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1.
Bol. malariol. salud ambient ; 62(6): 1142-1146, dic. 2022. tab.
Article in Spanish | LILACS, LIVECS | ID: biblio-1426866

ABSTRACT

El brote reciente de viruela símica ha despertado el interés de la comunidad internacional por su creciente número de contagiados en países no endémicos. Entre sus síntomas se encuentran la fiebre, dolor de cabeza, fatiga, dolor muscular, exantema y linfadenoma. La cavidad bucal es el lugar en el que suelen aparecer los primeros signos de la enfermedad. Por tanto, el objetivo de este trabajo fue establecer las principales manifestaciones orales de la viruela del mono y enumerar algunas recomendaciones de prevención. Para ello, se hizo una revisión bibliográfica entre 2012 y 2022 en la base de datos PubMed, usando las palabras clave, en inglés, monkeypox, oral manifestation y transmission. Se garantizó que, de los 14 documentos seleccionados, al menos el 80%, fueran publicaron en 2022. Las manifestaciones orales más frecuentes fueron: úlcera eritematosa, vesículas-ulcerosas y las asociadas a linfadenopatía (disfagia, odinofagia y faringitis). Entre las recomendaciones se encuentran: uso de mascarilla N95 y visores faciales, lavado constante de manos y espacios y atención de contagiados solo por eventos agudos (urgencias). Aunque no se ha confirmado, es posible que el Tecovirimat sea de ayuda en pacientes con sintomatología grave. Se concluye que es necesario que los odontólogos sepan distinguir los signos orales de la enfermedad para que contribuyan a cortar la cadena de contagio y deriven prontamente a los sospechosos para que se hagan las pruebas diagnósticas y las terapias medicamentosas de manera oportuna(AU)


The recent outbreak of monkeypox has aroused the interest of the international community due to its growing number of infections in non-endemic countries. Its symptoms include fever, headache, fatigue, muscle pain, rash, and lymphadenoma. The oral cavity is the place where the first signs of the disease usually appear. Therefore, the objective of this work was to establish the main oral manifestations of monkeypox and list some prevention recommendations. For this, a bibliographic review was carried out between 2012 and 2022 in the PubMed database, using the keywords, in English, monkeypox, oral manifestation and transmission. It was guaranteed that, of the 14 selected documents, at least 80% would be published in 2022. The most frequent oral manifestations were: erythematous ulcer, ulcer-vesicles and those associated with lymphadenopathy (dysphagia, odynophagia and pharyngitis). Among the recommendations are: use of N95 mask and face visors, constant washing of hands and spaces, and attention to those infected only due to acute events (emergencies). Although it has not been confirmed, it is possible that Tecovirimat is helpful in patients with severe symptoms. It is concluded that it is necessary for dentists to know how to distinguish the oral signs of the disease so that they contribute to breaking the chain of contagion and promptly refer suspects to diagnostic tests and drug therapies in a timely manner(AU)


Subject(s)
Deglutition Disorders/prevention & control , Pharyngitis/prevention & control , Oral Ulcer/prevention & control , Dental Offices , Monkeypox/prevention & control , Lymphadenopathy/prevention & control , Review Literature as Topic
2.
Journal of Peking University(Health Sciences) ; (6): 289-293, 2022.
Article in Chinese | WPRIM | ID: wpr-936149

