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1.
J Orthop Surg Res ; 18(1): 654, 2023 Sep 04.
Artigo em Inglês | MEDLINE | ID: mdl-37667295

RESUMO

BACKGROUND AND OBJECTIVES: Local anesthetics (LAs) are widely used to infiltrate into surgical wounds for postoperative analgesia. Different adjuvants like dexamethasone and dexmedetomidine, when added to LA agents, could improve and prolong analgesia. The aim of this trial was to evaluate the analgesic efficacy and opioid-sparing properties of dexamethasone and dexmedetomidine when added to ropivacaine for wound infiltration in transforaminal lumbar interbody fusion (TLIF). METHODS: We conducted a controlled study among 68 adult patients undergoing TLIF, which was prospective, randomized and double-blind in nature. The participants were divided into four equal groups at random. Group R was given 150 mg of 1% ropivacaine (15 mL) and 15 mL of normal saline. Group R + DXM received 150 mg of 1% ropivacaine (15 mL) and 10 mg of dexamethasone (15 mL). Group R + DEX received 150 mg of 1% ropivacaine (15 mL) and 1 µg/kg of dexmedetomidine (15 mL). Lastly, group R + DXM + DEX was given 150 mg of 1% ropivacaine (15 mL), 10 mg of dexamethasone and 1 µg/kg of dexmedetomidine (15 mL). The primary focus was on the length of pain relief provided. Additionally, secondary evaluations included the amount of hydromorphone taken after surgery, the numerical rating scale and safety assessments within 48 h after the operation. RESULTS: Based on the p value (P > 0.05), there was no significant variance in the duration of pain relief or the total usage of hydromorphone after surgery across the four groups. Similarly, the numerical rating scale scores at rest and during activity at 6-, 12-, 24- and 48-h post-surgery for all four groups showed no difference (P > 0.05). However, the incidence of delayed anesthesia recovery was slightly higher in group R + DEX and group R + DXM + DEX when compared to group R or group R + DXM. Furthermore, there were no significant differences between the four groups in terms of vomiting, nausea, dizziness or delayed anesthesia recovery. CONCLUSION: For wound infiltration in TLIF, the addition of dexamethasone and dexmedetomidine to ropivacaine did not result in any clinically significant reduction in pain or opioid consumption and could prompt some side effects.


Assuntos
Adjuvantes Anestésicos , Analgesia , Dexametasona , Dexmedetomidina , Fusão Vertebral , Adulto , Humanos , Analgesia/métodos , Analgésicos Opioides , Dexametasona/administração & dosagem , Dexmedetomidina/administração & dosagem , Hidromorfona , Vértebras Lombares/cirurgia , Dor , Estudos Prospectivos , Ropivacaina/administração & dosagem , Fusão Vertebral/efeitos adversos , Adjuvantes Anestésicos/administração & dosagem , Dor Pós-Operatória/etiologia , Dor Pós-Operatória/prevenção & controle , Anestesia Local/métodos
2.
BMC Pregnancy Childbirth ; 21(1): 121, 2021 Feb 09.
Artigo em Inglês | MEDLINE | ID: mdl-33563234

RESUMO

BACKGROUND: Anesthesia in lactating women is frequently indicated for time-sensitive procedures such as postpartum tubal ligation. Ketamine and diazepam are two of the most commonly used anesthetic agents in low resource settings, but their safety profile in lactating women has not been established. METHODS: Medical records of post-partum tubal ligations between 2013 and 2018 at clinics of the Shoklo Malaria Research Unit were reviewed for completeness of key outcome variables. Logistic regression identified presence or absence of associations between drug doses and adverse neonatal outcomes: clinically significant weight loss (≥95th percentile) and neonatal hyperbilirubinemia requiring phototherapy. RESULTS: Of 358 records reviewed, 298 were lactating women with singleton, term neonates. There were no severe outcomes in mothers or neonates. On the first postoperative day 98.0% (290/296) of neonates were reported to be breastfeeding well and 6.4% (19/298) had clinically significant weight loss. Phototherapy was required for 13.8% (41/298) of neonates. There was no association between either of the outcomes and increasing ketamine doses (up to 3.8 mg/kg), preoperative oral diazepam (5 mg), or increasing lidocaine doses (up to 200 mg). Preoperative oral diazepam resulted in lower doses of intraoperative anesthetics. Doses of intravenous diazepam above 0.1 mg/kg were associated with increased risk (adjusted odds ratio per 0.1 mg/kg increase, 95%CI) of weight loss (1.95, 95%CI 1.13-3.35, p = 0.016) and jaundice requiring phototherapy (1.87, 95%CI 1.11-3.13, p = 0.017). CONCLUSIONS: In resource-limited settings ketamine use appears safe in lactating women and uninterrupted breastfeeding should be encouraged and supported. Preoperative oral diazepam may help reduce intraoperative anesthetic doses, but intravenous diazepam should be used with caution and avoided in high doses in lactating women.


