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1.
Ann Vasc Surg ; 38: 212-219, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27521821

ABSTRACT

BACKGROUND: Venous ulcers are common complications of chronic venous insufficiency that result in severe physical and mental suffering to patients. The oral administration of diosmin/hesperidin has been used as adjuvant therapy in the treatment of chronic venous insufficiency. The purpose of this study was to evaluate and compare the effect of pycnogenol and diosmin/hesperidin on the healing of venous ulcers. METHODS: This longitudinal, prospective, randomized clinical trial was conducted with 30 adult patients with venous ulcers from a vascular surgery outpatient clinic of a university hospital. The patients were randomly allocated to 2 groups: Group 1 (n = 15) was treated with pycnogenol (50 mg orally, 3 times daily) and Group 2 (n = 15) was treated with diosmin/hesperidin (450/50 mg orally, twice daily). They were assessed every 15 days for 90 days. During follow-up visits, photo-documentation was obtained and the ulcer area and circumference of the affected limb were measured. Friedman's test and Mann-Whitney test were used to compare ulcer areas and circumference of affected limbs between and within groups at different time points. The level of significance was set at 5% (P < 0.05) for all tests. RESULTS: Both the pycnogenol and diosmin/hesperidin treatments had a similar effect on the healing of venous ulcers and led to a significant decrease in the circumference of affected limbs (P < 0.0001). CONCLUSION: The results suggest that pycnogenol has an adjuvant effect on the healing of venous ulcers, similar to diosmin/hesperidin.


Subject(s)
Diosmin/therapeutic use , Flavonoids/therapeutic use , Hesperidin/therapeutic use , Varicose Ulcer/drug therapy , Wound Healing/drug effects , Administration, Oral , Aged , Brazil , Diosmin/administration & dosage , Diosmin/adverse effects , Drug Administration Schedule , Drug Combinations , Female , Flavonoids/administration & dosage , Flavonoids/adverse effects , Hesperidin/administration & dosage , Hesperidin/adverse effects , Humans , Longitudinal Studies , Male , Middle Aged , Plant Extracts , Prospective Studies , Time Factors , Treatment Outcome , Varicose Ulcer/diagnosis
2.
Acta Cir Bras ; 34(6): e201900601, 2019 Aug 19.
Article in English | MEDLINE | ID: mdl-31432992

ABSTRACT

PURPOSE: To evaluate PBS®MCIMMO cement in the filling of bone defects. METHODS: Thirty-six adult male Wistar rats were divided into three groups of twelve individuals each (group 1, group 2 and group 3). In all groups, a bone failure in the femur was induced, 2.0 mm wide and 7.0 mm deep. In group 1, the PBS®MCIMMO cement was applied to the bone defect produced and a titanium implant (CONNECTION®) 1.5 mm thick and 6 mm long was installed. In group 2, only the PBS® CIMMO cement was installed. In group 3, only bone failure was performed. Kruskal Wallis tests were performed to compare the mean area among the three groups. RESULTS: In all comparisons, significance was observed for group 2 (p = 0.0014-0.0026). CONCLUSION: The PBS®CIMMO cement induced bone neoformation, and integration between the newly formed bone, cement, and implant was observed.


Subject(s)
Biocompatible Materials/administration & dosage , Bone Cements , Bone Regeneration/physiology , Bone Substitutes/administration & dosage , Ceramics , Femur/surgery , Materials Testing , Animals , Longitudinal Studies , Male , Models, Animal , Prospective Studies , Rats , Rats, Wistar
3.
Acta Cir Bras ; 23(1): 107-11, 2008.
Article in Portuguese | MEDLINE | ID: mdl-18278401

ABSTRACT

PURPOSE: This research explains ethics aspects of experiments in animals and human beings. CONTENTS: It is considered to be a very important issue because it focuses on the mental, spiritual, social and physical well being of humans, without forgetting the animal rights. The majority of the international health research codes mentions that human research must be based on previous laboratory animal testing or on scientific evidences. The author is reviewing the ethics concepts in humans and animal testing. He refers to the international policies for medical research on human beings, Helsinki Declaration, 8.080 and 8.142 of the 1990 federal law, 9.974 of the 1995 federal law and also to the 196/96 Health Department Resolution. Then, a historical retrospective is drawn about the first attempt to establish regulation on animal testing, which happened in the mid of the 19th Century, in London. He also emphasizes that some of the criteria used at that time remains up to the present. The first ethics commission in animal testing was established in Sweeden in 1979 and in the United States in 1984. In Brazil, the ethics animal testing committees were established in the early 90s. Since May 1979, there is the 6.638 Federal Law which establishes regulations for the practice of animal use in research or teaching. This law is still waiting to be enforced. In addition to it, there are some drafts being analyzed by the Congress to regulate the use of animal for the purpose of teaching and researching. Finally the policies adopted by the Brazilian College of Animal Experiments are presented by the author. CONCLUSIONS: The professors, post-graduates, residents and medical students , as well as other students from health related courses enrolled in human and animal testing researches must be aware of ethics principles aiming to protect researchers, research subjects and the animals selected for scientific work.


Subject(s)
Animal Experimentation/ethics , Biomedical Research/ethics , Ethics, Research , Human Experimentation/ethics , Animal Experimentation/legislation & jurisprudence , Animal Rights , Animals , Biomedical Research/legislation & jurisprudence , Brazil , Ethics Committees , Human Experimentation/legislation & jurisprudence , Human Rights , Humans
4.
Acta Cir Bras ; 33(11): 1027-1036, 2018 Nov.
Article in English | MEDLINE | ID: mdl-30517329

ABSTRACT

PURPOSE: To compare two suture threads, poliglecaprone 25 and nylon, used as intradermal suture for skin closure in women undergoing their first cesarean section. METHODS: This is a randomized clinical trial. A total of 60 women undergoing their first cesarean section were enrolled and prospectively assessed. They were randomly allocated to group I (n=30), which received an intradermal suture with nylon 4.0 or to group II (n=30), which had an intradermal suture with poliglecaprone 25, 4.0. The main author took standardized photographs of the scar 6 months after the operation. Four independent raters, two senior obstetricians and two senior plastic surgeons (a male and a female physician from each specialty) assessed the photographs.The panelists rated the scar according to Trimbos scale, composed by the subscales hypertrophy, color and width of the scar. RESULTS: At baseline, patients in both groups were similar regarding age and body mass index. Five patients withdraw the study, four from group and one from group II. Scars of patients from group II were significantly less hypertrophic (p=0.001), thinner (p=0.019) and had more acceptable color (p=0.019). CONCLUSION: The intradermal suture with poliglecaprone 25 for skin closure after cesarean incision provides better aesthetic result.


