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Abstract Foam has been used worldwide as a vehicle for the professional application of fluoride and hypothetically should have the same anticaries potential as conventional fluoride gel (F-gel) in terms of the formation of reaction products with enamel. Thus, the ability of Flúor Care® foam (FGM, Joinville, SC, Brazil, 12,300 ppm F, acidulated) to react with enamel was evaluated in comparison with Flúor gel® (DFL, Rio de Janeiro, RJ, Brazil, 12,300 ppm F, acidulated). Slabs (n=10/group) of sound enamel and with caries lesion were used, in which the concentrations of total fluoride (TF), and loosely (CaF2-like) and firmly (FAp) bound types were determined. The importance of agitation during application was previously tested. The determinations were made with fluoride ion-specific electrode and the results were expressed in μg F/cm² of the treated enamel area. ANOVA and Tukey tests were used to analyze the difference among treatments, independently for sound and carious enamel. The agitation of the products during application significantly increased the reactivity of the foam (p<0.05), but not that of the gel (p>0.05). The foam did not differ from F-gel (p>0.05) concerning the formation of TF and CaF2-like in sound or carious enamel. Regarding FAp, the foam did not differ from F-gel (p>0.05) in the carious enamel, but the concentration in the sound was lower (p<0.05). The results show that this commercial fluoride foam tested needs to be agitated during application to improve its reactivity with enamel, which raises a question about other brands.

Resumo A espuma tem sido utilizada mundialmente como veículo para aplicação profissional de fluoreto e hipoteticamente deveria ter o mesmo potencial anticárie que o gel fluoretado convencional (F-gel) em termos de formação de produtos de reação com o esmalte. Assim, a capacidade da espuma Flúor Care® (FGM, Joinville, SC, Brasil, 12.300 ppm F, acidulada) de reagir com o esmalte foi avaliada em comparação com o Flúor gel® (DFL, Rio de Janeiro, RJ, Brasil 12.300 ppm F, acidulado). Foram utilizados blocos (n=10/grupo) de esmalte hígido e com lesão de cárie, nos quais foram determinadas as concentrações de flúor total (FT), e os tipos de flúor fracamente (tipo-CaF2) e firmemente (FAp) ligados ao esmalte. A importância da agitação durante a aplicação foi previamente testada. As determinações foram feitas com eletrodo íon específico para fluoreto e os resultados foram expressos em μg F/cm² da área tratada do esmalte. A diferença entre os tratamentos foi analisada por ANOVA e Tukey (α=5%), independentemente para esmalte hígido e cariado. A agitação dos produtos durante a aplicação aumentou significativamente a reatividade da espuma (p<0,05), mas não a do gel (p>0,05). A espuma não diferiu do F-gel (p>0,05) quanto à formação de FT e tipo-CaF2 no esmalte hígido ou cariado. Em relação à FAp, a espuma não diferiu do F-gel (p>0,05) no esmalte cariado, mas a concentração no hígido foi menor (p<0,05). Os resultados mostram que esta espuma fluoretada comercial testada precisa ser agitada durante a aplicação para melhorar sua reatividade com o esmalte, o que levanta questão sobre outras marcas.

RESUMO

Although fluoride varnish (FV) and acidulated phosphate fluoride gel (APF-gel) are considered clinically effective to reduce caries, in vitro studies have shown that FV reacts slowly with enamel because most NaF present in the formulation is not solubilized in the FV. Therefore, we conducted a clinical study to evaluate if the time that FV remains on dental surfaces could overcome its slower chemical reactivity when compared with APF-gel. Sixty-eight volunteers were randomly allocated into 4 groups: negative control (Control, no treatment), APF-gel application (1.23% F applied for 4 min), and FV application (Duraphat®, 2.26% F) for 4 h (FV-4h) or 24 h (FV-24 h). To evaluate fluoride formed and retained on enamel, acid biopsies were made on the buccal surfaces of the maxillary central incisors before, at the end of the application of fluoride products (immediately after gel application, or after 4 or 24 h of varnish application), and after 7 and 28 days. Fluoride concentration in dental biofilm was also analyzed before and up to 28 days after initial application. The data were analyzed by 2-way ANOVA, considering treatment and time as factors. The APF-gel and FV-24h groups formed greater fluoride concentration on enamel than the FV-4h and the control group at the end of application (p = 0.0001), with no difference from each other (p = 0.99). The groups did not differ regarding fluoride in biofilm fluid (p = 0.73) and solids (p = 0.40). In conclusion, FV needs to remain in contact with the teeth for prolonged times (>4 h) to reach the same reactivity obtained by a 4-min application of APF-gel.

