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1.
RFO UPF ; 26(2): 262-274, 20210808. ilus
Article in Portuguese | LILACS, BBO | ID: biblio-1452533

ABSTRACT

Objetivo: Verificar, por meio de uma revisão de literatura, a efetividade do uso do fluoreto de sódio como dessensibilizante para casos de sensibilidade induzida por clareamento dental. Resultados: O clareamento dentário tornou-se um dos procedimentos estéticos mais procurados na odontologia. Atualmente, existem duas técnicas supervisionadas por dentistas: o clareamento caseiro e o de consultório. Os materiais mais utilizados são o peróxido de carbamida e o de hidrogênio, respectivamente. O clareamento dental baseia-se na premissa de que o peróxido de hidrogênio penetra na estrutura dentária para interagir com os cromóforos orgânicos. Embora o protocolo de clareamento exija o uso de agentes oxidantes de baixa concentração, a sensibilidade dentária ainda está presente e pode ser considerado o principal efeito adverso da técnica de clareamento. Para minimizar este problema, a aplicação tópica de dessensibilizantes antes e após o clareamento dentário tem mostrado bons resultados na redução da intensidade de sensibilidade. Considerações finais: Mediante revisão apresentada, constatou-se que fluoreto de sódio quando utilizado após o protocolo clareador, como dessensibilizante, não elimina a sensibilidade, mas diminui a intensidade da dor. Quando utilizado antes do clareamento dental, não apresenta resultados positivos. Ademais, salienta-se que quando o fluoreto é incorporado no gel clareador, resulta em menor desmineralização do esmalte dentário.(AU)


Objective: To verify, through a literature review, the effectiveness of using sodium fluoride as a desensitizer for cases of sensitivity induced by tooth whitening. Literature review: Teeth whitening has become one of the most desired aesthetic procedures in dentistry. Currently, there are two techniques supervised by dentists: home whitening and office whitening. The most used materials are carbamide peroxide and hydrogen peroxide, respectively. Teeth whitening is based on the premise that hydrogen peroxide penetrates the tooth structure to interact with organic chromophores. Although the whitening protocol requires the use of low concentration oxidizing agents, tooth sensitivity is still present and can be considered the main adverse effect of the whitening technique. To minimize this problem, the topical application of desensitizers before and after tooth whitening has shown good results in reducing the intensity of sensitivity. Final considerations: Upon the review presented, it was found that sodium fluoride, when used after the whitening protocol, as a desensitizer, does not eliminate sensitivity, but reduces the intensity of pain. When used before tooth whitening, it has no positive results. Furthermore, it should be noted that when fluoride is incorporated into the whitening gel, less enamel demineralization is induced.(AU)


Subject(s)
Humans , Tooth Bleaching/methods , Sodium Chloride/therapeutic use , Dentin Desensitizing Agents/therapeutic use , Dental Enamel/drug effects , Dentin Sensitivity/prevention & control , Tooth Bleaching Agents/chemistry
2.
Acta cir. bras ; 30(12): 852-857, Dec. 2015. graf
Article in English | LILACS | ID: lil-769504

ABSTRACT

ABSTRACT PURPOSE: To evaluate the effects of the low-level laser therapy applying Laser on the tissue repair in ulcer carriers due to diabetes. METHODS: Sixteen type II diabetic patients, ulcer carriers in the lower limbs, participated in the research from which eight were in the control group and eight were submitted to the low-level laser therapy with a pulsed wave form, visible ray, wave length of 632.8 nm, 30 mW peak power, (Laser - HTM). The application time was of 80 (4J/cm2) seconds. The application was punctual without contact (approximately 1mm of distance), the pen being held in a perpendicular position related to the wound, in equidistant points. There were 12 appointments, of which three were done weekly in alternated days. Photograph records and an application of the brief inventory of pain were done before and after 30 days of follow-up. RESULTS: There was a significant decrease in the size of the wound when compared to the control group (p<0.05). The pain was also reported as having an intense improvement in the treated group. CONCLUSION: The low-level laser treatment seems to be an efficient method, viable, painless and of low costs concerning the tissue repair ulcers in a diabetic foot.


Subject(s)
Humans , Diabetic Foot/radiotherapy , Foot Ulcer/radiotherapy , Low-Level Light Therapy/methods , /complications , Pain Measurement , Sodium Chloride/therapeutic use , Wound Healing/radiation effects
3.
Pesqui. vet. bras ; 35(1): 95-98, 01/2015. tab, graf
Article in English | LILACS | ID: lil-746559

ABSTRACT

The study aimed to compare the effects of intraosseous infusion of lactated Ringer's and 0.9% sodium chloride solutions on the electrolytes and acid-base balance in pigeons submitted to humerus osteosynthesis. Eighteen pigeons were undergoing to isoflurane anesthesia by an avalvular circuit system. They were randomly assigned into two groups (n=9) receiving lactated Ringer's solution (LR) or 0.9% sodium chloride (SC), in a continuous infusion rate of 20mL/kg/h, by using an intraosseous catheter into the tibiotarsus during 60-minute anesthetic procedure. Heart rate (HR), and respiratory rate (RR) were measured every 10 min. Venous blood samples were collected at 0, 30 and 60 minutes to analyze blood pH, PvCO2, HCO3 -, Na+ and K+. Blood gases and electrolytes showed respiratory acidosis in both groups during induction, under physical restraint. This acidosis was evidenced by a decrease of pH since 0 min, associated with a compensatory response, observed by increasing of HCO3 - concentration, at 30 and 60 min. It was not observed any changes on Na+ and K+ serum concentrations. According to the results, there is no reason for choosing one of the two solutions, and it could be concluded that both fluid therapy solutions do not promote any impact on acid-base balance and electrolyte concentrations in pigeons submitted to humerus osteosynthesis...