Subject(s)
Cesarean Section/methods , Cicatrix , Dioxanes/therapeutic use , Nylons , Polyesters/therapeutic use , Suture Techniques , Sutures , Biocompatible Materials , Esthetics , Female , Humans , Prospective Studies , Reference Values , Reproducibility of Results , Statistics, Nonparametric , Treatment Outcome
5.
Acta Cir Bras ; 31(6): 422-7, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27355751

ABSTRACT

PURPOSE: To evaluate the clinical applicability of Pozzolana Biologic Silva cement (PBS(r)) in endodontic surgery. METHODS: Persistent apical periodontitis was diagnosed in 30 teeth of 12 patients by cone-beam computed tomography (CT). All patients had 2 or 4 affected teeth and underwent endodontic surgery with root-end filling. Patients with 2 affected teeth had one tooth (control) treated with mineral trioxide aggregate (MTA-Angelus(r)) as a root-end filling material, and the other tooth treated with PBS (experiment). When the patient had four affected teeth, two of them were treated with MTA and two with PBS. Six months after surgery, all patients were assessed by CT scan. Between-group comparisons of measurements were performed using the Wilcoxon test. RESULTS: Periradicular tissue regeneration was observed in all cases. Significant within-group differences in long axes of the lesion were found in the bucco-palatal direction (PBS group, p=0.0012; MTA group, p=0.024) and coronal-apical direction (PBS group, p=0.0007; MTA group, p=0.0015) between pre- and postoperative measurements. CONCLUSIONS: Pozzolana Biologic Silva cement can be used in the treatment of persistent periradicular lesions. The clinical use of PBS as a root-end filling material may be an alternative to MTA. PBS has additives, which provide enhanced strength.


Subject(s)
Aluminum Compounds/therapeutic use , Biocompatible Materials/therapeutic use , Calcium Compounds/therapeutic use , Dental Cements/therapeutic use , Oxides/therapeutic use , Periapical Periodontitis/surgery , Root Canal Filling Materials/therapeutic use , Silicates/therapeutic use , Adolescent , Adult , Apicoectomy/methods , Cone-Beam Computed Tomography , Drug Combinations , Humans , Middle Aged , Periapical Periodontitis/diagnostic imaging , Postoperative Period , Prospective Studies , Regeneration/physiology , Tooth Root/diagnostic imaging , Tooth Root/surgery , Young Adult
6.
Acta Cir Bras ; 30(2): 160-4, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25714696

ABSTRACT

PURPOSE: To assess periradicular lesions clinically and by computed tomography (CT) after endodontic surgery using either Portland cement or mineral trioxide aggregate (MTA) as a root-end filling material. METHODS: Three patients diagnosed with periradicular lesions by cone-beam CT underwent endodontic surgery with root-end filling. Patient A was treated with MTA as the root-end filling material, patient B was treated with Portland cement and patient C had two teeth treated, one with MTA and the other with Portland cement. Six months after surgery, the patients were assessed clinically and by CT scan and the obtained results were compared. RESULTS: Periradicular tissue regeneration was observed in all cases, with no significant differences in bone formation when comparing the use of MTA and Portland cement as root-end filling materials. CONCLUSION: Both mineral trioxide aggregate and Portland cement were successful in the treatment of periradicular lesions.


Subject(s)
Aluminum Compounds/therapeutic use , Calcium Compounds/therapeutic use , Dental Cements/therapeutic use , Oxides/therapeutic use , Periapical Diseases/surgery , Root Canal Filling Materials/therapeutic use , Root Canal Therapy/methods , Silicates/therapeutic use , Tooth Root/surgery , Adult , Drug Combinations , Female , Humans , Male , Materials Testing , Periapical Diseases/diagnostic imaging , Pilot Projects , Postoperative Period , Prospective Studies , Reproducibility of Results , Time Factors , Tomography, X-Ray Computed/methods , Tooth Root/diagnostic imaging , Treatment Outcome , Young Adult
7.
Acta cir. bras ; 34(6): e201900601, 2019. tab, graf
Article in English | LILACS | ID: biblio-1019269

ABSTRACT

Abstract Purpose To evaluate PBS®MCIMMO cement in the filling of bone defects. Methods Thirty-six adult male Wistar rats were divided into three groups of twelve individuals each (group 1, group 2 and group 3). In all groups, a bone failure in the femur was induced, 2.0 mm wide and 7.0 mm deep. In group 1, the PBS®MCIMMO cement was applied to the bone defect produced and a titanium implant (CONNECTION®) 1.5 mm thick and 6 mm long was installed. In group 2, only the PBS® CIMMO cement was installed. In group 3, only bone failure was performed. Kruskal Wallis tests were performed to compare the mean area among the three groups. Results In all comparisons, significance was observed for group 2 (p = 0.0014-0.0026). Conclusion The PBS®CIMMO cement induced bone neoformation, and integration between the newly formed bone, cement, and implant was observed.