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Abstract Introduction and objective: Toothpastes should contain chemically soluble fluoride to have anti-caries efficacy. This study aimed at determining how much of the total fluoride (TF) concentration in the five top-selling children/family Colombian-toothpaste brands corresponds to total chemically soluble fluoride (TSF). Materials and methods: a convenience sample of three tubes of each of the following five toothpaste brands were obtained from three different chain stores, one-per-store, in five Colombian cities (n=3/brand/city): Colgate-Smiles-6+, Kolynos-Super-Blanco, Fortident-Cuatriacción, Colgate-Triple-Acción, Fluocardent. TF (sum of all toothpaste's fluoride) and TSF (toothpaste's chemically soluble fluoride) concentrations were determined in each fresh toothpaste sample (before expiry date) using a standardized ion-specific electrode direct-technique protocol. TF concentration was compared with the manufacturers' declared concentration. The difference between TF and TSF's concentrations purchased in different cities was compared with a one-way ANOVA (5%). Results: Most toothpastes' TF concentration complied with what was declared in the label. One toothpaste had a non-compatible fluoride/abrasive fluoride formulation and TSF < TF; however, it still complied with the minimum TSF requirement to exert a caries-preventive effect (>1000 ppm). Toothpastes' TF and TSF concentrations did not differ between cities (p>0.05). Conclusion: Fresh samples of highly distributed toothpaste brands sold in five Colombian-cities contain chemically available fluoride concentrations with the potential to control and prevent dental caries.

Resumen Introducción y objetivo: las cremas dentales requieren de la disponibilidad de fluoruro químicamente soluble para tener efecto anticaries. Este estudio tuvo como objetivo determinar qué parte de la concentración total de fluoruro (FT) en las cinco marcas de pastas dentales colombianas para niños/familias más vendidas corresponde al fluoruro total químicamente soluble (FTS). Materiales y métodos: se recolectaron tres tubos de cinco marcas diferentes en tres supermercados de cadena; una por tienda, en cinco ciudades colombianas (n=3/marca/ciudad): Colgate-Smiles-6+, Kolynos-Super-Blanco, Fortident-Cuatriacción, Colgate-Triple-Acción, Fluocardent. Las concentraciones de FT y FST se determinaron en cada una de las muestras frescas utilizando técnica directa con electrodo específico y un protocolo estandarizado. La concentración de FT se comparó con la concentración declarada por el fabricante. Se compararon las diferencias entre las concentraciones de FT y FST de la misma marca compradas en diferentes ciudades a con un análisis ANOVA (α=5%). Resultados: La mayoría de las cremas dentales cumplió con la concentración de FT declarada en la etiqueta. Una de las cremas dentale tenía una formulación de fluoruro/abrasivo no compatible y TSF <TF; sin embargo, aún cumplía con el requisito mínimo de TSF para ejercer un efecto preventivo de caries (> 1000 ppm). Las concentraciones de TF y TSF de las pastas de dientes no difirieron entre las ciudades (p> 0.05). Conclusión: Las muestras frescas de cremas dentales de las marcas más vendidas en cinco ciudades colombianas contienen concentraciones de fluoruro químicamente disponibles con el potencial de controlar y prevenir la caries dental.

Resumo Introdução e objetivo: os cremes dentais requerem a disponibilidade de fluoreto quimicamente solúvel para ter um efeito anticárie. O presente estudo determinou a proporção de fluoreto total (FT) que corresponde ao fluoreto total quimicamente solúvel (FST) em cinco marcas de creme dental amplamente distribuídas na Colômbia. Materiais e métodos: três tubos de cinco marcas diferentes foram coletados em três supermercados da rede; uma por loja, em cinco cidades colombianas (n = 3 / marca / cidade): Colgate-Smiles-6 +, Kolynos-Super-Blanco, Fortident-Quad, Colgate-Triple-Action, Fluocardent. As concentrações de FT e FST foram determinadas em cada uma das amostras frescas, utilizando a técnica direta com eletrodo específico e um protocolo padronizado. A concentração de FT foi comparada com a concentração declarada pelo fabricante. As diferenças entre as concentrações de FT e FST da mesma marca comprada em diferentes cidades foram comparadas com a análise ANOVA (α = 5%). Resultados: a maioria das marcas possui concentrações de flúor que atendem à concentração declarada pelo fabricante. Uma marca contém uma formulação de sal abrasivo e fluoreto quimicamente não compatível e FST menor que FT; no entanto, as amostras frescas atenderam à concentração necessária para exercer um efeito anticárie (> 1000 ppm). As concentrações de FT e TSF não foram significativamente diferentes entre amostras da mesma marca compradas em diferentes cidades (p> 0,05). Conclusão: as amostras frescas (analisadas antes do prazo de validade) das cinco marcas de creme dental com maior distribuição na Colômbia contêm concentrações de fluoreto quimicamente solúvel, com potencial para controlar e prevenir a cárie dentária.

