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1.
J Formos Med Assoc ; 122(8): 723-730, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-36623972

RESUMO

BACKGROUND/PURPOSE: Acute oral mucositis (OM) is a painful complication of concurrent chemoradiotherapy (CCRT). This severe adverse symptom may impact on patient's quality of life, lead to malnutrition. Thus, finding more effective methods in OM management is very important. The purpose of this study is to evaluate the efficacy of polyacrylate silver salt/Polyvinylpyrrolidone-based liquid oral gel (named as polyacrylate silver salt oral gel) in improving the symptomatic relief of CCRT-induced oral mucositis and oral dysfunction in neck and head cancer patients. METHODS: In this study, 24 oral cancer patients underwent CCRT and having OM grade 2 or higher were randomly assigned into the test group and the control group. Both groups followed Multinational Association of Supportive Care in Cancer and International Society of Oral Oncology (MASCC/ISOO) clinical practice guidelines for the management of mucositis, but adding rinsing with 15 g oral gel right after oral hygiene treaded the test group. Clinical OM and oral function were assessed weekly for 4 consecutive weeks till 5-10 days after the completion of radiotherapy. For evaluation, Common Terminology Criteria for Adverse Events (CTCAE) v3.0 was used for collecting the data of OM grade. RESULTS: The results showed that polyacrylate silver salt oral gel had better effect for relieving the oral mucositis. There were statistically significant differences in OM grades (1.59 vs. 2.8, p < 0.0001) between the test group and the control group. CONCLUSION: Our clinical studies demonstrated that polyacrylate silver salt oral gel is an effective interventional option in terms of rapid mucositis healing.


Assuntos
Neoplasias de Cabeça e Pescoço , Mucosite , Estomatite , Humanos , Mucosite/induzido quimicamente , Mucosite/tratamento farmacológico , Povidona/efeitos adversos , Prata/efeitos adversos , Qualidade de Vida , Neoplasias de Cabeça e Pescoço/radioterapia , Estomatite/tratamento farmacológico , Estomatite/etiologia , Quimiorradioterapia/efeitos adversos , Quimiorradioterapia/métodos
2.
Surg Today ; 48(7): 680-686, 2018 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-29516276

RESUMO

PURPOSE: Laparoscopic distal pancreatectomy has proven to be feasible and safe. Moreover, robotic surgery provides unique advantages for pancreatic procedures, although single-incision robotic pancreatic surgery is rarely discussed. We applied the single-port modified platform to accomplish robotic distal pancreatectomy in a series of patients. METHODS: The subjects of this study were ten patients who underwent robotic distal pancreatectomy in our hospital between July 1, 2015 and Dec 31, 2016. All patients were placed supine in the reverse Trendelenburg position with the legs abducted. Surgery was performed via a trans-umbilical 5.0-cm incision, using a modified single-port platform (LAGIPORT®) combined with the da Vinci Si Surgical System. The three arms and scope (30-degree up) were inserted through the LAGIPORT® and positioned in a triangle. Endoscopic ultrasound was used to localize the tumor and plan the resection margin. We recorded the surgical time, operation time, blood loss, postoperative pain score, hospital stay, and complications. RESULTS: The surgical time was 236 ± 32 min, the operation time was 172 ± 30 min, and the blood loss was 149 ± 65 ml. All patients underwent robot-assisted distal pancreatectomy without conversion. The average pain score on postoperative day (POD) 3 was 4.5 ± 1. Complications included subsplenic hematoma (n = 1) and minor pancreatic leakage (n = 2). There was no surgical mortality. CONCLUSIONS: Our results demonstrate the safety and efficiency of robotic single-incision distal pancreatectomy via the modified platform (LAGIPORT®).


Assuntos
Pancreatectomia/instrumentação , Neoplasias Pancreáticas/cirurgia , Procedimentos Cirúrgicos Robóticos/instrumentação , Adulto , Idoso , Fístula Anastomótica/epidemiologia , Perda Sanguínea Cirúrgica/estatística & dados numéricos , Feminino , Hematoma/epidemiologia , Humanos , Tempo de Internação , Masculino , Pessoa de Meia-Idade , Duração da Cirurgia , Dor Pós-Operatória/epidemiologia , Pancreatectomia/métodos , Complicações Pós-Operatórias/epidemiologia , Procedimentos Cirúrgicos Robóticos/métodos , Segurança , Esplenopatias/epidemiologia , Decúbito Dorsal , Resultado do Tratamento
3.
J Endod ; 30(3): 131-4, 2004 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-15055427

RESUMO

Our previous in vitro study indicated that Nd:YAG laser irradiation on dentin could melt normal dentin surface and close the exposed dentinal tubule orifices without creating surface cracks. This study evaluated the morphologic changes of hypersensitive dentin after Nd:YAG laser irradiation. Thirty patients with clinically diagnosed cervical dentin hypersensitive teeth were treated with a Nd:YAG laser of 30 mJ intensity at 10 pulses per second for 2 min. An impression of the sensitive area was taken before and after laser treatment and then examined with a scanning electron microscope. The impression of the dentin surface after Nd:YAG laser treatment showed no protrusive rods, in contrast with the presence of numerous rods before laser irradiation. Because protrusive rods are a measure of open dentinal tubules, we interpret these data to support the hypothesis that Nd:YAG laser irradiation at specifications of 30 mJ, 10 pulses per second, and 2 min can be used to seal the exposed dentinal tubules.


Assuntos
Sensibilidade da Dentina/terapia , Terapia a Laser , Adolescente , Dentina/ultraestrutura , Feminino , Humanos , Masculino , Microscopia Eletrônica de Varredura , Pessoa de Meia-Idade , Neodímio
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