Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/9695
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dc.contributor.authorMinov, Jordanen_US
dc.contributor.authorStoleski, Sashoen_US
dc.contributor.authorKaradzinska-bislimovska, Jovankaen_US
dc.contributor.authorPetrova, Tatjanaen_US
dc.contributor.authorVasilevska, Kristinen_US
dc.contributor.authorMijakoski, Draganen_US
dc.contributor.authorJesenak, Milosen_US
dc.date.accessioned2020-12-09T19:43:01Z-
dc.date.available2020-12-09T19:43:01Z-
dc.date.issued2020-09-15-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/9695-
dc.description.abstractBACKGROUND: Patients with non-cystic fibrosis bronchiectasis (BE) have frequent exacerbations that are causes of significant morbidity and sometimes mortality, and which it is desirable to prevent. AIM: We aimed to assess the effects of pleuran on the incidence and duration of exacerbations in patients with BE. METHODS: A prospective, observational, open-label, and active-controlled study was realized as a comparison of the frequency and duration of exacerbations between a group of patients with BE (30 patients, 14 males and 16 females, aged 44–72 years) who received a combination supplement containing pleuran 100 mg, Vitamin C 60 mg and zinc 5 mg over a 3-month period and a group of patients with BE (31 patients, 15 males and 16 females, aged 45–74 years) treated over a 3-month period with a combination supplement containing Vitamin C 60 mg and zinc 5 mg. RESULTS: Over the study period, altogether 46 exacerbations were documented (19 in the patients receiving pleuran and 27 in the patients who did not receive pleuran), nine of which required hospital treatment (four in the patients receiving pleuran [21.5%] and five in the patients who did not receive pleuran [18.6%]). The mean number of exacerbations over the study period was significantly lower in the patients receiving pleuran (0.6 ± 0.4) as compared to the mean number in the patients who did not receive pleuran (0.8 ± 0.3) (p = 0.0297). The mean duration of exacerbations, expressed in days, needed for cure or clinical improvement in the patients receiving pleuran (11.2 ± 1.7 days) was significantly shorter than that of exacerbations in the patients who did not receive pleuran (12.4 ± 1.3 days) (p = 0.0029). We found significantly lower incidence and significantly shorter duration of exacerbations in the patients with BE who received pleuran as compared to their incidence and duration in the patients with BE who did not receive pleuran. CONCLUSION: Our findings indicated a need for further investigations in this domain to define the possible role of pleuran in the prevention of BE exacerbations.en_US
dc.language.isoenen_US
dc.publisherScientific Foundation SPIROSKI, Skopje, Republic of Macedoniaen_US
dc.relation.ispartofOpen Access Macedonian Journal of Medical Sciencesen_US
dc.subjectBronchiectasisen_US
dc.subjectDurationen_US
dc.subjectExacerbationen_US
dc.subjectIncidenceen_US
dc.subjectPleuranen_US
dc.titleEffects of Pleuran (β-glucan from Pleurotus ostreatus) Supplementation on Incidence and Duration of Bronchiectasis Exacerbationsen_US
dc.typeArticleen_US
dc.identifier.doi10.3889/oamjms.2020.5266-
item.grantfulltextopen-
item.fulltextWith Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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