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Ultrasound (US) and X-ray imaging are diagnostic methods that are commonly used to image internal body structures. Several organic and inorganic imaging contrast agents are commercially available. However, their synthesis and purification remain challenging, in addition to posing safety issues. Here, we report on the promise of widespread, safe, and easy-to-produce particulate calcium fluoride (part-CaF2) as a bimodal US and X-ray contrast agent. Pure and highly crystalline part-CaF2 is obtained using a cheap commercial product. Scanning electron microscopy (SEM) depicts the morphology of these particles, while energy-dispersive X-ray spectroscopy (EDS) confirms their chemical composition. Diffuse reflectance ultraviolet-visible spectroscopy highlights their insulating behavior. The X-ray diffraction (XRD) pattern reveals that part-CaF2 crystallizes in the face-centered cubic cell lattice. Further analyses regarding peak broadening are performed using the Scherrer and Williamson-Hall (W-H) methods, which pinpoint the small crystallite size and the presence of lattice strain. X-ray photoelectron spectroscopy (XPS) solely exhibits specific peaks related to CaF2, confirming the absence of any contamination. Additionally, in vitro cytotoxicity and in vivo maximum tolerated dose (MTD) tests prove the biocompatibility of part-CaF2. Finally, the results of the US and X-ray imaging tests strongly signal that part-CaF2 could be exploited in bimodal bioimaging applications. These findings may shed a new light on calcium fluoride and the opportunities it offers in biomedical engineering.

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Aim: Evaluate the effect of adhesives systems combined with desensitizer agents on the microtensile bond strength (µTBS) of a composite resin to dentin. Methods: Cervical dentin of thirty-two human molars were used to simulate hypersensitivity areas. The teeth were divided into four groups (n=8), according to the type of adhesive system and desensitizer agents. No desensitizer was used in the control (Clearfil SE Bond ­ CS). Two experimental groups were pretreated with either MS Coat Bond (MS) or Biofluorid 12 (BF) immediately prior to bonding with CS. The last group corresponded to Gluma Comfort Bond + Desensitizer (GC) application. After dentin treatments, a composite block was built-up on dentin surface and after 24 hours teeth were serially sectioned to obtain bonded bean specimens. Beams were stored in water for 24 hours or one year. Subsequently, the specimens were submitted to the µTBS test. Data were analyzed by two-way mixed ANOVA and Bonferroni's test (α = 0.05). Results: At 24 hours, there was no significant difference in µTBS among groups. However, at one year, dentin treated with MS or BF demonstrated significantly lower µTBS of CS to dentin compared to control and GC, which kept their µTBS stable. Conclusion: The effect of MS and BF desensitizer agents on the µTBS of CS to dentin did not reduce the µTBS at 24 hours, but it decreases significantly after one year

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Abstract: Iontophoresis is a noninvasive technique, based on the application of a constant low-intensity electric current to facilitate the release of a variety of drugs, whether ionized or not, through biological membranes. The objective of this research was to evaluate the effect of iontophoresis using different electric current intensities on the uptake of fluoride in dental enamel with artificial caries lesions. In this in vitro operator-blind experiment, bovine enamel blocks (n = 10/group) with caries-like lesions and predetermined surface hardness were randomized into 6 groups: placebo gel without fluoride applied with a current of 0.8 mA (negative control), 2% NaF gel without application of any current, and 2% NaF gel applied with currents of 0.1, 0.2, 0.4 and 0.8 mA. Cathodic iontophoresis was applied for 4 min. The concentration of loosely bound fluoride (calcium fluoride) and firmly bound fluoride (fluorapatite) was determined. The results were analyzed by the nonparametric Kruskal-Wallis and Dunn tests. Iontophoresis at 0.8 mA, combined with the application of fluoridated gel (2% NaF), increased fluoride uptake in enamel with caries-like lesions, as either calcium fluoride or fluorapatite.