ABSTRACT

OBJECTIVE@#To explore the effectiveness and feasibility of dexamethasone combined with oxybuprocaine hydrochloride gel on the prevention of postoperative sore throat after nasal endoscopy.@*METHODS@#In the study, 60 patients with American Society of Anesthesiologist (ASA) physical statuses Ⅰ to Ⅱ, aged 18 to 72 years, scheduled for elective nasal endoscope surgery under general anesthesia requiring endotracheal intubation were randomly divided into dexamethasone combined with oxybuprocaine hydrochloride gel group (G group, n=30) and control group (C group, n=30). The patients in the G group received dexamethasone 0.1 mg/kg before induction and the oxybuprocaine gel was applied to the endotracheal catheter cuff and the front end within 15 cm. The patients in the C group received the same dose of saline and the saline was applied to the endotracheal catheter cuff and the front end within 15 cm. Then, all the patients in the two groups received the same induction and anesthesia maintainance. The operation time, anesthesia time, emergence time, extubation time and departure time were recorded. The intraoperative infusion volume, blood loss volume, propofol, remifentanil, rocuronium dosage were also recorded. The adverse reactions such as intraoperative hypotension, bradycardia and postoperative agitation were recorded. The postoperative sore throat score was recorded at the end of operation and 4 h, 8 h, 12 h, and 24 h after operation.@*RESULTS@#Compared with the C group, the emergence time [(8.4±3.9) min vs. (10.8±4.7) min], extubation time [(8.8±3.7) min vs. (11.9±4.8) min], and departure time [(20.0±5.3) min vs. (23.0±5.8) min] were significantly shorter, and the propofol dosage [(11.8±1.8) mg/kg vs. (15.9±4.6) mg/kg], remifentanil dosage [(10.9±4.7) μg/kg vs. (14.1±3.6) μg/kg] were significantly less in the G group, and there was no difference of rocuronium dosage in the two groups. Compared with the C group the incidence of intraoperative hypotension [10%(3/30) vs. 30%(9/30)], bradycardia [16.7%(5/30) vs. 20%(6/30)] and postoperative agitation [6.7%(2/30) vs. 23.3%(7/30)] were significantly lower in the C group. The postoperative sore throat score at the end of operation, 4 h, 8 h, 12 h and 24 h after operation in the G group were significantly lower than in the C group respectively [0 (0, 1) vs. 1 (1, 2), 0 (0, 0) vs. 1 (1, 2), 0 (0, 0) vs. 1 (1, 2), 0 (0, 0) vs. 1 (0.75, 1), 0 (0, 0) vs. 1 (0, 1)].@*CONCLUSION@#Dexamethasone combined with oxybuprocaine hydrochloride gel was effective and feasible on the prevention of postoperative sore throat after nasal endoscopy.


Subject(s)
Adolescent , Adult , Aged , Humans , Middle Aged , Young Adult , Bradycardia/drug therapy , Dexamethasone/therapeutic use , Endoscopy/adverse effects , Hypotension/drug therapy , Intubation, Intratracheal/adverse effects , Pain/drug therapy , Pharyngitis/prevention & control , Postoperative Complications/prevention & control , Procaine/analogs & derivatives , Propofol , Remifentanil , Rocuronium
3.
Rev. bras. anestesiol ; 66(3): 242-248, May.-June 2016. tab, graf
Article in English | LILACS | ID: lil-782883

ABSTRACT

ABSTRACT Postoperative sore throat is a common complication after endotracheal intubation. After tracheal intubation, the incidence of sore throat varies from 14.4% to 50%. The aim of the study was to compare between benzydamine hydrochloride gel, lidocaine 5% gel and lidocaine 10% spray on the endotracheal tube cuff as regards postoperative sore throat. The present study was carried out on 124 patients admitted to Alexandria university hospitals for lumbar fixation surgery requiring general anesthesia. Patients were randomly allocated into 4 groups. Benzydamine hydrochloride gel, 5% lidocaine hydrochloride gel, 10% lidocaine hydrochloride spray, or normal saline were applied on endotracheal tube cuffs before endotracheal intubation. The patients were examined for sore throat (none, mild, moderate, or severe) at 0, 1, 6, 12, and 24 h after extubation. The results were collected, analyzed and presented in table and figure. The highest incidence of postoperative sore throat occurred at 6 h after extubation in all groups. There was a significantly lower incidence of postoperative sore throat in the benzydamine group than 5% lidocaine gel, 10% lidocaine spray, and normal saline groups. The benzydamine group had significantly decreased severity of postoperative sore throat compared with the 10% lidocaine, 5% lidocaine, and normal saline groups at observation time point. Compared with the 5% lidocaine the 10% lidocaine group had significantly increased incidence and severity of postoperative sore throat after extubation. Compared with normal saline the 10% lidocaine group had increased incidence of postoperative sore throat. There were no significant differences among groups in local or systemic side effects. So in conclusion, benzydamine hydrochloride gel on the endotracheal tube cuff is a simple and effective method to reduce the incidence and severity of postoperative sore throat. Application of 10% lidocaine spray should be avoided because of worsening of postoperative sore throat where incidence increased but not the severity in relation to 5% lidocaine gel. Applying 5% lidocaine on the endotracheal tube cuff does not prevent postoperative sore throat but its application is better than lidocaine 10% spray or saline.


