Abstract Objective To describe a cohort of placenta accreta spectrum (PAS) cases from a tertiary care institution and compare the maternal outcomes before and after the creation of a multidisciplinary team (MDT). Methods Retrospective study using hospital databases. Identification of PAS cases with pathological confirmation between 2010 and 2021. Division in two groups: standard care (SC) group – 2010–2014; and MDT group – 2015–2021. Descriptive analysis of their characteristics and maternal outcomes. Results During the study period, there were 53 cases of PAS (24 - SC group; 29 - MDT group). Standard care group: 1 placenta increta and 3 percreta; 12.5% (3/24) had antenatal suspicion; 4 cases had a peripartum hysterectomy – one planned due to antenatal suspicion of PAS; 3 due to postpartum hemorrhage. Mean estimated blood loss (EBL) was 2,469 mL; transfusion of packed red blood cells (PRBC) in 25% (6/24) - median 7.5 units. Multidisciplinary team group: 4 cases of placenta increta and 3 percreta. The rate of antenatal suspicion was 24.1% (7/29); 9 hysterectomies were performed, 7 planned due to antenatal suspicion of PAS, 1 after intrapartum diagnosis of PAS and 1 after uterine rupture following a second trimester termination of pregnancy. The mean EBL was 1,250 mL, with transfusion of PRBC in 37.9% (11/29) - median 2 units. Conclusion After the creation of the MDT, there was a reduction in the mean EBL and in the median number of PRBC units transfused, despite the higher number of invasive PAS disorders.

Resumo Objetivo Descrever uma coorte de casos do espectro do acretismo placentário (PAS) de uma instituição terciária e comparar os resultados maternos antes e depois da criação de uma equipa multidisciplinar (MDT). Métodos Estudo retrospectivo utilizando bancos de dados hospitalares. Identificação de casos de PAS com confirmação patológica entre 2010 e 2021. Divisão em dois grupos: grupo Standard Care (SC) – 2010–2014; e grupo MDT – 2015–2021. Análise descritiva de suas características e desfechos maternos. Resultados Durante o período do estudo, houve 53 casos de PAS (24 - grupo SC; 29 - grupo MDT). Grupo Standard Care: 1 placenta increta e 3 percretas; 12,5% (3/24) tiveram suspeita anteparto; 4 casos tiveram histerectomia periparto – uma eletiva devido à suspeita anteparto de PAS; 3 devido a hemorragia pós-parto. A média de perda hemática estimada (EBL) foi de 2.469 mL; transfusão de concentrado eritrocitário (PRBC) em 25% (6/24) - mediana 7,5 unidades. Equipa multidisciplinar: 4 casos de placenta increta e 3 percretas. A taxa de suspeita anteparto foi de 24,1% (7/29); foram realizadas 9 histerectomias, 7 eletivas por suspeita anteparto de PAS, 1 após diagnóstico intraparto de PAS e 1 após rotura uterina após interrupção da gravidez no segundo trimestre. A EBL média foi de 1.250 mL, com transfusão de PRBC em 37,9% (11/29) - mediana de 2 unidades. Conclusão Após a criação da MDT, houve redução na média de EBL e na mediana do número de unidades de PRBC transfundidas, apesar do maior número de PAS invasivos.

Resumo Este estudo tem por objetivo avaliar o potencial oferecido pelo jogo Chapeuzinho Vermelho Desplugada como recurso didático para o desenvolvimento do pensamento computacional em alunos com deficiência visual. A metodologia consiste em uma abordagem qualitativa, com objetivos exploratório/descritivos. Os sujeitos são três estudantes com deficiência visual congênita. O instrumento de pesquisa utilizado foi a observação participante, por meio do diário de campo. Para analisar os dados, empregou-se a análise categorial, a partir de quatro categorias: decomposição, reconhecimento de padrões, abstração e algoritmo. A partir da discussão dos resultados encontrados, é possível concluir que o jogo de tabuleiro Chapeuzinho Vermelho Desplugada apresenta potencial para o desenvolvimento de conceitos do pensamento computacional, com uma atividade que promova a Linguagem de Programação Desplugada, por meio do uso de recursos didáticos acessíveis, favorecendo o desenvolvimento cognitivo, o raciocínio lógico/matemático na resolução de problemas e a inclusão.