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Calcium fluoride (CaF2), in both natural and synthetic forms, has been exhaustively studied and explored as thermoluminescent (TL) detector. However its sensitivity to ambient light points to the applicability of CaF2 as OSL (Optically Stimulated Luminescence) detector, increasing the research about its luminescent properties. Although some properties to employ CaF2 detectors with OSL technique have been already demonstrated, there is a lack of some essential information as the OSL response to different types and energy of ionizing radiation. In order to extend the use of Brazilian natural CaF2 with OSL technique, we evaluated the efficiency and dosimetric properties of cold pressed CaF2:NaCl pellets. The CaF2 detectors presented good reproducibility and negligible fading of the signal over one month after irradiation. The dose response using OSL, TL and residual TL showed linear behavior for different radiation beams (protons, photons and alpha and beta particles), being equivalent to the results obtained with BeO and MTS (LiF) detectors through OSL and TL technique respectively. Moreover, differences were observed in OSL efficiency according the beam type and energy; CaF2 detectors presented a higher OSL and TL sensitivities to protons, photons and beta particles than to alpha particles. The energy response to photons obtained using OSL and residual TL intensities present an over response at lower photon energy similar to TL energy response. In addition, differences in the OSL curve shapes were observed according to radiation type and energy, pointing to the possibility of applying this material in mixed radiation fields and to estimate average LET (Linear Energy Transfer).

RESUMO

Abstract Casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) complexes are anticariogenic and capable of remineralizing the early stages of enamel lesions. The use of fluoride prevents dental decay and the association of CPP-ACP with fluoride can increase remineralization. Objective: To evaluate the effect of CPP-ACP and CPP-ACPF creams associated with a fluoride dentifrice to prevent enamel demineralization in a pH cyclic model. Material and Methods: Previously selected by surface microhardness (SH) analysis, human enamel blocks (n = 56) were submitted to daily treatment with dentifrice in a pH-cycling model. The enamel blocks were divided into four groups; G1: Crest™ Cavity Protection - Procter & Gamble (1,100 ppmF of NaF); G2: Crest™ +MI Paste (MP) - Recaldent™ GC Corporation Tokyo, Japan); G3: Crest™ + MI Paste Plus (MPP) - Recaldent™ 900 ppm as NaF, GC Corporation Tokyo, Japan), and G4: control, saliva. Specimens were soaked alternatively in a demineralizing solution and in artificial saliva for 5 d. The fluoride dentifrice, with proportion of 1:3 (w/w), was applied three times for 60 s after the remineralization period. The undiluted MP and MPP creams were applied for 3 m/d. After cycling, SH was re-measured and cross section microhardness measurements were taken. Results: The SH values observed for the groups G3 (257±70), G1 (205±70), and G2 (208±84) differed from the G4 group (98±110) (one-way ANOVA and Tukey's post hoc test). There were no differences between the groups G1xG2, G2xG3, and G1xG3 for demineralization inhibition. The percentage of volume mineral showed that, when applied with fluoride dentifrice, MPP was the most effective in preventing enamel demineralization at 50 µ from the outer enamel surface (Kruskal-Wallis and Mann Whitney p<0.05). Conclusion: Fluoride dentifrice associated with CPP-ACPF inhibited subsurface enamel demineralization.

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High fluoride dentifrice (FD; 5,000 ppm F) has been recommended to arrest root dentine lesions and to control enamel caries in high-risk patients. Also, standard FD (1,100 ppm F) in combination with professional fluoride application has been recommended to control dentine caries, but the effect of this combination on enamel has been considered modest. Considering the lack of evaluation comparing the use of 5,000 ppm FD (5,000-FD) versus acidulated phosphate fluoride (APF) application combined with 1,100 ppm FD (1,100-FD) on the inhibition and repair of caries lesions in both enamel and dentine, we conducted this in situ, double-blind, crossover study of 3 phases of 14 days. In each phase, 18 volunteers wore palatal appliances containing enamel and root dentine specimens, either sound or carious, to evaluate the effect of the treatments on the inhibition or repair of caries lesions, respectively. The treatments were non-FD (negative control), 5,000-FD, or 1 APF gel application on dental specimens combined with 1,100-FD used twice per day (APF + 1,100-FD). The reduction of demineralization and enhancement of remineralization were assessed by surface and cross-sectional hardness. Fluoride concentration was determined on dental specimens and on the formed biofilm. For enamel, APF + 1,100-FD and 5,000-FD did not differ regarding the inhibition of demineralization and repair of caries lesions. However, for dentine the difference between these treatments was inconclusive because while APF + 1,100-FD was more effective than 5,000-FD in caries lesion reduction and repair, 5,000-FD was more effective than APF + 1,100-FD in the reduction of surface demineralization. Therefore, the findings show that the combination of APF + 1,100-FD is as effective as 5,000-FD in enamel inhibition of demineralization and enhancement of remineralization.