RESUMO A dor de garganta pós-operatória (DGPO) é uma complicação comum após a intubação traqueal. Em seguida a esse procedimento, a incidência de dor de garganta varia de 14,4 a 50%. O objetivo do estudo foi comparar os efeitos da aplicação de cloridrato de benzidamina em gel, lidocaína a 5% em gel e lidocaína a 10% em spray no balonete do tubo endotraqueal, no que diz respeito à dor de garganta pós-operatória. O presente estudo foi feito com 124 pacientes internados em hospitais universitários de Alexandria para cirurgia de fixação lombar que necessitavam de anestesia geral. Os pacientes foram aleatoriamente alocados em quatro grupos. Procedeu-se à aplicação de cloridrato de benzidamina em gel, cloridrato de lidocaína a 5% em gel, cloridrato de lidocaína a 10% em spray ou salina normal nos balonetes do TET antes da intubação endotraqueal. Os pacientes foram examinados para dor de garganta (nenhuma, leve, moderada ou intensa) a 0, uma, seis, 12 e 24 horas após a extubação. Os resultados foram coletados, analisados e apresentados em tabelas e figuras. A maior incidência de DGPO ocorreu seis horas após a extubação em todos os grupos. Houve incidência significativamente menor de DGPO no grupo de benzidamina versus grupos de lidocaína a 5% em gel, lidocaína a 10% em spray e salina normal. O grupo tratado com benzidamina exibiu redução significativa na intensidade da DGPO, em comparação com os grupos de lidocaína a 10%, lidocaína a 5% e salina normal no ponto no tempo de observação. Em comparação com lidocaína a 5%, o grupo tratado com lidocaína a 10% exibiu incidência e intensidade significativamente aumentadas na DGPO após a extubação. Em comparação com salina normal, o grupo tratado com lidocaína a 10% exibiu maior incidência de DGPO. Não foram observadas diferenças significativas entre grupos quanto a efeitos colaterais locais ou sistêmicos. Assim, em conclusão, o uso de cloridrato de benzidamina em gel no balonete do TET é um método simples e eficaz para reduzir a incidência e a gravidade da DGPO. Deve-se evitar a aplicação de lidocaína a 10% em spray, devido ao agravamento da DGPO, visto ter ocorrido aumento na incidência, mas não na severidade, em relação à lidocaína a 5% em gel. A aplicação de lidocaína a 5% no balonete do TET não impede a ocorrência da DGPO, mas a sua aplicação oferece melhores resultados do que lidocaína a 10% em spray, ou solução salina.


Subject(s)
Humans , Male , Female , Adult , Postoperative Complications/prevention & control , Benzydamine/therapeutic use , Intubation, Intratracheal/adverse effects , Lidocaine/therapeutic use , Severity of Illness Index , Administration, Inhalation , Nebulizers and Vaporizers , Benzydamine/administration & dosage , Pharyngitis/prevention & control , Treatment Outcome , Dose-Response Relationship, Drug , Gels/therapeutic use , Anesthetics, Local/administration & dosage , Anesthetics, Local/therapeutic use , Lidocaine/administration & dosage , Middle Aged , Anti-Inflammatory Agents/administration & dosage , Anti-Inflammatory Agents/therapeutic use
4.
Rev. bras. anestesiol ; 65(6): 450-454, Nov.-Dec. 2015. tab
Article in Portuguese | LILACS | ID: lil-769890

ABSTRACT

BACKGROUND: Laryngeal mask airway is still accompanied by complications such as sore throat. In this study, effects of three methods of reducing postoperative sore throat were compared with the control group. METHODS: 240 patients with ASA I, II candidates for cataract surgery were randomly divided into four same groups. No supplementary method was used in the control group. In the second, third and fourth groups, lidocaine gel, washing cuff before insertion, and washing mouth before removing laryngeal mask airway were applied, respectively. Anesthesia induction was done with fentanyl, atracurium, and propofol and maintained with propofol infusion. The incidence of sore throat was evaluated during the recovery, 3-4 h later and after 24 h using verbal analog scale. The data were analyzed by t-test, analysis of variance and chi-square using SPSS V11.5. RESULTS: Age, gender, duration of surgery and cuff pressure were the same in all the four groups. Incidence of sore throat at recovery room was highest in the control group (43.3%) and lowest in the washing mouth group (25%). However, no significant statistical difference was observed between these four groups (recovery, p = 0.30; discharge, p = 0.31; examination, p = 0.52). In this study, increased duration of operation had a significant relationship with the incidence of sore throat (p = 0.041). CONCLUSION: Sore throat is a common postoperative problem, but no special method has been found completely efficient yet. In this study, cuff washing, lidocaine gel, and mouth washing before removing laryngeal mask airway were not helpful for sore throat.