Assuntos
Aleitamento Materno , Diazepam/administração & dosagem , Ketamina/administração & dosagem , Período Pós-Parto , Esterilização Tubária , Adjuvantes Anestésicos/administração & dosagem , Adulto , Analgésicos/administração & dosagem , Feminino , Humanos , Recém-Nascido , Lactação , Pessoa de Meia-Idade , Pré-Medicação , Estudos Retrospectivos , Tailândia , Adulto Jovem
3.
Respiration ; 99(9): 789-799, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33207359

RESUMO

BACKGROUND: Medical thoracoscopy is the gold standard for the diagnosis of pleural diseases. To date, no consensus exists regarding the choice of sedative and analgesic agents in patients undergoing local anesthetic thoracoscopy (LAT), and questions are raised as to whether sedatives may add to respiratory side effects. OBJECTIVE: The aim of the study was to test the hypothesis that administration of midazolam associated with lidocaine versus lidocaine alone in patients with LAT adds to respiratory side effects. METHODS: We randomly assigned 80 patients to a 1:1 study to 2 groups: local anesthesia by lidocaine (n = 40) versus lidocaine and midazolam (n = 40), with the primary end point being the mean lowest oxygen saturation. The secondary end points were cardiovascular parameters, complications, days of drainage, hospital stay, and patients' quality of life (QoL) as assessed by a visual analog scale (VAS). RESULTS: The mean age of all patients was 66.6 ± 13.1 years. The study comprised 50 males (62.5%). No difference was observed in the demographics between the 2 groups. No significant difference was observed between the 2 groups in oxygen saturation (primary end point). A significant difference was observed in favor of the midazolam group regarding the QoL assessed by VAS. CONCLUSION: Midazolam does not add to respiratory side effects when it is used with lidocaine for LAT, while patients' QoL is actually improved in this group. Therefore, in our department, we changed our startegy in favor of the association of lidocaine and midazolam.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Anestesia Local , Anestésicos Locais/administração & dosagem , Lidocaína/administração & dosagem , Pneumopatias/diagnóstico , Midazolam/administração & dosagem , Qualidade de Vida , Toracoscopia/métodos , Adjuvantes Anestésicos/efeitos adversos , Idoso , Anestésicos Locais/efeitos adversos , Feminino , Humanos , Lidocaína/efeitos adversos , Masculino , Midazolam/efeitos adversos , Pessoa de Meia-Idade , Manejo da Dor/métodos , Derrame Pleural/diagnóstico
4.
Pan Afr Med J ; 35: 62, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32537066

RESUMO

Spinal anesthesia is a widely used regional anesthesia for many infra-umbilical surgical procedures with proven efficacy and safety. However, although rare, some neurologic complications can occur with potentially life threatening consequences. Among them, lower cranial nerve palsies have been rarely reported in the literature. We report such a case in a 75-year-old man with transient dysphagia, dysphonia and spinal accessory nerve palsy occurring four days after spinal anesthesia for transurethral resection of the prostate. His symptoms completely resolved spontaneously within 2 weeks. The possibility of lower cranial nerve palsies should be added to the potential complications during or following spinal anesthesia with bupivacaine-fentanyl combination. Although transitional, this complication may occur few days after the procedure and need to be promptly recognized, carefully evaluated and treated by conservative measures.


Assuntos
Raquianestesia/efeitos adversos , Doenças dos Nervos Cranianos/etiologia , Ressecção Transuretral da Próstata/métodos , Adjuvantes Anestésicos/administração & dosagem , Adjuvantes Anestésicos/efeitos adversos , Idoso , Raquianestesia/métodos , Anestésicos Locais/administração & dosagem , Anestésicos Locais/efeitos adversos , Bupivacaína/administração & dosagem , Bupivacaína/efeitos adversos , Fentanila/administração & dosagem , Fentanila/efeitos adversos , Humanos , Masculino
5.
Pulmonology ; 25(1): 9-14, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29898873

RESUMO

If the seemingly less invasive semi-flexible pleuroscopes are combined with strategies of conscious sedation and local anesthesia the pleuroscopy has the potential to reach an increasing number of hospital settings. Local experiences can provide valuable information pertaining to the reproducibility of this technique in different scenarios. We performed a retrospective analysis of the clinical records of all patients that had undergone local anesthetic semi-flexible pleuroscopy in our unit between February 2015 and July 2017. Data on demographics, previous biochemical, cytological and histopathological analysis, procedure details, diagnostic and therapeutic results, complications and mortality were collected from all patients. Statistical analysis was performed using SPSS v23. A total of 30 patients were included. They were mainly male (66.7%), with a median age of 72 years (minimum 19 years, maximum 87 years). All presented with exudative pleural effusions and the exam was performed for diagnostic reasons. Pleural tissue was obtained in all patients and the overall diagnostic accuracy was 93.3%. Malignancy was the chief group of diagnosis (66.7%), followed by pleural tuberculosis (13.3%). The procedure was well tolerated and self-limited subcutaneous emphysema was the only complication registered (13.3%). No deaths were associated with the procedure. Our results globally overlap those of wider series and reinforce the perception that local anesthetic semi-flexible pleuroscopy is a well-tolerated, safe and highly accurate diagnostic and therapeutic tool which has proved to be both feasible and effective in our experience.