O presente estudo avaliou os efeitos da infusão das soluções de Ringer lactato ou cloreto de sódio 0,9%, no equilíbrio ácido-base e hidroeletrolítico de pombos submetidos à osteossíntese de úmero. Foram utilizados 18 animais, os quais foram submetidos à anestesia por isofluorano, e mantidos em circuito avalvular durante o período anestésico (60 min). Os animais foram distribuídos aleatoriamente em dois grupos (n=9) recebendo Ringer lactato (LR) ou cloreto de sódio 0,9% (SC), administradas na taxa de 20mL/kg/h pela via intraóssea (tibiotarso). Foram monitoradas as frequências cardíaca e respiratória a cada 10 minutos e colhidas amostras sanguíneas venosas aos 0, 30 e 60 min de anestesia, obtendo-se a partir destas, valores de pH sanguíneo, bicarbonato (HCO3), pressão venosa de CO2 (PvCO2), sódio (Na+) e potássio (K+). Os valores referentes ao equilíbrio ácido-base indicam que houve acidose respiratória em ambos os grupos, a qual foi decorrente do processo de indução sob contenção física, caracterizada por diminuição no pH desde o 0 min, associado ao aumento compensatório nos valores de HCO3 -, nos momentos 30 e 60 min. No entanto, no que se refere aos valores obtidos de Na+ e K+ séricos, durante a infusão de ambos os fluidos, não foram observadas alterações que justifiquem a predileção por alguma destas soluções. Diante destes resultados conclui-se que a escolha entre uma das soluções avaliadas não promoveu impacto sob o equilíbrio ácido-base e hidroeletrolítico de pombos submetidos a osteossíntese de úmero...


Subject(s)
Animals , Acid-Base Equilibrium , Sodium Chloride/therapeutic use , Columbidae/surgery , Fracture Fixation, Internal/veterinary , Humeral Fractures/veterinary , Water-Electrolyte Balance , Anesthesia, Inhalation/veterinary , Isoflurane/administration & dosage
4.
Acta cir. bras ; 29(7): 429-437, 07/2014. tab, graf
Article in English | LILACS | ID: lil-714573

ABSTRACT

PURPOSE: To evaluate the healing of skin wounds induced experimentally in rats using a crystalline cellulose membrane (Veloderm(r)). METHODS: Thirty-two rats were divided into two groups: control group (CG) wounds treated with a solution of 0.9% sodium chloride and Veloderm(r) group (VG) wounds treated with a crystalline cellulose membrane. The rats were evaluated at different times over twenty-six days. RESULTS: Weight loss was observed in the animals from both groups in the early stages, with greater weight in the VG animals at the end. Times of predominant hypothermia, pink color of the wound in both groups over all time points, increased granulation tissue in the CG animals, the presence of slight oozing from the wound and feature in the VG animals, more serous exudation of the bloody feature, greater wound contraction and pain in the CG animals and an absence of pain and earlier complete wound healing in the VG rats were also observed. CONCLUSION: The crystalline cellulose membrane is effective in the treatment of wounds in rats, easy to use, protects and maintains the humidity of the wound, decreases pain, eases the visualization and control of the evolution of the lesion. .


Subject(s)
Animals , Male , Polysaccharides/therapeutic use , Skin/drug effects , Skin/injuries , Wound Healing/drug effects , Cellulose/therapeutic use , Exudates and Transudates , Granulation Tissue , Rats, Wistar , Reproducibility of Results , Sodium Chloride/therapeutic use , Time Factors , Treatment Outcome , Wound Healing/physiology
5.
Arch. argent. pediatr ; 111(4): 281-287, ago. 2013. ilus, tab
Article in Spanish | LILACS | ID: lil-694644

ABSTRACT

Introducción. Las soluciones hipotónicas se han vinculado a la producción de hiponatremia iatrogénica. Objetivos. Evaluar las variaciones en el sodio sérico (NaS) tras la administración de una solución de mantenimiento intravenosa isotónica (NaCl al 0,9% en dextrosa al 5%) en comparación con una solución de mantenimiento hipotónica (NaCl al 0,45% en dextrosa al 5%). Material y métodos. Ensayo clínico aleatorizado, doble ciego y controlado. Se enrolaron pacientes pediátricos con una estadía esperada en la unidad de cuidados intensivos mayor de 24 horas, NaS normal y líquidos intravenosos > 80% de los líquidos totales de mantenimiento. La concentración sérica de Na se midió antes de colocar la solución de mantenimiento y al reducir la administración de ésta a < 80% del total del aporte. Resultados. Se incorporaron 63 pacientes, que fueron asignados en forma aleatoria a recibir una solución de mantenimiento hipotónica (n= 32) o isotónica (n= 31). Las características basales fueron similares en ambos grupos. No hubo diferencias con respecto a la cantidad de solución administrada (grupo hipotónico 865 ± 853 ml; grupo isotónico 778 ± 649 ml, p= 0,654) o el tiempo de infusión (grupo hipotónico: 24 ± 10,8 horas; grupo isotónico: 27,6 ± 12,8 horas, p= 0,231). Se encontró una diferencia en el NaS luego de la administración de las soluciones de mantenimiento (grupo hipotónico: 137,8 ± 4,3 mmol/L; grupo isotónico: 140,0 ± 4,1 mmol/L, p= 0,04). Ninguna de las dos soluciones de mantenimiento aumentó el riesgo de hiponatremia (Na 145 mmol/L). Conclusiones. Ambas soluciones de mantenimiento, en 24 horas de infusión, no aumentaron el riesgo de producir hiponatremia iatrogénica.


Introduction. Hypotonic fluids have been associated with the development of iatrogenic hyponatremia. Objectives. To assess variations in serum sodium (sNa) following the intravenous administration of isotonic maintenance fuids (0.9% NaCl/5% dextrose) compared to hypotonic maintenance fuids (0.45% NaCl/5% dextrose). Material and Methods. Randomized, controlled, double-blind clinical trial. Pediatric patients with an expected length of stay in the intensive care unit of more than 24 hours were enrolled, with normal serum Na, and IV fuids >80% of total maintenance fuids. Serum Na level was measured before administering maintenance fuids and when reducing the administration to <80% of total fuids. Results. The study included 63 patients who were randomly assigned to receive hypotonic (n= 32) or isotonic (n= 31) maintenance fuids. Baseline characteristics were similar in both groups. There were no differences in terms of volume of fuid administered (hypotonic group: 865 ± 853 mL; isotonic group: 778 ± 649 mL; p= 0.654) or infusion duration (hypotonic group: 24 ± 10.8 hours; isotonic group: 27.6 ± 12.8 hours; p= 0.231). A difference was found in the serum Na following the administration of maintenance fuids (hypotonic group: 137.8 ± 4.3 mmol/L; isotonic group: 140.0 ± 4.1 mmol/L, p= 0.04). None of these two maintenance fuids increased the risk of hyponatremia (Na 145 mmol/L). Conclusions. Neither hypotonic nor isotonic maintenance fluids increased the risk of developing iatrogenic hyponatremia with the 24 hour infusion.


