Pub Date : 2025-11-06DOI: 10.1186/s41182-025-00832-3
Josue Rivadeneira, Carlos Manterola, Luis Alvarado, Paola Simbaña-Garcia
Background: Hepatic cystic echinococcosis (HCE) remains a significant public health issue in endemic countries. Although recurrence is a recognized challenge, its independent impact on adverse clinical outcomes such as postoperative complications (POC), mortality, and length of hospital stay (LHS) remains poorly studied in Latin America. This study aimed to assess the risk of POC, mortality, and LHS in patients with recurrence of HCE.
Methods: We conducted a retrospective cohort study of patients who underwent surgery for HCE between 1993 and 2019 at two centers in southern Chile. Patients with recurrence (exposed group) were compared to those undergoing primary surgery (non-exposed group). The primary outcome was the presence of POC; secondary outcomes included mortality and LHS. Crude and adjusted relative risks (RR) with 95% confidence intervals were estimated using Poisson regression with robust errors. Linear regression models were applied to assess the effect of recurrence on LHS.
Results: A total of 154 patients with 271 cysts were included. Recurrence was identified in 43 patients (27.9%). POC occurred in 18.2% of the total cohort and were significantly more frequent in the recurrence group (41.9% vs. 9.0%, p < 0.001). Adjusted RR for POC in the presence of recurrence was 5.1 (95% CI 2.7-9.9). Mortality was higher in patients with recurrence (7.0% vs. 2.7%, RR: 2.6; 95% CI 0.5-12.3), though not statistically significant. LHS was 1 day longer in the recurrence group (7.3 ± 4.5 vs. 5.6 ± 3.4; p = 0.02), but this association lost significance in regression models.
Conclusions: Recurrence of HCE increases the risk of POC. While trends toward higher mortality and prolonged LHS were observed, these did not reach statistical significance. These findings underscore the importance of long-term follow-up and the need to identify prognostic factors for recurrence to optimize outcomes in patients with HCE in endemic regions.
{"title":"Impact of recurrence of hepatic cystic echinococcosis on postoperative outcomes in an endemic region of Chile: a retrospective cohort study.","authors":"Josue Rivadeneira, Carlos Manterola, Luis Alvarado, Paola Simbaña-Garcia","doi":"10.1186/s41182-025-00832-3","DOIUrl":"10.1186/s41182-025-00832-3","url":null,"abstract":"<p><strong>Background: </strong>Hepatic cystic echinococcosis (HCE) remains a significant public health issue in endemic countries. Although recurrence is a recognized challenge, its independent impact on adverse clinical outcomes such as postoperative complications (POC), mortality, and length of hospital stay (LHS) remains poorly studied in Latin America. This study aimed to assess the risk of POC, mortality, and LHS in patients with recurrence of HCE.</p><p><strong>Methods: </strong>We conducted a retrospective cohort study of patients who underwent surgery for HCE between 1993 and 2019 at two centers in southern Chile. Patients with recurrence (exposed group) were compared to those undergoing primary surgery (non-exposed group). The primary outcome was the presence of POC; secondary outcomes included mortality and LHS. Crude and adjusted relative risks (RR) with 95% confidence intervals were estimated using Poisson regression with robust errors. Linear regression models were applied to assess the effect of recurrence on LHS.</p><p><strong>Results: </strong>A total of 154 patients with 271 cysts were included. Recurrence was identified in 43 patients (27.9%). POC occurred in 18.2% of the total cohort and were significantly more frequent in the recurrence group (41.9% vs. 9.0%, p < 0.001). Adjusted RR for POC in the presence of recurrence was 5.1 (95% CI 2.7-9.9). Mortality was higher in patients with recurrence (7.0% vs. 2.7%, RR: 2.6; 95% CI 0.5-12.3), though not statistically significant. LHS was 1 day longer in the recurrence group (7.3 ± 4.5 vs. 5.6 ± 3.4; p = 0.02), but this association lost significance in regression models.</p><p><strong>Conclusions: </strong>Recurrence of HCE increases the risk of POC. While trends toward higher mortality and prolonged LHS were observed, these did not reach statistical significance. These findings underscore the importance of long-term follow-up and the need to identify prognostic factors for recurrence to optimize outcomes in patients with HCE in endemic regions.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"153"},"PeriodicalIF":3.5,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12590839/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145459930","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}
Pub Date : 2025-11-06DOI: 10.1186/s41182-025-00828-z
Gildas Wounounou, Alfred B Tiono, Bernhards Ogutu, Christine Manyando, Issaka Sagara, Stefan Schneitter, Quique Bassat, Myriam El Gaaloul, Anne Claire Marrast, Ivan Demin, Cornelis Winnips, Celine Risterucci, Sophie Hugot, Georg Hofstetter, Zhiyan Qian, Guoqin Su, Jie Zhang, Katalin Csermak Renner, Marc Cousin, Vinay Kumar Venishetty, Sarfaraz Sayyed, Preetam Gandhi, Berenger Kabore
Background: Treatment recommendations for malaria in infants of < 5 kg body weight (BW) are not evidence-based. Due to pharmacokinetic characteristics of this population, weight-based dose adjustments for antimalarials may be suboptimal. The 20 mg artemether:120 mg lumefantrine dispersible tablet, even with dose adjustment, may lead to artemether over-exposure and reduced lumefantrine exposure in patients < 5 kg. PBPK modelling predicted that a 1:12 artemether:lumefantrine ratio dispersible tablet should match efficacious and safe drug exposures in patients 5- < 15 kg treated with the current artemether-lumefantrine dispersible tablet: the CALINA study used an exposure-matching approach to confirm that drug exposures were comparable.
Methods: Sequential age cohorts (Cohort 1: > 28 days; Cohort 2: 1-28 days) of patients < 5 kg with Plasmodium falciparum malaria received the new artemether-lumefantrine dispersible tablet (each dose 5 mg artemether: 60 mg lumefantrine) twice daily for 3 days. Artemether Cmax, and lumefantrine C168h and Cmax were compared with historical data from patients 5- < 15 kg treated with the current artemether-lumefantrine dispersible tablet. The primary endpoint was met if the 90% CI for artemether Cmax contained the LS mean value from historical data (101 ng/mL). PCR-corrected and uncorrected ACPR at Days 15, 29 and 43 and parasite clearance time were evaluated. Adverse events, laboratory evaluations, and developmental assessments were performed.