Abstract This study aims to evaluate the potential offered by the Red Riding Hood Unplugged game as a didactic resource for the development of computational thinking in students with visual impairments. The methodology consists of a qualitative approach, with exploratory/descriptive objectives. The subjects are three students with congenital visual impairment. The research instrument used was participant observation, through a field diary. To analyze the data, categorical analysis was used, based on four categories, decomposition, pattern recognition, abstraction and algorithm. From the discussion of the results found, it is possible to conclude that the Unplugged Little Red Riding Hood board game has potential for the development of concepts of computational thinking, with an activity that promotes the Unplugged Programming Language, through the use of accessible didactic resources, favoring cognitive development, logical/mathematical reasoning in problem solving and inclusion.

Overview and aims: Placenta Accreta Spectrum disorders are the leading cause of emergency hysterectomy in developed countries and are associated with high maternal morbidity and mortality (60% and 7%, respectively). The objective of our study was to review cases of PAS disorders occurring in the last 8 years (2010-2017) in a tertiary care centre, evaluating the forms of treatment chosen and the maternal and fetal outcomes. Methods: Retrospective cross-sectional study using hospital databases (Obscare®, SClinico®) to identify cases of placenta accreta during the study period. Diagnosis was made based on the histological study of placentas submitted for anatomo-pathological study. Results: During the study period, 38 cases of a PAS disorder were diagnosed in 20,910 births (1.8 / 1000), a number that is possibly underestimated. There were 8 women with a previous caesarean section and 6 had placenta previa (2 of them with previous caesarean section). There was ultrasound suspicion of a PAS disorder in 3 cases; of the 4 most severe cases (3 percretas and 1 increta), there was an ultrasound suspicion in 2. Regarding method of delivery, 21 births were by caesarean section and 16 by vaginal delivery. There was 1 case of spontaneous uterine rupture at 20 weeks' gestation with fetal loss; gestational age of birth varied between 32 and 41 weeks; 5 peri-partum hysterectomies were performed; transfusions of blood derivatives were required in 8 women. As for the newborns, there were 8 cases of prematurity and 7 hospitalisations in the Neonatal Intensive Care Unit; fetal death was observed in 2 cases. Conclusion: This case series demonstrate the high prevalence of PAS disorders and the great morbidity associated with it. Adequate antepartum care is essential in women with riskfactors to make the diagnosis timely, thus enabling a multidisciplinary approach with better maternal and fetal outcomes.

Overview and Aims: The last decade brought relevant insights into the pathophysiology of preeclampsia (PE), namely the role of the circulating levels of placental growth factor (PlGF) and soluble Fms-like tyrosine kinase-1 (sFlt-1). The purpose of this study is to estimate the financial impact of introducing the sFlt-1/PlGF ratio for the evaluation of women with suspicion of PE in the Portuguese National Healthcare System (SNS). Study Design: budget impact study evaluating short-term costs associated with the introduction of the sFlt-1/PlGF ratio from the SNS payer's perspective. The time horizon for the study is 1 year. Population: The target population consists of women presenting to the healthcare system with signs or symptoms suggestive of preeclampsia (estimated in 8500 subjects). Methods: A decision-tree model was used to estimate the budget impact of the introduction of the sFlt-1/PlGF ratio in the SNS. The model compares the management costs in the current clinical practice (“no test” scenario) vs. current diagnostic procedures plus the sFlt-1/PlGF ratio (“test” scenario). Clinical inputs have been derived primarily from literature review and, where data was unavailable, expert opinion. Resources and unit costs have been obtained from Portugal-specific sources. Results: In the current standard practice (no test), total costs were estimated to be e9 863 264 (e1160 per patient), with unnecessary admissions representing about e3,5 million. Total costs in the test scenario sum up to e9 781 194 (e1150 per patient), representing a cost saving to the system of e82 070 (e10 per patient), mainly due to a reduction of false positives and related unnecessary hospitalizations of women not developing PE. Conclusions: There is favorable economic evidence about the introduction of the sFlt- 1/PlGF ratio in the SNS. The generated savings appear to offset the costs related to the test.