Subject(s)
Female , Humans , Infant , Male , Critical Illness/therapy , Sodium Chloride/administration & dosage , Double-Blind Method , Hypotonic Solutions/therapeutic use , Infusions, Intravenous , Prospective Studies , Saline Solution, Hypertonic/therapeutic use , Sodium Chloride/therapeutic use , Sodium/blood
6.
Arch. argent. pediatr ; 111(4): 281-7, ago. 2013.
Article in Spanish | LILACS, BINACIS | ID: biblio-1159560

ABSTRACT

INTRODUCTION: Hypotonic fluids have been associated with the development of iatrogenic hyponatremia. OBJECTIVES: To assess variations in serum sodium (sNa) following the intravenous administration of isotonic maintenance fluids (0.9


dextrose) compared to hypotonic maintenance fluids (0.45


dextrose). MATERIAL AND METHODS: Randomized, controlled, double-blind clinical trial. Pediatric patients with an expected length of stay in the intensive care unit of more than 24 hours were enrolled, with normal serum Na, and IV fluids >80


of total maintenance fluids. Serum Na level was measured before administering maintenance fluids and when reducing the administration to <80


of total fluids. RESULTS: The study included 63 patients who were randomly assigned to receive hypotonic (n= 32) or isotonic (n= 31) maintenance fluids. Baseline characteristics were similar in both groups. There were no differences in terms of volume of fluid administered (hypotonic group: 865 ± 853 mL; isotonic group: 778 ± 649 mL; p= 0.654) or infusion duration (hypotonic group: 24 ± 10.8 hours; isotonic group: 27.6 ± 12.8 hours; p= 0.231). A difference was found in the serum Na following the administration of maintenance fluids (hypotonic group: 137.8 ± 4.3 mmol/L; isotonic group: 140.0 ± 4.1 mmol/L, p= 0.04). None of these two maintenance fluids increased the risk of hyponatremia (Na 145 mmol/L). CONCLUSIONS: Neither hypotonic nor isotonic maintenance fluids increased the risk of developing iatrogenic hyponatremia with the 24 hour infusion.


Subject(s)
Sodium Chloride/administration & dosage , Critical Illness/therapy , Sodium Chloride/therapeutic use , Prospective Studies , Female , Humans , Infusions, Intravenous , Infant , Male , Double-Blind Method , Saline Solution, Hypertonic/therapeutic use , Hypotonic Solutions/therapeutic use , Sodium/blood
7.
Rev. bras. anestesiol ; 63(3): 258-261, maio-jun. 2013. ilus, tab
Article in Portuguese | LILACS | ID: lil-675842

ABSTRACT

JUSTIFICATIVA E OBJETIVO: Comparar o efeito da administração profilática de solução salina normal com o efeito hipotensor de propofol em pacientes do sexo feminino programadas para procedimentos ginecológicos. MÉTODO: Foram randomicamente alocadas em dois grupos 69 pacientes, ASA I-II. O Grupo 1 recebeu 5 mL.kg-1 de solução salina a 0,9% 10 minutos antes da indução e o Grupo 2 não recebeu nada (controle). A anestesia foi induzida com propofol e fentanil e depois mantida com propofol e remifentanil. As variáveis hemodinâmicas foram mensuradas pré- e pós-indução da anestesia geral. RESULTADOS: Após a indução, ambos os grupos apresentaram queda significativa da pressão arterial média (p < 0,001) e redução também significativa da frequência cardíaca (p < 0,02 no grupo de estudo e p < 0,001 no grupo de controle). A pressão arterial média pré-indução teve uma queda de mais de 25% em 35% dos pacientes do grupo controle em comparação com apenas 17% dos pacientes que receberam a solução salina (p < 0,04). CONCLUSÃO: A administração profilática de solução salina pode diminuir a porcentagem de pacientes que apresentam queda significativa da pressão arterial após a indução de propofol em anestesia geral.


BACKGROUND AND OBJECTIVE: To compare the effect of prophylactic administration of normal saline against the hypotensive effect of propofol in female patients booked for gynecological procedures. METHOD: Sixty nine ASA (I, II) patients were randomly allocated into two groups, group 1 received 5 mL.kg-1 of 0.9% normal saline 10 minutes before induction, whereas group 2 received nothing (control). Anesthesia was induced with propofol and fentanyl then maintained with propofol and remifentanil. We measured hemodynamic variables pre and post general anesthesia induction. RESULTS: Both groups had significant drops in post induction mean arterial blood pressure (P < 0.001). Also both groups had significant drops in post induction heart rate ((P < 0.02 in sample group and P < 0.001 in control group), and 35% of patients in the control group had more than 25% drop in the pre induction mean arterial blood pressure, compared with only 17% of patients in the saline group (P < 0.04). CONCLUSION: The prophylactic administration of normal saline could decrease the percentage of patients who had a significant drop in their blood pressure after propofol induction of general anesthesia.


JUSTIFICATIVA Y OBJETIVO: Comparar el efecto de la administración profiláctica de solución salina normal con el efecto hipotensor de propofol en pacientes del sexo femenino programadas para procedimientos ginecológicos. MÉTODO: Sesenta y nueve pacientes con ASA I-II fueron ubicados aleatoriamente en dos grupos. El Grupo 1 recibió 5 mL.kg-1 de solución salina al 0,9% 10 minutos antes de la inducción y el Grupo 2 no recibió nada. La anestesia fue inducida con propofol y fentanilo y después se mantuvo con propofol y remifentanilo. Las variables hemodinámicas fueron mensuradas antes y después de la inducción de la anestesia general. RESULTADOS: Después de la inducción, ambos grupos presentaron una caída significativa de la presión arterial promedio (p < 0,001) y una reducción también significativa de la frecuencia cardíaca (p < 0,02 en el grupo de estudio y p < 0,001 en el grupo de control). La presión arterial promedio pre inducción tuvo una caída de más del 25% en 35% de los pacientes del grupo control en comparación con solamente un 17% de los pacientes que recibieron la solución salina (p < 0,04). CONCLUSIÓN: La administración profiláctica de la solución salina normal puede disminuir el porcentaje de pacientes que presentan una caída significativa de la presión arterial después de la inducción de propofol en la anestesia general.