Results: In Cohort 1 (N = 22), geometric mean artemether Cmax was 68.0 ng/mL (90% CI 45.1,103 ng/mL); therefore, Cmax was comparable to that in historical data, meeting the primary endpoint. In Cohort 2 (N = 6), there were too few patients for formal analysis, but geometric mean artemether Cmax was comparable to that in Cohort 1 (62.2 ng/mL, 90% CI 33.6,115 ng/mL). In both cohorts, lumefantrine C168h and Cmax were comparable to historical data. PCR-corrected Day 29 ACPR was 95.5% and 100% in Cohorts 1 and 2, respectively. Treatment was well-tolerated. Developmental assessments at 12 months of age were within the normal range.
Conclusions: The optimized dose of artemether-lumefantrine (5 mg/60 mg) achieves the exposures required for optimal efficacy and safety in patients < 5 kg body weight with P. falciparum malaria, consistent with those in patients 5- < 15 kg treated with the current dispersible tablet (20 mg/120 mg).
{"title":"Pharmacokinetics, safety and efficacy of an optimized dose of artemether-lumefantrine in the treatment of acute uncomplicated Plasmodium falciparum malaria in neonates and infants of less than 5 kg body weight: a multicentre, open-label, single-arm phase 2/3 study (CALINA).","authors":"Gildas Wounounou, Alfred B Tiono, Bernhards Ogutu, Christine Manyando, Issaka Sagara, Stefan Schneitter, Quique Bassat, Myriam El Gaaloul, Anne Claire Marrast, Ivan Demin, Cornelis Winnips, Celine Risterucci, Sophie Hugot, Georg Hofstetter, Zhiyan Qian, Guoqin Su, Jie Zhang, Katalin Csermak Renner, Marc Cousin, Vinay Kumar Venishetty, Sarfaraz Sayyed, Preetam Gandhi, Berenger Kabore","doi":"10.1186/s41182-025-00828-z","DOIUrl":"10.1186/s41182-025-00828-z","url":null,"abstract":"<p><strong>Background: </strong>Treatment recommendations for malaria in infants of < 5 kg body weight (BW) are not evidence-based. Due to pharmacokinetic characteristics of this population, weight-based dose adjustments for antimalarials may be suboptimal. The 20 mg artemether:120 mg lumefantrine dispersible tablet, even with dose adjustment, may lead to artemether over-exposure and reduced lumefantrine exposure in patients < 5 kg. PBPK modelling predicted that a 1:12 artemether:lumefantrine ratio dispersible tablet should match efficacious and safe drug exposures in patients 5- < 15 kg treated with the current artemether-lumefantrine dispersible tablet: the CALINA study used an exposure-matching approach to confirm that drug exposures were comparable.</p><p><strong>Methods: </strong>Sequential age cohorts (Cohort 1: > 28 days; Cohort 2: 1-28 days) of patients < 5 kg with Plasmodium falciparum malaria received the new artemether-lumefantrine dispersible tablet (each dose 5 mg artemether: 60 mg lumefantrine) twice daily for 3 days. Artemether C<sub>max</sub>, and lumefantrine C<sub>168h</sub> and C<sub>max</sub> were compared with historical data from patients 5- < 15 kg treated with the current artemether-lumefantrine dispersible tablet. The primary endpoint was met if the 90% CI for artemether C<sub>max</sub> contained the LS mean value from historical data (101 ng/mL). PCR-corrected and uncorrected ACPR at Days 15, 29 and 43 and parasite clearance time were evaluated. Adverse events, laboratory evaluations, and developmental assessments were performed.</p><p><strong>Results: </strong>In Cohort 1 (N = 22), geometric mean artemether C<sub>max</sub> was 68.0 ng/mL (90% CI 45.1,103 ng/mL); therefore, C<sub>max</sub> was comparable to that in historical data, meeting the primary endpoint. In Cohort 2 (N = 6), there were too few patients for formal analysis, but geometric mean artemether C<sub>max</sub> was comparable to that in Cohort 1 (62.2 ng/mL, 90% CI 33.6,115 ng/mL). In both cohorts, lumefantrine C<sub>168h</sub> and C<sub>max</sub> were comparable to historical data. PCR-corrected Day 29 ACPR was 95.5% and 100% in Cohorts 1 and 2, respectively. Treatment was well-tolerated. Developmental assessments at 12 months of age were within the normal range.</p><p><strong>Conclusions: </strong>The optimized dose of artemether-lumefantrine (5 mg/60 mg) achieves the exposures required for optimal efficacy and safety in patients < 5 kg body weight with P. falciparum malaria, consistent with those in patients 5- < 15 kg treated with the current dispersible tablet (20 mg/120 mg).</p><p><strong>Trial registry: </strong>Clinicaltrials.gov: NCT04300309.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"151"},"PeriodicalIF":3.5,"publicationDate":"2025-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12590907/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145459997","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}
Pub Date : 2025-11-03DOI: 10.1186/s41182-025-00845-y
L O Busari, A S Babalola, Q O Adeshina, O G Dauda, Z O Iwalewa, G O Ige, G B Jokanola, C T Aroyehun, M M Abdulsalam, Y O Yusuff, R A Oyewusi, I O Awoniyi, O A Surakat, A O Adeogun, A M Rufai, K A Fasasi, M A Adeleke
Background: Aedes mosquitoes are primary vectors of arboviral diseases, such as dengue, chikungunya, and Zika, posing major threats to tropical public health. Understanding their spatial distribution and resistance status is vital for sustainable control. This study investigated the mapping of breeding habitats, species composition, and insecticide susceptibility in Aedes populations from Osun State, Nigeria.
Methods: Larval surveys across a rural community identified 36 potential habitats, of which 27.8% were positive for Aedes breeding. A total of 3500 larvae were collected, reared to adult stage, morphologically identified and subjected to WHO-standard insecticide bioassays.