Abstract Human Papillomavirus (HPV) has considerable tropism for epithelial and mucosal tissues and can therefore be found in several anatomical sites, including the oral cavity. This study aimed to investigate the presence of HPV-DNA and the most frequent viral types in patients using full dentures, compare to patients not using full dentures and to associate its presence with socio-epidemiological and behavioral factors. The study consisted of 90 patients with or without full dentures at the time of collection, treated at a public dental clinic. The samples were obtained by exfoliating the oral cavity, and analyzed for HPV-DNA using the nested PCR with PGMY09/11 (450-bp), and general primers GP5+/GP6+ (150-bp). Genotyping was performed by specific-type PCR to HPV 6, 11, 16, 18, 31, 33, and 45; and Restriction Fragment Length Polymorphism (RFLP). Pearson’s Chi-square test (x 2 ) or Fisher’s exact test were applied and significant variables in these tests were analyzed by multinomial logistic regression analysis to estimate odds ratio (OR). HPV-DNA was detected in 27.7% of samples and, among those obtained from patients using full dentures, positivity for HPV-DNA was 41.9% (p = 0.025). The most frequent viral types were low-risk HPV 6 and 11, and high-risk HPV 31 and 45. Patients who used full dentures had an odds ratio of 2.1 to be positive for HPV DNA. Our results indicate the need for periodic dental follow-up of patients with full dentures in order to preserve the basic conditions of oral health, and also to monitor the appearance of lesions with malignant potential.

RESUMO Introdução: O papilomavírus humano (HPV) está intimamente associado ao câncer cervical, e a presença de coinfecções, como por Chlamydia trachomatis, Gardnerella vaginalis e Trichomonas vaginalis, pode potencializar ou facilitar a infecção por HPV. As mulheres profissionais do sexo são consideradas vulneráveis à aquisição dessas infecções devido à exposição aos fatores de risco. Objetivo: Determinar a infecção por HPV, os tipos virais e as coinfecções em amostras autocoletadas de mulheres profissionais do sexo. Métodos: Amostras autocoletadas de mulheres profissionais do sexo, do canal vaginal e da cérvice uterina, foram submetidas a detecção do HPV-ácido desoxirribonucleico (DNA), genotipagem viral por reação em cadeia da polimerase (PCR) tipo específica e restriction fragment length polymorphism (RFLP) e detecção de coinfecção. Resultados: O HPV-DNA foi detectado em 19,4% das amostras, sendo os tipos HPV 31, 6 e 53 os mais frequentes. Houve predominância de HPV de alto risco (HR-HPV) e elevada presença de infecções múltiplas (84,6%). A presença de coinfecções foi observada tanto para HPV e C. trachomatis quanto para HPV e G. vaginalis. Observou-se também que mulheres profissionais do sexo que não fazem uso de preservativos e aquelas que não realizam o exame citológico rotineiramente estão predispostas à aquisição da infecção causada pelo HPV. Conclusão: Os resultados obtidos ressaltam a importância de estudos mais abrangentes entre as populações vulneráveis, objetivando estabelecer medidas para a conscientização sobre os riscos de aquisição das infecções sexualmente transmitidas, bem como auxiliar estudos futuros para introdução de vacinas contra o HPV com maior cobertura de tipos virais.

ABSTRACT Introduction: Human papillomavirus (HPV) is intimately associated with cervical cancer, and the presence of coinfections, such as with Chlamydia trachomatis, Gardnerella vaginalis and Trichomonas vaginalis, may potentiate or facilitate HPV infection. Female sex workers are considered vulnerable to the acquisition of these infections due to exposure to risk factors. Objective: To determine HPV infection, viral types and coinfections in self-collected samples from female sex workers. Methods: Self-collected samples from female sex workers, of vaginal canal and uterine cervix, were subjected to HPV-deoxyribonucleic acid (DNA) detection, viral genotyping by type-specific polymerase chain reaction (PCR), restriction fragment length polymorphism (RFLP), and the detection of coinfection. Results: HPV-DNA was detected in 19.4% of the samples, and HPV 31, 6, and 53 were the most frequently detected types. There was a predominance of high-risk oncogenic HPV (HR-HPV) and a strong presence of simultaneous infections with multiple HPV types (84.6%). Coinfections with both HPV and C. trachomatis, and HPV and G. vaginalis were detected. The variables that were statistically associated with HPV infection and the presence of multiple infections were non-use of condoms and non-compliance with regular cervical cytology screening. Conclusion: The results highlight the importance of more comprehensive studies among vulnerable populations, aiming to establish measures to raise awareness about the risks of contracting sexually transmitted infections, as well as to support future studies for introducing HPV vaccines with wider coverage of viral types.