Subject(s)
Animals , Male , Biocompatible Materials/administration & dosage , Bone Cements , Bone Regeneration/physiology , Materials Testing , Ceramics , Bone Substitutes/administration & dosage , Femur/surgery , Prospective Studies , Longitudinal Studies , Rats, Wistar , Models, Animal
8.
Acta cir. bras ; 33(11): 1027-1036, Nov. 2018. tab, graf
Article in English | LILACS | ID: biblio-973478

ABSTRACT

Abstract Purpose: To compare two suture threads, poliglecaprone 25 and nylon, used as intradermal suture for skin closure in women undergoing their first cesarean section. Methods: This is a randomized clinical trial. A total of 60 women undergoing their first cesarean section were enrolled and prospectively assessed. They were randomly allocated to group I (n=30), which received an intradermal suture with nylon 4.0 or to group II (n=30), which had an intradermal suture with poliglecaprone 25, 4.0. The main author took standardized photographs of the scar 6 months after the operation. Four independent raters, two senior obstetricians and two senior plastic surgeons (a male and a female physician from each specialty) assessed the photographs.The panelists rated the scar according to Trimbos scale, composed by the subscales hypertrophy, color and width of the scar. Results: At baseline, patients in both groups were similar regarding age and body mass index. Five patients withdraw the study, four from group and one from group II. Scars of patients from group II were significantly less hypertrophic (p=0.001), thinner (p=0.019) and had more acceptable color (p=0.019). Conclusion: The intradermal suture with poliglecaprone 25 for skin closure after cesarean incision provides better aesthetic result.


Subject(s)
Humans , Female , Polyesters/therapeutic use , Sutures , Cesarean Section/methods , Suture Techniques , Cicatrix , Dioxanes/therapeutic use , Nylons , Reference Values , Biocompatible Materials , Prospective Studies , Reproducibility of Results , Treatment Outcome , Statistics, Nonparametric , Esthetics
9.
Acta Cir Bras ; 27(11): 809-14, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23117614

ABSTRACT

PURPOSE: To evaluate the use of Portland cements with additives as furcation perforation repair materials and assess their biocompatibility. METHODS: The four maxillary and mandibular premolars of ten male mongrel dogs (1-1.5 years old, weighing 10-15 kg) received endodontic treatment (n=80 teeth). The furcations were perforated with a round diamond bur (1016 HL). The perforations involved the dentin, cementum, periodontal ligament, and alveolar bone. A calcium sulfate barrier was placed into the perforated bone to prevent extrusion of obturation material into the periradicular space. The obturation materials MTA (control), white, Type II, and Type V Portland cements were randomly allocated to the teeth. Treated teeth were restored with composite resin. After 120 days, the animals were sacrificed and samples containing the teeth were collected and prepared for histological analysis. RESULTS: There were no significant differences in the amount of newly formed bone between teeth treated with the different obturation materials (p=0.879). CONCLUSION: Biomineralization occurred for all obturation materials tested, suggesting that these materials have similar biocompatibility.


Subject(s)
Dental Cements/therapeutic use , Furcation Defects/drug therapy , Root Canal Filling Materials/therapeutic use , Root Canal Obturation/methods , Tooth Root/injuries , Aluminum Compounds/therapeutic use , Animals , Bicuspid , Biocompatible Materials/chemistry , Biocompatible Materials/therapeutic use , Bone Regeneration , Calcium Compounds/therapeutic use , Calcium Sulfate/chemistry , Calcium Sulfate/therapeutic use , Dental Cements/chemistry , Dogs , Drug Combinations , Male , Materials Testing , Oxides/therapeutic use , Root Canal Filling Materials/chemistry , Silicates/therapeutic use , Time Factors
10.
Acta cir. bras ; 31(6): 422-427, graf
Article in English | LILACS | ID: lil-785019

ABSTRACT

ABSTRACT PURPOSE: To evaluate the clinical applicability of Pozzolana Biologic Silva cement (PBS(r)) in endodontic surgery. METHODS: Persistent apical periodontitis was diagnosed in 30 teeth of 12 patients by cone-beam computed tomography (CT). All patients had 2 or 4 affected teeth and underwent endodontic surgery with root-end filling. Patients with 2 affected teeth had one tooth (control) treated with mineral trioxide aggregate (MTA-Angelus(r)) as a root-end filling material, and the other tooth treated with PBS (experiment). When the patient had four affected teeth, two of them were treated with MTA and two with PBS. Six months after surgery, all patients were assessed by CT scan. Between-group comparisons of measurements were performed using the Wilcoxon test. RESULTS: Periradicular tissue regeneration was observed in all cases. Significant within-group differences in long axes of the lesion were found in the bucco-palatal direction (PBS group, p=0.0012; MTA group, p=0.024) and coronal-apical direction (PBS group, p=0.0007; MTA group, p=0.0015) between pre- and postoperative measurements. CONCLUSIONS: Pozzolana Biologic Silva cement can be used in the treatment of persistent periradicular lesions. The clinical use of PBS as a root-end filling material may be an alternative to MTA. PBS has additives, which provide enhanced strength.


Subject(s)
Humans , Adolescent , Adult , Middle Aged , Young Adult , Oxides/therapeutic use , Periapical Periodontitis/surgery , Biocompatible Materials/therapeutic use , Calcium Compounds/therapeutic use , Aluminum Compounds/therapeutic use , Dental Cements/therapeutic use , Apicoectomy/methods , Periapical Periodontitis/diagnostic imaging , Postoperative Period , Regeneration/physiology , Tooth Root/surgery , Tooth Root/diagnostic imaging , Prospective Studies , Drug Combinations , Cone-Beam Computed Tomography
11.
Acta Cir Bras ; 25(6): 479-84, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21120277

ABSTRACT

PURPOSE: Clinical, radiological and histological evaluation of root perforations treated with mineral trioxide aggregate (MTA) or Portland cements, and calcium sulfate barrier. METHODS: One molar and 11 premolar teeth of a male mongrel dog received endodontic treatment and furcations were perforated with a high-speed round bur and treated with a calcium sulfate barrier. MTA, Portland cement type II (PCII) and type V (PCV), and white Portland cement (WPC) were used as obturation materials. The teeth were restored with composite resin and periapical radiographs were taken. The animal was euthanized 120 days post-surgery for treatment evaluation. RESULTS: Right lower first premolar (MTA), right lower third premolar (PCV), left lower second premolar (MTA), and right lower second premolar (WPC): clinically normal, slightly radio-transparent area on the furcation, little inflammatory infiltrate, and new-bone formation. Left lower third premolar (PCII), right upper first premolar (WPC), right upper third premolar (PCII), and left upper first molar (PCV): clinically normal, radiopaque area on the furcation, and new-bone formation. Right upper second premolar (MTA), left upper second premolar (WPC), left upper third premolar (PCII): presence of furcation lesion, large radiolucent area, and intense inflammatory infiltrate. CONCLUSION: All obturation materials used in this study induced new-bone formation.