Assuntos
Anestesia Local/efeitos adversos , Anestésicos Locais/efeitos adversos , Derrame Pleural/diagnóstico por imagem , Toracoscopia/instrumentação , Adjuvantes Anestésicos/administração & dosagem , Adulto , Idoso , Idoso de 80 Anos ou mais , Anestésicos Locais/administração & dosagem , Feminino , Humanos , Masculino , Midazolam/administração & dosagem , Pessoa de Meia-Idade , Pleura/patologia , Derrame Pleural/etiologia , Derrame Pleural/metabolismo , Derrame Pleural/patologia , Reprodutibilidade dos Testes , Estudos Retrospectivos , Enfisema Subcutâneo/etiologia , Toracoscópios/tendências , Toracoscopia/efeitos adversos , Toracoscopia/métodos
6.
Am J Cardiol ; 122(6): 1095-1097, 2018 09 15.
Artigo em Inglês | MEDLINE | ID: mdl-30072130

RESUMO

Patients undergoing invasive cardiac catheterization (ICC) can experience anxiety and pain. A common practice in the United States is to administer benzodiazepines and opioids for conscious sedation to relieve these symptoms. Music may reduce anxiety and pain perception. We sought to evaluate the role of music in lieu of pharmacotherapy for conscious sedation during elective ICC. A retrospective data analysis was performed on patients who underwent ICC and received music therapy ± intravenous sedation/analgesics based on patient's preference compared with control patients who were offered and received intravenous sedation/analgesics based on patient's preference. A total of 161 patients were analyzed, 49 in the music arm, and 112 in the control arm. Baseline characteristics were similar in the 2 groups except that the rate of drug addiction, back pain, post-traumatic stress disorder, and hearing loss were higher in the control group when compared with the music arm. 42 (86%) of the patients in the music group and 29 (26%) of the control group received no sedation or analgesia in the periprocedural period. The average dose of midazolam (0.7 mg vs 0.1 mg, p <0.0001) and fentanyl (39.5 mcg vs 3 mcg, p <0.0001) was higher in the control than the music arm, respectively. 42 (86%) of patients receiving music therapy believed music was helpful in reducing their stress/anxiety levels. In conclusion, music may serve as adjunctive/alternative intervention to pharmacotherapy in relieving anxiety and stress for patients undergoing elective ICC.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Cateterismo Cardíaco , Sedação Consciente/métodos , Fentanila/administração & dosagem , Hipnóticos e Sedativos/administração & dosagem , Midazolam/administração & dosagem , Musicoterapia , Idoso , Feminino , Humanos , Masculino , Estudos Retrospectivos , Resultado do Tratamento
7.
Saudi Med J ; 39(6): 579-585, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29915852

RESUMO

OBJECTIVES: To assess the effects of magnesium on the depth of anesthesia and to determine the effects of magnesium on incidence of awareness and postoperative pain after caesarean section.  Methods: The study was designed as a double-blind, controlled, randomized study and conducted in Hacettepe University Hospital, Ankara, Turkey  between January 2015 and March 2016. A total of 100 pregnant healthy women who were between 17 and 41 years old, ASA II, and scheduled for an elective cesarean section with general anesthesia were included in the study. After induction, sevoflurane was used for maintenance in Group S and desflurane in Group D (control groups). At Group S-M and Group D-M (study groups), magnesium infusion was started with sevoflurane and desflurane anesthesia respectively. Minimum alveolar concentration of sevoflurane and desflurane were kept constant. Bispectral index scores (BIS), fentanyl consumption and postoperative visual analogue scale (VAS) values were recorded. All of the patients had been followed-up for awareness until the postoperative first year. Results: Demographic variables of the patients were similar. BIS values were significantly higher in control groups throughout the operation (p less than 0.001). No significant difference was detected for intraoperative fentanyl consumption and awareness incidence. VAS values were significantly lower in study groups (p less than 0.05). Conclusion: Magnesium infusion provided significantly lower intraoperative BIS values and lower postoperative VAS scores. We believe that magnesium can be useful as an adjuvant to general anesthesia.


Assuntos
Adjuvantes Anestésicos , Anestesia Geral/métodos , Anestesia Obstétrica/métodos , Consciência no Peroperatório , Sulfato de Magnésio , Dor Pós-Operatória/etiologia , Adjuvantes Anestésicos/administração & dosagem , Adolescente , Adulto , Anestésicos Inalatórios , Cesárea/efeitos adversos , Monitores de Consciência , Desflurano , Método Duplo-Cego , Feminino , Fentanila/administração & dosagem , Humanos , Consciência no Peroperatório/diagnóstico , Isoflurano/análogos & derivados , Éteres Metílicos , Gravidez , Sevoflurano , Adulto Jovem
8.
Oral Maxillofac Surg ; 22(2): 225-230, 2018 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-29752604

RESUMO

INTRODUCTION: The aim of this clinical study was to evaluate and compare the relative efficacy of two different dosages of dexamethasone, i.e., 4 and 8 mg injected submucosally to reduce postoperative discomfort after mandibular third molar surgery. METHODOLOGY: A prospective randomized study was conducted on 45 patients requiring surgical removal of an impacted third molar. Selected patients were divided randomly into three groups of 15 patients each: group I patients received one regimen single dose of 4 mg dexamethasone submucosally, group II received one regimen single dose of 8 mg dexamethasone submucosally, and group III (control group), no dexamethasone was given but only received injection of normal saline submucosally after establishing local anesthesia. The postoperative sequelae were assessed on the second and seventh postoperative day. RESULT: As compared to group III, groups I and II showed statistically significant reduction in pain and swelling whereas no statistically significant difference was found between the test groups. CONCLUSION: It can be concluded that corticosteroids are effective in curtailing the postoperative edema of lower third molar surgery but have negligible analgesic effect. As no statistically significant difference is found between both the regimes of dexamethasone, i.e., 4 and 8 mg so within the confines of our study, it may be concluded that 4 mg dexamethasone can be given safely to reduce the postoperative edema after the third molar surgery.