Results: Two species were identified: Aedes aegypti (99.3%) and Aedes albopictus (0.7%), with Ae. aegypti strongly predominant (p < 0.05). Mortality rates following insecticide exposure ranged from 94 to 100%. Complete susceptibility was observed for permethrin, deltamethrin, and pirimiphos-methyl, while reduced mortality (94%) against alpha-cypermethrin indicated possible emerging resistance. The mapping of larval habitats revealed clustered breeding in rural communities, portending localized risk of arboviral transmission.
Conclusions: These findings highlight that while Aedes populations in the study area remain largely susceptible to conventional insecticides, early signals of resistance require proactive management by the state. Incorporating synergists into integrated vector control, alongside habitat surveillance and mapping, will be critical to sustaining insecticide effectiveness and reducing the burden of Aedes-borne diseases in Osun State and Nigeria at large.
{"title":"Spatial distribution and insecticide resistance of Aedes mosquitoes in Osun State: implications for vector control.","authors":"L O Busari, A S Babalola, Q O Adeshina, O G Dauda, Z O Iwalewa, G O Ige, G B Jokanola, C T Aroyehun, M M Abdulsalam, Y O Yusuff, R A Oyewusi, I O Awoniyi, O A Surakat, A O Adeogun, A M Rufai, K A Fasasi, M A Adeleke","doi":"10.1186/s41182-025-00845-y","DOIUrl":"10.1186/s41182-025-00845-y","url":null,"abstract":"<p><strong>Background: </strong>Aedes mosquitoes are primary vectors of arboviral diseases, such as dengue, chikungunya, and Zika, posing major threats to tropical public health. Understanding their spatial distribution and resistance status is vital for sustainable control. This study investigated the mapping of breeding habitats, species composition, and insecticide susceptibility in Aedes populations from Osun State, Nigeria.</p><p><strong>Methods: </strong>Larval surveys across a rural community identified 36 potential habitats, of which 27.8% were positive for Aedes breeding. A total of 3500 larvae were collected, reared to adult stage, morphologically identified and subjected to WHO-standard insecticide bioassays.</p><p><strong>Results: </strong>Two species were identified: Aedes aegypti (99.3%) and Aedes albopictus (0.7%), with Ae. aegypti strongly predominant (p < 0.05). Mortality rates following insecticide exposure ranged from 94 to 100%. Complete susceptibility was observed for permethrin, deltamethrin, and pirimiphos-methyl, while reduced mortality (94%) against alpha-cypermethrin indicated possible emerging resistance. The mapping of larval habitats revealed clustered breeding in rural communities, portending localized risk of arboviral transmission.</p><p><strong>Conclusions: </strong>These findings highlight that while Aedes populations in the study area remain largely susceptible to conventional insecticides, early signals of resistance require proactive management by the state. Incorporating synergists into integrated vector control, alongside habitat surveillance and mapping, will be critical to sustaining insecticide effectiveness and reducing the burden of Aedes-borne diseases in Osun State and Nigeria at large.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"150"},"PeriodicalIF":3.5,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12581341/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145431909","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}
Pub Date : 2025-11-02DOI: 10.1186/s41182-025-00830-5
Ghulam Raza Mohammadyan, Seyed Aria Nejadghaderi, Hamid Sharifi, Mohammad Mehdi Gouya, Seyed Mohsen Zahraei, AliAkbar Haghdoost
Background: Global vaccine coverage improved substantially. In Afghanistan, routine immunization has been expanding since 1978 but remains inadequate, contributing to consistently high under-five mortality rates. This time-trend analysis focused on national routine childhood immunization coverage and the number of Expanded Programme on Immunization (EPI) centers in Afghanistan from 1999 to 2023.
Methods: Data were drawn from World Health Organization/United Nations Children's Fund (WHO/UNICEF) estimates and the "Gavi, the Vaccine Alliance" administrative reports (1999-2018). Seven vaccines were assessed: third dose of polio vaccine (Pol3), first and second doses of measles-containing vaccine (MCV1, MCV2), first and third doses of diphtheria-tetanus-pertussis vaccine (DTP1, DTP3), Bacillus Calmette-Guérin (BCG), and third dose of hepatitis B vaccine (HepB3). Linear spline regression, with knots in 2006 and 2018, was validated.
Results: Between 1999 and 2023, coverage of all seven vaccines increased. WHO/UNICEF data showed Pol3 rising from 27% to 68%, MCV1 from 31% to 55%, DTP1 from 15.2% to 67%, DTP3 from 27% to 60%, and BCG from 38% to 68%, with MCV2 growing from 2% to 42% and HepB3 peaking at 67%. Spline regression revealed rapid growth from 1999 to 2006, slower increases from 2007 to 2018, and declines from 2019 to 2023. Gavi data mirrored these patterns, with DTP3 rising by 7.96% annually from 1999 to 2006 and DTP1 falling by 0.30% from 2007 to 2018. EPI centers expanded by 159.78 per year (2001-2006) and 74.12 (2007-2018).
Conclusions: Afghanistan's immunization coverage increased substantially until 2006, grew more slowly from 2007 to 2018, and declined after 2019. These patterns highlight the vulnerability of routine immunization programs to contextual challenges and suggest that sustaining coverage will require continued strengthening of routine services, monitoring subnational disparities, and implementing conflict-sensitive strategies.