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There is no consensus about the clinical recommendation of the time that Duraphat® varnish should be maintained on enamel surfaces without suffering mechanical disturbance by the patient. Considering the importance of calcium fluoride (CaF2)-like reservoirs on the anticaries effect of professional fluoride application, an in vitro study was designed to test the reactivity of Duraphat® varnish with enamel forming these reservoirs as a function of time. Since most fluoride in Duraphat® varnish is insoluble to react and form products on enamel, the relative contribution of the varnish soluble and insoluble fluoride fractions to the reactivity was also evaluated. For this, whole-varnish, containing soluble and insoluble fluoride (total fluoride concentration of 23699±384 µg F/g), or centrifuged varnish, containing only soluble fluoride (fluoride concentration of 258±97 µg F/g), were applied in a standardized manner on enamel slabs (n=8/varnish group/time), which were immersed in continuously renewed artificial saliva for up to 36 h. CaF2-like reservoirs formed on enamel by varnish application were extracted using 1 M KOH and fluoride concentration was measured with ion specific electrode. The results were expressed as µg F/cm2 of enamel area. Whole varnish formed significantly higher fluoride concentration on enamel than centrifuged varnish, reaching maximum concentration at 24 h (22.0±4.5 µg F/cm2). Centrifuged varnish reached maximum concentration at 6 h (3.20±0.81 µg F/cm2). In conclusion, a longer varnish retention time than the usually recommended could improve the anticaries effect of Duraphat® varnish, allowing that NaF particles, initially insoluble in the varnish matrix, prolong the reactivity with enamel.

Não há consenso sobre a recomendação clínica do tempo que o verniz Duraphat® deve ser mantido nas superfícies de esmalte sem ter perturbação mecânica pelo paciente. Considerando a importância dos reservatórios tipo fluoreto de cálcio (“CaF2”) no efeito anticárie da aplicação profissional de fluoreto, um estudo in vitro foi delineado para testar a reatividade do verniz Duraphat® com o esmalte na formação desses reservatórios em função do tempo. Como a maioria do fluoreto no verniz Duraphat® é insolúvel para reagir e formar produtos no esmalte, também se avaliou a contribuição relativa das frações solúvel e insolúvel do verniz na reatividade. Assim, verniz total, contendo fluoreto solúvel e insolúvel (concentração total de 23699±384 µg F/g), ou verniz centrifugado, contendo somente o fluoreto solúvel (concentração de 258±97 µg F/g), foram aplicados de maneira padronizada sobre blocos de esmalte (n =8/grupo de verniz/tempo), os quais foram imersos em saliva artificial com renovação continua por até 36 h. Os reservatórios tipo “CaF2” formados no esmalte pela aplicação do verniz foram extraídos com KOH 1 M e a concentração de F foi medida utilizando um eletrodo específico. Os resultados foram expressos como µg F/cm2. O verniz total formou significativamente maior concentração de fluoreto no esmalte que o verniz centrifugado, atingindo concentrações máximas após 24 h (22,0±4,5 µg F/cm2 de área de esmalte). O verniz centrifugado apresentou a máxima formação após 6 h (3,20 ± 0,81 µg F/cm2). Em conclusão, um tempo maior de retenção do que habitualmente recomendado poderia melhorar o efeito anticárie do verniz Duraphat®, pois partículas de NaF, inicialmente insolúveis na matriz do mesmo, possibilitam uma reatividade prolongada do verniz com o esmalte em função do tempo.