JUSTIFICATIVA: A máscara laríngea ainda é relacionada a complicações como a dor de garganta. Neste estudo, os efeitos de três métodos para reduzir a dor de garganta, no período pós-operatório, foram comparados com o grupo controle. MÉTODOS: Duzentos e quarenta candidatos,com estado físico ASA I-II, foram aleatoriamente divididos em quatro grupos iguais para a cirurgia de catarata.com estado físico ASA I-II, candidatos para a cirurgia de catarata foram aleatoriamente divididos em quatro grupos iguais. Nenhum método complementar foi usado no grupo controle. No segundo, terceiro e quarto grupos, os métodos utilizados foram: Aplicação de gel de lidocaína, lavagem do manguito antes da inserção e lavagem da boca antes de remover a máscara laríngea, respectivamente. A anestesia foi induzida com fentanil, atracúrio e propofol e mantida com propofol. A incidência de dor de garganta foi avaliada durante a recuperação, 3-4 h depois e após 24 h usando uma escala verbal analógica. Teste-t, análise de variância e teste do qui-quadrado foram usados para a análise dos dados por meio do programa estatístico SPSS V11.5. RESULTADOS: Idade, gênero, tempo de cirurgia e pressão do manguito foram semelhantes em todos os quatro grupos. Na sala de recuperação, a incidência de dor de garganta foi maior no grupo controle (43,3%) e mais baixa no grupo lavagem da boca (25%). No entanto, não houve diferença estatisticamente significante entre os quatro grupos (recuperação, p = 0,30; alta, p = 0,31; exame, p = 0,52). Neste estudo, o tempo mais longo de cirurgia apresentou relação significativa com a incidência de dor de garganta (p = 0,041). CONCLUSÃO: Dor de garganta é um problema pós-operatório comum, mas nenhum método em especial foi considerado totalmente eficiente. Neste estudo, a lavagem do manguito, a aplicação de gel de lidocaína e a lavagem de boca antes de remover a máscara laríngea não foram úteis para evitar a dor de garganta.


Subject(s)
Humans , Female , Aged , Postoperative Complications/prevention & control , Sodium Chloride/administration & dosage , Pharyngitis/prevention & control , Laryngeal Masks/adverse effects , Lidocaine/therapeutic use , Mouthwashes , Gels , Middle Aged
5.
Anaesthesia, Pain and Intensive Care. 2013; 17 (1): 18-21
in English | IMEMR | ID: emr-142490

ABSTRACT

To study and investigate the efficacy of intra-cuff alkalinized lidocaine in the prevention of the endotracheal tube [ETT] induced emergence phenomena in children.Fifty children, ages 6-12 years, ASA physical status I-II, scheduled for elective dental surgery under N2O free general anesthesia with an expected duration of 120 min or more, were randomly assigned one of the two groups [25 patients each]; lidocaine group in which the cuff of ETT was inflated with a mixture of lidocaine 2% and sodium bicarbonate 8.4% and the saline group, in which tube cuff was inflated with 0.9% saline solution.There were significant reduction in the incidence and severity [p=0.005 and p= 0.014] of cough at extubation and in the PACU [P=0.048 and P=0.014]. The incidence and severity of postoperative sore throat was also reduced in the lidocaine group compared to the saline group [p=0.025 and 0.031 respectively]. Moreover, there was a significant prolongation of the time to spontaneous ventilation before extubation in the lidocaine compared to the control group [16.4 +/- 3.1 min and 9.4 +/- 1.7 min respectively] with p value < 0.0001. Intra-cuff alkalinized lidocaine reduces the incidence of cough, sore throat, improved ETT tolerance and inducing smooth extubation in paediatric patients, but prolongs time to spontaneous ventilation before extubation


Subject(s)
Humans , Male , Female , Lidocaine/administration & dosage , Postoperative Complications/prevention & control , Anesthesia, General , Pharyngitis/prevention & control , Prospective Studies , Single-Blind Method
6.
Journal of Zanjan University of Medical Sciences and Health Services. 2008; 15 (61): 11-20
in Persian | IMEMR | ID: emr-112623