{"title":"Trends of routine childhood vaccination status in Afghanistan over the last two decades (1999-2023).","authors":"Ghulam Raza Mohammadyan, Seyed Aria Nejadghaderi, Hamid Sharifi, Mohammad Mehdi Gouya, Seyed Mohsen Zahraei, AliAkbar Haghdoost","doi":"10.1186/s41182-025-00830-5","DOIUrl":"10.1186/s41182-025-00830-5","url":null,"abstract":"<p><strong>Background: </strong>Global vaccine coverage improved substantially. In Afghanistan, routine immunization has been expanding since 1978 but remains inadequate, contributing to consistently high under-five mortality rates. This time-trend analysis focused on national routine childhood immunization coverage and the number of Expanded Programme on Immunization (EPI) centers in Afghanistan from 1999 to 2023.</p><p><strong>Methods: </strong>Data were drawn from World Health Organization/United Nations Children's Fund (WHO/UNICEF) estimates and the \"Gavi, the Vaccine Alliance\" administrative reports (1999-2018). Seven vaccines were assessed: third dose of polio vaccine (Pol3), first and second doses of measles-containing vaccine (MCV1, MCV2), first and third doses of diphtheria-tetanus-pertussis vaccine (DTP1, DTP3), Bacillus Calmette-Guérin (BCG), and third dose of hepatitis B vaccine (HepB3). Linear spline regression, with knots in 2006 and 2018, was validated.</p><p><strong>Results: </strong>Between 1999 and 2023, coverage of all seven vaccines increased. WHO/UNICEF data showed Pol3 rising from 27% to 68%, MCV1 from 31% to 55%, DTP1 from 15.2% to 67%, DTP3 from 27% to 60%, and BCG from 38% to 68%, with MCV2 growing from 2% to 42% and HepB3 peaking at 67%. Spline regression revealed rapid growth from 1999 to 2006, slower increases from 2007 to 2018, and declines from 2019 to 2023. Gavi data mirrored these patterns, with DTP3 rising by 7.96% annually from 1999 to 2006 and DTP1 falling by 0.30% from 2007 to 2018. EPI centers expanded by 159.78 per year (2001-2006) and 74.12 (2007-2018).</p><p><strong>Conclusions: </strong>Afghanistan's immunization coverage increased substantially until 2006, grew more slowly from 2007 to 2018, and declined after 2019. These patterns highlight the vulnerability of routine immunization programs to contextual challenges and suggest that sustaining coverage will require continued strengthening of routine services, monitoring subnational disparities, and implementing conflict-sensitive strategies.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"149"},"PeriodicalIF":3.5,"publicationDate":"2025-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12581220/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145431938","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}
Pub Date : 2025-10-30DOI: 10.1186/s41182-025-00822-5
Serge Akpodji, Clément Agbangla, Germain Gil Padonou, Zul-Kifl Affolabi, Zinsou Côme Koukpo, Constantin Adoha, Steve Zinsou Hougbe, André Sominahouin, Filémon Tokponnon, Razaki A Osse, Olivier Oussou, Bruno Adjottin, Esdras Mahoutin Odjo, Boulais Yovogan, Roseric Azondékon, Albert Salako, Martin Akogbéto
Background: To help with planning malaria vector control in Benin, the National Malaria Control Program launched a study to update the distribution of major malaria vectors and their role in Plasmodium falciparum transmission. The study aimed to go beyond the standard entomological inoculation rate (EIR) by incorporating the average sporozoite load of the mosquitoes. This is because the parasite load is a key factor in a successful infection. The research proposed combining the average P. falciparum sporozoite load with EIR to better determine the vectors' true contribution to malaria transmission.
Methods: The study was conducted across 18 communes in Benin. Within each commune, two villages were chosen for mosquito collection using human landing catches (HLC) and pyrethrum spray catches (PSC). Heads and thoraxes from female Anopheles gambiae s.l. and Anopheles funestus mosquitoes were analyzed for the Plasmodium falciparum circumsporozoite antigen using the ELISA/CSP method. The corresponding carcasses were used for species identification via PCR. The P. falciparum sporozoite load was quantified in CSP ELISA-positive mosquitoes using the NZYTech real-time PCR kit. The contribution of vectors to P. falciparum transmission was first estimated by considering both their infection and bite rates. Subsequently, the relative contribution to transmission was further assessed by correlating the P. falciparum sporozoite load of the primary vectors with EIR.
Results: Anopheles coluzzii is responsible for 63.01% of malaria transmission, with an EIR of 87.7 infecting bites per person per year. This is followed by Anopheles gambiae, which accounts for 36.7% of transmission and has an EIR of 51.1 infecting bites per person per year. The contribution of Anopheles funestus is 0.24%. The study found that An. gambiae carries a higher load of Plasmodium falciparum sporozoites than An. coluzzii. Specifically, approximately 30% of An. gambiae individuals carried more than 10,000 sporozoites in their salivary glands, while less than 10% of An. coluzzii individuals had a comparable load.
Conclusion: This study clarifies the true contribution of malaria vectors to Plasmodium falciparum transmission by linking sporozoite load to the EIR. The findings will allow for a more accurate assessment of the vectors' role in P. falciparum transmission in Benin.
{"title":"Spatial and temporal distribution of four malaria vector species and their relative contributions to Plasmodium falciparum transmission along the south-north transect of Benin, West Africa.","authors":"Serge Akpodji, Clément Agbangla, Germain Gil Padonou, Zul-Kifl Affolabi, Zinsou Côme Koukpo, Constantin Adoha, Steve Zinsou Hougbe, André Sominahouin, Filémon Tokponnon, Razaki A Osse, Olivier Oussou, Bruno Adjottin, Esdras Mahoutin Odjo, Boulais Yovogan, Roseric Azondékon, Albert Salako, Martin Akogbéto","doi":"10.1186/s41182-025-00822-5","DOIUrl":"10.1186/s41182-025-00822-5","url":null,"abstract":"<p><strong>Background: </strong>To help with planning malaria vector control in Benin, the National Malaria Control Program launched a study to update the distribution of major malaria vectors and their role in Plasmodium falciparum transmission. The study aimed to go beyond the standard entomological inoculation rate (EIR) by incorporating the average sporozoite load of the mosquitoes. This is because the parasite load is a key factor in a successful infection. The research proposed combining the average P. falciparum sporozoite load with EIR to better determine the vectors' true contribution to malaria transmission.</p><p><strong>Methods: </strong>The study was conducted across 18 communes in Benin. Within each commune, two villages were chosen for mosquito collection using human landing catches (HLC) and pyrethrum spray catches (PSC). Heads and thoraxes from female Anopheles gambiae s.l. and Anopheles funestus mosquitoes were analyzed for the Plasmodium falciparum circumsporozoite antigen using the ELISA/CSP method. The corresponding carcasses were used for species identification via PCR. The P. falciparum sporozoite load was quantified in CSP ELISA-positive mosquitoes using the NZYTech real-time PCR kit. The contribution of vectors to P. falciparum transmission was first estimated by considering both their infection and bite rates. Subsequently, the relative contribution to transmission was further assessed by correlating the P. falciparum sporozoite load of the primary vectors with EIR.</p><p><strong>Results: </strong>Anopheles coluzzii is responsible for 63.01% of malaria transmission, with an EIR of 87.7 infecting bites per person per year. This is followed by Anopheles gambiae, which accounts for 36.7% of transmission and has an EIR of 51.1 infecting bites per person per year. The contribution of Anopheles funestus is 0.24%. The study found that An. gambiae carries a higher load of Plasmodium falciparum sporozoites than An. coluzzii. Specifically, approximately 30% of An. gambiae individuals carried more than 10,000 sporozoites in their salivary glands, while less than 10% of An. coluzzii individuals had a comparable load.</p><p><strong>Conclusion: </strong>This study clarifies the true contribution of malaria vectors to Plasmodium falciparum transmission by linking sporozoite load to the EIR. The findings will allow for a more accurate assessment of the vectors' role in P. falciparum transmission in Benin.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"147"},"PeriodicalIF":3.5,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12573912/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410122","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}
Background: Primary liver cancer (PLC) ranks as the third leading cause of cancer-related mortality worldwide, posing a serious global public health burden. Hepatocellular carcinoma (HCC) is the most common subtype, accounting for approximately 75%-85% of all PLC cases. In recent years, environmental pollution has emerged as a potential risk factor for PLC. However, a systematic bibliometric analysis of global research trends in this field remains lacking. This study aims to perform a comprehensive bibliometric analysis to explore global trends in the field of environmental pollution and PLC research from 2000 to 2025.
