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Acceptability and safety of thermal ablation for the treatment of precancerous cervical lesions in Honduras.


ABSTRACT: OBJECTIVE:To evaluate the acceptability and safety of thermal ablation (TA) for the treatment of precancerous cervical lesions in women in Honduras. METHODS:Human papillomavirus (HPV) and visual inspection with acetic acid (VIA) screen-positive eligible women received TA. After treatment, women rated the level of pain experienced during treatment using the Wong-Baker FACES® pain-rating scale from 0 to 10. Short-term safety outcomes that could require medical attention were assessed one month after treatment. RESULTS:A total of 319 women received TA treatment. The average pain rating was 2.5 (95% CI: 2.3-2.8), and 85% rated their pain levels as less than 6. No significant differences in low (below 6) or high (6 and above) pain were found by age or number of biopsies performed, but there was a significant difference by the number of TA applications (P < 0.01). When asked if they would recommend this treatment, all women said they would. At the one-month follow-up visit, the most common reported discomforts were bleeding (10%) and cramping (8.4%); 11 women reported severe lower abdominal pain, and none required medical attention. CONCLUSIONS:TA is safe and acceptable to patients as a treatment option for precancerous cervical lesions in low-resource settings.

SUBMITTER: Sandoval M 

PROVIDER: S-EPMC6916631 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Acceptability and safety of thermal ablation for the treatment of precancerous cervical lesions in Honduras.

Sandoval Manuel M   Slavkovsky Rose R   Bansil Pooja P   Jeronimo Jose J   Lim Jeanette J   Figueroa Jacqueline J   de Sanjose Silvia S  

Tropical medicine & international health : TM & IH 20191121 12


<h4>Objective</h4>To evaluate the acceptability and safety of thermal ablation (TA) for the treatment of precancerous cervical lesions in women in Honduras.<h4>Methods</h4>Human papillomavirus (HPV) and visual inspection with acetic acid (VIA) screen-positive eligible women received TA. After treatment, women rated the level of pain experienced during treatment using the Wong-Baker FACES® pain-rating scale from 0 to 10. Short-term safety outcomes that could require medical attention were assesse  ...[more]

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