Assuntos
Adjuvantes Anestésicos/uso terapêutico , Anestesia Dentária/métodos , Anestesia Local/métodos , Anti-Inflamatórios/uso terapêutico , Dexametasona/uso terapêutico , Dente Serotino/cirurgia , Dor Pós-Operatória/prevenção & controle , Extração Dentária , Dente Impactado/cirurgia , Adjuvantes Anestésicos/administração & dosagem , Adulto , Anti-Inflamatórios/administração & dosagem , Dexametasona/administração & dosagem , Feminino , Humanos , Injeções , Masculino , Método Simples-Cego , Extração Dentária/efeitos adversos , Extração Dentária/métodos , Adulto Jovem
9.
Anesth Analg ; 126(4): 1170-1175, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29239940

RESUMO

BACKGROUND: The relatively short duration of effect of local anesthetics has been addressed by encapsulation in drug delivery systems. Codelivery with a single compound that produces an adjuvant effect on nerve block but without intrinsic local anesthetic properties can further prolong the nerve block effect. Here, we investigated whether codelivery of more than 1 encapsulated adjuvant compound can further enhance nerve blockade. METHODS: Liposomes loaded with bupivacaine (Bup), dexamethasone phosphate (DexP), or dexmedetomidine (DMED) were synthesized and its in vitro drug release profiles were determined. Animals (Sprague-Dawley rats) were injected with liposomal Bup (Lipo-Bup) and adjuvants at the sciatic nerve and underwent a modified hot plate test to assess the degree of nerve block. The duration of block was monitored and the tissue reaction was assessed. RESULTS: Coinjection of Lipo-Bup with liposomal DexP (Lipo-DexP) and liposomal DMED (Lipo-DMED) prolonged the duration of sciatic nerve block 2.9-fold compared to Lipo-Bup alone (95% confidence interval, 1.9- to 3.9-fold). The duration of the block using this combination was significantly increased to 16.2 ± 3.5 hours compared to Lipo-Bup with a single liposomal adjuvant (8.7 ± 2.4 hours with Lipo-DMED, P = .006 and 9.9 ± 5.9 hours with Lipo-DexP, P = .008). The coinjection of Lipo-Bup with liposomal adjuvants decreased tissue inflammation (P = .014) but did not have a significant effect on myotoxicity when compared to Lipo-Bup alone. Coinjection of Lipo-Bup with unencapsulated adjuvants prolonged the duration of nerve block as well (25.0 ± 6.3 hours; P < .001) however was accompanied by systemic side effects. CONCLUSIONS: Codelivery of Lipo-DexP and Lipo-DMED enhanced the efficacy of Lipo-Bup. This benefit was also seen with codelivery of both adjuvant molecules in the unencapsulated state, but with marked systemic toxicity.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Anestesia Local/métodos , Anestésicos Combinados/administração & dosagem , Anestésicos Locais/administração & dosagem , Bupivacaína/administração & dosagem , Dexametasona/administração & dosagem , Dexmedetomidina/administração & dosagem , Bloqueio Nervoso/métodos , Nervo Isquiático/efeitos dos fármacos , Adjuvantes Anestésicos/toxicidade , Anestesia Local/efeitos adversos , Anestésicos Combinados/toxicidade , Anestésicos Locais/toxicidade , Animais , Bupivacaína/toxicidade , Dexametasona/toxicidade , Dexmedetomidina/toxicidade , Liberação Controlada de Fármacos , Cinética , Lipossomos , Masculino , Bloqueio Nervoso/efeitos adversos , Limiar da Dor/efeitos dos fármacos , Ratos Sprague-Dawley , Fatores de Tempo
10.
J Craniofac Surg ; 29(2): 286-288, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-29084114

RESUMO

Fracture of nasal bone is among the most common facial bone fractures. Reduction of nasal bone fracture is able to be performed under local or general anesthesia. The aim of this study is to compare monitored anesthetic care (MAC) and general anesthesia (GA) based on intraoperative vital signs, and the adverse effects after closed reduction of nasal bone fractures.The authors performed a retrospective study of 45 patients who underwent a closed reduction of nasal bone fracture between January 1, 2016 and December 31, 2016. Patients are divided into an MAC group (n = 17) or GA group (n = 28). A sore throat, postoperative pain scores, nausea, vomiting, hospital stay, operation time, and the result of surgery are compared between the groups. All the patients have interviewed their satisfaction of aesthetic and functional outcome.The operation time and hospital stay were lower in the MAC group. There is no difference in a sore throat, postoperative pain score, and the result of surgery significantly. In the MAC and GA groups, there was no statistically significant difference in the postoperative cosmetic and functional satisfaction scores.Closed reduction of nasal bone fracture using MAC is as safe and efficient as GA. However, MAC anesthesia may not be feasible if airway discomfort due to bleeding is expected, or fracture is severe and multiple manipulations are required. Therefore, MAC is considered to be a good alternative when patients undergoing short-term or small operations do not prefer general anesthesia.


