Utilidad de los enjuagues con povidona yodada y peróxido de hidrógeno en pacientes con COVID-19 / Utility of mouth rinses with povidone-iodine and hydrogen peroxide in patients with COVID-19

Introducción: La povidona yodada y el peróxido de hidrógeno podrían ser eficaces contra el SARS-CoV-2. Métodos: Estudio observacional de seguimiento prospectivo (EPA-AS) en 88 pacientes (43±17 años, 55% varones) con SARS-CoV-2 en muestras nasofaríngeas (RT-PCR). Treinta y uno recibieron enjuagues/gargarismos con povidona yodada cada 8h 2 días consecutivos, 17 con la misma pauta de peróxido de hidrógeno y 40 controles sin enjuagues. Se repitió PCR a los 3, 11 y 17 días. Resultados: Tras la intervención no hubo diferencias en la carga viral: povidona yodada (4,3±2,7 copias/ml), peróxido de hidrógeno (4,6±2,9 copias/ml), controles (4,4±3,0 copias/ml). El porcentaje de pacientes con una 2.ª PCR negativa fue 27% povidona yodada, 23% peróxido de hidrógeno y 32% controles; en la 3.ª PCR 62%, 54% y 58% respectivamente y en la 4.ª PCR, 81%, 75% y 81%. Conclusión: Nuestros resultados no apoyan la utilidad de los enjuagues de estos 2 antisépticos en pacientes con COVID-19.(AU)

Introduction: Povidone-iodine and hydrogen peroxide could be effective in against SARS-CoV-2. Methods: A “non-interventional trial” in 88 patients (43±17 yrs, 55% men) with SARS-CoV-2 in nasopharyngeal swabs (RT-PCR). 31 received mouth rinses/gargling with povidone-iodine (every 8h, two consecutive days), 17 with mouth rinses/gargling of hydrogen peroxide, and 40 controls. PCR were repeated at 3, 11 and 17 days. Results: After intervention the viral load (Log10copies/ml) remained similar in povidone-iodine (4.3±2.7copies/ml), hydrogen peroxide (4.6±2.9copies/ml; p=0.40) and controls (4.4±3.0copies/ml). The percentage of patients with a negative result in the second PCR was 27% in povidone-iodine group, 23% in hydrogen peroxide and 32% in controls; in the third PCR, 62%, 54% and 58% respectively; and in the fourth PCR, 81%, 75% and 81%. Conclusion: Our results do not support the clinical usefulness of mouth rinses/gargling with povidone-iodine or hydrogen peroxide in patients with COVID-19.(AU)

Utility of mouth rinses with povidone-iodine and hydrogen peroxide in patients with COVID-19.

INTRODUCTION: Povidone-iodine and hydrogen peroxide could be effective in against SARS-CoV-2. METHODS: A "non-interventional trial" in 88 patients (43±17 yrs., 55% men) with SARS-CoV-2 in nasopharyngeal swabs (RT-PCR). 31 received mouth rinses/gargling with povidone-iodine (every 8h, two consecutive days), 17 with mouth rinses/gargling of hydrogen peroxide, and 40 controls. Were repeated PCR in 3, 11 and 17 days. RESULTS: After intervention the viral load (Log10 copies/ml) remained similar in povidone-iodine (4.3±2.7 copies/ml), hydrogen peroxide (4.6±2.9 copies/ml; p=0.40) and controls (4.4±3.0 copies/ml). The percentage of patients with a negative result in the second PCR was 27% in povidone-iodine group, 23% in hydrogen peroxide and 32% in controls; in the third PCR, 62%, 54% y 58% respectively; and in the fourth PCR, 81%, 75% y 81%. CONCLUSION: Our results do not support the clinical usefulness of mouth rinses/gargling with povidone-iodine or hydrogen peroxide in patients with COVID-19.