ABSTRACT

Tracheal intubation can result in trauma and nerve damage which may also account for postoperative throat symptoms such as hoarseness and dysphagia. The effects of beclomethasone inhaler and intravenous lidocaine in prevention of the above symptoms were documented in previous studies. The aim of the present study is comparison of the effects of beclomethasone inhaler with various clinically used dosages of intravenous lidocaine prior to endotracheal intubation on the incidence and severity of postoperative sore throat, cough, sputum, hoarseness, and dysphagia. A total of 120 patients undergoing elective operations were enrolled in this randomized double-blind clinical trial. Patients were assigned to one of four treatment modalities: lidocaine 1mg/kg [group L[1]], lidocaine 1.5 mg/kg [group L[2]], a dose of 50 micrograms beclomethasone inhaler [Group B], and normal saline [Group C]. Incidence and severity of sore throat, cough, sputum, hoarseness, and dysphagia were compared between the groups before leaving the operating room, 1 hr later, at the time of the first postoperative drink or meal [for assessment of dysphagia], and in the morning after the surgery. In all time intervals of evaluating postoperative symptoms, the incidence and severity of sore throat were significantly lower in groups L2 and B than in group C [P <0.05]. One and twenty hours after emergence of anesthesia, the incidence and severity of cough were significantly lower in groups L[2] and B than in group C [P <0.05]. The incidence and severity of sore throat or cough was not significantly different between groups L2 and B. Throughout the study, the incidence and severity of sputum were significantly lower in group B than in group C [P <0.05]. Beclomehtasone in comparison with intravenous lidocaine prior to intubation decreases the postoperative sore throat and cough. In addition, beclomethasone inhaler decreases the incidence and severity of postoperative sputum


Subject(s)
Humans , Beclomethasone , Nebulizers and Vaporizers , Injections, Intravenous , Hoarseness/prevention & control , Intubation, Intratracheal/adverse effects , Lidocaine , Deglutition Disorders/prevention & control , Pharyngitis/prevention & control , Cough/prevention & control , Double-Blind Method , Preoperative Care , Clinical Trial
7.
São Paulo med. j ; 125(6): 322-328, Nov. 2007. graf, tab
Article in English | LILACS | ID: lil-476090

ABSTRACT

CONTEXT AND OBJECTIVE: High intracuff pressure in endotracheal tubes (ETs) may cause tracheal lesions. The aim of this study was to evaluate the effectiveness and safety of endotracheal tube cuffs filled with air or with alkalinized lidocaine. DESIGN AND SETTING: This was a prospective clinical study at the Department of Anesthesiology, Faculdade de Medicina de Botucatu, Universidade Estadual Paulista. METHODS: Among 50 patients, ET cuff pressures were recorded before, 30, 60, 90 and 120 minutes after starting and upon ending nitrous oxide anesthesia. The patients were randomly allocated to two groups: Air, with ET cuff inflated with air to attain a cuff pressure of 20 cmH2O; and Lido, with ET cuff filled with 2 percent lidocaine plus 8.4 percent sodium bicarbonate to attain the same pressure. ET discomfort before tracheal extubation, and sore throat, hoarseness and coughing incidence were studied at the time of discharge from the post-anesthesia care unit, and sore throat and hoarseness were studied 24 hours after anesthesia. RESULTS: Pressures in Lido cuffs were significantly lower than in Air cuffs (p < 0.05). Tracheal complaints were similar for the two groups, except for lower ET discomfort and sore throat incidence after 24 hours and lower systolic arterial pressure at the time of extubation in the Lido group (p < 0.05). CONCLUSION: ET cuffs filled with alkalinized lidocaine prevented the occurrence of high cuff pressures during N2O anesthesia and reduced ET discomfort and postoperative sore throat incidence. Thus, alkalinized lidocaine-filled ET cuffs seem to be safer than conventional air-filled ET cuffs.


CONTEXTO E OBJETIVO: Os tubos traqueais são dispositivos utilizados para manutenção da ventilação. A hiperinsuflação do balonete do tubo traqueal, causada pela difusão do óxido nitroso (N2O), pode determinar lesões traqueais, que se manifestam clinicamente como odinofagia, rouquidão e tosse. A lidocaína, quando injetada no balonete do tubo traqueal, difunde-se através de sua parede, determinando ação anestésica local na traquéia. O objetivo foi avaliar a efetividade e a segurança do balonete do tubo traqueal preenchido com ar comparado com o balonete preenchido com lidocaína, considerando os desfechos: sintomas cardiovasculatórios (HAS, taquicardia); odinofagia, tosse, rouquidão e tolerância ao tubo traqueal. TIPO DE ESTUDO E LOCAL: Estudo clínico prospectivo, realizado no Departamento de Anestesiologia da Faculdade de Medicina da Unesp, campus de Botucatu. MÉTODOS: A pressão do balonete do tubo traqueal foi medida, entre 50 pacientes, antes, 30, 60, 90 e 120 minutos após o início da inalação de N2O anestésico. As pacientes foram distribuídas aleatoriamente em dois grupos: Air, em que o balonete foi inflado com ar para obtenção de pressão de 20 cm H2O, e Lido, em que o balonete foi preenchido com lidocaína a 2 por cento mais bicarbonato de sódio a 8,4 por cento para obtenção da mesma pressão. O desconforto antes da extubação, e manifestações clínicas como dor de garganta, rouquidão e tosse foram registrados no momento da alta da unidade de cuidados pós-anestésicos, e dor de garganta e rouquidão foram avaliadas também 24 horas após a anestesia. RESULTADOS: Os valores da pressão no balonete em G2 foram significativamente menores do que os de Air em todos os tempos de estudo, a partir de 30 minutos (p < 0,001). A proporção de pacientes que reagiu ao tubo traqueal no momento da desintubação foi significantemente menor em Lido (p < 0,005). A incidência de odinofagia foi significantemente menor em Lido no primeiro dia de pós-operatório...