Overview and aims: Kidney transplantation has brought a new hope to women with end stage renal disease (ESRD) who wish to become pregnant, as it can improve the reproductive function and restore fertility. A successful pregnancy after kidney transplant is possible, at expenses of high rates of maternal and fetal morbidity. The objective of the study is to investigate the impact of renal transplantation in obstetric and neonatal outcomes as well as the effect of pregnancy itself in the graft. Study design: Retrospective study and descriptive analysis Methods and population: Retrospective study of nine pregnancies in eight renal transplant recipients between 1995 and 2015 in Centro Hospitalar São João. We evaluated the pre-pregnancy and post-delivery renal function, outcomes of gestation, as well as maternal and fetal complications. Results: The average time between transplant and pregnancy was 51.1 ± 25.3 months. The most common complications were urinary tract infections (7 cases), preterm delivery (6 cases), fetal growth restriction (3 cases), and pre-eclampsia (2 cases). One case of intrauterine fetal death was recorded. The cesarean section rate was 66.7%. There were two cases of graft dysfunction, which resolved in the postpartum period, without rejection or graft loss. In one patient, graft dysfunction recurred five months post-delivery due to native kidney disease relapse. Currently, one year after delivery, her creatinine plasmatic level is 2.2 mg/dL. Conclusions: This study suggests that successful pregnancy is possible in renal transplant recipients. Neverthless, these pregnancies should be considered at high risk and we must be alert to the complications that may occur

RESUMO Introdução: A infecção persistente por papilomavírus humano (HPV) é a principal causa do câncer cervical e suas lesões precursoras, e a resposta imune inadequada está entre os fatores que contribuem para a persistência viral. Isso pode ser influenciado por células T regulatórias (Treg) e pela produção de citocinas imunossupressoras, como o fator de transformação de crescimento beta (TGF-β) e a interleucina 10 (IL-10). Objetivo: Estabelecemos o perfil de resposta predominante, resposta Th1 ou imunossupressora, no microambiente tecidual, pela detecção de interferon gama (IFN-γ), TGF-β, e IL-10, bem como a coexpressão do receptor da cadeia alfa da IL-2 (CD25) e do forkhead box P3 (FOXP3). Método: Setenta e quatro amostras de biópsias de cérvice uterina, submetidas à detecção do ácido desoxirribonucleico (DNA) de HPV e à análise histopatológica, foram utilizadas nas reações de imuno-histoquímica para detectar IFN-γ, TGF-β, IL-10 e CD25/FOXP3 em linfócitos. Resultados: O microambiente das amostras de lesões intraepiteliais escamosas de alto grau (HSIL) com elevado números de partículas virais (≥ 10.000 cópias/ml) continha elevado número de células CD25/FOXP3+, TGF-β+, IL-10+ e IFN-γ+. Conclusão: A coexpressão de CD25/FOXP3 e a expressão de TGF-β nas amostras HSIL sugerem a existência de células Treg nesses locais, embora a expressão de IFN-γ tenha sido observada em várias células. Nossos dados sugerem que essa citocina pode estar relacionada com a manutenção do microambiente imunossuprimido, favorecendo a infecção persistente por HPV e a progressão para carcinoma.

ABSTRACT Introduction: Human papillomavirus (HPV) persistent infection is the leading cause of cervical cancer and its precursor lesions, and the inappropriate immune response is among the factors that contribute to viral persistence. This may be influenced by regulatory T (Treg) cells and the production of immunosuppressive cytokines, such as transforming growth factor beta (TGF-β) and interleukin-10 (IL-10). Objective: We established the profile of the predominant response, Th1 or immunosuppressive response, in the tissue microenvironment, by detecting interferon-gamma (IFN-γ), TGF-β, and IL-10, as well as the co-expression of IL-2 receptor alpha (CD25) and forkhead box P3 (FOXP3). Methods: Seventy-four samples from uterine cervix biopsies that underwent HPV deoxyribonucleic acid (DNA) detection and histopathology analysis were immunostained to detect CD25/FOXP3, IFN-γ and suppressive cytokines in lymphocytes. Results: The microenvironment of high-grade squamous intraepithelial lesion (HSIL) samples with high numbers of viral particles (≥ 10,000 copies/ml) contained high numbers of CD25/FOXP3+, TGF-β+, IL-10+, and IFN-γ+ cells. Conclusion: The co-expression of CD25/FOXP3 and the expression of TGF-β, and IL-10 in HSIL samples suggest the existence of Treg cells in these locations, although IFN-γ expression was observed in several cells in these samples. Our data suggest that this cytokine could be related to immunosuppressed microenvironment maintenance, favoring the persistent HPV infection and the progression to carcinoma.

