RESUMEN
This study aimed to investigate the effects on fracture healing of locally applied boric acid (BA) with and without low-level laser therapy (LLLT). A unicortical femoral defect was surgically created on the anterolateral surface of proximal femur of each subject. The subjects, totaling 56 Wistar albino rats, were randomly allocated into four groups (n = 14 each): control, LLLT (λ = 905 µm, 10,000 Hz, 25 mW, and peak power 25 W), BA (40 mg/kg), and BA + LLLT groups. On the 30th day, the highest radiological score was recorded for the BA + LLLT group (3.63 [2-4]), followed by the BA (3.38 [2.75-3.75]), control (3 [2-3.25]), and LLLT (2.5 [1.25-3]) groups. On days 15 and 30 post-surgery, malondialdehyde levels were significantly lower among the BA + LLLT group compared to the control group (p < 0.001). On day 30, superoxide dismutase, catalase, and alkaline phosphatase levels were highest in the BA + LLLT group compared to the control group (p < 0.001). When the histopathological, immunofluorescence, and immunohistochemical findings on the 15th and 30th days were compared with the control group, a statistically significant difference was found for the BA and BA + LLLT groups (p Ë 0.05). This study suggests that locally applied BA with LLLT may accelerate fracture healing.
Asunto(s)
Terapia por Láser , Terapia por Luz de Baja Intensidad , Animales , Ratas , Ácidos Bóricos/farmacología , Ácidos Bóricos/uso terapéutico , Curación de Fractura , Ratas WistarRESUMEN
BACKGROUND: Boron neutron capture therapy (BNCT) selectively kills tumor cells while sparing adjacent normal cells. Boric acid (BA)-mediated BNCT showed therapeutic efficacy in treating hepatocellular carcinoma (HCC) in vivo. However, DNA damage and corresponding responses induced by BA-mediated BNCT remained unclear. This study aimed to investigate whether BA-mediated BNCT induced DNA double-strand breaks (DSBs) and to explore DNA damage responses in vitro. MATERIALS AND METHODS: Huh7 Human HCC cells were treated with BA and irradiated with neutrons during BA-BNCT. Cell survival and DNA DSBs were examined by clonogenic assay and expression of phosphorylated H2A histone family member X (γH2AX), respectively. The DNA damage response was explored by determining the expression levels of DNA repair- and apoptosis-associated proteins and conducting a cell-cycle analysis. RESULTS: DNA DSBs induced by BA-mediated BNCT were primarily repaired through the homologous recombination pathway. BA-mediated BNCT induced G2/M arrest and apoptosis in HCC. CONCLUSION: Our findings may enable the identification of radiosensitizers or adjuvant drugs for potentiating the therapeutic effectiveness of BA-mediated BNCT for HCC.
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Ácidos Bóricos/uso terapéutico , Terapia por Captura de Neutrón de Boro/métodos , Carcinoma Hepatocelular/radioterapia , Roturas del ADN de Doble Cadena , Reparación del ADN , Neoplasias Hepáticas/radioterapia , Fármacos Sensibilizantes a Radiaciones/uso terapéutico , Proteínas Reguladoras de la Apoptosis/metabolismo , Ácidos Bóricos/farmacocinética , Carcinoma Hepatocelular/genética , Carcinoma Hepatocelular/metabolismo , Caspasa 3/metabolismo , Línea Celular Tumoral , Supervivencia Celular/efectos de la radiación , Reparación del ADN por Unión de Extremidades , Proteínas de Unión al ADN/metabolismo , Activación Enzimática , Histonas/metabolismo , Humanos , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/metabolismo , Fármacos Sensibilizantes a Radiaciones/farmacocinética , Reparación del ADN por RecombinaciónRESUMEN
PURPOSE: Ovarian ischemia-reperfusion (IR) damage continues to be a serious infertility problem. The oxidative stress plays central role in the development of IR injuries. Activation of antioxidants decreases IR injuries; however, the efficacy of antioxidant agents remains controversial. Unfortunately, there has been no evidence for medicinal use of boric acid (BA) and propolis (Prop) on ovarian IR injury on rats so far. This study will provide to reveal the potential applications of the Prop and BA in ovarian IR therapy. METHODS: The Sprague-Dawley rats were randomized into five groups: I-control, II-IR, 3 h of ischemia and 3 h of reperfusion, III and IV-a signal dose of oral BA (7 mg/kg) and Prop (100 mg/kg) alone 1 h before induction of IR, V-Prop and BA together 1 h before induction of IR. SOD (superoxide dismutase), CAT (catalase), GSH (glutathione), MPO (myeloperoxidase), MDA (malondialdehyde), and IL-6 (interleukin-6) levels were quantified by ELISA and the TNF-α (tumor necrosis factor-α), 8-OHdG (8-hydroxylo-2'-deoxyguanosin) and Caspase-3 expressions were performed by immunohistochemical analyses. RESULTS: BA and Prop pretreatment significantly reduced MPO, MDA, and IL-6 levels and pathologic score in IR rats, with no effects in control group. These agents used in therapy also decreased TNF-α, 8-OHdG and Caspase-3 protein expressions increased by IR. Furthermore, BA and Prop combination showed significant ameliorative effects on ovary injury caused by IR through acting as an antioxidant, anti-inflammatory and antiapoptotic agent. CONCLUSION: BA and Prop alone and especially in combination could be developed as therapeutic agents against ovary IR injury.