Subject(s)
Adolescent , Adult , Female , Humans , Middle Aged , Young Adult , Anesthetics, Local/administration & dosage , Intubation, Intratracheal/instrumentation , Lidocaine/administration & dosage , Nitrous Oxide/administration & dosage , Pharyngitis/etiology , Administration, Inhalation , Anesthesia, Inhalation , Cough/etiology , Hoarseness/etiology , Intubation, Intratracheal/adverse effects , Intubation, Intratracheal/standards , Oxygen/administration & dosage , Pharyngitis/prevention & control , Prospective Studies , Trachea/injuries , Young Adult
8.
Middle East Journal of Anesthesiology. 2007; 19 (1): 197-204
in English | IMEMR | ID: emr-84507

ABSTRACT

Tracheal intubation for general anesthesia often leads to traumatization of the airway mucosa resulting in postoperative sore throat, hoarseness and cough. This study was undertaken to determine the effects of betamethasone gel in reducing these complications. One hundred patients [ASA I-II] to undergo endotracheal intubation, were randomly divided equally into two groups; 50 Case [Group A]. 50 Control [Group B]. The tracheal tubes for Case Group A were lubricated with 0.05% betamethasone gel and for the Control Group B with KY gel. Patients were interviewed at end of procedures and 1 and 24 hour after extubation. The incidence and severity of sore throat, hoarseness and cough, 1 and 24 hours postoperatively was reduced significantly in Case Group A. Betamethasone gel, when was used for lubrication of endotracheal tubes pre-operatively, was shown to be effective in decreasing postoperative sore throat, hoarseness, and cough


Subject(s)
Humans , Male , Female , Betamethasone/administration & dosage , Betamethasone , Gels , Pharyngitis/prevention & control , Hoarseness/prevention & control , Cough/prevention & control , Double-Blind Method
9.
Armaghane-danesh. 2005; 9 (36): 1-8
in Persian | IMEMR | ID: emr-69946

ABSTRACT

Sore-throat and hoarseness are the most common complication after endotracheal intubation which take place 12-24 hr after operation. Different studies have reported the incidence of these complications between 24-90%. Increase of heat on the trachea will raise the blood pressure in the local capillaries and therefore induce better blood supplementation to the local tissues. This study aimed to evaluate the effect of local heat on the incidence of sore- throat and hoarseness after endotracheal intubations. One hundred and sixty patients aging 15 -50 years old, candidate for elective surgeries under general anesthesia, were randomly divided into two groups. Patients for head and neck surgeries were excluded from the study. Methods of intubation, type, size, cuff pressure of ETT, method of anesthesia and time of operation were the same for all patients. During the operation time, local heat was applied on the external surface of trachea [up to 40 [oc] by using electrical blanket for the patients in the study group. 24 hr after operation all the patients were visited by anesthesiologist for evaluating the sore- throat and hoarseness. The incidence of sore-throat in the control group was 65% versus 40% in the study group [p<0.05]. Moreover the incidence of hoarseness was 66.2% in the control group versus 10% in the case group. Application of local heat [40[oc] on the external surface of trachea can effectively decreases the incidence of postoperative sore - throat and hoarseness


Subject(s)
Humans , Hoarseness/prevention & control , Pharyngitis/prevention & control , Hot Temperature , Postoperative Complications , Hoarseness/etiology , Pharyngitis/etiology , Incidence , Hoarseness/epidemiology , Pharyngitis/epidemiology
10.
Article in English | IMSEAR | ID: sea-40471