Subject(s)
Aluminum Compounds/pharmacology , Biocompatible Materials/pharmacology , Calcium Compounds/pharmacology , Calcium Sulfate/pharmacology , Dental Cements/pharmacology , Oxides/pharmacology , Root Canal Filling Materials/pharmacology , Silicates/pharmacology , Tooth Root/injuries , Animals , Biocompatible Materials/adverse effects , Dogs , Drug Combinations , Male , Models, Animal , Molar/diagnostic imaging , Molar/drug effects , Molar/injuries , Osteogenesis/drug effects , Radiography , Random Allocation , Tooth Root/diagnostic imaging
12.
Acta cir. bras ; 30(2): 160-164, 02/2015. tab, graf
Article in English | LILACS | ID: lil-741024

ABSTRACT

PURPOSE: To assess periradicular lesions clinically and by computed tomography (CT) after endodontic surgery using either Portland cement or mineral trioxide aggregate (MTA) as a root-end filling material. METHODS: Three patients diagnosed with periradicular lesions by cone-beam CT underwent endodontic surgery with root-end filling. Patient A was treated with MTA as the root-end filling material, patient B was treated with Portland cement and patient C had two teeth treated, one with MTA and the other with Portland cement. Six months after surgery, the patients were assessed clinically and by CT scan and the obtained results were compared. RESULTS: Periradicular tissue regeneration was observed in all cases, with no significant differences in bone formation when comparing the use of MTA and Portland cement as root-end filling materials. CONCLUSION: Both mineral trioxide aggregate and Portland cement were successful in the treatment of periradicular lesions. .


Subject(s)
Adult , Female , Humans , Male , Young Adult , Aluminum Compounds/therapeutic use , Calcium Compounds/therapeutic use , Dental Cements/therapeutic use , Oxides/therapeutic use , Periapical Diseases/surgery , Root Canal Filling Materials/therapeutic use , Root Canal Therapy/methods , Silicates/therapeutic use , Tooth Root/surgery , Drug Combinations , Materials Testing , Pilot Projects , Postoperative Period , Prospective Studies , Periapical Diseases , Reproducibility of Results , Time Factors , Treatment Outcome , Tomography, X-Ray Computed/methods , Tooth Root
13.
Rev Bras Anestesiol ; 58(6): 614-22, 2008.
Article in English, Portuguese | MEDLINE | ID: mdl-19082408

ABSTRACT

BACKGROUND AND OBJECTIVES: Prophylaxis of postoperative nausea and vomiting has been the subject of several studies. The objective of the present study was to compare anti-emetics, and their association, in the prevention of postoperative nausea and vomiting. METHODS: Seventy patients, ASA I and II, underwent epidural block associated with general anesthesia for gynecologic surgeries. Patients in the Metochlopramide Group (MG) received 20 mg of the drug; the Dexamethasone Group (DeG) received 8 mg; the Droperidol Group (DrG) received 1.25 mg; the Ondansetron Group (OG) received 8 mg; the Dexamethasone-Ondansetron Group (DeOG) received 8 mg and 4 mg, respectively; the Droperidol-Ondansetron Group (DrOG) received 1.25 mg and 4 mg, respectively; the Dexamethasone-Droperidol-Ondansetron Group (DeDrOG) received 8 mg, 0.625 mg, and 4 mg. The presence of nausea and vomiting was evaluated at 6, 12, 24, and 36 hours after the end of the surgery. RESULTS: The total incidence of episodes of nausea per group is as follows: 4 in DeDrOG, 6 in OG, 6 in DrOG, 11 in DeG, 11 in DeOG, 18 in MG, and 22 in DrG. The Chi-square and Fisher exact tests indicated statistically significant differences between DrG and DeG, DOG, DrOG, DeOG, and DeDrOG; between MG and OG, DrOG, and DeDrOG; and between DeOG and DeDrOG. And the incidence of vomiting was: 3 in OG, 3 in DeDrOG, 6 in DrOG, 7 in DeG, 7 in DeOG, and 10 in DrG, and 13 in G. There was a statistically significant difference between DrG and OG and DeDrOG; and between MG and OG and DeDrOG. CONCLUSIONS: The association dexamethasone-droperidol-ondansetron and ondansetron alone were more effective in the prophylaxis of nausea and vomiting.


Subject(s)
Antiemetics/therapeutic use , Gynecologic Surgical Procedures , Postoperative Nausea and Vomiting/prevention & control , Adult , Antiemetics/administration & dosage , Drug Therapy, Combination , Female , Humans
14.
Rev Bras Anestesiol ; 57(1): 8-18, 2007 Feb.
Article in English, Portuguese | MEDLINE | ID: mdl-19468614

ABSTRACT

BACKGROUND AND OBJECTIVES: The association of drugs with different mechanisms of action in the dorsal horn of the spinal cord decreases postoperative pain, with a reduction in the incidence of side effects. The aim of this study was to evaluate postoperative analgesia and sedation by epidural S(+) ketamine and S(+) ketamine-morphine associated with ropivacaine in subcostal cholecystectomy. METHODS: Seventy patients of both genders, physical status ASA I and II, participated in this study. The following drugs were administered epidurally: 0.75% ropivacaine associated with 0.9% sodium chloride in the Control Group (CG); 0.75% ropivacaine associated with S(+) ketamine (0.5 mg kg(-1)) in the Ketamine Group (KG); 0.75% ropivacaine associated with S(+) ketamine (0.5 mg kg(-1)) and morphine (2 mg) in the Ketamine-Morphine Group2 (KMG2); 0.75% ropivacaine associated with S(+) ketamine (0.5 mg kg(-1)) and morphine (3 mg) in the Ketamine-Morphine Group3 (KMG3). Analgesia and sedation were evaluated 2h, 6h, and 24h after the end of the surgery. RESULTS: Sedation was observed up to 2 hours after the end of the procedure in KG, KMG2, and KMG3. Analgesia was effective in CG up to 2 hours after the surgery, at 2h and 6h in KG, and at 2h, 6h, and 24h, in KMG2 and KMG3. CONCLUSIONS: S(+) ketamine and the associations S(+) ketamine-morphine promoted sedation up to 2h after the end of the surgical procedure. S(+) ketamine promoted analgesia especially at the moment of the 2h observation, and the associations of S(+) ketamine-morphine promoted analgesia especially at 2h and 6h after the surgery.