Subject(s)
Female , Humans , Anesthesia, General , Anesthetics, Intravenous/adverse effects , Blood Pressure/drug effects , Gynecologic Surgical Procedures , Hypotension/chemically induced , Hypotension/prevention & control , Propofol/adverse effects , Sodium Chloride/therapeutic use , Prospective Studies , Single-Blind Method
8.
Braz. dent. j ; 24(3): 188-193, May-Jun/2013. tab, graf
Article in English | LILACS | ID: lil-681867

ABSTRACT

This study investigated the expression of extracellular matrix glycoproteins tenascin (TN) and fibronectin (FN) in pulp repair after capping with calcium hydroxide (CH), following different hemostasis protocols. Class I cavities with a pulp exposure were prepared in 42 human third molars scheduled for extraction. Different hemostatic agents (0.9% saline solution, 5.25% sodium hypochlorite and 2% chlorhexidine digluconate) were used and pulps were capped with CH cement. After 7, 30 or 90 days, teeth were extracted, formalin-fixed, and prepared for immunohistochemical technique. Hemostatic agents did not influence the expression of TN and FN. Both glycoproteins were found in the entire the pulp tissue and around collagen fibers, but were absent in the mineralized tissues. In the predentin, TN showed positive immunostaining and FN had a variable expression. Within 7 days post-treatment, a slightly more pronounced immunostaining on the pulp exposure site was observed. Within 30 days, TN and FN demonstrated a positive expression around the dentin barrier and at 90 days, a thin and linear expression of TN and FN was delimitating the reparative dentin. In conclusion, hemostatic agents did not influence TN and FN expression. Immunostaining for TN and FN was seen in different regions and periods, demonstrating their role in pulp repair.


Este estudo investigou a expressão das glicoproteínas Tenascina (TN) e Fibronectina (FN) da matriz extracelular no reparo pulpar após capeamento com hidróxido de cálcio (HC), seguindo diferentes protocolos de hemostasia. Cavidades de classe I com exposição pulpar foram preparadas em 42 terceiros molares humanos indicados para extração. Diferentes agentes hemostáticos (solução salina a 0,9%, hipoclorito de sódio a 5,25% e clorexidina a 2%) foram usados e as polpas foram capeadas com cimento de HC. Após 7, 30 ou 90 dias, os dentes foram extraídos, fixados em formalina e preparados para análise imunoistoquímica. Os agentes hemostáticos não influenciaram a expressão de TN e FN. Ambas glicoproteínas foram encontradas em todo tecido pulpar, ao redor das fibras colágenas e estiveram ausentes nos tecidos mineralizados. Na pré-dentina, a TN mostrou forte imunoexpressão e a FN teve uma expressão variável. Após 7 dias, foi observada uma expressão levemente mais pronunciada no lugar da exposição pulpar. Aos 30 dias, a TN e a FN demonstraram uma expressão mais forte sob a barreira dentinária e aos 90 dias, uma expressão fina e linear da TN e FN apresentava-se delimitando a dentina reparativa. Em conclusão, os agentes hemostáticos não influenciaram e expressão da TN e da FN. A imunoexpressão da TN e FN foi observada em diferentes regiões e períodos, demonstrando o seu papel no reparo pulpar.


Subject(s)
Adult , Humans , Young Adult , Dental Pulp Capping , Fibronectins/analysis , Hemostatics/therapeutic use , Pulp Capping and Pulpectomy Agents/therapeutic use , Tenascin/analysis , Bisphenol A-Glycidyl Methacrylate/chemistry , Calcium Hydroxide/therapeutic use , Chlorhexidine/analogs & derivatives , Chlorhexidine/therapeutic use , Collagen/analysis , Composite Resins/chemistry , Dental Pulp Exposure/therapy , Dental Pulp/chemistry , Dental Restoration, Permanent/methods , Dentin, Secondary/chemistry , Dentin/chemistry , Follow-Up Studies , Sodium Chloride/therapeutic use , Sodium Hypochlorite/therapeutic use , Tooth Extraction
9.
Int. braz. j. urol ; 39(1): 37-45, January-February/2013. tab, graf
Article in English | LILACS | ID: lil-670374

ABSTRACT

Objective: During partial nephrectomy, renal hypothermia has been shown to decrease ischemia induced renal damage which occurs from renal hilar clamping. In this study we investigate the infusion rate required to safely cool the entire renal unit in a porcine model using retrograde irrigation of iced saline via dual-lumen ureteral catheter. Materials and Methods: Renal cortical, renal medullary, bowel and rectal temperatures during retrograde cooling in a laparoscopic porcine model were monitored in six renal units. Iced normal saline was infused at 300 cc/hour, 600 cc/hour, 1000 cc/hour and gravity (800 cc/hour) for 600 seconds with and without hilar clamping. Results: Retrograde cooling with hilar clamping provided rapid medullary renal cooling and significant hypothermia of the medulla and cortex at infusion rates ≥ 600 cc/hour. With hilar clamping, cortical temperatures decreased at -0.9° C/min. reaching a threshold temperature of 26.9° C, and medullary temperatures decreased at -0.90 C/min. reaching a temperature of 26.1° C over 600 seconds on average for combined data at infusion rates ≥ 600 cc/hour. The lowest renal temperatures were achieved with gravity infusion. Without renal hilum clamping, retrograde cooling was minimal at all infusion rates. Conclusions: Significant renal cooling by gravity infusion of iced cold saline via a duel lumen catheter with a clamped renal hilum was achieved in a porcine model. Continuous retrograde irrigation with iced saline via a two way ureteral catheter may be an effective method to induce renal hypothermia in patients undergoing robotic assisted and/or laparoscopic partial nephrectomy. .