Povidona Yodada como Antiséptico Oral en la Reducción de la Carga Viral del SARS-CoV-2: Revisión de la Literatura

RESUMEN: Se ha sugerido que el uso de antisépticos orales podría reducir la carga viral del virus SARS-CoV-2 en los pacientes durante la atención dental, pero sin evidencia que avale su efectividad. Dada la vulnerabilidad del virus a la oxidac ión, se ha recomendado el uso de colutorios que contengan agentes oxidantes como la povidona yodada. El objetivo de la presente revisión fue determinar la efectividad del uso de povidona yodada como antiséptico oral en la disminución de la carga viral del virus SARS-CoV-2. Se realizó una búsqueda bibliográfica en PubMed, Biblioteca Virtual en Salud, SciELO, Web of Science y EBSCO host. Se incluyeron estudios clínicos en pacientes con COVID-19 y estudios in vitro con cepas del virus que utilizaran colutorios de povidona yodada como forma de intervención, publicados entre enero del 2019 y enero del 2021. La selección de los artículos se realizó en dos etapas por dos autores de manera independiente. Luego de eliminar los artículos duplicados, se mantuvieron 53 referencias. Finalmente se incluyeron 2 estudios in vivo y 5 estudios in vitro para la revisión cualitativa. En los estudios in vitro, todas las concentraciones de povidona yodada evidenciaron una actividad virucida eficaz en los distintos tiempos de exposición, donde la mínima concentración efectiva correspondió a 0,5 % en 15 segundos. Los estudios in vivo presentaron resultados positivos hacia el uso de povidona yodada, pero con tamaños muestrales pequeños y una gran heterogeneidad en su metodología. En conclusión el uso profiláctico de povidona yodada como colutorio contra el virus SARS-CoV-2 es respaldado por los trabajos in vitro, con tiempos de aplicación fácilmente realizables en la atención dental, pero se requiere de un mayor número de ensayos controlados aleatorizados para comprobar su efectividad en la práctica clínica.

ABSTRACT: It has been suggested that the use of oral antiseptics could reduce the viral load of SARS-CoV-2 virus in patients during dental care, but without evidence to support its effectiveness. The objective of this study was to determine the effectiveness of povidone iodine mouthwash in reducing the viral load of SARS-CoV-2 virus. A literature search was conducted in PubMed, Biblioteca Virtual enSalud, SciELO, Web of Science and EBSCOhost. Clinical studies in patients with COVID-19 or in vitro studies with SARS-CoV-2 strains that used povidone-iodine mouthwash as a form of intervention, published between January 2019 and January 2021, were included. The selection of articles was carried out in two phases by two authors independently. After removing duplicate articles, 53 references were kept. Finally, 2 in vivo studies and 5 in vitro studies were included for the qualitative review. In the in vitro studies, all concentrations of povidone iodine showed effective virucidal activity at the different exposure times, where the minimum effective concentration corresponded to 0.5 % in 15 seconds. In vivo studies showed positive results towards the use of povidone iodine, but with small sample sizes and great heterogeneity in their methodology. The prophylactic use of povidone iodine mouthwash against the SARS-CoV- 2 virus is supported by in vitro studies, with application times easily achievable in dental care, but a large number of randomized controlled trials are required to verify its effectiveness in clinical practice.

Relación del uso de colutorios bucales con la disminución de la carga viral del SARS-CoV-2 en la práctica odontológica: tema de revision / Relationship of the use of mouthwashes with the decrease in the viral load of SARS-CoV-2 in dental practice: review topic

Resumen Actualmente, el odontólogo es uno de los profesionales de la salud con mayor riesgo de contagio de la COVID-19 debido a su contacto directo con la cavidad bucal. La alta exposición a los aerosoles, generados por los instrumentos rotatorios, en pacientes con la COVID-19, eleva el contacto con la carga viral del SARS-CoV-2 en los procedimientos de rutina. Se ha descrito que los colutorios bucales, previos a la atención odontológica, podrían ser soluciones efectivas para la reducción del contagio pese a su poca evidencia clínica. Los colutorios con cloruro de cetilpiridinio (CPC), peróxido de hidrógeno (H2O2), povidona yodada (PVP-I) y gluconato de clorhexidina (CHX) muestran un gran potencial para reducir la carga viral del SARS- CoV-2 en los aerosoles generados a partir de la saliva durante la consulta odontológica. Por lo expuesto, el presente artículo tuvo por objetivo hacer una revisión de la información científica actual sobre la relación del uso de los colutorios bucales con la disminución de la carga viral del SARS-CoV-2.