Methods: We conducted a bibliometric analysis using the Web of Science Core Collection database, covering studies published from January 2000 to March 2025. CiteSpace was used to analyze publication trends, global collaborations, and key research areas through network visualizations and co-occurrence analyses.
Results: A total of 562 publications were included in this study, with China and the United States identified as the leading contributors. Prominent institutions in this field include the National Institutes of Health (USA), National Cancer Institute (USA), and the Chinese Academy of Sciences. Among journals, Environmental Health Perspectives, Hepatology, and Cancer Research were the most frequently cited, indicating a close connection between environmental science and oncology. Keyword analysis revealed that research focuses not only on traditional pollutants such as air pollution and heavy metals, but also on emerging exposures including volatile organic compounds and drinking water contaminants. Mechanistic studies remain at the core of this field, with frequently occurring terms such as "oxidative stress", "gene expression", and "inflammation". Meanwhile, clinical research-related keywords like "epidemiology" and "follow-up" have become increasingly prominent in recent years, indicating a growing emphasis on population-based risk assessment.
Conclusions: This study highlights the growing research interest in the link between environmental pollution and PLC. Cross-disciplinary collaborations between environmental science, medicine, and public health are increasingly influencing the development of this field. Future research should focus on elucidating the carcinogenic mechanisms of pollutants and enhancing translational applications in public health.
背景:原发性肝癌(PLC)是全球癌症相关死亡的第三大原因,造成了严重的全球公共卫生负担。肝细胞癌(HCC)是最常见的亚型,约占所有PLC病例的75%-85%。近年来,环境污染已成为PLC的潜在风险因素。然而,对该领域的全球研究趋势进行系统的文献计量分析仍然缺乏。本研究旨在进行全面的文献计量分析,以探讨2000年至2025年环境污染和PLC研究领域的全球趋势。方法:我们使用Web of Science Core Collection数据库进行文献计量分析,涵盖2000年1月至2025年3月发表的研究。CiteSpace通过网络可视化和共现分析来分析出版趋势、全球合作和重点研究领域。结果:本研究共纳入562篇论文,其中中国和美国是主要贡献者。该领域的知名机构包括美国国立卫生研究院、美国国家癌症研究所和中国科学院。在期刊中,《环境健康展望》、《肝病学》和《癌症研究》是最常被引用的,这表明环境科学与肿瘤学之间有着密切的联系。关键词分析表明,研究不仅集中在传统污染物如空气污染和重金属,而且还集中在新兴暴露点如挥发性有机物和饮用水污染物。机制研究仍然是该领域的核心,经常出现“氧化应激”、“基因表达”和“炎症”等术语。与此同时,“流行病学”、“随访”等临床研究相关的关键词近年来日益突出,表明基于人群的风险评估越来越受到重视。结论:这项研究突出了环境污染与PLC之间联系的日益增长的研究兴趣。环境科学、医学和公共卫生之间的跨学科合作正日益影响着这一领域的发展。未来的研究应侧重于阐明污染物的致癌机制,并加强在公共卫生方面的转化应用。
{"title":"Global research trends and hotspots on environmental pollution and primary liver cancer: a bibliometric and visualized analysis.","authors":"Jingqin Hu, Xue Jiao, Yuchang Wang, Huiwen Yang, Xiaohan Zhang, Feng Jiang, Ping Li","doi":"10.1186/s41182-025-00820-7","DOIUrl":"10.1186/s41182-025-00820-7","url":null,"abstract":"<p><strong>Background: </strong>Primary liver cancer (PLC) ranks as the third leading cause of cancer-related mortality worldwide, posing a serious global public health burden. Hepatocellular carcinoma (HCC) is the most common subtype, accounting for approximately 75%-85% of all PLC cases. In recent years, environmental pollution has emerged as a potential risk factor for PLC. However, a systematic bibliometric analysis of global research trends in this field remains lacking. This study aims to perform a comprehensive bibliometric analysis to explore global trends in the field of environmental pollution and PLC research from 2000 to 2025.</p><p><strong>Methods: </strong>We conducted a bibliometric analysis using the Web of Science Core Collection database, covering studies published from January 2000 to March 2025. CiteSpace was used to analyze publication trends, global collaborations, and key research areas through network visualizations and co-occurrence analyses.</p><p><strong>Results: </strong>A total of 562 publications were included in this study, with China and the United States identified as the leading contributors. Prominent institutions in this field include the National Institutes of Health (USA), National Cancer Institute (USA), and the Chinese Academy of Sciences. Among journals, Environmental Health Perspectives, Hepatology, and Cancer Research were the most frequently cited, indicating a close connection between environmental science and oncology. Keyword analysis revealed that research focuses not only on traditional pollutants such as air pollution and heavy metals, but also on emerging exposures including volatile organic compounds and drinking water contaminants. Mechanistic studies remain at the core of this field, with frequently occurring terms such as \"oxidative stress\", \"gene expression\", and \"inflammation\". Meanwhile, clinical research-related keywords like \"epidemiology\" and \"follow-up\" have become increasingly prominent in recent years, indicating a growing emphasis on population-based risk assessment.</p><p><strong>Conclusions: </strong>This study highlights the growing research interest in the link between environmental pollution and PLC. Cross-disciplinary collaborations between environmental science, medicine, and public health are increasingly influencing the development of this field. Future research should focus on elucidating the carcinogenic mechanisms of pollutants and enhancing translational applications in public health.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"145"},"PeriodicalIF":3.5,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12574309/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410116","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}
Pub Date : 2025-10-30DOI: 10.1186/s41182-025-00823-4
Jingfang Cai, Ahiafor Maxwell, Boda Zhou
Background: Disease burden attributable to extreme high temperature requires more attention amid dramatic climate change, especially in South Asia and Southeast Asia.