Subject(s)
Animals , Hypothermia, Induced/methods , Ischemia/prevention & control , Kidney/blood supply , Nephrectomy/methods , Sodium Chloride/therapeutic use , Constriction , Kidney/injuries , Models, Animal , Reference Values , Reproducibility of Results , Swine , Temperature , Time Factors , Therapeutic Irrigation/methods , Urinary Catheterization/methods
10.
Arq. bras. cardiol ; 99(6): 1129-1134, dez. 2012. tab
Article in Portuguese | LILACS | ID: lil-662373

ABSTRACT

FUNDAMENTO: A exposição ao meio de contraste radiográfico pode causar comprometimento agudo da função renal. Há evidências limitadas e conflitantes de que a hidratação com bicarbonato de sódio previne a Nefropatia Induzida por Contraste (NIC) em pacientes submetidos a cateterismo cardíaco. OBJETIVO: O presente estudo teve como objetivo determinar se o bicarbonato de sódio é superior à hidratação com soro fisiológico para evitar a nefropatia em pacientes de risco submetidos a cateterismo cardíaco. MÉTODOS: Trezentos e um pacientes submetidos a intervenção coronariana percutânea ou angiografia coronariana com creatinina sérica > 1,2 mg/dL ou Taxa de Filtração Glomerular (TFG) < 50 mL/min, foram randomizados para receber hidratação com bicarbonato de sódio a partir de 1 hora antes do procedimento, e 6 horas após o procedimento, ou hidratação com solução salina a 0,9%. A NIC foi definida como um aumento de 0,5 mg/dL na creatinina em 48h. RESULTADOS: Dezoito pacientes (5,9%) desenvolveram nefropatia induzida por contraste: 9 pacientes no grupo do bicarbonato (6,1%) e 9 pacientes no grupo da solução salina (6,0%), p = 0,97. A variação na creatinina sérica foi semelhante em ambos os grupos, 0,01 ± 0,26 mg/dL no grupo do bicarbonato, e 0,01 ± 0,35 mg/dL no grupo da solução salina, p = 0,9. Não foi observada diferença estatística entre a alteração na taxa de filtração glomerular (0,89 ± 9 mL/ min vs. 2,29 ± 10 mL/min, p = 0,2, grupo do bicarbonato e grupo da solução salina, respectivamente). CONCLUSÃO: A hidratação com bicarbonato de sódio não foi superior ao soro fisiológico na prevenção a nefropatia induzida pelo contraste, em pacientes de risco submetidos a cateterismo cardíaco.


BACKGROUND: Radiographic contrast media exposition can cause acute renal function impairment. There is limited and conflicting evidence that hydration with sodium bicarbonate prevents contrast-induced nephropathy (CIN) in patients undergoing cardiac catheterization. OBJECTIVE: The present study was aimed at determining whether sodium bicarbonate is superior to hydration with saline to prevent nephropathy in patients at risk undergoing cardiac catheterization. METHODS: Three hundred and one patients undergoing coronary angiography or percutaneous coronary intervention with serum creatinine > 1.2mg/dL or glomerular filtration rate (GFR) < 50ml/min were randomized to receive hydration with sodium bicarbonate starting 1 hour before the procedure and 6 hours after the procedure, or hydration with 0.9% saline. CIN was defined as an increase of 0.5mg/dL in creatinine in 48h RESULTS: Eighteen patients (5.9%) developed contrast induced nephropathy: 9 patients in the bicarbonate group (6.1%) and 9 patients in the saline group (6.0%), p = 0.97. The change in serum creatinine was similar in both groups, 0.01 ± 0.26 mg/dL in the bicarbonate group and 0.01 ± 0.35 mg/dL in the saline group, p = 0.9. No statistical difference was observed between the change in glomerular filtration rate (0.89 ± 9 ml/min vs. 2.29 ± 10 ml/min, p = 0.2 bicarbonate group and saline group, respectively). CONCLUSION: Hydration with sodium bicarbonate was not superior to saline to prevent contrast media induced nephropathy in patients at risk undergoing cardiac catheterization.


Subject(s)
Aged , Female , Humans , Male , Middle Aged , Cardiac Catheterization , Contrast Media/adverse effects , Fluid Therapy/methods , Kidney Diseases/chemically induced , Kidney Diseases/prevention & control , Sodium Bicarbonate/therapeutic use , Creatinine/blood , Glomerular Filtration Rate/drug effects , Risk Factors , Statistics, Nonparametric , Sodium Chloride/therapeutic use , Time Factors , Treatment Outcome
11.
Journal of Korean Academy of Nursing ; : 791-798, 2012.
Article in Korean | WPRIM | ID: wpr-166595

ABSTRACT

PURPOSE: The purpose of this study was to analyze the effectiveness of saline solution vs. heparinized-saline for maintenance of arterial lines and to detect changes in platelet and aPTT as physiological indexes. METHODS: In this nonequivalent control group, non-synchronized, double-blind study the effects of heparinized and saline solution on the maintenance of arterial lines were compared. Fifty five patients received the heparinized solution and fifty nine patients received the saline solution. All patients who had surgery in K-university hospital between September and December 2011 were eligible for participation in the study. RESULTS: There was no statistically significant difference between the saline and the heparin group in the maintenance time of the arterial lines or the number of irrigations. There was no statistically significant difference between the groups in changes in the number of platelets and aPTT for interaction between the groups and time intervals. CONCLUSION: The results indicate that saline solution can be used as an irrigation solution for the maintenance of arterial lines of adult surgical patients, rather than heparinized-saline, in view of potential risk factors in the use of heparin.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Anticoagulants/therapeutic use , Central Nervous System Diseases/surgery , Digestive System Diseases/surgery , Double-Blind Method , Heparin/therapeutic use , Musculoskeletal Diseases/surgery , Partial Thromboplastin Time , Platelet Count , Respiratory Tract Diseases/surgery , Risk Factors , Sodium Chloride/therapeutic use , Vascular Access Devices
12.
Yonsei Medical Journal ; : 859-862, 2012.
Article in English | WPRIM | ID: wpr-93566

ABSTRACT

Cerebral salt wasting is characterized by inappropriate natriuresis and volume contraction with associated cerebral pathology. It is distinct from the syndrome of inappropriate antidiuretic hormone secretion, which is characterized by inappropriate retention of free water. We report a patient with a porencephalic cyst who developed cerebral salt wasting. His initial treatment was supplementation of water and salt, which did not improve natriuresis or volume contraction. Fludrocortisone administration effectively managed the cerebral salt wasting.