15.
Acta cir. bras ; 27(11): 809-814, Nov. 2012. ilus, tab
Article in English | LILACS | ID: lil-654249

ABSTRACT

PURPOSE: To evaluate the use of Portland cements with additives as furcation perforation repair materials and assess their biocompatibility. METHODS: The four maxillary and mandibular premolars of ten male mongrel dogs (1-1.5 years old, weighing 10-15 kg) received endodontic treatment (n=80 teeth). The furcations were perforated with a round diamond bur (1016 HL). The perforations involved the dentin, cementum, periodontal ligament, and alveolar bone. A calcium sulfate barrier was placed into the perforated bone to prevent extrusion of obturation material into the periradicular space. The obturation materials MTA (control), white, Type II, and Type V Portland cements were randomly allocated to the teeth. Treated teeth were restored with composite resin. After 120 days, the animals were sacrificed and samples containing the teeth were collected and prepared for histological analysis. RESULTS: There were no significant differences in the amount of newly formed bone between teeth treated with the different obturation materials (p=0.879). CONCLUSION: Biomineralization occurred for all obturation materials tested, suggesting that these materials have similar biocompatibility.


OBJETIVO: Avaliar o uso de cimentos Portland aditivados na reparação de perfurações radiculares e a biocompatibilidade destes materiais. MÉTODOS: Oitenta pré-molares, quatro da arcada dentária superior e quatro da arcada inferior de 10 cães machos, sem raça definida, com idade em torno de um a um ano e meio, pesando entre 10 e 15 kg foram submetidos a tratamento endodôntico, sendo realizadas perfurações nas furcas com broca de diamante 1016 HL. A cavidade envolveu dentina e cemento, como também periodonto e o osso alveolar. Na porção óssea da obturação, barreira de sulfato de cálcio foi utilizada evitando extravasamento do cimento para o espaço periodontal. Foi realizada a distribuição randomizada dos cimentos MTA (controle), Portland tipo II, Portland tipo V e Portland branco estrutural nas obturações. Os dentes foram restaurados com resina composta. Após 120 dias realizou-se eutanásia, retirada dos dentes, preparação e análise histológica. RESULTADOS: Entre os cimentos não houve diferença estatística significante quanto à neoformação óssea (p=0,879). CONCLUSÃO: Ocorreu biomineralização com os diferentes cimentos usados no estudo, sugerindo que estes são similares em termos de biocompatibilidade.


Subject(s)
Animals , Dogs , Male , Dental Cements/therapeutic use , Furcation Defects/drug therapy , Root Canal Filling Materials/therapeutic use , Root Canal Obturation/methods , Tooth Root/injuries , Aluminum Compounds/therapeutic use , Bicuspid , Bone Regeneration , Biocompatible Materials/chemistry , Biocompatible Materials/therapeutic use , Calcium Compounds/therapeutic use , Calcium Sulfate/chemistry , Calcium Sulfate/therapeutic use , Drug Combinations , Dental Cements/chemistry , Materials Testing , Oxides/therapeutic use , Root Canal Filling Materials/chemistry , Silicates/therapeutic use , Time Factors
16.
Rev Bras Anestesiol ; 55(5): 525-31, 2005 Oct.
Article in Portuguese | MEDLINE | ID: mdl-19468643

ABSTRACT

BACKGROUND AND OBJECTIVES: Low dose ketamine decreases nociception by blocking NMDA receptor channels. Alpha2-adrenergic receptor activation triggers intense analgesic response. This study aimed at evaluating the effects of epidural ketamine, clonidine and dexmedetomidine, in patients undergoing upper abdominal surgery. METHODS: Participated in this randomized double-blind study 70 patients of both genders, aged 18 to 50 years, physical status ASA I or II, submitted to subcostal cholecystectomy under general anesthesia associated to lumbar epidural anesthesia. Lumbar epidural anesthesia was randomly induced as follows: CONTROL GROUP: 20 mL of 0.75% ropivacaine and 1 mL of 0.9% saline solution (n = 10); Ketamine group: 20 mL of 0.75% ropivacaine and 0.5 mg.kg-1 ketamine (n = 20); Clonidine group: 20 mL of 0.75% ropivacaine and 1 mL clonidine (150 microg) (n = 20); Dexmedetomidine group: 20 mL of 0.75% ropivacaine and 2 microg.kg-1 dexmedetomidine (n = 20). Anesthesia was induced with etomidate, alfentanil and rocuronium and was maintained with isoflurane and alfentanil. Analgesia was evaluated by clinical signs and inhalational anesthetic inspired concentration was evaluated by anesthetic gases analysis during surgery. RESULTS: All patients receiving ketamine, clonidine or dexmedetomidine had heart rate and systemic blood pressure decrease and have not required perioperative analgesic complementation. For the same patients, isoflurane inspired concentration varied from 0.5vol% to 1vol% and there were no clinical signs or responses suggesting inadequate anesthetic levels. CONCLUSIONS: Epidural ketamine, clonidine or dexmedetomidine decreases alfentanil consumption and isoflurane inspired concentration in the intraoperative period of upper abdominal surgery.