Methods: We analyzed comprehensive estimates from the GBD 2021 Study, examining mortality and disability-adjusted life years (DALYs) across 369 diseases and 88 risk factors. This study employed joinpoint regression analysis and Age-Period-Cohort modeling to examine time trends from 1990 to 2021 and projected disease burden up to 2045 by incorporating demographic forecasts and a Bayesian Age-Period-Cohort model.
Results: South Asia and Southeast Asia contributed more than half of the global death number attributed to high temperature. In 2021, South Asia recorded 209,537 deaths and Southeast Asia recorded 32,230 deaths attributed to high temperatures. In South Asia and Southeast Asia, Pakistan bore the highest number and rate of deaths attributed to high temperature. The population above 55 and below 5 years in South Asia and Southeast Asia experienced higher disease burden attributed to high temperature. The leading cause of ASMR attributed to high temperature in South Asia and Southeast Asia was non-communicable diseases. Population growth and aging were the main drivers of ASMR increases in South Asia and Southeast Asia, while epidemiological changes contributed to a reduction in ASMR. Deaths attributed to high temperatures in South and Southeast Asia are projected to rise until 2045, with South Asia exceeding 400,000 and Southeast Asia approaching 100,000 deaths in 2045.
Conclusions: This study highlights the urgent need for region-specific, gender-specific and age-specific interventions to reduce high temperature-related disease burden in South Asia and Southeast Asia.
{"title":"Disease burden attributable to high temperature between 1990 and 2021 in South Asia and Southeast Asia, with projections to 2045.","authors":"Jingfang Cai, Ahiafor Maxwell, Boda Zhou","doi":"10.1186/s41182-025-00823-4","DOIUrl":"10.1186/s41182-025-00823-4","url":null,"abstract":"<p><strong>Background: </strong>Disease burden attributable to extreme high temperature requires more attention amid dramatic climate change, especially in South Asia and Southeast Asia.</p><p><strong>Methods: </strong>We analyzed comprehensive estimates from the GBD 2021 Study, examining mortality and disability-adjusted life years (DALYs) across 369 diseases and 88 risk factors. This study employed joinpoint regression analysis and Age-Period-Cohort modeling to examine time trends from 1990 to 2021 and projected disease burden up to 2045 by incorporating demographic forecasts and a Bayesian Age-Period-Cohort model.</p><p><strong>Results: </strong>South Asia and Southeast Asia contributed more than half of the global death number attributed to high temperature. In 2021, South Asia recorded 209,537 deaths and Southeast Asia recorded 32,230 deaths attributed to high temperatures. In South Asia and Southeast Asia, Pakistan bore the highest number and rate of deaths attributed to high temperature. The population above 55 and below 5 years in South Asia and Southeast Asia experienced higher disease burden attributed to high temperature. The leading cause of ASMR attributed to high temperature in South Asia and Southeast Asia was non-communicable diseases. Population growth and aging were the main drivers of ASMR increases in South Asia and Southeast Asia, while epidemiological changes contributed to a reduction in ASMR. Deaths attributed to high temperatures in South and Southeast Asia are projected to rise until 2045, with South Asia exceeding 400,000 and Southeast Asia approaching 100,000 deaths in 2045.</p><p><strong>Conclusions: </strong>This study highlights the urgent need for region-specific, gender-specific and age-specific interventions to reduce high temperature-related disease burden in South Asia and Southeast Asia.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"146"},"PeriodicalIF":3.5,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12573994/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410069","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}
Pub Date : 2025-10-30DOI: 10.1186/s41182-025-00826-1
Schawanya K Rattanapitoon, Patpicha Arunsan, Chutharat Thanchonnang, Nathkapach K Rattanapitoon
The study by Nikièma et al. demonstrates the absence of Wuchereria bancrofti infection in Anopheles mosquitoes a decade after cessation of mass drug administration (MDA) in Burkina Faso. This rare longitudinal evidence underscores the utility of molecular xenomonitoring (MX) as a sensitive early-warning tool that complements traditional transmission assessment surveys (TAS). MX enables detection of recrudescence earlier than human-based diagnostics, particularly in low-prevalence settings, and offers opportunities for integration with malaria vector surveillance. Ethical and operational challenges associated with human landing catches highlight the need for alternative trapping methods to maintain MX sensitivity safely. Sustaining lymphatic filariasis elimination globally will depend on institutionalizing MX alongside TAS, ensuring robust surveillance, and safeguarding long-term programmatic gains.