Asunto(s)
Antiinfecciosos/uso terapéutico , Ácidos Bóricos/uso terapéutico , Ovario/efectos de los fármacos , Própolis/uso terapéutico , Daño por Reperfusión/tratamiento farmacológico , Animales , Antiinfecciosos/farmacología , Ácidos Bóricos/farmacología , Femenino , Ovario/patología , Própolis/farmacología , Ratas , Ratas Sprague-Dawley , Daño por Reperfusión/patologíaRESUMEN
BACKGROUND: Bacterial vaginosis (BV) and vulvovaginal candidiasis (VVC) present serious reproductive health risks and management challenges, with poor control attributed to survival of treatment-resistant biofilm communities. Boric acid is used in various regimens for non-albicans VVC and recurrent BV. We investigated safety and efficacy of a novel boric acid-based vaginal anti-infective with enhanced antibiofilm activity (TOL-463) in treating BV and VVC. METHODS: In this phase 2 randomized, investigator-blinded trial conducted at 2 sexual health clinics, women with BV or VVC were randomly assigned (1:1) to 7 nights of TOL-463 vaginal gel or insert. The primary test of cure (TOC) was clinical cure at day 9-12; safety was assessed at TOC and day 21-30. RESULTS: One hundred six participants (53 with BV, 36 VVC, 17 both) were enrolled; most were African American (69%). Clinical cure rate of BV at TOC was 59% (95% confidence interval [CI], 41%-75%) for TOL-463 insert and 50% (95% CI, 31%-69%) for TOL-463 gel, and for VVC, 92% (95% CI, 67%-99%) for TOL-463 insert and 81% (95% CI, 57%-93%) for TOL-463 gel. Both products were safe and well tolerated with no secondary cases of VVC; vulvovaginal burning was the most common adverse event (9.6%). CONCLUSIONS: TOL-463, especially in vaginal insert form, is effective and safe in treating BV and VVC. Future studies should assess the potential role of TOL-463 as a biofilm disrupter in enhancing likelihood of cure relative to approved therapies, reducing recurrence rates, and combined with traditional antimicrobials. CLINICAL TRIALS REGISTRATION: NCT02866227.
Asunto(s)
Antiinfecciosos/uso terapéutico , Boratos/uso terapéutico , Ácidos Bóricos/uso terapéutico , Candidiasis Vulvovaginal/tratamiento farmacológico , Ácido Edético/análogos & derivados , Ácido Edético/uso terapéutico , Vaginosis Bacteriana/tratamiento farmacológico , Adolescente , Adulto , Antiinfecciosos/farmacología , Boratos/farmacología , Ácidos Bóricos/farmacología , Ácido Edético/farmacología , Femenino , Humanos , Persona de Mediana Edad , Adulto JovenRESUMEN
Boron is increasingly added to food supplements due to multiple effects that have been reported in mammals after boric acid administration. Among these effects are inflammatory process control, bone and muscle strength enhancement, protein expression regulation, and a decreased risk of developing some pathologies in which these processes are key, such as osteoporosis, dermatological inflammatory non-infectious maladies and diseases affecting the central nervous system. Experimental data have suggested that steroid hormone levels in plasma change after boric acid administration, but a clear mechanism behind these variations has not been established. We analyzed possibilities for these changes and hypothesized that boric acid disrupts the interactions between steroid hormones and several carriers in plasma. In particular, we proposed that there is an uncoupling of the interactions between sex hormone binding globulin (SHBG) and estrogens and testosterone and that there are alterations in the binding of hydrophobic ligands by other carrier proteins in plasma. Further experimental and computational studies are required to support the hypothesis that boric acid and probably other boron-containing compounds can displace steroid hormones from their plasma carriers. If such phenomena are confirmed, boron administration with a clear mechanism could be employed as a therapeutic agent in several diseases or physiological events that require modulation of steroid hormone levels in plasma.