17.
Rev. dor ; 11(1)jan.-mar. 2010.
Article in Portuguese | LILACS | ID: lil-562424

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: A anestesia geral é a técnica mais utilizada para a realização dos procedimentos cirúrgicos de tratamento do câncer de mama, sendo também empregadas anestesia regional e a associação de ambas as técnicas. Os objetivos deste estudo foram observar a presença de dor pós-operatória, a necessidade de analgésicos e o tempo de permanência hospitalar.MÉTODO: Após aprovação pelo Comitê de Ética em Pesquisa, participaram deste estudo aleatório e prospectivo, 40 pacientes do sexo feminino, com idade variando de 25 a 55 anos, peso entre 50 e 100 kg, estado físico ASA I e II, submetidas à mastectomia ou quadrantectomia com axilectomia, sob bloqueio interpleural associado à anestesia geral. As pacientes foram divididas em quatro grupos de 10. LMC: levobupivacaína - morfina - clonidina; RMC: ropivacaína - morfina - clonidina; LMK: levobupivacaína - morfina - cetamina; RMK - ropivacaína - morfina - cetamina. A indução da anestesia geral foi realizada com a administração de etomidato (0,2 mg.kg-1), alfentanil (30 µg.kg-1) e rocurônio (0,6 mg.kg-1) e a manutenção com oxigênio e isoflurano (0,5 vol% a 3,0 vol%). O bloqueio interpleural foi executado no EIC5, linha axilar média, com agulha de Tuohy 17G, sendo administradas levobupivacaína a 0,5% (100 mg) com adrenalina 1:200.000 (5 µg.mL-1) ou ropivacaína 0,75% (150 mg), morfina (3 mg) e clonidina (150 µg) ou cetamina (0,5 mg.kg-1). A analgesia pós-operatória, analisada pela escala analógica visual (EAV), foi observada às 6h, 12h, 18h e 24h após o término do ato operatório.RESULTADOS: Quinze pacientes apresentaram dor pós-operatória leve, sendo: nos grupos LMC e RMC, uma entre 6 e 12h, uma entre 12 e 18h e duas entre 18 e 24h; no grupo LMK, duas até 6h, duas entre 6 e 12h e uma entre 12 e 18h; no grupo RMK, duas até 6h e quatro entre 6 e 12h. Utilizando o teste do Qui-quadrado observou-se diferença estatística significante entre o grupo LMC e os grupos LMK e RMK, assim como entre o grupo RMC e os grupos LMK e RMK. Aplicando o teste Exato de Fisher observou-se diferença estatística significante entre o tempo de observação até 6h e o tempo de 18-24h nos grupos LMC e RMC. Não ocorreram complicações relacionadas ao bloqueio interpleural. Foi necessário administrar somente dipirona para tratamento da dor pós-operatória.CONCLUSÃO: As pacientes que apresentaram dor pós-operatória necessitaram somente de analgésico comum (dipirona), sendo que todas tiveram alta hospitalar com 24h de pós-operatório.


BACKGROUND AND OBJECTIVES: General anesthesia is the most widely used technique for breast cancer surgical procedures, being also used regional anesthesia and the association of both techniques. This study aimed at observing the presence of postoperative pain, the need for analgesics and hospital stay length.METHOD: After the Research Ethics Committee approval, participated in this randomized prospective study 40 female patients aged 25 to 55 years, weighing between 50 and 100 kg, physical status ASA I and II, submitted to mastectomy or quadrantectomy with axillectomy, under interpleural block associated to general anesthesia. Patients were distributed in four groups of 10: LMC: levobupivacaine - morphine - clonidine; RMC: ropivacaine - morphine - clonidine; LMK: levobupivacaine - morphine - ketamine; RMK: ropivacaine - morphine - ketamine. General anesthesia was induced with etomidate (0.2 mg.kg-1), alfentanil (30 µg.kg-1) and rocuronium (0.6 mg.kg-1) and was maintained with oxygen and isoflurane (0.5 vol% at 3.0 vol%). Interpleural block was induced in EIC5, median axillary line, with Tuohy 17G needle, with 0.5% levobupivacaine (100 mg) with epinephrine 1:200,000 (5 µg.mL-1) or 0.75% ropivacaine (150 mg), morphine (3 mg) and clonidine (150 µg) or ketamine (0,5 mg.kg-1). Postoperative analgesia evaluated by the visual analog scale (VAS) was observed at 6h, 12h, 18h and 24h after surgery completion.RESULTS: Fifteen patients referred mild postoperative pain being: in groups LMC and RMC, one between 6 and 12 h, one between 12 and 18 h and two between 18 and 14 h; in group RMK, two up to 6 h and four between 6 and 12 h. Using Chi-square test, there has been statistically significant difference between group LMC and groups LMK and RMK, as well as between group RMC and groups LMK and RMK. Fisher's Exact test has shown statistically significant difference between observation time up to 6 h and time of 18-24 h in groups LMC and RMC. There were no interpleural block-related complications. Only dipirone was needed to treat postoperative pain.CONCLUSION: Patients with postoperative pain only needed common analgesics (dipirone) and all were discharged 24 hours after surgery completion


Subject(s)
Humans , Female , Adult , Middle Aged , Anesthetics/administration & dosage , Nerve Block/standards , Pain, Postoperative/drug therapy , Breast Neoplasms/surgery , Pleura , Amides/administration & dosage , Nerve Block/methods , Bupivacaine/administration & dosage , Bupivacaine/analogs & derivatives , Clonidine/administration & dosage , Data Interpretation, Statistical , Double-Blind Method , Dipyrone/administration & dosage , Pain, Postoperative/prevention & control , Ketamine/administration & dosage , Length of Stay , Morphine/administration & dosage , Prospective Studies
18.
Rev. dor ; 11(2)abr.-jun. 2010.
Article in Portuguese | LILACS | ID: lil-562454