Assuntos
Anestesia Geral , Anestesia Local , Redução Fechada , Osso Nasal/cirurgia , Fraturas Cranianas/cirurgia , Adjuvantes Anestésicos/administração & dosagem , Adulto , Feminino , Humanos , Hipnóticos e Sedativos/administração & dosagem , Tempo de Internação , Masculino , Monitorização Intraoperatória , Osso Nasal/lesões , Duração da Cirurgia , Estudos Retrospectivos , Adulto Jovem
11.
Urology ; 100: 27-32, 2017 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-27658661

RESUMO

OBJECTIVE: To investigate whether the use of a belladonna and opium (B&O) rectal suppository administered immediately before ureteroscopy (URS) and stent placement could reduce stent-related discomfort. METHODS: A randomized, double-blinded, placebo-controlled study was performed from August 2013 to December 2014. Seventy-one subjects were enrolled and randomized to receive a B&O (15 mg/30 mg) or a placebo suppository after induction of general anesthesia immediately before URS and stent placement. Baseline urinary symptoms were assessed using the American Urological Association Symptom Score (AUASS). The Ureteral Stent Symptom Questionnaire and AUASS were completed on postoperative days (POD) 1, 3, and after stent removal. Analgesic use intraoperatively, in the recovery unit, and at home was recorded. RESULTS: Of the 71 subjects, 65 had treatment for ureteral (41%) and renal (61%) calculi, 4 for renal urothelial carcinoma, and 2 were excluded for no stent placed. By POD3, the B&O group reported a higher mean global quality of life (QOL) score (P = .04), a better mean quality of work score (P = .05), and less pain with urination (P = .03). The B&O group reported an improved AUASS QOL when comparing POD1 with post-stent removal (P = .04). There was no difference in analgesic use among groups (P = .67). There were no episodes of urinary retention. Age was associated with unplanned emergency visits (P <.00) and "high-pain" measure (P = .02) CONCLUSION: B&O suppository administered preoperatively improved QOL measures and reduced urinary-related pain after URS with stent. Younger age was associated with severe stent pain and unplanned hospital visits.


Assuntos
Atropa belladonna , Atropina/administração & dosagem , Ópio/administração & dosagem , Dor Pós-Operatória/prevenção & controle , Escopolamina/administração & dosagem , Stents/efeitos adversos , Ureteroscopia/efeitos adversos , Adjuvantes Anestésicos/administração & dosagem , Adulto , Idoso , Analgésicos Opioides/administração & dosagem , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Dor Pós-Operatória/etiologia , Parassimpatolíticos/administração & dosagem , Fitoterapia , Extratos Vegetais/administração & dosagem , Cuidados Pré-Operatórios , Estudos Prospectivos , Qualidade de Vida , Supositórios , Cálculos Urinários/cirurgia
12.
J Endod ; 42(10): 1458-61, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-27507627

RESUMO

INTRODUCTION: The purpose of this prospective, randomized, double-blind study was to evaluate the effect of a buccal infiltration of sodium bicarbonate on the anesthetic success of the inferior alveolar nerve block (IANB) for mandibular first molars in patients with symptomatic irreversible pulpitis. METHODS: One hundred patients diagnosed with symptomatic irreversible pulpitis of a mandibular first molar were selected. The patients randomly received a buccal infiltration injection of either 0.7 mL 8.4% sodium bicarbonate with 0.3 mL 2% lidocaine containing 1:80,000 epinephrine or 0.7 mL sterile distilled water with 0.3 mL 2% lidocaine containing 1:80,000 epinephrine in a double-blind manner. After 15 minutes, all the patients received conventional IANB injection using 3.6 mL 2% lidocaine with 1:80,000 epinephrine. Access cavity preparation was initiated 15 minutes after the IANB injection. Lip numbness was a requisite for all the patients. Success was determined as no or mild pain on the basis of Heft-Parker visual analog scale recordings upon access cavity preparation or initial instrumentation. Data were analyzed using the t, chi-square and Mann-Whitney U tests. RESULTS: The success rate after the buccal infiltration of sodium bicarbonate was 78%, whereas without the buccal infiltration of sodium bicarbonate it was 44% (P < .001). CONCLUSIONS: A buccal infiltration of 0.7 mL 8.4% sodium bicarbonate increased the success rate of IANBs in mandibular first molars with symptomatic irreversible pulpitis.