Subject(s)
Adolescent , Humans , Male , Fludrocortisone/therapeutic use , Hyponatremia/drug therapy , Natriuresis/physiology , Sodium Chloride/therapeutic use
13.
Acta cir. bras ; 26(1): 51-57, jan.-fev. 2011. ilus, tab
Article in English | LILACS | ID: lil-572234

ABSTRACT

Purpose: To compare the effects of vitamin E and 1 percent methylen blue solutions on prevention of experimentally induced adhesions in rats. Methods: Thirty seven female Spraque Dawley rats were randomized into four groups. First group was kept as sham operated group. An adhesion model was constituted on the left uterine horn of the other groups. The lesion areas of rats from the second, the third and the fourth groups were coated with 2 ml 0.9 percent saline solution (C group), 10 mg vitamin E (VE group) and 1 percent methylen blue solutions (MB group), respectively. Results: Histopathologically, adhesion scores, mononuclear cell infiltration, oedema and fibrosis were more prominent in the MB group compared with C and VE groups. There were no significant differences between the groups in tissue glutathione peroxidase (GPx), catalase (CAT) activities and glutation (GSH) level, these parameters were slightly increased in group with VE supplementation though. The administration of VE and MB significantly decreased NO (P<0.01) levels when compared to the C group. The level of malondialdehyde (MDA) in the VE group was significantly lower (P<0.05) than those of the Sh and C groups. Conclusion: Intraperitoneal methylen blue solutions treatments were more effective according to vitamin E in preventing the formation of intra-abdominal adhesion in a rat uterine horn model.


Objetivo: Comparar os efeitos da vitamina E e 1 por cento da solução de azul de metileno na prevenção de aderências induzidas em ratos. Métodos: Trinta e sete ratos fêmeas Spraque Dawley foram distribuídos em quatro grupos. O primeiro grupo foi mantido como grupo sham. O modelo de aderência foi realizado no corno uterino esquerdo nos outros grupos. As áreas da lesão dos ratos do segundo, terceiro e quarto grupos foram revestidas com 2 ml de solução salina 0,9 por cento (Grupo C), 10 mg de vitamina E (Grupo VE) e solução de azul de metileno 1 por cento (Grupo MB), respectivamente. Resultados: Histopatologicamente, o escore das aderências, infiltração celular mononuclear, edema e fibrose foram mais proeminentes no grupo MB em comparação aos grupos C e VE. Não houve diferença significante entre os grupos na peroxidase da glutatione do tecido (GPx), atividade da catalase (CAT) e o nível de glutation (GSH). Estes parâmetros foram ligeiramente aumentados no grupo com suplemento da VE. A administração da VE e do MB diminuiu significantemente os níveis quando quando comparada ao Grupo C. O nível de malondialdeído no grupo VE foi significantemente mais baixo do que nos grupos sham e C. Conclusão: A administração intraperitoneal da solução de azul de metileno foi mais eficaz de acordo com a vitamina E na prevenção de aderências intra-abdominais no corno uterino de ratos.


Subject(s)
Animals , Female , Rats , Methylene Blue/therapeutic use , Postoperative Complications/prevention & control , Uterine Diseases/prevention & control , Vitamin E/therapeutic use , Vitamins/therapeutic use , Catalase/analysis , Glutathione Peroxidase/analysis , Glutathione/analysis , Lipid Peroxidation , Malondialdehyde/analysis , Nitric Oxide/analysis , Postoperative Complications/pathology , Random Allocation , Rats, Sprague-Dawley , Sodium Chloride/therapeutic use , Tissue Adhesions/etiology , Tissue Adhesions/pathology , Tissue Adhesions/prevention & control , Uterine Diseases/etiology , Uterine Diseases/metabolism
14.
Rev. cuba. farm ; 44(4): 465-475, oct.-dic. 2010.
Article in Spanish | LILACS | ID: lil-584550

ABSTRACT

Se desarrolló una formulación para uso oftálmico, que contenía cloruro de sodio al 5 por ciento, estable desde el punto de vista físico, químico y microbiológico. Se realizaron los estudios de formulación correspondientes, seleccionándose la composición y procedimiento tecnológico más adecuados. Además, se estudió la efectividad antimicrobiana de los preservativos antimicrobianos empleados según se establece en la Farmacopea de los Estados Unidos 30 y se comprobó la seguridad del uso de este medicamento a través de los resultados del ensayo de irritabilidad oftálmica. Se elaboraron 3 lotes del medicamento y se envasaron en frascos plásticos de polietileno de baja densidad con tapa de polipropileno de alta densidad y se almacenaron a temperatura ambiente durante 24 meses; se estudió su estabilidad física y química por el método acelerado y de vida de estante. Se comprobó su estabilidad microbiológica a cada uno de los lotes elaborados, al inicio y final del estudio, según se establece en la Farmacopea de los Estados Unidos 30, y se obtuvieron resultados satisfactorios. Todos los resultados cumplieron con los límites de calidad establecidos en la literatura oficial para este tipo de forma farmacéutica, por lo que se concluyó que el medicamento desarrollado está correctamente formulado desde el punto de vista galénico con un tiempo de vida útil de 24 meses almacenado bajo las condiciones estudiadas, demostrado según el otorgamiento del certificado de registro por el organismo regulador (Centro Estatal para el Control de Medicamentos, CECMED). Finalmente el medicamento fue introducido al nivel industrial sin que se presentaran problemas tecnológicos


A formula for ophthalmic use was developed containing 5 percent sodium chloride stable from the physical, chemical and microbiological point of view. Studies of corresponding formulae were conducted selecting the more suitable composition and technological procedure. Also, the antimicrobial effectiveness of animicrobials preservatives used according to United States Pharmacopeia was studied demonstrating the safe use of this drug by the results of the ophthalmic irritability trial. Three batchs of this drug were elaborated packing in low density polyethylene plastic flasks with a high density polypropylene top stored at room temperature during 24 monhts and its physical and cchemical stability was studied y accelerated method and of shield-life. At onset and the end of study microbiological stability was demonstrate in each of batches made (30), according to USP with satisfactory results. All results fulfill with the established quality limits in official literature for this type of pharmaceutical way concluding that this developeddrug is appropriately formulated fro the doctoral point of view with a useful life time of 24 months stored under study conditions, demonstrated according to award of registry certificate by regulator institution (State Center for Drugs' Control, CECMED). Finally, the drug was introduced at industrial level without technological problems


Subject(s)
Chemistry, Pharmaceutical , Sodium Chloride/therapeutic use , Drug Stability , Ophthalmic Solutions
15.
J. bras. nefrol ; 32(3): 292-302, jul.-set. 2010. tab
Article in Portuguese | LILACS | ID: lil-562925