{"title":"Molecular xenomonitoring highlights post-MDA surveillance priorities for sustained Wuchereria bancrofti elimination in Burkina Faso.","authors":"Schawanya K Rattanapitoon, Patpicha Arunsan, Chutharat Thanchonnang, Nathkapach K Rattanapitoon","doi":"10.1186/s41182-025-00826-1","DOIUrl":"10.1186/s41182-025-00826-1","url":null,"abstract":"<p><p>The study by Nikièma et al. demonstrates the absence of Wuchereria bancrofti infection in Anopheles mosquitoes a decade after cessation of mass drug administration (MDA) in Burkina Faso. This rare longitudinal evidence underscores the utility of molecular xenomonitoring (MX) as a sensitive early-warning tool that complements traditional transmission assessment surveys (TAS). MX enables detection of recrudescence earlier than human-based diagnostics, particularly in low-prevalence settings, and offers opportunities for integration with malaria vector surveillance. Ethical and operational challenges associated with human landing catches highlight the need for alternative trapping methods to maintain MX sensitivity safely. Sustaining lymphatic filariasis elimination globally will depend on institutionalizing MX alongside TAS, ensuring robust surveillance, and safeguarding long-term programmatic gains.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"148"},"PeriodicalIF":3.5,"publicationDate":"2025-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12574178/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410113","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}
Pub Date : 2025-10-29DOI: 10.1186/s41182-025-00819-0
Shu Yang, Shu Yang, Jun Guo, Peng Li, Yuling Xu, Fei Hu, Yiting Cui, Ai Peng, Yangqing Liu, Yibing Fan, Shihui Peng, Hui Li, Peng Huang
Background: Scrub typhus is an important zoonotic disease with rising incidence globally. Meteorological factors may influence its transmission dynamics. However, inconsistencies across studies and limited quantitative evidence highlight the need for further investigation.
Objective: To systematically evaluate the linear and nonlinear associations between various meteorological factors and scrub typhus incidence, explore lagged effects and potential sources of heterogeneity, and analyze inconsistencies in existing findings.
Method: We searched PubMed, Scopus, Web of Science, and Embase for studies published up to February 2025. Relevant articles were identified based on predefined inclusion and exclusion criteria. We conducted linear meta-analyses to assess the effects of unit changes in meteorological factors and dose-response meta-analyses to evaluate cumulative lagged risks across different exposure levels. Subgroup and sensitivity analyses were conducted to explore sources of heterogeneity and assess result robustness.
Results: Seventeen studies were included, covering China, Korea, Laos, and India. Eleven studies contributed to linear meta-analyses, and six to dose-response analyses. Ambient temperature (RR 1.08, 95% CI 1.02-1.16), land surface temperature (RR 1.06, 95% CI 1.02-1.09), precipitation (RR 1.01, 95% CI 1.01-1.02), relative humidity (RR 1.07, 95% CI 1.04-1.11), and atmospheric pressure (RR 1.06, 95% CI 0.91-1.23) were positively associated with the risk of scrub typhus. Wind speed (RR 0.59, 95% CI 0.49-0.71) and sunshine duration (RR 0.92, 95% CI 0.77-1.10) exhibited negative associations. Dose-response meta-analysis revealed inverted U-shaped relationships for ambient temperature and relative humidity, and a unimodal pattern for precipitation, with risk increasing continuously at high levels. Significant lag effects were observed: precipitation had the most immediate effect (lag0: RR 1.05), while ambient temperature (lag1: RR 1.18) and relative humidity (lag2: RR 1.28) peaked with a 1- to 2-month delay. Geographic variation was identified as a major source of between-study heterogeneity.
Conclusion: Although this study has certain limitations, including the small number of included studies, their concentration mainly in China, and the presence of substantial heterogeneity, the results provide evidence of linear and nonlinear associations between meteorological factors and scrub typhus incidence, and highlight the roles of geographical variation and lag effects. These findings offer quantitative evidence and scientific support for disease prevention and control in the context of climate change.
背景:恙虫病是一种重要的人畜共患疾病,全球发病率呈上升趋势。气象因素可能影响其传播动态。然而,研究之间的不一致性和有限的定量证据突出了进一步调查的必要性。目的:系统评价各种气象因素与恙虫病发病率的线性和非线性关系,探索滞后效应和异质性的潜在来源,分析现有研究结果的不一致之处。方法:检索PubMed、Scopus、Web of Science和Embase,检索截止到2025年2月发表的研究。根据预先确定的纳入和排除标准确定相关文章。我们进行了线性荟萃分析来评估气象因素单位变化的影响,并进行了剂量-反应荟萃分析来评估不同暴露水平的累积滞后风险。进行亚组分析和敏感性分析以探索异质性来源并评估结果的稳健性。结果:纳入17项研究,涵盖中国、韩国、老挝和印度。11项研究用于线性荟萃分析,6项用于剂量-反应分析。环境温度(RR 1.08, 95% CI 1.02-1.16)、地表温度(RR 1.06, 95% CI 1.02-1.09)、降水(RR 1.01, 95% CI 1.01-1.02)、相对湿度(RR 1.07, 95% CI 1.04-1.11)和大气压力(RR 1.06, 95% CI 0.91-1.23)与恙虫病发病风险呈正相关。风速(RR 0.59, 95% CI 0.49 ~ 0.71)与日照时数(RR 0.92, 95% CI 0.77 ~ 1.10)呈负相关。剂量-反应荟萃分析显示,环境温度和相对湿度呈倒u型关系,降水呈单峰模式,在高水平下风险持续增加。观察到显著的滞后效应:降水具有最直接的影响(lag0: RR 1.05),而环境温度(lag1: RR 1.18)和相对湿度(lag2: RR 1.28)在1至2个月后达到峰值。地理差异被认为是研究间异质性的主要来源。结论:虽然本研究存在一定的局限性,包括纳入的研究数量少、主要集中在中国,且存在较大的异质性,但研究结果证明了气象因素与丛林斑疹伤寒发病率之间存在线性和非线性关联,并突出了地理变异和滞后效应的作用。这些发现为气候变化背景下的疾病预防和控制提供了定量证据和科学支持。
{"title":"Associations between meteorological factors and scrub typhus incidence: a systematic review and meta-analysis of linear and nonlinear dose-response relationships.","authors":"Shu Yang, Shu Yang, Jun Guo, Peng Li, Yuling Xu, Fei Hu, Yiting Cui, Ai Peng, Yangqing Liu, Yibing Fan, Shihui Peng, Hui Li, Peng Huang","doi":"10.1186/s41182-025-00819-0","DOIUrl":"10.1186/s41182-025-00819-0","url":null,"abstract":"<p><strong>Background: </strong>Scrub typhus is an important zoonotic disease with rising incidence globally. Meteorological factors may influence its transmission dynamics. However, inconsistencies across studies and limited quantitative evidence highlight the need for further investigation.</p><p><strong>Objective: </strong>To systematically evaluate the linear and nonlinear associations between various meteorological factors and scrub typhus incidence, explore lagged effects and potential sources of heterogeneity, and analyze inconsistencies in existing findings.