Overview and Aims: pregnancy in women with chronic kidney disease (CKD), particularly in terminal CKD, remains a rare event. There are scarce reports of pregnancy in women undergoing peritoneal dialysis. Our study aims to evaluate the outcomes of pregnancies in women with CKD diagnosed at Hospital São João during the study period. Study design: retrospective case series. Population: pregnant women with chronic kidney disease diagnosed between January 2005 and December 2013. Methods: pregnancies in women with severe CKD (GFR <30mL in/1.73m2) were identified by using hospital electronic platforms with evaluation of maternal and fetal outcomes. Results: during the study period 4 cases of pregnancy in women with CKD were identified, including one of a woman in peritoneal dialysis prior to pregnancy - case 1. Case 1 progressed to hemodialysis at 17 weeks (due to haemoperitoneum subsequent to trauma by the peritoneal dialysis catheter) and had an eutocic late preterm delivery at 35 weeks. Case 2 began hemodialysis at 22 weeks, and was submitted to urgent cesarean section at 29 weeks. Case 3 started hemodialysis at 21 weeks, having also undergone urgent cesarean section at 31 weeks. Case 4 began hemodialysis at 21 weeks, presenting with an episode of hepatotoxicity secondary to darbopoietin at 26 weeks. Delivery occurred by Caesarean section at 32 weeks. Conclusion: despite the high fetal morbidity documented, with the strategies adopted there was no fetal or neonatal mortality. The monitoring of these pregnant in specialized consultation favored the positive outcomes.

Resumo Pacientes pediátricos, principalmente internados em unidades de terapia intensiva (UTI) neonatal, são altamente vulneráveis aos erros de medicação. O objetivo deste trabalho foi conhecer a frequência dos erros de prescrição em uma UTI neonatal de um hospital universitário, bem como os pacientes susceptíveis, os tipos de erros e os medicamentos envolvidos. As variáveis prescritas relacionadas aos medicamentos foram comparadas com a base utilizada como referência para a prescrição na unidade (Neofax). Participaram do estudo 150 recém-nascidos. Foram analisadas 489 prescrições, 1.491 itens de medicamentos, correspondendo a 46 fármacos. A taxa de erros de prescrição foi de 43,5%. Foram encontrados erros de dose, intervalo, diluente e tempo de infusão, distribuídos em sete classes terapêuticas. A ocorrência de erros foi maior em recém-nascidos pré-termos. Os erros de diluente e de dose foram os mais frequentes. As classes de medicamentos mais envolvidas nos erros foram os anti-infecciosos e aqueles que atuam nos sistemas nervoso e cardiovascular.

Abstract Pediatric patients, especially those admitted to the neonatal intensive care unit (ICU), are highly vulnerable to medication errors. This study aimed to measure the prescription error rate in a university hospital neonatal ICU and to identify susceptible patients, types of errors, and the medicines involved. The variables related to medicines prescribed were compared to the Neofax prescription protocol. The study enrolled 150 newborns and analyzed 489 prescription order forms, with 1,491 medication items, corresponding to 46 drugs. Prescription error rate was 43.5%. Errors were found in dosage, intervals, diluents, and infusion time, distributed across 7 therapeutic classes. Errors were more frequent in preterm newborns. Diluent and dosing were the most frequent sources of errors. The therapeutic classes most involved in errors were antimicrobial agents and drugs that act on the nervous and cardiovascular systems.

Resumen Pacientes pediátricos, principalmente internados en unidades de terapia intensiva (UTI) neonatal, son altamente vulnerables a los errores de medicación. El objetivo de este estudio fue conocer la frecuencia de los errores de prescripción en una UTI neonatal de un hospital universitario así como, los pacientes susceptibles, los tipos de errores y los medicamentos involucrados. Las variables prescritas relacionadas a los medicamentos fueron comparadas con la base utilizada como referencia para la prescripción en la unidad (Neofax). Participaron en el estudio 150 recién nacidos. Se analizaron 489 prescripciones, 1.491 ítems de medicamentos, correspondiendo a 46 fármacos. La tasa de errores de prescripción fue de un 43,5%. Fueron encontrados errores de dosis, intervalo, diluyente y tiempo de infusión, distribuidos en 7 clases terapéuticas. La ocurrencia de errores fue mayor en recién nacidos prematuros. Los errores de diluyente y de dosis fueron los más frecuentes. Las clases de medicamentos más involucrados en los errores fueron los anti-infecciosos y aquellos que actúan en el sistema nervioso y cardiovascular.