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O uso de glicosímetros portáteis é mundialmente consagrado em seres humanos, sendo considerado uma excelente forma de acompanhamento de pacientes com diabetes melito ou que recebem fluidoterapia glicosada. No entanto, estes precisam ser mais bem avaliados na medicina veterinária, para determinar a eficácia das diferentes marcas entre as diversas espécies de animais. O objetivo deste estudo foi comparar os diferentes métodos de dosagem glicêmica e avaliar a utilização dos glicosímetros humanos portáteis em 71 aves, utilizando três anticoagulantes: heparina lítica, fluoreto e ácido edético (EDTA). De forma geral, a marca OneTouch Ultra Mini ® obteve os parâmetros de glicemia mais fidedignos quando comparados aos dados obtidos por colorimetria, em relação ao glicosímetro da marca Accu-Chek Active ®.(AU)

Portable blood glucose meters are used worldwide in humans, and are considered an excellent tool for monitoring patients that have diabetes or that receive fluidotherapy containing glucose. However, these glucometers need to be better evaluated in veterinary medicine, in order to determine the effectiveness of different brands when applied to different animal species. The aim of this study was to compare different methods of dosing glycemic values and evaluate the use of human portable glucometers in 71 birds, using three anticoagulants: lithium heparin, fluoride and edetic acid (EDTA). In general, the parameters obtained with the OneTouch Ultra Mini ® brand glucose meter were more reliable when compared to data obtained by colorimetry, in comparison to the Accu-Chek ® Active glucometer.(AU)

La utilización de glucómetros portátiles está consagrada mundialmente en los seres humanos, considerándoselos una excelente forma de control para pacientes con diabetes mellitus, o en aquellos que reciben fluidoterapia con glucosa. No obstante, estos aparatos tienen que ser mas bién analizados en medicina veterinaria, afín de determinar la eficiencia de las diferentes marcas en diferentes especies de animales. El objetivo de este estudio fue comparar los diferentes métodos de evaluación de la glucemia y evaluar la utilización de glucómetros humanos portátiles en 71 aves, utilizando tres tipos de anticoagulantes: heparina lítica, fluoruro y EDTA. En términos generales, la marca OneTouch Ultra Mini® fue la que obtuvo los parámetros de glucemia mas fidedignos en comparación a la marca Accu-Chek Active®, en relación a los datos obtenidos por colorimetría.(AU)

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O uso de glicosímetros portáteis é mundialmente consagrado em seres humanos, sendo considerado uma excelente forma de acompanhamento de pacientes com diabetes melito ou que recebem fluidoterapia glicosada. No entanto, estes precisam ser mais bem avaliados na medicina veterinária, para determinar a eficácia das diferentes marcas entre as diversas espécies de animais. O objetivo deste estudo foi comparar os diferentes métodos de dosagem glicêmica e avaliar a utilização dos glicosímetros humanos portáteis em 71 aves, utilizando três anticoagulantes: heparina lítica, fluoreto e ácido edético (EDTA). De forma geral, a marca OneTouch Ultra Mini ® obteve os parâmetros de glicemia mais fidedignos quando comparados aos dados obtidos por colorimetria, em relação ao glicosímetro da marca Accu-Chek Active ®.

Portable blood glucose meters are used worldwide in humans, and are considered an excellent tool for monitoring patients that have diabetes or that receive fluidotherapy containing glucose. However, these glucometers need to be better evaluated in veterinary medicine, in order to determine the effectiveness of different brands when applied to different animal species. The aim of this study was to compare different methods of dosing glycemic values and evaluate the use of human portable glucometers in 71 birds, using three anticoagulants: lithium heparin, fluoride and edetic acid (EDTA). In general, the parameters obtained with the OneTouch Ultra Mini ® brand glucose meter were more reliable when compared to data obtained by colorimetry, in comparison to the Accu-Chek ® Active glucometer.

La utilización de glucómetros portátiles está consagrada mundialmente en los seres humanos, considerándoselos una excelente forma de control para pacientes con diabetes mellitus, o en aquellos que reciben fluidoterapia con glucosa. No obstante, estos aparatos tienen que ser mas bién analizados en medicina veterinaria, afín de determinar la eficiencia de las diferentes marcas en diferentes especies de animales. El objetivo de este estudio fue comparar los diferentes métodos de evaluación de la glucemia y evaluar la utilización de glucómetros humanos portátiles en 71 aves, utilizando tres tipos de anticoagulantes: heparina lítica, fluoruro y EDTA. En términos generales, la marca OneTouch Ultra Mini® fue la que obtuvo los parámetros de glucemia mas fidedignos en comparación a la marca Accu-Chek Active®, en relación a los datos obtenidos por colorimetría.

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