Abstract It is currently known that the dentist is one of the health professionals with the highest risk of contagion of COVID-19 due to its direct contact with the oral cavity. High exposure to aerosols generated by rotating instruments in COVID-19 patients increases contact with the SARS-CoV-2 viral load in routine procedures. It has been described that mouthwashes prior to dental care could be effective solutions to reduce contagion despite their little clinical evidence. Mouthwashes with cetylpyridinium chloride (CPC), hydrogen peroxide (H2O2), povidone-iodine (PVP-I) and chlorhexidine gluconate (CHX) show great potential to reduce the viralload of SARS-CoV-2 in the aerosols generated from saliva during the dental visit. Therefore, the objective of this article was to review the current scientific information on the relationship of the use of mouthwashes with the decrease in the viral load of SARS-CoV-2.

Administración oral accidental de povidona yodada a un neonato: a propósito de un caso / Accidental oral administration of povidone iodine in a newborn: Case report

Las soluciones yodadas se utilizan ampliamente como antiséptico para el tratamiento y la prevención de infecciones en las heridas. La povidona yodada, una de las soluciones yodadas de aplicación tópica que más se encuentra en los botiquines de emergencia, podría producir anomalías graves, como disfunción tiroidea. La intoxicación por povidona yodada es poco frecuente; entre los efectos notificados previamente se incluyen complicaciones del uso tópico durante procedimientos quirúrgicos. Se describe el caso de un neonato que recibió povidona yodada por vía oral accidentalmente, sin signos ni síntomas de toxicidad después de la ingesta.

Iodine solutions are widely used as antiseptic for treating and preventing wound infections. Povidone iodine, one of the most common topical iodine solutions in emergency kits, can lead to several abnormalities as thyroid dysfunction. Povidone iodine poisoning is unusual and previously reported effects are mainly complications of topical usage during surgical procedures. Here we present the case of a newborn that was accidentally given oral povidone iodine, showing no signs or symptoms of toxicity after ingestion.

[Randomised clinical trial to compare two tracheotomy care methods in an Intensive Care Unit]. / Ensayo clínico aleatorizado para la comparación de dos métodos de cura de traqueotomía en una Unidad de Cuidados Intensivos.

INTRODUCTION: Tracheotomy is a common technique in Intensive Care Units (ICU). It is known that nursing care during and after that procedure is directly related to its success, by reducing the possible complications to a minimum, such as the stoma infection, and contributing to a favourable outcome in critical patients. OBJECTIVES: To compare the use of polyhexanide (PLX) versus saline+povidone iodine (PY) as antiseptics and infection incidence in tracheostomies performed in Intensive Care Units. MATERIAL AND METHOD: A 2-year, experimental, randomised, open-label trial carried out in a multidiscipline ICU with 32 beds. The study was approved by the Research Ethics Committee of Principality of Asturias. RESULTS: The overall infection rate observed for every hundred patients was 1.34 (95% CI; 0.81-2.01), with 1.46 when using PLX and 1.21 for PY (P=.685). CONCLUSIONS: In spite of the experimental treatment (PLX) was shown to be effective in other types of wounds in our study. No significant differences were found between this technique and the standard one. Since there is no national registry of tracheotomy- associated infections, it is not possible to know whether the rate observed is within the usual parameters.

Central retinal artery occlusion after phacoemulsification under peribulbar anaesthesia: Pathogenic hypothesis.

CLINICAL CASE: A 77-year-old patient had uneventful cataract surgery in the right eye under peribulbar anaesthesia. The next day, a severe and progressive eyelid swelling was noted, caused by an unknown allergic reaction to povidone-iodine. The allergic signs dissapeared by the fifth day, but amaurosis and a cherry-red spot were detected. Doppler ultrasound and CT angiography confirmed an 80% ipsilateral internal carotid artery stenosis. DISCUSSION: Retinal vascular occlusion after orbital loco-regional anaesthesia is rare. When this complication occurs, carotid disease, and local or systemic factors, should be evaluated.