Asunto(s)
Boro/uso terapéutico , Globulina de Unión a Hormona Sexual/metabolismo , Esteroides/uso terapéutico , Ácidos Bóricos/química , Ácidos Bóricos/uso terapéutico , Boro/química , Proteínas Portadoras/metabolismo , Estrógenos/metabolismo , Glicoproteínas/metabolismo , Humanos , Inflamación/etiología , Ligandos , Modelos Teóricos , Osteoporosis/etiología , Multimerización de Proteína , Testosterona/metabolismoRESUMEN
INTRODUCTION: Clinicians are increasingly challenged by patients with refractory vulvovaginal candidiasis (VVC) caused by azole-resistant Candida species. Fluconazole resistant C.albicans is a growing and perplexing problem following years of indiscriminate drug prescription and unnecessary drug exposure and for which there are few therapeutic alternatives. Regrettably, although the azole class of drugs has expanded, new classes of antifungal drugs have not been forthcoming, limiting effective treatment options in patients with azole resistant Candida vaginitis. AREAS COVERED: This review covers published data on epidemiology, pathophysiology and treatment options for women with azole-resistant refractory VVC. EXPERT OPINION: Fluconazole resistant C.albicans adds to the challenge of azole resistant non-albicans Candida spp. Both issues follow years of indiscriminate drug prescription and unnecessary fluconazole exposure. Although an understanding of azole resistance in yeast has been established, this knowledge has not translated into useful therapeutic advantage. Treatment options for such women with refractory symptoms are extremely limited. New therapeutic options and strategies are urgently needed to meet this challenge of azole drug resistance.
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Antifúngicos/uso terapéutico , Candidiasis Vulvovaginal/tratamiento farmacológico , Fluconazol/uso terapéutico , Inhibidores de 14 alfa Desmetilasa/farmacología , Inhibidores de 14 alfa Desmetilasa/uso terapéutico , Antifúngicos/farmacología , Ácidos Bóricos/farmacología , Ácidos Bóricos/uso terapéutico , Candida/efectos de los fármacos , Candida/aislamiento & purificación , Candidiasis Vulvovaginal/microbiología , Candidiasis Vulvovaginal/patología , Farmacorresistencia Fúngica/efectos de los fármacos , Femenino , Fluconazol/farmacología , Humanos , Pruebas de Sensibilidad MicrobianaRESUMEN
This study presents a case report of a female patient with symptomatic refractory Trichomonas vaginalis infection who was not able to clear her infection with high-dose oral metronidazole, oral tinidazole, intra-vaginal zinc sulfate, intra-vaginal metronidazole, intra-vaginal tinidazole, and intra-vaginal boric acid. She was unable to tolerate intra-vaginal paromomycin. A combination of intravenous metronidazole, oral tinidazole liquid suspension, and intra-vaginal boric acid for 14 days subsequently achieved a complete symptomatic and laboratory cure.
Asunto(s)
Antiprotozoarios/administración & dosificación , Antitricomonas/administración & dosificación , Ácidos Bóricos/administración & dosificación , Metronidazol/administración & dosificación , Tinidazol/administración & dosificación , Vaginitis por Trichomonas/tratamiento farmacológico , Trichomonas vaginalis/efectos de los fármacos , Administración Intravaginal , Administración Intravenosa , Adulto , Antiprotozoarios/uso terapéutico , Antitricomonas/uso terapéutico , Ácidos Bóricos/uso terapéutico , Femenino , Derivación Gástrica , Humanos , Metronidazol/uso terapéutico , Tinidazol/uso terapéutico , Resultado del Tratamiento , Trichomonas vaginalis/aislamiento & purificaciónRESUMEN
OBJECTIVES: To compare the clinical effectiveness and adverse events for 3 per cent boric acid in 70 per cent alcohol versus 1 per cent clotrimazole solution in the treatment of otomycosis. METHODS: A total of 120 otomycosis patients were randomly assigned to receive either 1 per cent clotrimazole solution (intervention group) or 3 per cent boric acid in 70 per cent alcohol (control group) at the Khon Kaen Hospital ENT out-patient department. Treatment effectiveness was determined based on the otomicroscopic absence of fungus one week after therapy, following a single application of treatment. RESULTS: After 1 week of treatment, there were data for 109 participants, 54 in the clotrimazole group and 55 in the boric acid group. The absolute difference in cure rates between 1 per cent clotrimazole solution and 3 per cent boric acid in 70 per cent alcohol was 17.9 per cent (95 per cent confidence interval, 2.3 to 33.5; p = 0.028) and the number needed to treat was 6 (95 per cent confidence interval, 3.0 to 43.4). Adverse events for the two agents were comparable. CONCLUSION: One per cent clotrimazole solution is more effective than 3 per cent boric acid in 70 per cent alcohol for otomycosis treatment.