ABSTRACT

INTRODUÇÃO: A incidência da nefropatia por contraste tem aumentado simultaneamente ao aumento da sua utilização com fins diagnósticos e de intervenção terapêutica. A sua incidência na população geral é baixa, porém aumenta exponencialmente em pacientes com fatores de risco como diabetes e doença renal prévia. Várias estratégias têm sido utilizadas na tentativa de prevenir a nefropatia por contraste. Hidratação com solução fisiológica, contraste de baixa osmolalidade ou iso-osmolar e infusão de bicarbonato de sódio são consideradas como as mais eficazes. OBJETIVO: O objetivo deste trabalho é revisar a literatura pertinente sobre prevenção de nefropatia do contraste e estudar, de forma inicial, a eficácia da hidratação a base de bicarbonato de sódio a 1,3 por cento comparada à hidratação a base de cloreto de sódio a 0,9 por cento na prevenção da nefrotoxicidade do contraste em pacientes de alto risco para o seu desenvolvimento. MATERIAIS E MÉTODOS: Foi analisada a literatura por meio de busca sistemática no banco de dados PubMed usando as palavras-chave bicarbonato, nefrotoxicidade, contraste e insuficiência renal aguda e, adicionalmente, foram estudados 27 pacientes, portadores de diabetes mellitus e/ou doença renal crônica prévia e diagnosticados com algum tipo de câncer. RESULTADOS: Nenhum dos pacientes desenvolveu nefropatia do contraste, caracterizada como aumento de 0,5 mg/ dL e/ou de 25 por cento na creatinina basal. CONCLUSÃO: A revisão de literatura sugere fortemente que o uso de bicarbonato de sódio é eficaz na prevenção de nefropatia por contraste. Em relação ao estudo randomizado e controlado o soro fisiológico e o bicarbonato de sódio apresentaram eficácia similar quanto à prevenção de nefrotoxicidade do contraste. No entanto, o pequeno número de pacientes não permite conclusões definitivas.


INTRODUCTION: The incidence of contrast-induced nephropathy has increased simultaneously with the increase in contrast medium use in diagnostic and interventional procedures. The incidence of contrast-induced nephropathy in the general population is low, but increases exponentially in patients with risk factors, such as diabetes and chronic kidney disease. Several strategies have been used in order to prevent contrast-induced nephropathy. The most efficient strategies are saline hydration (0.9 percent or 0.45 percent), use of low-or iso-osmolality contrast medium, and sodium bicarbonate infusion. OBJECTIVE: The aim of this study was to review the pertinent literature and to assess the efficacy of hydration with 1.3 percent sodium bicarbonate compared with hydration with 0.9 percent saline solution in preventing contrastinduced nephropathy in high-risk patients. MATERIAL AND METHODS: A systematic search of the literature was conducted in PubMed by using the following keywords: bicarbonate, nephropathy, contrast medium, and acute kidney failure. In addition, 27 patients with diabetes and/or chronic kidney disease, diagnosed with some kind of cancer were randomized for study. RESULTS: None of the patients developed contrast-induced nephropathy characterized as a 0.5 mg/ dL-increase and/or a relative 25 percent-increase in baseline creatinine. CONCLUSIONS: The literature review strongly suggested that sodium bicarbonate is effective in preventing contrast-induced nephropathy. Regarding the randomized study, saline solution and bicarbonate solution had similar efficacy in preventing contrast-induced nephropathy. However, the small number of patients does not allow definite conclusions.


Subject(s)
Aged , Humans , Contrast Media/adverse effects , Kidney Diseases/chemically induced , Kidney Diseases/prevention & control , Sodium Bicarbonate/therapeutic use , Sodium Chloride/therapeutic use , Solutions
16.
Int. braz. j. urol ; 36(2): 183-189, Mar.-Apr. 2010. tab
Article in English | LILACS | ID: lil-548378

ABSTRACT

INTRODUCTION: Transurethral resection syndrome is an uncommon but potentially life threatening complication. Various irrigating solutions have been used, normal saline being the most physiological. The recent availability of bipolar cautery has permitted the use of normal saline irrigation. MATERIAL AND METHODS: In a randomized prospective study, we compared the safety and efficacy of bipolar cautery (using 0.9 percent normal saline irrigation) versus conventional monopolar cautery (using 1.5 percent glycine irrigation). Pre and postoperative hemoglobin (Hb) and hematocrit values were compared. Hemodynamics and arterial oxygen saturation were monitored throughout the study. Safety end points were changes in serum electrolytes, osmolarity and Hb/PCV (packed cell volume). Efficacy parameters were the International Prostate Symptom Score (IPSS) and Qmax (maximum flow rate in mL/sec) values. RESULTS: Mean preoperative prostate size on ultrasound was 60 ± 20cc. Mean resected weight was 17.6 ± 10.8 g (glycine) and 18.66 ± 12.1 g (saline). Mean resection time was 56.76 ± 14.51 min (glycine) and 55.1 ± 13.3 min (saline). The monopolar glycine group showed a greater decline in serum sodium and osmolarity (4.12 meq/L and 5.14 mosmol/L) compared to the bipolar saline group (1.25 meq/L and 0.43 mosmol/L). However, this was not considered statistically significant. The monopolar glycine group showed a statistically significant decline in Hb and PCV (0.97 gm percent, 2.83, p < 0.005) as compared to the bipolar saline group (0.55 gm percent and 1.62, p < 0.05). Patient follow- up (1,3,6 and 12 months postoperatively) demonstrated an improvement in IPSS and Qmax in both the groups. CONCLUSION: We concluded that bipolar transurethral resection of prostate is clinically comparable to monopolar transurethral resection of prostate with an improved safety profile. However, larger number of patients with longer follow up is essential.


Subject(s)
Humans , Male , Middle Aged , Prostate/surgery , Prostatic Hyperplasia/surgery , Sodium/blood , Transurethral Resection of Prostate/methods , Glycine Agents/therapeutic use , Glycine/metabolism , Postoperative Care , Preoperative Care , Potassium/blood , Prostatic Hyperplasia/blood , Prostatic Hyperplasia/pathology , Sodium Chloride/therapeutic use , Treatment Outcome , Therapeutic Irrigation/methods , Transurethral Resection of Prostate/adverse effects , Transurethral Resection of Prostate/standards
17.
An. bras. dermatol ; 84(3): 229-236, jul. 2009. ilus, tab
Article in English, Portuguese | LILACS | ID: lil-521746