Incidência de infecção do trato urinário relacionada ao cateterismo vesical de demora: um estudo de coorte / Incidence of catheter-related urinary tract infecions: a cohort study / Incidencia de infección del tracto urinario relacionada con cateterismo vesical de demora: estudio de cohorte

Estudo de coorte não concorrente com informações de 301 de pacientes internados em centros de terapia intensiva de dois hospitais públicos de Belo Horizonte. O objetivo foi analisar os aspectos epidemiológicos das infecções do trato urinário em pacientes submetidos ao cateterismo vesical de demora, estimar a taxa de incidência nos dois hospitais, identificar possíveis fatores de risco relacionados à infecção e aos microrganismos causadores. A amostra constituiu-se de todos os pacientes internados nas duas unidades e que foram submetidos ao cateterismo vesical de demora no período de seis meses. Dos 301 pacientes, 23 desenvolveram infecção, sendo 56,52% do sexo masculino e com idade superior a 60 anos. A incidência global de infecção do trato urinário foi de 6,70 infecções/1.000 cateteres-dia. O hospital que utilizou água e sabão para a higiene periuretral apresentou maior incidência do que o hospital que utilizou antisséptico (14,01 e 3,05 infecções/1.000 cateteres-dia, respectivamente). O fator de risco identificado foi a higienização periuretral com água e sabão. Os microrganismos mais prevalentes nas uroculturas foram Pseudomonas aeruginosa (17,39%) Candida sp. (13,04%), Escherichia coli (13,04%), e Proteus mirabilis (8,70%). O resultado encontrado neste estudo contradiz os achados da literatura e reforça a necessidade de estudos primários que identifiquem a solução mais eficaz para a realização da limpeza periuretral com vistas à redução da infecção do trato urinário relacionada ao cateterismo vesical de demora.

This is a non-concurrent cohort study that uses data from 301 patients admitted to the intensive care unit of two public hospitals in Belo Horizonte.It aimed at analysing epidemiological aspects of urinary tract infections amongst patients with indwelling bladder catheterization, evaluatingthe incidence rate of the infection in the two hospitals and identifying possible risk factors related to the infection. Sample consisted of patientsthat underwent indwelling catheterization for a period of six months. Of the 301 patients, 23 developed infection: 56.52% were male and aged60 years and over. The overall incidence of urinary tract infection was 6.70 infections/1000 catheter-days. The hospital using water and soap forperiurethral cleaning presented higher incidence of urinary infection than the hospital using antiseptic (14.01 and 3.05 infections/1000 catheterdays, respectively). Risk factor identified was periurethral cleaning with soap and water. The most prevalent microorganisms in urine cultures were Pseudomonas aeruginosa (17.39%), Candida sp. (13.04%), Escherichia coli (13.04%), and Proteus mirabilis (8.70%). This study results contradict theliterature which demonstrates the need for primary research aimed at identifying the most effective solution for periurethral cleaning in order toreduce catheter-related urinary tract infections.

Estudio de cohorte no concurrente con información de 301 pacientes internados en centros de terapia intensiva de dos hospitales públicos de BeloHorizonte. El objetivo fue analizar la epidemiología de las infecciones del tracto urinario en pacientes sometidos a cateterismo vesical permanente,estimar la tasa de incidencia en cada hospital, identificar posibles factores de riesgo relacionados con las infecciones del tracto urinario e identificarlos microorganismos causantes de la infección. La muestra estuvo constituida por todos los pacientes de las unidades sometidos a cateterismovesical permanente en un período de seis meses. De los 301 pacientes, 23 desarrollaron la infección, siendo 56,52% del sexo masculino y edad superiora 60 años. La incidencia global de infección del tracto urinario fue de 6,70 infecciones/1.000 catéteres/día. El hospital que utilizó agua y jabón para lalimpieza periuretral presentó mayor incidencia que el hospital que utilizó antiséptico (14,01 y 3,05infecciones/1.000 catéteres/día, respectivamente).El factor de riesgo identificado fue la utilización de la técnica de limpieza con agua y jabón. Los microorganismos más prevalentes en los urocultivos fueron Pseudomonas aeruginosa (17,39%) Candida sp. (13,04%), Escherichia coli (13,04%), and Proteus mirabilis (8,70%). El resultado encontradocontradice los de la literatura y refuerza la necesidad de estudios primarios que identifiquen la solución más eficaz para la limpieza periuretral conel fin de reducir la infección del tracto urinario relacionada con el cateterismo vesical permanente.