Asunto(s)
Antifúngicos/uso terapéutico , Ácidos Bóricos/uso terapéutico , Clotrimazol/uso terapéutico , Otomicosis/tratamiento farmacológico , Adulto , Antifúngicos/administración & dosificación , Ácidos Bóricos/administración & dosificación , Clotrimazol/administración & dosificación , Conducto Auditivo Externo , Femenino , Humanos , Instilación de Medicamentos , Masculino , Persona de Mediana Edad , Resultado del TratamientoRESUMEN
BACKGROUND: To compare different therapeutic supportive approaches in patients with burning mouth syndrome. A prospective study was carried out for this purpose. MATERIALS AND METHODS: The study involved 56 patients with burning mouth syndrome. They were randomly assigned to treatment with capsaicin, alpha-lipoic acid or lysozyme-lactoperoxidase (test drugs) or boric acid (control group). Symptoms were scored after 60 days treatment and 60 days after drug discontinuation. RESULTS: At the end of the treatment period, there was a significant reduction in the symptom scores of all of the patients who received the test drugs (P<0.01), and at the end of the follow-up period in the test groups as a whole (P<0.01); the reduction was not significant when considering each test group separately after the treatment period. All of the treatments were more effective than boric acid and there was no significant difference in the symptom scores of the control group at either of the study time-points. CONCLUSIONS: Our results demonstrate the similar effectiveness of capsaicin and alpha-lipoic acid in controlling the symptoms of burning mouth syndrome. Lysozyme-lactoperoxidase may be effective in the supportive care of BMS patients with xerostomia. The transitory effect observed after discontinuing drug administration justifies the use of prolonged therapy in chronically affected patients.
Asunto(s)
Síndrome de Boca Ardiente/tratamiento farmacológico , Administración Oral , Administración Tópica , Antioxidantes/administración & dosificación , Antioxidantes/uso terapéutico , Ácidos Bóricos/administración & dosificación , Ácidos Bóricos/uso terapéutico , Capsaicina/administración & dosificación , Capsaicina/uso terapéutico , Femenino , Estudios de Seguimiento , Humanos , Lactoperoxidasa/administración & dosificación , Lactoperoxidasa/uso terapéutico , Masculino , Persona de Mediana Edad , Antisépticos Bucales/uso terapéutico , Muramidasa/administración & dosificación , Muramidasa/uso terapéutico , Dimensión del Dolor , Placebos , Estudios Prospectivos , Fármacos del Sistema Sensorial/administración & dosificación , Fármacos del Sistema Sensorial/uso terapéutico , Método Simple Ciego , Comprimidos , Ácido Tióctico/administración & dosificación , Ácido Tióctico/uso terapéuticoRESUMEN
OBJECTIVE: This study seeks to identify practices of self-medication in the treatment of ocular emergencies. We examine patients' use of both homemade preparations and manufactured products before seeking specialized care. MATERIALS AND METHODS: We conducted a cross-sectional analytic survey of consecutive patients seen in the ophthalmology emergency room of a teaching hospital. RESULTS: The sample included 561 subjects, 51.3% males and 48.7% females, with a mean age of 39.8 years. Prior to seeking emergency care, 40.5% reported self-medicating; 29.4% used a homemade preparation (13.9% referred to an industrialized product like boric acid as a homemade preparation), and 11.1% used a manufactured product. The most frequently used products included a boric acid solution (53.3%), a normal saline solution (35.7%), herbal infusions (6.1%) and breast milk (4.8%). Viral conjunctivitis was the most frequent diagnosis (24.4%), followed by the presence of a corneal foreign body (7.4%). No significant differences were found in the self-treatment of ocular injuries according to gender (p = 0.95), level of education (p = 0.21) or age (p = 0.14). In addition, self-medication practices were not related to the medically judged severity of the condition. CONCLUSION: Patients often attempt to treat conditions that require ophthalmologic emergency care by self-medicating with homemade or manufactured products. The most widely used products include boric acid, normal saline, leaf infusions and breast milk. This behavior occurs independently of educational level, gender, age or the nature of the ocular condition. Self-medication is a culturally driven practice that is used even in cases of acute ocular injuries.