ABSTRACT

PURPOSE OF THE STUDY: To determine the efficacy of lubrication of the endotracheal tube cuff with Chamomile extract (Kamillosan M) before intubation on postoperative sore throat and hoarseness. MATERIAL AND METHOD: The authors randomly assigned 161 patients ASA (American Society of Anesthesiologists) physical status I, II elective surgical, orthopedic, gynecological or urological into 2 groups. The study group received 10 puffs of total 370 mg of Chamomile extract (Kamillosan M spray) lubricated at cuff of endotracheal tube while the control group did not receive any lubrication before intubation. Standard general anesthesia with tracheal intubation was given in both groups. Sore throat and hoarseness were recorded in post anesthetic care unit and at 24 h after operation. RESULTS: One hundred and sixty-one ASA physical status I, II elective surgical patients were recruited. Forty one out of 81 patients (50.6%) in the Chamomile group, scored no postoperative sore throat in the post-anesthesia care unit compared with 45 out of 80 patients (56.3%) in the control group p=0.386. Postoperative sore throat and hoarseness both in the postanesthesia care unit and at 24 h postoperation were not statistically different. There was no statistically significant relationship between sore throat or hoarseness and postoperative nausea or vomiting, ASA physical status, gender, history of smoking, grade of laryngoscopic view, number of intubation attempts, condition during intubation, use of oral airway and couching during extubation. CONCLUSION: Lubrication of endotracheal tube cuff with Chamomile extract spray before intubation can not prevent post operative sore throat and hoarseness.


Subject(s)
Adult , Double-Blind Method , Drug Combinations , Female , Hoarseness/prevention & control , Humans , Intubation, Intratracheal , Lubrication , Male , Middle Aged , Oils, Volatile/administration & dosage , Pain, Postoperative/prevention & control , Pharyngitis/prevention & control , Phytotherapy , Plant Extracts/administration & dosage , Sesquiterpenes/administration & dosage
11.
Journal of the Royal Medical Services. 2003; 10 (2): 38-40
in English | IMEMR | ID: emr-62736

ABSTRACT

To compare the frequency and severity of sore throat and hoarseness following inflation of the endotracheal cuff using air or saline. A double-blined, randomized controlled trial in 63 intubated patients was conducted at Queen Alia Military Hospital in 1999. Patients were included if they were ASA 1-3, aged 18 years or older scheduled for operation below the neck which were expected to last longer than one hour. Following placement of the tracheal tube, the cuff was inflated slowly [using air or saline], until no leak was felt and was connected to a three-way stopcock, extension tubing and connection to a pressure transducer. Intra-cuff pressures were compared to assess any change due to inward diffusion of nitrous oxide. The frequency of significant sore throat and/or hoarseness overall was 15%. There were no statistically significant difference between the groups [air 15%, saline 14.5%]. In the air group mean, intra-cuff pressure increased significantly [start 14 mmHg, end 40 mmHg], while in the saline group there was no significant increase [start 12.7 mmHg, end 14.6 mmHg]. The substitution of saline reliably results in sustained low intra-cuff pressure but high tracheal pressure, but is not an immportant factor in the development of sore throat or hoarseness postoperatively within the pressure range and duration of the operations


Subject(s)
Humans , Male , Female , Pharyngitis/prevention & control , Hoarseness/prevention & control , Air , Sodium Chloride , Postoperative Period , Randomized Controlled Trials as Topic , Neck/surgery
12.
Article in English | IMSEAR | ID: sea-42620

ABSTRACT

A randomized, double-blind study was carried out to assess the effect of 111 mg of Chamomile extract spray compared with normal saline spray (placebo) administered before intubation on post-operative sore throat and hoarseness. One hundred and sixty-one ASA (American Society of Anesthesiologists) physical status I, II elective surgical patients were recruited. Forty-two out of 80 patients (52.5%) in the Chamomile group scored no post-operative sore throat in the post-anesthesia care unit compared with 41 out of 81 patients (50.6%) in the placebo group, p=0.159. Post-operative sore throat and hoarseness both in the post-anesthesia care unit and 24 hour after operation were not statistically different. There was no statistically significant relationship between sore throat or hoarseness and ASA physical status, sex, history of smoking, grade of laryngoscopic view, number of intubation attempts, condition during intubation and condition of extubation. However, there was significant correlation between use of oral airway and sore throat in the post-anesthesia care unit and 24 hours after operation (p=0.031 and 0.002 respectively). Chamomile extract spray administered before intubation, therefore, can not prevent post-operative sore throat and hoarseness.