[Use of collagen-polyvinylpirrolidone in the treatment of Parry-Romberg syndrome.] / Colágeno-polivinilpirrolidona para tratar el síndrome de Parry-Romberg.

Background: Parry-Romberg syndrome is characterized by the presence of progressive hemifacial atrophy that affects the growth and development of structures on one side of the face. Our objective was to introduce collagen-polyvinylpirrolidone as a new therapeutic option for Parry-Romberg syndrome in two clinical cases. Clinical cases: two women, aging 56 and 28 years old, with facial hypocrhomic lesions, and right and left fronto-malar sunken area respectively, treated with topic steroids + penicilamina, fat grafts and silicone implants without improvement. We used collagen-polyvinylpirrolidone and they showed improvement: after six months there were not clinical or esthetical complications. Conclusions: collagen-polivinilpirrolidone could be a new therapeutic option for Parry-Romberg syndrome with good clinical and esthetical results. It is easy to apply and it has few side effects and without complications.

Introducción: el síndrome de Parry-Romberg está caracterizado por la presencia de atrofia hemifacial progresiva, afección del crecimiento y desarrollo de las estructuras de un lado de la cara. El objetivo de este trabajo es describir nuestra experiencia con el colágeno polivinilpirrolidona para tratar el síndrome de Parry-Romberg. Casos clínicos: dos mujeres de 56 y 28 años de edad, con manchas hiperpigmentadas y hundimiento frontomalar derecho e izquierdo, respectivamente, manejadas con esteroides tópicos más penicilamina, injertos grasos e implantes de silicón, sin mejoría. Se decidió iniciar tratamiento con colágeno-polivinilpirrolidona, con lo que se logró una mejoría clínica y estética sin complicaciones después de seis meses de seguimiento. Conclusiones: el colágeno polivinilpirrolidona es una opción terapéutica para el síndrome de Parry-Romberg que ofrece buenos resultados clínicos y estéticos, es de fácil administración, sin complicaciones y mínimos efectos secundarios.

Acute skin lesions after surgical procedures: a clinical approach.

In the hospital setting, dermatologists are often required to evaluate inflammatory skin lesions arising during surgical procedures performed in other departments. These lesions can be of physical or chemical origin. Povidone iodine is the most common reported cause of such lesions. If this antiseptic solution remains in contact with the skin in liquid form for a long period of time, it can give rise to serious irritant contact dermatitis in dependent or occluded areas. Less common causes of skin lesions after surgery include allergic contact dermatitis and burns under the dispersive electrode of the electrosurgical device. Most skin lesions that arise during surgical procedures are due to an incorrect application of antiseptic solutions. Special care must therefore be taken during the use of these solutions and, in particular, they should be allowed to dry.

Effectiveness of 10% povidone-iodine drying time before Peripheral Intravascular Catheter insertion: preliminary results from an explorative quasi-experimental study / Eficácia de iodopovidona a 10% de acordo com tempo de secagem antes da inserção do cateter intravenoso periférico: resultados preliminares de um estudo exploratório quasi-experimental / Eficacia del tiempo de secado de la yodopovidona al 10% antes de la inserción de catéter venoso periférico: resultados preliminares de un estudio exploratorio casi-experimental

AIM: to investigate the effectiveness of 10% povidone-iodine after a 30-second or 2-minute drying time on microbial count reduction at the point of a Peripheral Intravascular Catheter (PIC) insertion. A quasi-experimental design was adopted. In total, 53 patients were enrolled, 25 were exposed to a 2-m drying time and 28 to a 30-s drying time. From the preliminary results of this study, no differences in the occurrence of contamination have emerged between patients receiving 30-s and 2-m drying time for 10% povidone-iodine solutions.