Asunto(s)
Conjuntivitis Viral/tratamiento farmacológico , Cuerpos Extraños en el Ojo/tratamiento farmacológico , Automedicación , Adolescente , Adulto , Ácidos Bóricos/uso terapéutico , Brasil/epidemiología , Niño , Preescolar , Conjuntivitis Viral/epidemiología , Estudios Transversales , Servicio de Urgencia en Hospital , Cuerpos Extraños en el Ojo/epidemiología , Femenino , Atención Domiciliaria de Salud/estadística & datos numéricos , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Leche Humana , Medicamentos sin Prescripción/clasificación , Medicamentos sin Prescripción/uso terapéutico , Oftalmología , Extractos Vegetales/uso terapéutico , Automedicación/clasificación , Automedicación/estadística & datos numéricos , Cloruro de Sodio/uso terapéutico , Adulto JovenRESUMEN
OBJECTIVE: This study seeks to identify practices of self-medication in the treatment of ocular emergencies. We examine patients' use of both homemade preparations and manufactured products before seeking specialized care. MATERIALS AND METHODS: We conducted a cross-sectional analytic survey of consecutive patients seen in the ophthalmology emergency room of a teaching hospital. RESULTS: The sample included 561 subjects, 51.3 percent males and 48.7 percent females, with a mean age of 39.8 years. Prior to seeking emergency care, 40.5 percent reported self-medicating; 29.4 percent used a homemade preparation (13.9 percent referred to an industrialized product like boric acid as a homemade preparation), and 11.1 percent used a manufactured product. The most frequently used products included a boric acid solution (53.3 percent), a normal saline solution (35.7 percent), herbal infusions (6.1 percent) and breast milk (4.8 percent). Viral conjunctivitis was the most frequent diagnosis (24.4 percent), followed by the presence of a corneal foreign body (7.4 percent). No significant differences were found in the self-treatment of ocular injuries according to gender (p = 0.95), level of education (p = 0.21) or age (p = 0.14). In addition, self-medication practices were not related to the medically judged severity of the condition. CONCLUSION: Patients often attempt to treat conditions that require ophthalmologic emergency care by self-medicating with homemade or manufactured products. The most widely used products include boric acid, normal saline, leaf infusions and breast milk. This behavior occurs independently of educational level, gender, age or the nature of the ocular condition. Self-medication is a culturally driven practice that is used even in cases of acute ocular injuries.
Asunto(s)
Adolescente , Adulto , Niño , Preescolar , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Persona de Mediana Edad , Adulto Joven , Conjuntivitis Viral/tratamiento farmacológico , Cuerpos Extraños en el Ojo/tratamiento farmacológico , Automedicación , Ácidos Bóricos/uso terapéutico , Brasil/epidemiología , Estudios Transversales , Conjuntivitis Viral/epidemiología , Servicio de Urgencia en Hospital , Cuerpos Extraños en el Ojo/epidemiología , Atención Domiciliaria de Salud/estadística & datos numéricos , Leche Humana , Medicamentos sin Prescripción/clasificación , Medicamentos sin Prescripción/uso terapéutico , Oftalmología , Extractos Vegetales/uso terapéutico , Automedicación/clasificación , Automedicación/estadística & datos numéricos , Cloruro de Sodio/uso terapéutico , Adulto JovenRESUMEN
BACKGROUND: Recalcitrant vaginal trichomoniasis is extremely distressing for patients and frustrating for physicians because there are no current guidelines for treatment. Numerous studies have shown that an increase in vaginal pH creates a better environment for the growth of Trichomonas vaginalis. We describe two patients with recalcitrant trichomoniasis who were successfully treated using vaginal acidification. CASES: The first patient with trichomoniasis had a severe reaction to metronidazole, but the infection subsequently resolved after treatment with a combination of boric acid and clotrimazole. The second patient with resistant trichomoniasis had been treated unsuccessfully with multiple courses of metronidazole but was treated successfully with vaginal acidification using boric acid. CONCLUSION: A process of vaginal acidification resulted in resolution of recalcitrant Trichomonas vaginalis in two patients.