Resumo Pacientes pediátricos, principalmente internados em unidades de terapia intensiva (UTI) neonatal, são altamente vulneráveis aos erros de medicação. O objetivo deste trabalho foi conhecer a frequência dos erros de prescrição em uma UTI neonatal de um hospital universitário, bem como os pacientes susceptíveis, os tipos de erros e os medicamentos envolvidos. As variáveis prescritas relacionadas aos medicamentos foram comparadas com a base utilizada como referência para a prescrição na unidade (Neofax). Participaram do estudo 150 recém-nascidos. Foram analisadas 489 prescrições, 1.491 itens de medicamentos, correspondendo a 46 fármacos. A taxa de erros de prescrição foi de 43,5%. Foram encontrados erros de dose, intervalo, diluente e tempo de infusão, distribuídos em sete classes terapêuticas. A ocorrência de erros foi maior em recém-nascidos pré-termos. Os erros de diluente e de dose foram os mais frequentes. As classes de medicamentos mais envolvidas nos erros foram os anti-infecciosos e aqueles que atuam nos sistemas nervoso e cardiovascular.

Abstract Pediatric patients, especially those admitted to the neonatal intensive care unit (ICU), are highly vulnerable to medication errors. This study aimed to measure the prescription error rate in a university hospital neonatal ICU and to identify susceptible patients, types of errors, and the medicines involved. The variables related to medicines prescribed were compared to the Neofax prescription protocol. The study enrolled 150 newborns and analyzed 489 prescription order forms, with 1,491 medication items, corresponding to 46 drugs. Prescription error rate was 43.5%. Errors were found in dosage, intervals, diluents, and infusion time, distributed across 7 therapeutic classes. Errors were more frequent in preterm newborns. Diluent and dosing were the most frequent sources of errors. The therapeutic classes most involved in errors were antimicrobial agents and drugs that act on the nervous and cardiovascular systems.

Resumen Pacientes pediátricos, principalmente internados en unidades de terapia intensiva (UTI) neonatal, son altamente vulnerables a los errores de medicación. El objetivo de este estudio fue conocer la frecuencia de los errores de prescripción en una UTI neonatal de un hospital universitario así como, los pacientes susceptibles, los tipos de errores y los medicamentos involucrados. Las variables prescritas relacionadas a los medicamentos fueron comparadas con la base utilizada como referencia para la prescripción en la unidad (Neofax). Participaron en el estudio 150 recién nacidos. Se analizaron 489 prescripciones, 1.491 ítems de medicamentos, correspondiendo a 46 fármacos. La tasa de errores de prescripción fue de un 43,5%. Fueron encontrados errores de dosis, intervalo, diluyente y tiempo de infusión, distribuidos en 7 clases terapéuticas. La ocurrencia de errores fue mayor en recién nacidos prematuros. Los errores de diluyente y de dosis fueron los más frecuentes. Las clases de medicamentos más involucrados en los errores fueron los anti-infecciosos y aquellos que actúan en el sistema nervioso y cardiovascular.

Women infected with human papillomavirus (HPV) are at a higher risk of developing cervical lesions. In the current study, self and clinician-collected vaginal and cervical samples from women were processed to detect HPV DNA using polymerase chain reaction (PCR) with PGMY09/11 primers. HPV genotypes were determined using type-specific PCR. HPV DNA detection showed good concordance between self and clinician-collected samples (84.6%; kappa = 0.72). HPV infection was found in 30% women and genotyping was more concordant among high-risk HPV (HR-HPV) than low-risk HPV (HR-HPV). HPV16 was the most frequently detected among the HR-HPV types. LR-HPV was detected at a higher frequency in self-collected; however, HR-HPV types were more frequently identified in clinician-collected samples than in self-collected samples. HPV infections of multiple types were detected in 20.5% of clinician-collected samples and 15.5% of self-collected samples. In this study, we demonstrated that the HPV DNA detection rate in self-collected samples has good agreement with that of clinician-collected samples. Self-collected sampling, as a primary prevention strategy in countries with few resources, could be effective for identifying cases of HR-HPV, being more acceptable. The use of this method would enhance the coverage of screening programs for cervical cancer.