OBJETIVO: investigar a eficácia da solução iodopovidona a 10% sobre a redução da contagem microbiana no ponto de inserção do Cateter Venoso Periférico após tempo de secagem de 30s ou 2 min. MÉTODO: desenho quase-experimental. Foram incluídos 53 pacientes no estudo: 25 foram expostos a 2min de secagem e 28 foram expostos a 30s de secagem. RESULTADOS: Os resultados preliminares não apresentaram diferenças na ocorrência de contaminação entre os pacientes que foram submetidos a 30s ou 2min de secagem após desinfecção com solução de iodopovidona a 10%.

OBJETIVO: para investigar la eficacia de una solución yodopovidona al 10% tras tiempo de secado de 30 segundos o 2 minutos en la reducción del contaje microbiano en el local de inserción del Catéter Venoso Periférico, fue adoptado un diseño casi-experimental. Al total, fueron incluidos 53 pacientes, 25 expuestos a 2 min. de secado y 28 a 30 segundos. Con base en los resultados preliminares, no se encontraron diferencias en la ocurrencia de contaminaciones entre pacientes sometidos a un tiempo de secado de 30 s. o de 2 min tras desinfección con solución de yodopovidona al 10%.

A prospective study demonstrating the effect of 5 percent povidone-iodine application for anterior segment intraocular surgery in Paraguay / Estudio prospectivo demostrando el efecto de la instilación de yodo povidona al 5 por ciento previo a cirugía de segmento anterior en Paraguay

PURPOSE: To determine the conjunctival bacterial flora in cataract surgery patients and the effect of presurgical irrigation with 5 percent povidone-iodine solution. METHODS: Three samples from the inferior conjunctival fornix of the eye to be operated were obtained at baseline before washing (T0) with 10 ml 5 percent povidone-iodine solution, immediately after washing (T1), and upon completion of surgery (T2). Bacteria from the samples were inoculated in blood agar, chocolate agar, and thioglycolate broth. RESULTS: A total of 221 patients (n=224 eyes) with a mean age of 67 ± 13 years were included in the study. Bacteria from the (T0) samples were successfully grown in 73.2 percent of the thioglycolate agars, 21.0 percent of the blood agars, and 19.2 percent of the chocolate agars. Compared with T1 samples, the use of povidone-iodine wash translated into a 60.8 percent reduction (from 73.2 percent to 12.5 percent) in colonization of the conjunctiva (p<0.001), while no significant difference was found between the T1 and T2 samples. Conclusion: Conjunctival irrigation with a 5 percent povidone-iodine solution effectively reduces conjunctival flora and is therefore strongly recommended as a means of preventing postsurgical endophthalmitis following cataract surgery.

OBJETIVO: Determinar la flora bacteriana de la conjuntiva en los pacientes a ser sometidos a cirugía de catarata y el efecto del lavado prequirúrgico con yodo povidona al 5 por ciento sobre dichos microorganismos. MÉTODOS: Se tomaron 3 muestras del fondo de saco conjuntival del ojo a ser operado de catarata antes (T0) de la irrigación de la conjuntiva con 10 ml de yodo povidona al 5 por ciento, como control, inmediatamente después (T1) y al término de la cirugía (T2). Se realizaron cultivos en agar sangre, agar chocolate y en caldo de tioglicolato. RESULTADOS: Se incluyeron en el estudio 221 pacientes (n=24 ojos) con un promedio de edad de 67 ± 13 años. El porcentaje de crecimiento bacteriano en (T0) fue de 73,2 por ciento en tioglicolato, 21 por ciento en agar sangre y 19,2 por ciento en agar chocolate. Al compararlo con (T1) el efecto de la yodo povidona se tradujo en una reducción del 60,8 por ciento (de 73,2 por ciento a 12,5 por ciento) en la colonización conjuntival (p<0.001). Entre las muestras de los tiempos T1 y T2 no hubo diferencia significativa en cuanto al crecimiento bacteriano. CONCLUSIÓN: El lavado conjuntival con yodo povidona al 5 por ciento reduce de forma efectiva la flora conjuntival por lo cual se recomienda fuertemente como método preoperatorio, como una de las medidas preventivas de la endoftalmitis posquirúrgica en cirugías de catarata.