ABSTRACT

FUNDAMENTOS: Na última década, as indicações de uso tópico de compostos com ácidos graxos essenciais (AGE-TG) para o tratamento de feridas aumentaram no Brasil, e houve declínio das indicações do açúcar. OBJETIVOS: Estudar o efeito da aplicação de solução fisiológica de cloreto de sódio a 0,9 por cento, de açúcar e de AGE-TG sobre feridas experimentalmente induzidas em ratos. MÉTODOS: Foi induzida uma ferida de 400 mm2 no dorso de cada rato Wistar, constituindo três grupos tratados separadamente com solução fisiológica de cloreto de sódio a 0,9 por cento, açúcar e AGE-TG. Todos os animais receberam curativo oclusivo sobre a lesão, trocado a cada 24 horas. As aferições realizadas em quatro momentos consistiram na determinação do percentual de redução das áreas das feridas, da reação inflamatória celular, da ordenação do colágeno e da densidade de colágeno dos tipos I e III nas cicatrizes. RESULTADOS: A cicatrização ocorreu igualmente nos grupos estudados, mas o açúcar modulou positivamente a reação inflamatória entre o 7º e 14º dias. No 20º dia, não houve diferenças na quantidade de colágeno dos tipos I e III entre os grupos tratados. CONCLUSÕES: As feridas cicatrizaram nos três grupos. O grupo açúcar apresentou uma modulação positiva da resposta inflamatória celular. Não houve diferenças na quantidade de colágeno dos tipos I e III ao final do experimento nos grupos tratados.


BACKGROUND: In the last 10 years, the use of essential fatty acids (EFA) compounds for the treatment of wounds has increased in Brazil, while there has been reducing indication for the use of sugar. OBJECTIVE: The aim of this study was to evaluate the response to saline, sugar and EFA on induced wounds in rats. METHODS: A wound of 400 mm2 was produced on the back of each Wistar rat. The rats were divided into three groups, each being treated with either saline, sugar or EFA. All the animals received a closed dressing on the wounds, changed daily. Measures were taken in four moments, and the values of wound area reduction by healing, cellular inflammatory response, collagen ordering and types I and III collagen density were assessed. RESULTS: The wound healing was equal in all the three groups, but sugar promoted an inflammatory response modulation between the 7th and 14th days. On the 20th post-operative day, there were no differences between the three treated groups concerning types I and III collagen. CONCLUSIONS: The wounds healed in the three groups. The sugar group promoted effective cellular inflammatory response modulation. There were no differences between all the treated groups regarding types I and III collagen at the end of this study.


Subject(s)
Animals , Male , Rats , Fatty Acids, Essential/therapeutic use , Fibrillar Collagens/biosynthesis , Sodium Chloride/therapeutic use , Sucrose/therapeutic use , Wound Healing/drug effects , Fibrillar Collagens/drug effects , Rats, Wistar , Time Factors
18.
Clinics ; 64(8): 735-741, 2009. graf, tab
Article in English | LILACS | ID: lil-523991

ABSTRACT

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.


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , Young Adult , Conjunctivitis, Viral/drug therapy , Eye Foreign Bodies/drug therapy , Self Medication , Boric Acids/therapeutic use , Brazil/epidemiology , Cross-Sectional Studies , Conjunctivitis, Viral/epidemiology , Emergency Service, Hospital , Eye Foreign Bodies/epidemiology , Home Nursing/statistics & numerical data , Milk, Human , Nonprescription Drugs/classification , Nonprescription Drugs/therapeutic use , Ophthalmology , Plant Extracts/therapeutic use , Self Medication/classification , Self Medication/statistics & numerical data , Sodium Chloride/therapeutic use , Young Adult
19.
Rev. chil. radiol ; 14(1): 14-19, 2008. ilus, tab
Article in Spanish | LILACS | ID: lil-516231

ABSTRACT

lleocolic intussusception is an important cause of acute abdomen in infants. When there is no surgical indication, reduction under fluorosco-pic vision has been the main radiologic treatment performed in our country. Ultrasound examination is broadly used as a diagnostic method but reports on local experiences with ultrasound for guidance in intussusception reduction have not been recorded. A series of five cases of successful hydrostatic reduction performed under ultrasonographic control is presented and images of different stages of the reduction process are shown. Our aim is to promote a change in monitoring procedures so as to avoid the use of ionizing radiation.


La invaginación ileocólica es una causa importante de abdomen agudo en lactantes y su tratamiento de elección en nuestro medio es la reducción bajo visión fluoroscópica, cuando no existe indicación quirúrgica. El ultrasonido es utilizado como método de diagnóstico y su uso como guía para la reducción de la invaginación no ha sido comunicado en nuestro medio. Se presenta una pequeña serie de 5 casos de reducciones hidrostáticas exitosas efectuadas bajo control ultrasonográfico y se muestran imágenes de ultrasonido características de las diferentes etapas de la desinvaginación, con el objeto de estimular el cambio de método de monitorización en este procedimiento, evitando el uso de radiación ionizante.


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Colonic Diseases/therapy , Colonic Diseases , Ileal Diseases/therapy , Ileal Diseases , Intussusception/therapy , Intussusception , Sodium Chloride/therapeutic use , Enema , Hydrostatic Pressure , Treatment Outcome
20.
Article in English | IMSEAR | ID: sea-45372

ABSTRACT

OBJECTIVE: To compare bowel preparation quality and patient tolerance of two common enema solutions for flexible sigmoidoscopy. MATERIAL AND METHOD: Three hundred adults were randomized to receive a hypertonic sodium chloride or hypertonic sodium phosphate enema regime, each consisting of two enemas administered 60 and 30 min before the procedure. Patients completed surveys on preparation comfort. Patients and endoscopist were blinded to the preparation used During the procedure, the endoscopist took pictures of the mucosa and intraluminal content. All pictures were later evaluated by a single doctor who graded the quality of the preparation. RESULTS: There were no serious complications during or following the procedures. The preparation quality was rated as excellent or good by 76.9% of the hypertonic sodium chloride group and 72.9% of the hypertonic sodium phosphate group (p = 0.423). The hypertonic sodium chloride enema was associated with more abdominal discomfort (p = 0.018). CONCLUSION: Both enemas were safe for all patients with no statistical difference between the qualities of the two bowel preparations. Both preparations performed their bowel-cleaning function well and were suitable for the preparation of patients before flexible sigmoidoscopy. The less expensive hypertonic sodium chloride solution may be an option for hospitals where budgetary considerations are important.


Subject(s)
Cathartics , Colon , Enema/methods , Female , Humans , Hypotonic Solutions , Magnesium Compounds , Male , Middle Aged , Sigmoidoscopy/methods , Sodium Chloride/therapeutic use
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