Subject(s)
Administration, Topical , Adolescent , Adult , Aged , Chamomile , Chi-Square Distribution , Female , Follow-Up Studies , Hoarseness/prevention & control , Humans , Intubation, Intratracheal/adverse effects , Male , Middle Aged , Pain Measurement , Pharyngitis/prevention & control , Plant Extracts/administration & dosage , Postoperative Complications/prevention & control , Preoperative Care/methods , Primary Prevention/methods , Probability , Reference Values , Statistics, Nonparametric , Treatment Outcome
13.
Pediatria (Säo Paulo) ; 20(3): 191-210, jul.-set. 1998. ilus, tab
Article in Portuguese | LILACS | ID: lil-228023

ABSTRACT

Os autores analisam aspectos diagnosticos e terapeuticos relacionados as faringites agudas e recorrentes da crianca, a luz dos relatos da literatura e da experiencia dos medicos da Divisao de Pediatria do Hospital Universitario da Universidade de Sao Paulo


Subject(s)
Humans , Child, Preschool , Pharyngitis/diagnosis , Recurrence , Tonsillitis/diagnosis , Antibiotic Prophylaxis , Bacteriological Techniques , Follow-Up Studies , Bacterial Infections/diagnosis , Bacterial Infections/prevention & control , Pharyngitis/complications , Pharyngitis/etiology , Pharyngitis/prevention & control , Pharyngitis/therapy , Risk Factors , Tonsillitis/complications , Tonsillitis/etiology , Tonsillitis/prevention & control , Tonsillitis/therapy
14.
Rev. SOCERJ ; 9(2): 74-7, abr.-jun. 1996.
Article in Portuguese | LILACS | ID: lil-266156

ABSTRACT

A dor de gargante, sintoma muito comum nas crianças, tem como principal etiologia vírus e bactérias. Constituti-se na maior imprortância o diagnóstico correto do agente etiológico, pois a faringoamigdalite causada pelo streptococco beta hemolítico do Grupo A é responsável pelo desencadeamento posterior da febre reumática. Os sintomas da amigdalite estreptocócica podem ser característicos ou apresentar variaçöes de acordo com a faixa etária. Para diagnóstico diferencial utiliza-se os testes rápidos, a cultura de orofaringe e a dosagem de anticorpos específicos tais como o antiestreptolisina O. Em suma, o tratamento visa a erradicaçäo do estreptococco beta hemolítico do Grupo A, sendo a droga de escolha a penicilina benzatina ou a eritrominica nos casos comprovados de alergia a penicilina.


Subject(s)
Humans , Child , Streptococcal Infections/complications , Streptococcal Infections/therapy , Pharyngitis/diagnosis , Pharyngitis/prevention & control , Pharyngitis/therapy , Rheumatic Fever , Tonsillitis/diagnosis , Tonsillitis/prevention & control , Tonsillitis/therapy , Erythromycin/therapeutic use , Penicillin G Benzathine/adverse effects , Penicillin G Benzathine/therapeutic use , Drug Prescriptions
15.
Rev. SOCERJ ; 9(2): 81-7, abr.-jun. 1996. tab
Article in Portuguese | LILACS | ID: lil-266158

ABSTRACT

A profilaxia primária continua sendo a principal arma na prevençäo de febre reumática. Uma única injeçäo é eficaz e elimina o problema da falta de adesäo observada com os antibióticos orais. A profilaxia secundária também fornece maior segurança e menores índices de recidivas quando a droga empregada é a penicilina benzatina. A eficácia, a facilidade de administraçäo e do baixo custo säo fatores importantíssimos e suficientes para recomendarem o uso dessa droga na prevençäo da febre reumática, principalmente nos países pobres, onde os recursos econômicos säo poucos e a prevalência da febre reumática é alta. Casos fatais devidos a alergia a penicilina existem mais säo raros. A maior parte das histórias clínicas de alergia näo coincidem com os resultados dos testes empregados atualmente no diagnóstico e a possibilidade de reaçöes às cadeias laterais dos compostos semi-sintéticos vem crescendo. Acreditamos que num futuro próximo seräo utilizados testes para detecçäo de reaçöes a qualquer tipo de peniciplina. As reaçöes graves, incluíndo as fatais, säo raríssimas em pacientes menores de 12 anos e sem problemas cardíacos. Os riscos de febre reumática no nosso país säo muito maiores do que o observado com a alergia a penicilina e justificam a recomendaçäo dessa droga para a prevençäo da febre reumática.


Subject(s)
Humans , Child , Rheumatic Fever/complications , Rheumatic Fever/therapy , Hypersensitivity , Penicillins/adverse effects , Pharyngitis/prevention & control , Pharyngitis/therapy , Penicillin G Benzathine/adverse effects , Penicillin G Benzathine/therapeutic use , Drug Prescriptions , Risk Factors , Time Factors
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