Asunto(s)
Antiprotozoarios/uso terapéutico , Ácidos Bóricos/uso terapéutico , Clotrimazol/uso terapéutico , Vaginitis por Trichomonas/tratamiento farmacológico , Trichomonas vaginalis/efectos de los fármacos , Vagina/parasitología , Ácido Acético/uso terapéutico , Adulto , Animales , Antiinfecciosos Locales/uso terapéutico , Ácidos Bóricos/farmacología , Femenino , Violeta de Genciana/uso terapéutico , Humanos , Concentración de Iones de Hidrógeno , Persona de Mediana Edad , Recurrencia , Resultado del Tratamiento , Vagina/efectos de los fármacosRESUMEN
PURPOSE: To evaluate use conditions and detect contamination in bottles of boric acid solution. METHODS: A convenience sample of 42 recruited patients using boric acid solution came to the Ophthalmology Emergency Room of the São Paulo Hospital from February to March of 2003. Cultures were taken from material of the conjunctival sac, inner surface of bottle edge, inner part of cap and from 1 ml of boric acid solution of each bottle. RESULTS: Of the 42 boric acid solution bottles, 17 (40.5%) showed contamination: 1 (2.4%) in the solution, 17 (40.5%) in the inner cap and 6 (14.3%) in the inner part of the bottle edge. Of the 17 contaminated bottles, 10 (58.8%) were handled inappropriately and 13 (76.5%) of the bottles were not discharged after first use. The most common microorganisms found in the caps and edges of the bottles were Staphylococcus sp (69.6%), followed by Gram-positive bacillus (26.1%). Sixteen bottles (38.1%) had been opened more than a month ago and 5 (31.3%) of those showed contamination. The boric acid solution bottle directions shown on the labels were incomplete and not clear. The use of boric acid solution was on recommendation of their own, friends or relatives in 26 (61.9%) cases; pharmacists in 8 (19.0%) cases, ophthalmologists in 5 (11.9%) cases and general practitioners in 3 (7.1%) cases. CONCLUSION: In most cases, the topic use of boric acid solution was recommended by non-physicians. The bottles, in general, were handled inappropriately, and hence presented a much higher level of contamination that did the boric acid solution inside. The lower level of contamination in the solution is possibly associated with the anti-septic characteristics of the boric acid solution.
Asunto(s)
Ácidos Bóricos/uso terapéutico , Enfermedades de la Conjuntiva/tratamiento farmacológico , Contaminación de Medicamentos , Soluciones Oftálmicas/uso terapéutico , Adolescente , Adulto , Niño , Recuento de Colonia Microbiana , Conjuntiva/virología , Etiquetado de Medicamentos/normas , Embalaje de Medicamentos , Almacenaje de Medicamentos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Staphylococcus/aislamiento & purificación , Encuestas y Cuestionarios , Factores de TiempoRESUMEN
OBJETIVOS: Avaliar as condições de uso de água boricada e verificar a contaminação dos frascos e seu conteúdo. MÉTODOS: Foram selecionados, por critério de conveniência, quarenta e dois pacientes, usuários de água boricada, que compareceram ao Pronto-Socorro de Oftalmologia do Hospital São Paulo, em fevereiro e março de 2003. Foi colhido material para cultura do saco conjuntival, da superfície interna da borda do frasco, da superfície interna da tampa, além de 1 ml de solução do frasco. RESULTADOS: Dos 42 recipientes de água boricada, 17 (40,5 por cento) apresentavam contaminação, sendo 1 (2,4 por cento) no conteúdo liquido, 17 (40,5 por cento) na parte interna da tampa e 6 (14,3 por cento) na parte interna da borda do frasco. Dos 17 frascos contaminados, 10 (58,8 por cento) tiveram suas tampas manuseadas de maneira inadequada e 13 (76,5 por cento) frascos já haviam sido usados em outras ocasiões. Os microrganismos mais encontrados nas tampas e bordas foram Staphylococcus sp (69,6 por cento) e bacilos Gram-positivos (26,1 por cento). Dezesseis (38,1 por cento) frascos foram abertos há mais de um mês e, destes, 5 (31,3 por cento) apresentaram contaminação. A instrução de uso nos rótulos dos frascos era inconsistente. A utilização de água boricada foi por conta própria, por indicação de amigos ou parentes em 26 (61,9 por cento) casos; indicação de farmacêuticos em 8 (19,0 por cento); de oftalmologistas em 5 (11,9 por cento) e de clínicos gerais em 3 (7,1 por cento). CONCLUSÃO: A indicação de uso tópico oftálmico de água boricada foi feita, na maioria, por leigos. Os frascos, em geral, eram manipulados de maneira inadequada, apresentando contaminação em uma proporção de casos muito maior do que a contaminação do líquido. Essa porcentagem menor de contaminação do conteúdo provavelmente está associada às características anti-sépticas do produto.