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: Pesquisas empregando bloqueio interpleural com anestésico local, opioide e agonista Alfa2-adrenérgico ou bloqueador do receptor N-metil-D-aspartato (NMDA), observaram a ocorrência de analgesia pós-operatória em cirurgias de abdômen superior. O objetivo deste estudo foi observar a presença de dor no pós-operatório de cirurgias de colecistectomia por via subcostal.MÉTODO: Após aprovação pelo Comitê de Ética, participaram do experimento aleatório e prospectivo, 40 pacientes, de ambos os sexos, com idade variando de 18 a 50 anos, peso entre 50 e 100 kg, estado físico ASA I e II, submetidos à colecistectomia por via subcostal, sob anestesia geral associada ao bloqueio interpleural. Foram administradas levobupivacaína a 0,5% (100 mg) com adrenalina 1:200.000 (5 µg.mL-1) ou ropivacaína a 0,75% (150 mg), morfina (3 mg) e clonidina (3 µg.kg-1) ou cetamina (0,5 mg.kg-1), ao nível EIC7, na linha axilar média, com agulha de Tuohy 17G, por via interpleural. A indução da anestesia geral foi realizada com a injeção de etomidato (0,2 mg.kg-1), alfentanil (30 µg.kg-1) e rocurônio (0,6 mg.kg-1) e a manutenção com oxigênio e isoflurano (0,5 vol% a 3,0 vol%). A analgesia pós-operatória, analisada pela escala analógica visual (EAV), foi observada às 6h, 12h, 18h e 24h após o término do ato operatório.RESULTADOS: Apresentaram dor pós-operatória: grupo RMC (ropivacaína, morfina e clonidina), um até 6h, seis entre 6 e 12h e um entre 18 e 24h; grupo RMK (ropivacaína, morfina e cetamina), quatro até 6h, quatro entre 6 e 12h, um entre 12 e 18h e um entre 18 e 24h; grupo LMC (levobupivacaína, morfina e clonidina), quatro até 6h e quatro entre 6 e 12h; grupo LMK (levobupivacaína, morfina e cetamina, cinco até 6h, quatro entre 6 e 12h e um entre 12 e 18h. Aplicando o teste Exato de Fisher observou-se diferença estatística significante entre o tempo de observação até 6h e os demais no grupo RMC; entre o tempo de observação até 6h e os 12-18h e 18-24h nos grupos RMK e LMK. Não ocorreram complicações relacionadas ao bloqueio interpleural.CONCLUSÃO: A necessidade de associar opioide ao analgésico comum para abolir a dor, em cirurgias de colecistectomia por via subcostal, ocorreu em número reduzido de pacientes.


BACKGROUND AND OBJECTIVES: Researches using interpleural block with local anesthetics, opioid and alpha2-adrenergic agonist or N-Methyl-D-aspartate (NMDA) receptor blocker have shown the presence of postoperative analgesia in upper abdominal surgeries. This study aimed at observing the presence of pain in the postoperative period of subcostal cholecystectomies. METHOD: After The Ethics Committee approval, participated in this randomized, prospective study 40 patients of both genders, aged 18 to 50 years, weighing between 50 and 100 kg, physical status ASA I and II, submitted to subcostal cholecystectomy under general anesthesia associated to interpleural block. The following drugs were administered: 0.5% levobupivacaine (100 mg) with 1:200.000 epinephrine (5 µg.mL-1) or 0.75% ropivacaine (150 mg), morphine (3 mg) and clonidine (3 µg.kg-1) or ketamine (0,5 mg.kg-1), at EIC7, in the medium axillary line with 17G Tuohy needle by interpleural route. General anesthesia was induced with etomidate (0.2 mg.kg-1), alfentanil (30 µg.kg-1) and rocuronium (0.6 mg.kg-1) and was maintained with oxygen and isoflurane (0.5 vol% at 3.0 vol%). Postoperative analgesia, evaluated by the visual analog scale (VAS), was observed at 6h, 12h, 18h and 24h after surgery completion.RESULTS: Postoperative pain was observed: one patient up to 6h, six between 6 and 12h and one between 18 and 24h in the RMC group (ropivacaine, morphine and clonidine); four patients up to 6h, four between 6 and 12h, one between 12 and 18h and one between 18 and 24h in the RMK group (ropivacaine, morphine and ketamine); four patients up to 6h, and four between 6 and 12h in the LMC group (levobupivacaine, morphine and clonidine); five patients up to 6h, four between 6 and 12h, and one between 12 and 18h in the LMK group (levobupivacaine, morphine and ketamine). Fisher's Exact test has shown statistically significant difference between 6h observation time and the others in the RMC group; between 6h observation time and 12-18h and 18-24h in RMK and LMK groups. There were no interpleural block-related complications.CONCLUSION: Only a small number of patients needed the association of opioid to normal analgesics to abolish pain in subcostal cholecystectomy surgeries.

19.
Acta cir. bras ; 25(6): 479-484, nov.-dez. 2010. ilus
Article in English | LILACS | ID: lil-567275

ABSTRACT

PURPOSE: Clinical, radiological and histological evaluation of root perforations treated with mineral trioxide aggregate (MTA) or Portland cements, and calcium sulfate barrier. METHODS: One molar and 11 premolar teeth of a male mongrel dog received endodontic treatment and furcations were perforated with a high-speed round bur and treated with a calcium sulfate barrier. MTA, Portland cement type II (PCII) and type V (PCV), and white Portland cement (WPC) were used as obturation materials. The teeth were restored with composite resin and periapical radiographs were taken. The animal was euthanized 120 days post-surgery for treatment evaluation. RESULTS: Right lower first premolar (MTA), right lower third premolar (PCV), left lower second premolar (MTA), and right lower second premolar (WPC): clinically normal, slightly radio-transparent area on the furcation, little inflammatory infiltrate, and new-bone formation. Left lower third premolar (PCII), right upper first premolar (WPC), right upper third premolar (PCII), and left upper first molar (PCV): clinically normal, radiopaque area on the furcation, and new-bone formation. Right upper second premolar (MTA), left upper second premolar (WPC), left upper third premolar (PCII): presence of furcation lesion, large radiolucent area, and intense inflammatory infiltrate. CONCLUSION: All obturation materials used in this study induced new-bone formation.


