavailability of the diagnostic test in our setting. Given a sibling's documented successful response to methylprednisolone for a similar presentation, a brief course of low-dose intravenous methylprednisolone (1mg/kg/day in 2 divided doses) (off-label use) was cautiously initiated. This resulted in a rapid and significant improvement in the neonate's hyperbilirubinemia. Methylprednisolone was prescribed for 3 days after which it was discontinued. Following close observation for 3 days and confirmation of no neurological sequelae, the neonate was discharged home in stable condition. Managing severe, worsening NNJ, especially with multiple aetiologies, is complex. Standard therapies may be inadequate. While promising, immunomodulatory therapies like IVIG may be limited in resource-poor settings. Methylprednisolone shows potential but lacks strong clinical evidence. Well-designed studies are essential to explore its safety and efficacy, particularly in developing countries with limited treatment options.

新生儿黄疸(NNJ),特别是由于ABO血型不合,是一个主要的全球卫生问题。光疗是标准的治疗方法,重症患者需进行换血。然而,在一些婴儿中,这些疗法可能无效,需要额外的免疫调节治疗。发展中国家获得这些治疗的机会有限,造成了严重的差距,加剧了黄疸的严重程度。一个22小时出生的足月新生儿在15小时内出现了快速进展的严重新生儿高胆红素血症(NNJ),符合基于母婴血型不一致(母亲:O型,婴儿:b阳性)的ABO不相容。尽管最初进行了积极的光疗和交换输血治疗,但NNJ的改善有限。脓毒症和G6PD缺乏被认为是潜在的影响因素,尽管由于在我们的环境中无法获得诊断测试,G6PD缺乏的确证测试被推迟。鉴于一位兄弟姐妹对甲基强的松龙治疗类似症状的成功反应,我们谨慎地开始了一个短疗程的低剂量静脉注射甲基强的松龙(1mg/kg/天,分2次使用)(标签外使用)。这导致了新生儿高胆红素血症的快速和显著改善。甲强的松龙开了3天,之后停药。密切观察3 d,确认无神经系统后遗症,病情稳定出院。管理严重、恶化的NNJ,特别是多种病因的NNJ,是复杂的。标准疗法可能是不够的。虽然很有希望,但像IVIG这样的免疫调节疗法在资源贫乏的环境中可能受到限制。甲基强的松龙显示出潜力,但缺乏强有力的临床证据。精心设计的研究对于探索其安全性和有效性至关重要,特别是在治疗选择有限的发展中国家。
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引用次数: 0
Prevalence and Determinants of Singleton Stillbirths at a Tertiary Hospital in Port-Harcourt, Nigeria. 尼日利亚哈科特港一家三级医院单胎死产的患病率和决定因素
Pub Date : 2024-11-06 eCollection Date: 2024-09-01 DOI: 10.60787/nmj-v65i3.528
Peter Abiye Awoyesuku, Chinweowa Ohaka, Paul Ledee Kua, Kenneth Eghuan Okagua, Lewis Barinadaa Lebara, Leziga Dimkpa Ndii

Background: Nigeria makes a substantial contribution to the global burden of stillbirths. Stillbirth accounts for about 50% of perinatal mortality and the stillbirth rate is an indicator of the quality of antenatal and intrapartum care. The study sought to determine the prevalence and determinants of stillbirths.

Methodology: This was a retrospective, unmatched case-control study over two years from May 2022 to April 2024. Cases were women with stillbirths that occurred at a gestational age of ≥28 weeks, while controls were women with livebirths, in a 1 case for 2 controls ratio. Data extracted from the hospital records, using a predesigned collection form, included demographic, medical, obstetric and neonatal characteristics as exposure variables. Data was analysed with SPSS version 25, using descriptive and inferential statistics. Multivariate logistics regression was used to determine adjusted odds ratios with 95% confidence intervals and a P-value of <0.05.

Results: There were 3,425 livebirths and 120 stillbirths, giving a stillbirth rate of 35 per 1000 livebirths. Analysis was performed for 114 cases and corresponding 228 controls, 6 cases were excluded for incomplete data. Maternal age ranged from 20-48 years and parity from 0-7, with no statistical difference between either group (P=0.982 and P=0.638 respectively). There were 58(50.9%) macerated and 56(49.1%) fresh stillbirths, with 21(37.5%) of the fresh stillbirths alive at presentation. Factors associated with stillbirth after multivariate analysis included unbooked status (aOR=9.64; P=0.0001), vaginal delivery (aOR=2.04; P=0.034), abruptio placenta (aOR=25.58; P=0.007), preterm delivery at GA ≤36weeks (aOR=3.26; P=0.012), and low birth weight <2500g (aOR=3.53; P=0.016). Obstructed labour and ruptured uterus were significant in bivariate analysis but could not be fitted into multivariate analysis because of non-occurrence in controls.

Conclusion: The stillbirth rate at our Centre was 35 per 1000 livebirths. Associated factors for stillbirth were unbooked status, vaginal delivery, abruptio placenta, preterm delivery and birth weight <2500g.

背景:尼日利亚对全球死产负担作出了重大贡献。死产约占围产期死亡率的50%,死产率是产前和产时护理质量的一个指标。该研究旨在确定死产的患病率和决定因素。方法:这是一项回顾性的、无与伦比的病例对照研究,从2022年5月到2024年4月为期两年。病例为胎龄≥28周的死产妇女,对照组为活产妇女,比例为1例2例。使用预先设计的收集表格从医院记录中提取的数据包括作为暴露变量的人口、医疗、产科和新生儿特征。数据分析采用SPSS 25版,采用描述性统计和推理统计。多变量logistic回归用于确定校正优势比,95%置信区间和p值结果:有3425例活产和120例死产,死产率为每1000例活产35例。114例病例和228例对照进行分析,6例因资料不完整而被排除。产妇年龄20 ~ 48岁,胎次0 ~ 7岁,两组间差异无统计学意义(P=0.982、P=0.638)。浸泡死产58例(50.9%),新鲜死产56例(49.1%),新鲜死产21例(37.5%)分娩时存活。多因素分析后,与死产相关的因素包括未预约状态(aOR=9.64;P=0.0001),阴道分娩(aOR=2.04;P=0.034),胎盘早剥(aOR=25.58;P=0.007), GA≤36周早产(aOR=3.26;P=0.012),低出生体重P=0.016)。难产和子宫破裂在双因素分析中具有显著性,但由于在对照组中未发生,因此不能用于多因素分析。结论:本中心死产率为35 / 1000。死产的相关因素包括未预约分娩、阴道分娩、胎盘早剥、早产和出生体重
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Nigerian medical journal : journal of the Nigeria Medical Association
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