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一项关于泛醇鼻喷雾剂在内镜鼻窦手术后对慢性鼻窦炎患者进行术后治疗疗效的随机、前瞻性、双盲研究。

A randomized, prospective, double-blind study of the efficacy of dexpanthenol nasal spray on the postoperative treatment of patients with chronic rhinosinusitis after endoscopic sinus surgery.

作者信息

Tantilipikorn Pongsakorn, Tunsuriyawong Prayuth, Jareoncharsri Perapun, Bedavanija Anan, Assanasen Paraya, Bunnag Chaweewan, Metheetrairut Choakchai

机构信息

Division of Rhinology & Allergy, Department of Otorhinolaryngology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 2012 Jan;95(1):58-63.

Abstract

OBJECTIVE

To assess the efficacy of dexpanthenol nasal spray compared with normal saline spray in the postoperative treatment of patients with chronic rhinosinusitis (CRS) who underwent endoscopic sinus surgery (ESS).

MATERIALS AND METHOD

A prospective, randomized controlled study was conducted in CRS patients who underwent ESS. The enrolled patients had never been operated intranasally. These patients received either dexpanthenol or normal saline nasal spray intranasally four times a day for six weeks post-operatively.

RESULTS

Fifty CRS patients were recruited in the present study. Age ranged from 23 to 63 years (means 43.4 +/- 11.2 years). Forty-four percent of patients were diagnosed as CRS without nasal polyps (NP) (CRSs NP) and 56% were CRS with NP (CRSw NP). Twenty-five cases were randomly assigned to use dexpanthenol nasal spray whereas the other 25 cases used normal saline nasal spray. The preoperative severity of CRS, determined by the computerized tomography (CT) scan scoring system of Lund-McKay was 13.9 +/- 6.2 in the dexpanthenol group and 13.6 +/- 6.9 in the normal saline group, which were not statistically different (p > 0.05). The endoscopic scoring was 10.2 +/- 2 in the dexpanthenol group and 10.7 +/- 3 in the normal saline group, which were not statistically different (p > 0.05). The mucociliary transit time improvement (time difference between pre- and post-treatment by nasal spray) was 8.4 +/- 3.3 minutes in the dexpanthenol group and 1.7 +/- 1.2 minutes in the normal saline group, which were statistically different (p < 0.05).

CONCLUSION

The majority of the postoperative symptom scores and all of the endoscopic scores of the dexpanthenol group were not statistically different from those of the normal saline group. However, dexpanthenol nasal spray has superior efficacy compared with normal saline nasal spray on improvement of mucociliary clearance and nasal discharge in the postoperative care of CRS patients after ESS.

摘要

目的

评估右泛醇鼻喷雾剂与生理盐水喷雾剂相比,在接受鼻内镜手术(ESS)的慢性鼻窦炎(CRS)患者术后治疗中的疗效。

材料与方法

对接受ESS的CRS患者进行一项前瞻性随机对照研究。入选患者从未接受过鼻内手术。这些患者在术后六周内每天接受四次右泛醇或生理盐水鼻喷雾剂鼻内给药。

结果

本研究招募了50例CRS患者。年龄范围为23至63岁(平均43.4±11.2岁)。44%的患者被诊断为无鼻息肉的CRS(CRSsNP),56%为有鼻息肉的CRS(CRSwNP)。25例患者被随机分配使用右泛醇鼻喷雾剂,而另外25例使用生理盐水鼻喷雾剂。根据Lund-McKay计算机断层扫描(CT)评分系统确定的CRS术前严重程度,右泛醇组为13.9±6.2,生理盐水组为13.6±6.9,差异无统计学意义(p>0.05)。内镜评分右泛醇组为10.2±2,生理盐水组为10.7±3,差异无统计学意义(p>0.05)。右泛醇组的黏液纤毛转运时间改善(鼻喷雾剂治疗前后的时间差)为8.4±3.3分钟,生理盐水组为1.7±1.2分钟,差异有统计学意义(p<0.05)。

结论

右泛醇组的大多数术后症状评分和所有内镜评分与生理盐水组相比差异无统计学意义。然而,在ESS术后CRS患者的护理中,右泛醇鼻喷雾剂在改善黏液纤毛清除和鼻涕方面比生理盐水鼻喷雾剂具有更好的疗效。

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