</p><p><strong>Method: </strong>We searched PubMed, Scopus, Web of Science, and Embase for studies published up to February 2025. Relevant articles were identified based on predefined inclusion and exclusion criteria. We conducted linear meta-analyses to assess the effects of unit changes in meteorological factors and dose-response meta-analyses to evaluate cumulative lagged risks across different exposure levels. Subgroup and sensitivity analyses were conducted to explore sources of heterogeneity and assess result robustness.</p><p><strong>Results: </strong>Seventeen studies were included, covering China, Korea, Laos, and India. Eleven studies contributed to linear meta-analyses, and six to dose-response analyses. Ambient temperature (RR 1.08, 95% CI 1.02-1.16), land surface temperature (RR 1.06, 95% CI 1.02-1.09), precipitation (RR 1.01, 95% CI 1.01-1.02), relative humidity (RR 1.07, 95% CI 1.04-1.11), and atmospheric pressure (RR 1.06, 95% CI 0.91-1.23) were positively associated with the risk of scrub typhus. Wind speed (RR 0.59, 95% CI 0.49-0.71) and sunshine duration (RR 0.92, 95% CI 0.77-1.10) exhibited negative associations. Dose-response meta-analysis revealed inverted U-shaped relationships for ambient temperature and relative humidity, and a unimodal pattern for precipitation, with risk increasing continuously at high levels. Significant lag effects were observed: precipitation had the most immediate effect (lag0: RR 1.05), while ambient temperature (lag1: RR 1.18) and relative humidity (lag2: RR 1.28) peaked with a 1- to 2-month delay. Geographic variation was identified as a major source of between-study heterogeneity.</p><p><strong>Conclusion: </strong>Although this study has certain limitations, including the small number of included studies, their concentration mainly in China, and the presence of substantial heterogeneity, the results provide evidence of linear and nonlinear associations between meteorological factors and scrub typhus incidence, and highlight the roles of geographical variation and lag effects. These findings offer quantitative evidence and scientific support for disease prevention and control in the context of climate change.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"144"},"PeriodicalIF":3.5,"publicationDate":"2025-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12570654/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145402148","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}
Pub Date : 2025-10-27DOI: 10.1186/s41182-025-00840-3
Muhamad Khizar, Ehsanullah Alokozay, Muhammad Junaid, Najibullah Alokozay
We commend Oh et al.'s recent analysis of TB preventive treatment (TPT) in the Western Pacific Region, but note important gaps and ways forward. We first caution that reliance on routine program data may overestimate gains. For example, China's passive surveillance misses ≈20% of cases [1]. Prospective cohorts or integrated surveillance including clinical databases could validate coverage estimates. We also urge attention to overlooked risk groups beyond children and PLHIV (as highlighted by Oh et al. [2]), groups like healthcare workers, prisoners, and people with diabetes warrant targeted TPT pilots (e.g., occupational health or prison-based programs). In the Philippines, ~ 36% of TB patients first seek private care [3], so partnering with private clinics and pharmacies is essential to reach all contacts. Likewise, MDR-TB contacts were underemphasized; WHO now strongly recommends a 6-month levofloxacin regimen for MDR contacts [4]. We encourage pilot studies of this regimen (as in Mongolia [5]) and operational research on MDR-TPT. Finally, policy does not guarantee practice as Cambodia and Lao PDR have guidelines, yet stockouts and training gaps persist [6, 7]. Embedding TPT in universal health insurance and conducting cost effectiveness studies will support sustainable scale-up. In sum, by suggesting concrete examples and research strategies for each country, we aim to refine Oh et al.'s insights into actionable steps for TPT acceleration.
{"title":"Critical appraisal of progress and challenges in tuberculosis preventive treatment in the Western Pacific Region: a situational analysis of seven high tuberculosis burden countries.","authors":"Muhamad Khizar, Ehsanullah Alokozay, Muhammad Junaid, Najibullah Alokozay","doi":"10.1186/s41182-025-00840-3","DOIUrl":"10.1186/s41182-025-00840-3","url":null,"abstract":"<p><p>We commend Oh et al.'s recent analysis of TB preventive treatment (TPT) in the Western Pacific Region, but note important gaps and ways forward. We first caution that reliance on routine program data may overestimate gains. For example, China's passive surveillance misses ≈20% of cases [1]. Prospective cohorts or integrated surveillance including clinical databases could validate coverage estimates. We also urge attention to overlooked risk groups beyond children and PLHIV (as highlighted by Oh et al. [2]), groups like healthcare workers, prisoners, and people with diabetes warrant targeted TPT pilots (e.g., occupational health or prison-based programs). In the Philippines, ~ 36% of TB patients first seek private care [3], so partnering with private clinics and pharmacies is essential to reach all contacts. Likewise, MDR-TB contacts were underemphasized; WHO now strongly recommends a 6-month levofloxacin regimen for MDR contacts [4]. We encourage pilot studies of this regimen (as in Mongolia [5]) and operational research on MDR-TPT. Finally, policy does not guarantee practice as Cambodia and Lao PDR have guidelines, yet stockouts and training gaps persist [6, 7]. Embedding TPT in universal health insurance and conducting cost effectiveness studies will support sustainable scale-up. In sum, by suggesting concrete examples and research strategies for each country, we aim to refine Oh et al.'s insights into actionable steps for TPT acceleration.</p>","PeriodicalId":23311,"journal":{"name":"Tropical Medicine and Health","volume":"53 1","pages":"143"},"PeriodicalIF":3.5,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12557891/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145378704","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}