Assuntos
Anestesia Local/métodos , Nervo Mandibular/efeitos dos fármacos , Dente Molar/efeitos dos fármacos , Bloqueio Nervoso/métodos , Pulpite/fisiopatologia , Bicarbonato de Sódio/administração & dosagem , Adjuvantes Anestésicos/administração & dosagem , Administração Bucal , Adolescente , Adulto , Anestesia Dentária/métodos , Anestésicos Combinados/administração & dosagem , Anestésicos Locais/administração & dosagem , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Medição da Dor/efeitos dos fármacos , Estudos Prospectivos , Pulpite/tratamento farmacológico , Preparo de Canal Radicular/métodos , Bicarbonato de Sódio/farmacocinética , Adulto Jovem
13.
J Endod ; 41(1): 33-5, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25442722

RESUMO

INTRODUCTION: The purpose of this prospective, randomized, double-blind study was to compare the anesthetic efficacy of buffered with nonbuffered 2% lidocaine with 1:80,000 epinephrine solution for inferior alveolar nerve (IAN) block in patients with mandibular posterior teeth experiencing symptomatic irreversible pulpitis. METHODS: Eighty adult patients diagnosed with symptomatic irreversible pulpitis of a mandibular posterior tooth were selected. The patients received 2 cartridges of either 2% lidocaine with 1:80,000 epinephrine buffered with 0.18 mL 8.4% sodium bicarbonate or 2% lidocaine with 1:80,000 epinephrine with 0.18 mL sterile distilled water using conventional IAN block injections. Endodontic access preparation was initiated 15 minutes after injection. Lip numbness was required for all the patients. Success was determined as no or mild pain on the basis of Heft-Parker visual analog scale recordings upon access cavity preparation or initial instrumentation. Data were analyzed by the t, Mann-Whitney, and chi-square tests. RESULTS: The success rates were 62.5% and 47.5% for buffered and nonbuffered groups, respectively, with no significant differences between the two groups (P = .381). CONCLUSIONS: Buffering the 2% lidocaine with 1:80,000 epinephrine with 8.4% sodium bicarbonate did not improve the success of the IAN block in mandibular molars in patients with symptomatic irreversible pulpitis.


Assuntos
Lidocaína/administração & dosagem , Nervo Mandibular/efeitos dos fármacos , Bloqueio Nervoso/métodos , Pulpite/fisiopatologia , Bicarbonato de Sódio/administração & dosagem , Adjuvantes Anestésicos/administração & dosagem , Adulto , Anestesia Dentária/métodos , Anestesia Local/métodos , Anestésicos Combinados/administração & dosagem , Anestésicos Locais/administração & dosagem , Soluções Tampão , Método Duplo-Cego , Epinefrina/administração & dosagem , Feminino , Humanos , Lábio/inervação , Masculino , Pessoa de Meia-Idade , Dente Molar , Dor/tratamento farmacológico , Estudos Prospectivos , Pulpite/tratamento farmacológico , Preparo de Canal Radicular/métodos , Adulto Jovem
15.
Dermatol Surg ; 40(6): 603-9, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24852463

RESUMO

BACKGROUND: While patients' hypertensive problems are usually actively and effectively managed by their primary physician, the dermatologic surgeon can still be affected by hypertension where the condition is unrecognized or uncontrolled. Hypertension is an important contributor to both bleeding and hematoma formation during and after surgery, ultimately affecting functional and cosmetic outcomes. OBJECTIVE: To extensively review the literature on perioperative management of the hypertensive patient as relates to the dermatologic surgeon. MATERIALS AND METHODS: An updated and comprehensive literature review, focusing on current diagnostic guidelines, practice by specific dermatologic surgery groups and management recommendations, was conducted. RESULTS: Review of the literature does support generalized guidelines for the management of hypertensive patients in the Mohs Micrographic Surgery (MMS) setting; however data on implementation and outcomes by specific dermatologic surgery groups is variable and lacking. CONCLUSIONS: The treatment of nonmelanoma skin cancers with MMS is now routine, and fortunately can be performed quite safely. There are still improvements to be made however, in managing perioperative hypertension-both in making patients aware of their condition and in treating it effectively. Practicing these measures can promote patients' overall health and the efficiency of the dermatologic surgeon's practice.


Assuntos
Adjuvantes Anestésicos/efeitos adversos , Anestesia Local/efeitos adversos , Epinefrina/efeitos adversos , Hipertensão/etiologia , Cirurgia de Mohs , Período Perioperatório , Neoplasias Cutâneas/complicações , Adjuvantes Anestésicos/administração & dosagem , Anestesia Local/métodos , Perda Sanguínea Cirúrgica/prevenção & controle , Epinefrina/administração & dosagem , Humanos , Hipertensão/induzido quimicamente , Hipertensão/diagnóstico , Hipertensão/tratamento farmacológico , Metanálise como Assunto , Cirurgia de Mohs/efeitos adversos , Cirurgia de Mohs/métodos , Monitorização Intraoperatória/métodos , Guias de Prática Clínica como Assunto , Ensaios Clínicos Controlados Aleatórios como Assunto , Medição de Risco , Fatores de Risco , Neoplasias Cutâneas/cirurgia , Infecção da Ferida Cirúrgica/prevenção & controle , Resultado do Tratamento , Vasoconstritores/efeitos adversos , Hipertensão do Jaleco Branco/diagnóstico , Hipertensão do Jaleco Branco/tratamento farmacológico
16.
PLoS One ; 9(2): e88076, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24505383