PURPOSE: To evaluate use conditions and detect contamination in bottles of boric acid solution. METHODS: A convenience sample of 42 recruited patients using boric acid solution came to the Ophthalmology Emergency Room of the São Paulo Hospital from February to March of 2003. Cultures were taken from material of the conjunctival sac, inner surface of bottle edge, inner part of cap and from 1 ml of boric acid solution of each bottle. RESULTS: Of the 42 boric acid solution bottles, 17 (40.5 percent) showed contamination: 1 (2.4 percent) in the solution, 17 (40.5 percent) in the inner cap and 6 (14.3 percent) in the inner part of the bottle edge. Of the 17 contaminated bottles, 10 (58.8 percent) were handled inappropriately and 13 (76.5 percent) of the bottles were not discharged after first use. The most common microorganisms found in the caps and edges of the bottles were Staphylococcus sp (69.6 percent), followed by Gram-positive bacillus (26.1 percent). Sixteen bottles (38.1 percent) had been opened more than a month ago and 5 (31.3 percent) of those showed contamination. The boric acid solution bottle directions shown on the labels were incomplete and not clear. The use of boric acid solution was on recommendation of their own, friends or relatives in 26 (61.9 percent) cases; pharmacists in 8 (19.0 percent) cases, ophthalmologists in 5 (11.9 percent) cases and general practitioners in 3 (7.1 percent) cases. CONCLUSION: In most cases, the topic use of boric acid solution was recommended by non-physicians. The bottles, in general, were handled inappropriately, and hence presented a much higher level of contamination that did the boric acid solution inside. The lower level of contamination in the solution is possibly associated with the anti-septic characteristics of the boric acid solution.
Asunto(s)
Humanos , Masculino , Femenino , Niño , Adolescente , Adulto , Persona de Mediana Edad , Ácidos Bóricos/uso terapéutico , Enfermedades de la Conjuntiva/tratamiento farmacológico , Contaminación de Medicamentos , Soluciones Oftálmicas/uso terapéutico , Recuento de Colonia Microbiana , Conjuntiva/virología , Embalaje de Medicamentos , Prescripciones de Medicamentos , Almacenaje de Medicamentos , Etiquetado de Medicamentos/normas , Encuestas y Cuestionarios , Staphylococcus/aislamiento & purificaciónRESUMEN
Vulvovaginitis is a common inflammatory condition that can significantly disrupt a woman's life. The term vulvovaginitis actually encompasses a variety of inflammatory lower gential tract disorders that may be secondary to infection, irritation, allergy or systemic disease (Table 1). This article focuses on candida-caused vulvovaginitis, a condition known as vulvovaginitis candidiasis. Approximately 75% of U.S. women expreience vulvovaginitis candidiasis during thier reproductive years. Between 40% and 50% of these women have recurrent episodes, and 5% to 8% experience chronic candida infections. Approximately 3 million women have recurrent candidial infections. The prevalence of vulvovaginitis candiasis is expected to rise due to the growing number of non-C albicans species (which are immune to most antifungal medcationa) and as a result of more widespread antifungal resistance.
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Antifúngicos/uso terapéutico , Candidiasis Vulvovaginal/terapia , Terapias Complementarias/métodos , Antiinfecciosos Locales/uso terapéutico , Ácidos Bóricos/uso terapéutico , Candidiasis Vulvovaginal/diagnóstico , Candidiasis Vulvovaginal/epidemiología , Candidiasis Vulvovaginal/microbiología , Causalidad , Prescripciones de Medicamentos , Farmacorresistencia Fúngica , Femenino , Ajo , Humanos , Lactobacillus acidophilus , Medicamentos sin Prescripción/uso terapéutico , Prevalencia , Recurrencia , Autocuidado , Aceite de Árbol de Té/uso terapéutico , Resultado del Tratamiento , YogurAsunto(s)
Antiinfecciosos/farmacología , Antiinfecciosos/uso terapéutico , Ácidos Bóricos/farmacología , Ácidos Bóricos/uso terapéutico , Ciprofloxacina/farmacología , Ciprofloxacina/uso terapéutico , Otitis Media Supurativa/tratamiento farmacológico , Administración Tópica , Antiinfecciosos/administración & dosificación , Umbral Auditivo/fisiología , Ácidos Bóricos/administración & dosificación , Niño , Enfermedad Crónica , Ciprofloxacina/administración & dosificación , Países en Desarrollo , Trastornos de la Audición/diagnóstico , Trastornos de la Audición/etiología , Trastornos de la Audición/fisiopatología , Humanos , Kenia/epidemiología , Tamizaje Masivo/métodos , Otitis Media Supurativa/complicaciones , Otitis Media Supurativa/etnología , Dolor/diagnóstico , Dolor/etiología , Índice de Severidad de la Enfermedad , Membrana Timpánica/efectos de los fármacosRESUMEN
OBJECTIVE: To compare a topical quinolone antibiotic (ciprofloxacin) with a cheaper topical antiseptic (boric acid) for treating chronic suppurative otitis media in children. DESIGN: Randomized controlled trial. SETTING AND PARTICIPANTS: A total of 427 children with chronic suppurative otitis media enrolled from 141 schools following screening of 39 841 schoolchildren in Kenya. Intervention Topical ciprofloxacin (n = 216) or boric acid in alcohol (n = 211); child-to-child treatment twice daily for 2 weeks. MAIN OUTCOME MEASURES: Resolution of discharge (at 2 weeks for primary outcome), healing of the tympanic membrane, and change in hearing threshold from baseline, all at 2 and 4 weeks. RESULTS: At 2 weeks, discharge was resolved in 123 of 207 (59%) children given ciprofloxacin, and in 65 of 204 (32%) given boric acid (relative risk 1.86; 95% CI 1.48-2.35; P < 0.0001). This effect was also significant at 4 weeks, and ciprofloxacin was associated with better hearing at both visits. No difference with respect to tympanic membrane healing was detected. There were significantly fewer adverse events of ear pain, irritation, and bleeding on mopping with ciprofloxacin than boric acid. CONCLUSIONS: Ciprofloxacin performed better than boric acid and alcohol for treating chronic suppurative otitis media in children in Kenya.
