Conclusions & Recommendations
33.07.1 - Tanzania
Conclusion/Recommendation:
TEC encourages the Tanzanian health ministry to consider conducting a TSS+ in Chamwino DC South and Kongwa DC North evaluation units, given their long history of persistent/recrudescent TF. TEC recognizes that incorporating complementary indicator(s) adds time and cost to surveys, albeit with a view to save time and costs in the future by avoiding unnecessary MDA and subsequent surveys, and encourages the Tanzanian health ministry to discuss this recommendation with its partners and donors.
Action:
This recommendation has been shared with the Tanzanian trachoma program.
TEC 33
2025
Africa - East
Tanzania
33.08.1 - Central African Republic
Conclusion/Recommendation:
TEC encourages the CAR health ministry to consider conducting surveys that incorporate complementary indicators (“plus” surveys) in Bossangoa and Bouca in 2028 when their next impact survey is due, following completion of their newly-approved modified MDA strategy. TEC recognizes that incorporating complementary indicator(s) adds time and cost to surveys, albeit with a view to save time and costs in the future by avoiding unnecessary MDA and subsequent surveys, and encourages the CAR health ministry to discuss this recommendation with its partners and donors.
TEC noted that activities are sometimes delayed in CAR and further encourages the health ministry to discuss with partners their full funding needs to ensure adequate resources.
Action:
These recommendations were shared and reviewed with the program and partners during a visit to Bangui in September. To address the challenge of delayed activities in 2025, ITI and partners visited the program in Bangui to find solutions and plan all programmatic activities foreseen for 2025 and 2026. Given that funding may not be identified for all activities, the program will look for opportunities of integration with the NTD Coordination to reduce costs and maximize resources.
TEC 33
2025
Africa - Central/Southern
CAR
33.09.1 - Chad
Conclusion/Recommendation:
TEC noted the recent influx of refugees from Darfur (endemic for trachoma) across the border into Chad. TEC recommends to ITI to follow up with the Chad health ministry to understand the situation in refugee camps and have a dialogue about whether they would be interested in requesting azithromycin to treat refugees in camps where populations from Darfur had a TF prevalence warranting MDA.
TEC further noted that given the incredible progress made in Chad in reducing trachoma prevalence to below elimination thresholds in all other areas of the country, it is very unlikely that there is active ocular C. trachomatis infection remaining in the three districts with TF1-9 ≽5%. Therefore, if funding cannot be identified for implementing MDA in 2025/26, a “wait and see” strategy followed by a survey incorporating complementary indicator(s) is a very reasonable approach.
Action:
These recommendations were shared with the Chad program and discussed in person in Dakar during a side meeting of RAFET. For the first recommendation considering refugee camps, the program is interested in exploring this further and a representative from OPC Chad has been put in contact with TCC to discuss further.
TEC 33
2025
Africa - Central/Southern
Chad
32.01.1 - Senegal congratulations
Conclusion/Recommendation:
TEC congratulates the national program of Senegal on reaching the important milestone of completing their dossier for the validation of the elimination of trachoma as a public health problem. The strong political engagement displayed by the Senegal program in the fight against NTDs is well noted. TEC looks forward to hearing that the dossier has been submitted and validated by WHO.
Action:
No action needed. Elimination of trachoma as a public health problem in Senegal was formally announced by the WHO in July 2025.
TEC 32
2025
Africa - West
Senegal
32.02.1 - On delaying child MDAs for trachoma validation
Conclusion/Recommendation:
TEC reviewed the experience of national trachoma programs in areas that completed trachoma MDA and are awaiting impact or surveillance surveys, while also being targeted for MDA for child survival. Noting the validation requirement for a two-year antibiotic MDA free period before a TSS is in tension with the ethical mandate of MDA for child survival, TEC requested that WHO provide relevant guidance to affected countries.
Action:
WHO has provided the following guidance relevant to the Niger program: "In Madaoua 1 (most recent prevalence of TF in 1-9-year-olds 7.0%), Matamaye 3 (9.5%) and Mirriah 1 (8.9%) EUs in Niger, in the face of (1) the incipient programme to undertake six-monthly azithromycin MDA for child survival ("REACH"); and (2) the ongoing programme to undertake seasonal malaria chemoprophylaxis with sulfadoxine four times per year, there has been uncertainty on the part of the health ministry as to whether to continue to undertake specific MDA in the whole population for trachoma elimination purposes, and how to time future trachoma prevalence surveys. It was recommended that because of the uncertain future duration of these interventions, the trachoma survey schedule for such evaluation units could continue as though child survival MDA and seasonal malaria chemoprophylaxis was not being undertaken, with an accompanying commitment to undertake further surveillance in the EUs once those interventions cease."
TEC 32
2025
Africa - West
Niger, Nigeria
research
32.03.1 - Innovation around surveys in insecure areas
Conclusion/Recommendation:
TEC appreciated the progress in developing innovative ways to assess the need for intervention in areas of conflict, and encouraged ongoing development of methods to assess the need for, and deliver interventions in, areas of conflict. Options for this may include using local teams to conduct surveys, simultaneously collecting complementary indicators, and using paper-based surveys.
Action:
No action needed.
TEC 32
2025
insecurity, alternative indicators (Ct, serology)
32.04.1 - Delayed TIS, TF <5%
Conclusion/Recommendation:
The TEC reviewed data on trachoma impact surveys that have been delayed due to conflict and other factors. Such delays can postpone submission of the national dossier and thus the validation of the elimination of trachoma as a public health problem. When the recommended number of MDA rounds has been completed and trachoma impact surveys are delayed by more than 2.5 years, national programs may wish to consult WHO on whether such an impact survey may serve the function of a trachoma surveillance survey if the TF prevalence is <5%.
Action:
Districts where this was relevant were discussed throughout TEC 33.
TEC 32
2025
32.05.1 - Delayed TIS, TF≥5%
Conclusion/Recommendation:
In areas where trachoma impact surveys have been delayed for more than 2.5 years since MDA and the new TIS results indicate TF above threshold, TEC would consider a request from national programs for a drug donation for a modified MDA strategy (even if the district did not previously qualify as 'persistent' or 'recrudescent').
Action:
This information has been added into the 2025 Azithromycin Management Guide as a new category for areas that qualify for modified MDA.
TEC 32
2025
alternative treatment strategies
32.06.1 - Integrating trachoma and child survival MDA
Conclusion/Recommendation:
The TEC congratulates the REACH Network on their impressive progress in supporting national programs using azithromycin MDA to reduce child mortality. TEC is committed to support the emerging partnership between the child survival and trachoma communities. TEC reviewed preliminary information on geographic overlap of areas requiring MDA for trachoma elimination and child survival. The TEC encourages national health ministries to explore opportunities for integrating child survival and trachoma MDAs where possible.
Action:
TEC 32
2025
Niger, Nigeria
32.06.2 - Integrating trachoma and child survival MDA
Conclusion/Recommendation:
Recognizing both the potential advantages and challenges in ‘integrated’ MDA for both trachoma and child survival, as well as the need for more information, TEC recommends that ITI commission a white paper that analyzes the programmatic impact, cost, safety, supply chain, and operational implications of different options for integrated trachoma/child survival MDA. TEC looks forward to engaging in future conversations about how best to achieve integration.
Action:
ITI has commissioned the development of a white paper, and a first draft is available as of May 2025. In the coming months, the white paper draft will be finalized and circulated initially to TEC, WHO, and Pfizer for feedback and used to guide further discussion.
TEC 32
2025