OBJETIVO: Avaliar clínica, radiológica e histologicamente perfurações radiculares tratadas com MTA e cimentos Portland, com barreira de sulfato de cálcio. MÉTODOS: A amostra foi constituída por 11 dentes pré-molares e um molar de cão macho, sem raça definida. Após tratamento endodôntico realizaram-se perfurações nas furcas com broca esférica de alta rotação e barreira de sulfato de cálcio. Foram utiliados os cimentos MTA, Portland tipo II (CPII), Portland tipo V (CPV) e Portland branco estrutural (CPB). Os dentes foram restaurados com resina composta e submetidos a radiografias periapicais. O animal foi confinado por 120 dias e submetido à eutanásia para avaliações. RESULTADOS: Primeiro pré-molar inferior direito (MTA), terceiro pré-molar inferior direito (CPV), segundo pré-molar inferior esquerdo (MTA) e segundo pré-molar inferior direito (CPB): clinicamente normal; leve área radiotransparente na furca; pequeno infiltrado inflamatório e neoformação óssea. Terceiro pré-molar inferior esquerdo (CPII), primeiro pré-molar superior direito (CPB), terceiro pré-molar superior direito (CPII) e primeiro molar superior esquerdo (CPV): clinicamente normal; área radiopaca na furca; neoformação óssea. Segundo pré-molar superior direito (MTA), segundo pré-molar superior esquerdo (CPB) e terceiro pré-molar superior esquerdo (CPII): clinicamente com lesão na furca; intensa área radiolucida; infiltrado inflamatório intenso. CONCLUSÃO: Todos os cimentos induziram a neoformação óssea.


Subject(s)
Animals , Dogs , Male , Aluminum Compounds/pharmacology , Biocompatible Materials/pharmacology , Calcium Compounds/pharmacology , Calcium Sulfate/pharmacology , Dental Cements/pharmacology , Oxides/pharmacology , Root Canal Filling Materials/pharmacology , Silicates/pharmacology , Tooth Root/injuries , Biocompatible Materials/adverse effects , Drug Combinations , Models, Animal , Molar/drug effects , Molar/injuries , Molar , Osteogenesis/drug effects , Random Allocation , Tooth Root
20.
Rev. dor ; 11(4)out.-dez. 2010.
Article in Portuguese | LILACS | ID: lil-568559

ABSTRACT

JUSTIFICATIVA E OBJETIVOS: O retalho musculocutâneo transverso do reto abdominal (TRAM) permite uma reconstrução completamente autóloga. É um procedimento complexo, de grande porte, exigindo analgesia eficiente. O objetivo deste estudo foi relatar o uso do bloqueio interpleural, associado à anestesia geral, para mastectomia e reconstrução imediata com retalho TRAM.RELATOS DOS CASOS: Foram avaliadas três pacientes com 37, 43 e 49 anos, apresentando neoplasia mamária. A indução anestésica foi realizada com etomidato (0,2 mg.kg-1), alfentanil (30 µg.kg-1) e rocurônio (0,6 mg.kg-1), sendo a manutenção obtida pela administração de isoflurano (0,5vol% a 3,0vol%). No bloqueio interpleural foram administradas ropivacaína a 0,75% (150 mg), morfina (3 mg) e clonidina (3 µg.kg-1), ao nível do EIC5, na linha axilar média, com agulha de Tuohy 17G; as pacientes foram colocadas na posição céfalodeclive (20º) imediatamente antes da realização do bloqueio, permanecendo por aproximadamente 10 minutos. A intensidade da dor pós-operatória foi analisada pela escala analógica verbal, nas primeiras 24 horas. Durante o intraoperatório foi administrado isoflurano em doses superiores a 0,5% e inferiores a 3%. Com a associação das técnicas anestésicas utilizadas, as pacientes se queixaram de dor leve nas primeiras 24 horas após o término do procedimento anestésico-cirúrgico, necessitando somente de anti-inflamatório não hormonal (dipirona).CONCLUSÃO: A técnica do bloqueio interpleural é segura e de fácil realização em cirurgias de mastectomia e reconstrução mamária imediata com retalho TRAM. Reduz o consumo de fármacos utilizados no intraoperatório e a solicitação de analgésicos no pós-operatório imediato.


BACKGROUND AND OBJECTIVES: Transverse rectus abdominis myocutaneous flap allows for a totally autologous reconstruction (TRAM). It is a complex and major procedure requiring efficient analgesia. This study aimed at reporting the use of interpleural block associated to general anesthesia for mastectomy and immediate reconstruction with TRAM flap. CASES REPORTS: Three patients aged 37, 43 and 49 years with breast neoplasia were evaluated. Anesthesia was induced with used for interpleural block at the level of EIC5 on the medium axillary line with 17G Tuohy needle; patients were placed in the head-down position (20º) immediately before the block, remaining for approximately 10 minutes. Postoperative pain intensity was evaluated by the verbal analog scale in the first 24 hours. Isoflurane was administered in the perioperative period in doses above 0.5% and below 3%. With the association of the anesthetic techniques, patients reported mild pain during the first 24 hours after anesthetic-surgical procedure completion, needing only non-steroid anti-inflammatory drugs (dipirone).CONCLUSION: Interpleural block is a safe and easy technique for mastectomy and immediate breast reconstruction with TRAM flap. It decreases perioperative drugs consumption and the request for analgesia in the immediate postoperative period.etomidate (0.2 mg.kg-1), alfentanil (30 µg.kg-1) and rocuronium (0.6 mg.kg-1) and was maintained with isoflurane (0.5vol% to 3.0vol%). 0.75% ropivacaine (150 mg), morphine (3 mg) and clonidine (3 µg.kg-1) were used for interpleural block at the level of EIC5 on the medium axillary line with 17G Tuohy needle; patients were placed in the head-down position (20º) immediately before the block, remaining for approximately 10 minutes. Postoperative pain intensity was evaluated by the verbal analog scale in the first 24 hours. Isoflurane was administered in the perioperative period in doses above 0.5% and below 3%. With the association of the anesthetic techniques, patients reported mild pain during the first 24 hours after anesthetic-surgical procedure completion, needing only non-steroid anti-inflammatory drugs (dipirone).CONCLUSION: Interpleural block is a safe and easy technique for mastectomy and immediate breast reconstruction with TRAM flap. It decreases perioperative drugs consumption and the request for analgesia in the immediate postoperative period.

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