RESUMO

Lycium barbarum is used both as a food additive and as a medicinal herb in many countries, and L. barbarum polysaccharides (LBPs), a major cell component, are reported to have a wide range of beneficial effects including neuroprotection, anti-aging and anticancer properties, and immune modulation. The effects of LBPs on neuronal function, neurogenesis, and drug-induced learning and memory deficits have not been assessed. We report the therapeutic effects of LBPs on learning and memory and neurogenesis in scopolamine (SCO)-treated rats. LBPs were administered via gastric perfusion for 2 weeks before the onset of subcutaneous SCO treatment for a further 4 weeks. As expected, SCO impaired performance in novel object and object location recognition tasks, and Morris water maze. However, dual SCO- and LBP-treated rats spent significantly more time exploring the novel object or location in the recognition tasks and had significant shorter escape latency in the water maze. SCO administration led to a decrease in Ki67- or DCX-immunoreactive cells in the dentate gyrus and damage of dendritic development of the new neurons; LBP prevented these SCO-induced reductions in cell proliferation and neuroblast differentiation. LBP also protected SCO-induced loss of neuronal processes in DCX-immunoreactive neurons. Biochemical investigation indicated that LBP decreased the SCO-induced oxidative stress in hippocampus and reversed the ratio Bax/Bcl-2 that exhibited increase after SCO treatment. However, decrease of BDNF and increase of AChE induced by SCO showed no response to LBP administration. These results suggest that LBPs can prevent SCO-induced cognitive and memory deficits and reductions in cell proliferation and neuroblast differentiation. Suppression of oxidative stress and apoptosis may be involved in the above effects of LBPs that may be a promising candidate to restore memory functions and neurogenesis.


Assuntos
Adjuvantes Anestésicos/farmacologia , Antioxidantes/farmacologia , Medicamentos de Ervas Chinesas/farmacologia , Neurogênese/efeitos dos fármacos , Fármacos Neuroprotetores/farmacologia , Escopolamina/farmacologia , Adjuvantes Anestésicos/administração & dosagem , Adjuvantes Anestésicos/toxicidade , Animais , Antioxidantes/administração & dosagem , Apoptose/efeitos dos fármacos , Proteína Duplacortina , Medicamentos de Ervas Chinesas/administração & dosagem , Hipocampo/citologia , Hipocampo/efeitos dos fármacos , Lycium/química , Masculino , Aprendizagem em Labirinto/efeitos dos fármacos , Memória/efeitos dos fármacos , Fármacos Neuroprotetores/administração & dosagem , Ratos , Ratos Sprague-Dawley , Escopolamina/administração & dosagem , Escopolamina/toxicidade
17.
J Oral Maxillofac Surg ; 72(3): 474-80, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24268964

RESUMO

PURPOSE: The combination of α2-adrenoceptor agonists, such as dexmedetomidine (DEX) and clonidine, with local anesthetics has been found to extend the duration of peripheral nerve blocks, probably owing to the resultant local vasoconstriction in the peripheral nerves. However, because the clear elucidation of the effect of DEX requires examination of the local anesthetic effect with DEX alone and the combination of various concentrations of DEX with local anesthetics, we evaluated the local anesthetic effect of various concentrations of DEX alone and with a local anesthetic. MATERIALS AND METHODS: The present study assessed the tail-flick (TF) latencies after injection of the appropriate drug in male Sprague-Dawley rats, using an epidural model that allowed constant pain stimulation intensity, dispersion of the anesthetic, and a precise injection site and dose. Lidocaine alone, lidocaine with 2.5-ppm DEX, lidocaine with 5.0-ppm DEX, lidocaine with 7.5-ppm DEX, and DEX alone were administered at the predetermined dose. The TF latency changes over time were compared using repeated measures analysis of variance (ANOVA). Comparisons among the groups were analyzed using ANOVA followed by a post hoc Dunnett's multiple comparison test or Tukey's multiple comparison test. RESULTS: The addition of DEX to lidocaine increased the TF latency and dose-dependently prolonged its duration as follows: 0-ppm DEX, 20 minutes; 2.5-ppm, 40 minutes; 5.0-ppm, 40 minutes; and 7.5-ppm, 50 minutes. DEX alone did not change the TF latency. CONCLUSIONS: Our results have demonstrated that DEX dose-dependently enhances the local anesthetic action of lidocaine in a rat TF model.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Agonistas de Receptores Adrenérgicos alfa 2/administração & dosagem , Anestesia Dentária/métodos , Anestesia Local/métodos , Anestésicos Locais/administração & dosagem , Dexmedetomidina/administração & dosagem , Lidocaína/administração & dosagem , Animais , Relação Dose-Resposta a Droga , Injeções Epidurais , Masculino , Ratos , Ratos Sprague-Dawley
18.
Artigo em Inglês | MEDLINE | ID: mdl-22981094

RESUMO

OBJECTIVE: The aim of this study was to assess analgesic and adjuvant anesthetic effects of submucosal tramadol after third molar extraction. STUDY DESIGN: In this double-blind, split-mouth, placebo-controlled, single-dose, crossover investigation, 52 patients underwent mandibular third molar extraction under local anesthesia. Surgical side was randomly assigned to submucosal 2 mL 100 mg tramadol injection (group T) or normal saline solution (group P) immediately after surgery. Anesthetic blockade duration, time of intake and amount of analgesic rescue drug, and postoperative pain intensity were recorded immediately after anesthesia cessation and 4, 8, 24, 48, and 72 hours after surgery. Data were submitted to analysis of variance and Wilcoxon tests. RESULTS: Anesthetic blockade duration between groups was similar. Group T took significantly less rescue drug after 72 hours (P = .008). Time elapsed before first intake of rescue drug was longer (P = .006), and pain intensity was significantly lower (P = .001) in group T. CONCLUSIONS: Submucosal tramadol injection after oral surgery improved postoperative analgesia, but did not extend anesthetic action duration.


