AIM:To evaluate the effect of differ-ent frequencies 0.01%atropine eye drops on the ocular surface in adolescent myopia control.METH-ODS:A total of 84 adolescent patients with myopia were recruited for this study.They were randomly assigned to receive 0.01%atropine eye drops at dif-ferent frequencies(morning group,evening group,morning and evening group).During the treatment period,ocular and systemic adverse reactions were observed,spherical equivalent refraction(SER)and axial length(AX)were examined.Additionally,ocu-lar surface disease index(OSDI)questionnaire was obtained,tear meniscus height(TMH),non-inva-sive first tear film break-up time(NifBUT),non-inva-sive average tear film break-up time(NiaBUT),and meibomian gland atrophy score(MaS)were mea-sured by Keratograph 5M.RESULTS:During the 6-month treatment with 0.01%atropine eye drops,all adverse reaction symptoms were relatively mild and infrequent.Only one case of systemic reaction was reported,with temporary xerostomia.Six pa-tients reported discomfort such as ocular itching and dryness.The ocular reactions of photophobia and blurred near vision were slightly more com-mon in the morning and combined morning-eve-ning groups compared to the evening group,but there were no significant differences among the three groups(P>0.05).Compared to baseline,there were significant differences in SER and AX among the three groups after six months of treatment(P<0.05).Compared to baseline,no significant differ-ences were observed in the Morning group after six months of treatment in terms of OSDI score(P=0.656),TMH value(P=0.362),NifBUT(P=0.510),Ni-aBUT(P=0.700),and MaS(P=0.846).Similarly,no significant changes were found in the Evening group regarding OSDI score(P=0.429),TMH value(P=0.462),NifBUT(P=0.462),NiaBUT(P=0.598),and MaS(P=0.351).Additionally,in the Morning and evening group,no significant changes were de-tected in OSDI score(P=0.457),TMH value(P=0.748),NifBUT(P=0.197),NiaBUT(P=0.070),and MaS(P=0.802)after six months of treatment.CON-CLUSION:After six months of using 0.01%atropine eye drops with different frequencies in adolescent myopia control,there was no significant impact on the ocular surface.

AIM:To evaluate the effect of differ-ent frequencies 0.01%atropine eye drops on the ocular surface in adolescent myopia control.METH-ODS:A total of 84 adolescent patients with myopia were recruited for this study.They were randomly assigned to receive 0.01%atropine eye drops at dif-ferent frequencies(morning group,evening group,morning and evening group).During the treatment period,ocular and systemic adverse reactions were observed,spherical equivalent refraction(SER)and axial length(AX)were examined.Additionally,ocu-lar surface disease index(OSDI)questionnaire was obtained,tear meniscus height(TMH),non-inva-sive first tear film break-up time(NifBUT),non-inva-sive average tear film break-up time(NiaBUT),and meibomian gland atrophy score(MaS)were mea-sured by Keratograph 5M.RESULTS:During the 6-month treatment with 0.01%atropine eye drops,all adverse reaction symptoms were relatively mild and infrequent.Only one case of systemic reaction was reported,with temporary xerostomia.Six pa-tients reported discomfort such as ocular itching and dryness.The ocular reactions of photophobia and blurred near vision were slightly more com-mon in the morning and combined morning-eve-ning groups compared to the evening group,but there were no significant differences among the three groups(P>0.05).Compared to baseline,there were significant differences in SER and AX among the three groups after six months of treatment(P<0.05).Compared to baseline,no significant differ-ences were observed in the Morning group after six months of treatment in terms of OSDI score(P=0.656),TMH value(P=0.362),NifBUT(P=0.510),Ni-aBUT(P=0.700),and MaS(P=0.846).Similarly,no significant changes were found in the Evening group regarding OSDI score(P=0.429),TMH value(P=0.462),NifBUT(P=0.462),NiaBUT(P=0.598),and MaS(P=0.351).Additionally,in the Morning and evening group,no significant changes were de-tected in OSDI score(P=0.457),TMH value(P=0.748),NifBUT(P=0.197),NiaBUT(P=0.070),and MaS(P=0.802)after six months of treatment.CON-CLUSION:After six months of using 0.01%atropine eye drops with different frequencies in adolescent myopia control,there was no significant impact on the ocular surface.