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Antiinfecciosos Locales/uso terapéutico , Ciprofloxacina/uso terapéutico , Otitis Media Supurativa/tratamiento farmacológico , Adolescente , Ácidos Bóricos/uso terapéutico , Niño , Preescolar , Enfermedad Crónica , Países en Desarrollo , Método Doble Ciego , Femenino , Estudios de Seguimiento , Trastornos de la Audición/etiología , Humanos , Kenia , Masculino , Otitis Media Supurativa/complicaciones , Resultado del TratamientoRESUMEN
Vulvovaginal candidiasis is considered recurrent when at least four specific episodes occur in one year or at least three episodes unrelated to antibiotic therapy occur within one year. Although greater than 50 percent of women more than 25 years of age develop vulvovaginal candidiasis at some time, fewer than 5 percent of these women experience recurrences. Clinical evaluation of recurrent episodes is essential. Patients who self-diagnose may miss other causes or concurrent infections. Known etiologies of recurrent vulvovaginal candidiasis include treatment-resistant Candida species other than Candida albicans, frequent antibiotic therapy, contraceptive use, compromise of the immune system, sexual activity and hyperglycemia. If microscopic examination of vaginal secretions in a potassium hydroxide preparation is negative but clinical suspicion is high, fungal cultures should be obtained. After the acute episode has been treated, subsequent prophylaxis (maintenance therapy) is important. Because many patients experience recurrences once prophylaxis is discontinued, long-term therapy may be warranted. Patients are more likely to comply when antifungal therapy is administered orally, but oral treatment carries a greater potential for systemic toxicity and drug interactions.
Asunto(s)
Antifúngicos/uso terapéutico , Candidiasis Vulvovaginal/tratamiento farmacológico , Ácidos Bóricos/uso terapéutico , Candidiasis Vulvovaginal/diagnóstico , Candidiasis Vulvovaginal/etiología , Candidiasis Vulvovaginal/prevención & control , Clotrimazol/uso terapéutico , Interacciones Farmacológicas , Femenino , Fluconazol/uso terapéutico , Humanos , Cetoconazol/uso terapéutico , Educación del Paciente como Asunto , Recurrencia , Factores de Riesgo , Materiales de Enseñanza , Factores de Tiempo , Triazoles/uso terapéuticoRESUMEN
The association between the concentrations of various blood constituents and the responses of cows with milk fever following calcium borogluconate therapy was determined using analysis of variance. In cows which had not received herdsman treatment prior to sampling (n = 63), plasma potassium was the only constituent with a significant effect (p less than 0.01), the mean concentrations for cows classified as unassisted, assisted, or delayed, recoveries, and deaths ranging down from 4.3 to 2.8 mmol/l, respectively. In cows which had received treatment prior to sampling (n = 55) those making unassisted recoveries had significantly lower mean concentrations of serum total calcium than those making assisted recoveries (1.3 v 1.9 mmol/l, respectively, p less than 0.05), and cows making delayed recoveries had significantly lower mean plasma inorganic phosphate concentrations (0.3 mmol/l) than those making unassisted and assisted recoveries (both 0.7 mmol/l, p less than 0.05) and those subsequently dying (1.2 mmol/l, p less than 0.01). Response was not dependent on plasma potassium concentrations in the treated group of cows, and plasma sodium, serum magnesium, and erythrocyte sodium concentrations were not significant in either group of cows.