Assuntos
Adjuvantes Anestésicos/uso terapêutico , Analgésicos Opioides/uso terapêutico , Dente Serotino/cirurgia , Extração Dentária , Tramadol/uso terapêutico , Adjuvantes Anestésicos/administração & dosagem , Adolescente , Adulto , Analgésicos Opioides/administração & dosagem , Anestesia Local/métodos , Estudos Cross-Over , Método Duplo-Cego , Feminino , Humanos , Injeções , Masculino , Mandíbula/cirurgia , Medição da Dor , Dor Pós-Operatória/prevenção & controle , Placebos , Estudos Prospectivos , Tramadol/administração & dosagem
19.
Oral Maxillofac Surg ; 18(3): 325-9, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23740399

RESUMO

INTRODUCTION: Local anesthetics are generally much less effective when administered in inflamed tissues. PURPOSE: This study was conducted to validate the addition of sodium bicarbonate in local anesthetics to increase its effectiveness as local infiltrations in teeth associated with periapical infections. METHODS: Two hundred subjects requiring extraction of maxillary teeth with periapical infections were enrolled. These subjects were divided in two groups of 100 subjects each. One group received local infiltration with 2 % lignocaine and 1:80,000 adrenaline, and the other group received local infiltration with sodium bicarbonate as an adjunct to the above mentioned local anesthetic solution. All extractions were performed using a consistent intra-alveolar technique by a single operator. Both the patient and the operator were blinded to the contents of local anesthetic solution. Data related to the onset of action of local anesthesia, pain experienced by the patient while undergoing extraction on two scales-"the visual analog scale and the verbal response scale", and any requirement of repeated injections during the procedure was recorded. RESULTS: Clinical and statistical data confirmed that the addition of sodium bicarbonate in local anesthetics did increase the efficacy of local anesthesia in inflamed tissues. CONCLUSION: It has been observed in this study that the action of sodium bicarbonate in local anesthetics increases the pH levels of these solutions, thus possibly making them more effective in an acidic environment.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Anestesia Dentária/métodos , Anestesia Local/métodos , Anestésicos Locais/administração & dosagem , Doenças Periapicais/fisiopatologia , Bicarbonato de Sódio/administração & dosagem , Fístula Dentária/complicações , Método Duplo-Cego , Epinefrina/administração & dosagem , Humanos , Concentração de Íons de Hidrogênio , Injeções , Lidocaína/administração & dosagem , Maxila/cirurgia , Medição da Dor/métodos , Extração Dentária/métodos , Odontalgia/complicações , Vasoconstritores/administração & dosagem
20.
J Pharm Sci ; 102(11): 4159-72, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24114833

RESUMO

With the aid of experimental design, we developed and characterized nanoemulsions for parenteral drug delivery. Formulations containing a mixture of medium-chain triglycerides and soybean oil as oil phase, lecithin (soybean/egg) and polysorbate 80 as emulsifiers, and 0.1 M phosphate buffer solution (pH 8) as aqueous phase were prepared by cold high-pressure homogenization. To study the effects of the oil content, lecithin type, and the presence of diazepam as a model drug and their interactions on physicochemical characteristics of nanoemulsions, a three factor two-level full factorial design was applied. The nanoemulsions were evaluated concerning droplet size and size distribution, surface charge, viscosity, morphology, drug-excipient interactions, and physical stability. The characterization revealed the small spherical droplets in the range 195 -220 nm with polydispersity index below 0.15 and zeta potential between -30 and - 60 mV. Interactions among the investigated factors, rather than factors alone, were shown to more profoundly affect nanoemulsion characteristics. In vivo pharmacokinetic study of selected diazepam nanoemulsions with different oil content (20%, 30%, and 40%, w/w) demonstrated fast and intense initial distribution into rat brain of diazepam from nanoemulsions with 20% and 30% (w/w) oil content, suggesting their applicability in urgent situations.


Assuntos
Adjuvantes Anestésicos/administração & dosagem , Adjuvantes Anestésicos/farmacocinética , Encéfalo/metabolismo , Diazepam/administração & dosagem , Diazepam/farmacocinética , Emulsões/química , Veículos Farmacêuticos/química , Adjuvantes Anestésicos/química , Animais , Diazepam/química , Emulsificantes/química , Lecitinas/química , Masculino , Polissorbatos/química , Ratos , Ratos Wistar , Solubilidade , Óleo de Soja/química , Triglicerídeos/química
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