Objective:To examine the efficacy of uniportal video-assisted thoracoscopic surgery in the treatment of tuberculous destroyed lung.Methods:This is a retrospective case series study. The clinical data of 33 patients with tuberculous destroyed lung who had received uniportal video-assisted thoracoscopic pulmonary resection from June 2020 to May 2022 in Department of Surgery, Wuhan Pulmonary Hospital were retrospectively analyzed. There were 13 males and 20 females, aged (47.5±16.2) years (range: 19 to 68 years). The course of the disease was from 15 days to 8 years. All 33 cases had pleural adhesions, including 30 cases with total pleural adhesions and atresia. There were 21 cases of calcification of the thoracic lymph node, 17 cases of aspergillus infection, 4 cases of drug-resistant tuberculosis. The surgical incision was located at the midline of the fifth intercostal axilla, length 4 to 5 cm. The principle of separating pleural adhesions was easy first and difficult later, and then appropriate procedures were selected to resect the diseased lung based on the exploration situation. There were 12 cases that underwent superior lobectomy, 11 cases that underwent superior lobectomy and dorsal segmentectomy, 3 cases that underwent inferior lobectomy, 3 cases that underwent pneumonectomy, 2 cases that underwent middle and inferior lobectomy, and 1 case that underwent superior lobectomy, dorsal segmentectomy and basal segment wedgectomy. The surgical techniques, perioperative evaluation and treatment, management of complications, and the outcome were summarized.Results:Six cases were converted to thoracoscope assisted small incision or thoracotomy. For 27 cases who successfully underwent uniportal VATS, the operation time was (238.7±76.8) minutes (range: 60 to 420 minutes), the intraoperative bleeding was (400.4±315.9) ml (range: 50 to 1 200 ml). The duration of postoperative drainage was (12.7±8.3) days (range: 3 to 42 days). The postoperative hospital stay was (15.2±7.9) days (range: 6 to 43 days). Persistent postoperative pulmonary leakage occurred in 12 cases. There were 2 cases of active thoracic bleeding, one of which was cured with conservative treatment. The other case underwent secondary operation. One case of bronchopleural fistula was cured after continuous thoracic drainage to control infection and implantation of one-way bronchial valve through a fiberoptic bronchoscope.Conclusion:For selected patients with tuberculous destroyed lung, choosing the reasonable surgical procedures and techniques, the uniportal VATS could reduce surgical trauma.

Objective:To examine the efficacy of uniportal video-assisted thoracoscopic surgery in the treatment of tuberculous destroyed lung.Methods:This is a retrospective case series study. The clinical data of 33 patients with tuberculous destroyed lung who had received uniportal video-assisted thoracoscopic pulmonary resection from June 2020 to May 2022 in Department of Surgery, Wuhan Pulmonary Hospital were retrospectively analyzed. There were 13 males and 20 females, aged (47.5±16.2) years (range: 19 to 68 years). The course of the disease was from 15 days to 8 years. All 33 cases had pleural adhesions, including 30 cases with total pleural adhesions and atresia. There were 21 cases of calcification of the thoracic lymph node, 17 cases of aspergillus infection, 4 cases of drug-resistant tuberculosis. The surgical incision was located at the midline of the fifth intercostal axilla, length 4 to 5 cm. The principle of separating pleural adhesions was easy first and difficult later, and then appropriate procedures were selected to resect the diseased lung based on the exploration situation. There were 12 cases that underwent superior lobectomy, 11 cases that underwent superior lobectomy and dorsal segmentectomy, 3 cases that underwent inferior lobectomy, 3 cases that underwent pneumonectomy, 2 cases that underwent middle and inferior lobectomy, and 1 case that underwent superior lobectomy, dorsal segmentectomy and basal segment wedgectomy. The surgical techniques, perioperative evaluation and treatment, management of complications, and the outcome were summarized.Results:Six cases were converted to thoracoscope assisted small incision or thoracotomy. For 27 cases who successfully underwent uniportal VATS, the operation time was (238.7±76.8) minutes (range: 60 to 420 minutes), the intraoperative bleeding was (400.4±315.9) ml (range: 50 to 1 200 ml). The duration of postoperative drainage was (12.7±8.3) days (range: 3 to 42 days). The postoperative hospital stay was (15.2±7.9) days (range: 6 to 43 days). Persistent postoperative pulmonary leakage occurred in 12 cases. There were 2 cases of active thoracic bleeding, one of which was cured with conservative treatment. The other case underwent secondary operation. One case of bronchopleural fistula was cured after continuous thoracic drainage to control infection and implantation of one-way bronchial valve through a fiberoptic bronchoscope.Conclusion:For selected patients with tuberculous destroyed lung, choosing the reasonable surgical procedures and techniques, the uniportal VATS could reduce surgical trauma.

Objective: To observe the clinical efficacy of moxibustion at Baihui (GV20) plus Tuina (Chinese therapeutic massage) for children with postnasal drip syndrome (PNDS).Methods: A total of 60 cases were divided into an observation group and a control group according to the random number table method, with 30 cases in each group. Cases in the control group received mometasone furoate nasal spray and nasal irrigation with 0.9％ normal saline. Cases in the observation group received additional moxibustion at Baihui (GV20) plus Tuina at the head and face. All the cases were treated for four consecutive weeks. The clinical efficacy and traditional Chinese medicine (TCM) symptoms score were compared between the two groups. Results: The total effective rate of the observation group was 93.3％ while that of the control group was 70.0％. The difference between the two groups was statistically significant (P<0.05). After treatment, the TCM symptom scores in both groups declined significantly, showing a statistical difference from that before treatment (P<0.05), and the score of the observation group was notably lower than that of the control group (P<0.05). Conclusion: The clinical efficacy of moxibustion at Baihui (GV20) plus Tuina at the head and face on the basis of nasal spray with Western medicine is more significant than that of Western medicine alone for PNDS in children.