2018
DOI: 10.1007/s13126-018-0456-0
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The Effect of Bacillus Coagulans and Galactomannans on the Quality of Life of Patients Undergoing Laparoscopic Sleeve Gastrectomy: A Randomized Controlled Clinical Trial

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Cited by 8 publications
(18 citation statements)
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“…Out of the 59 studies, 36 studies applied a pre-post design (baseline measurements provided) (Group 1: n = 23 [ 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 ]; Group 2: n = 10 [ 60 , 61 , 62 , 63 , 64 , 65 , 66 , 67 , 68 , 69 ]; Group 3: n = 4 [ 70 , 71 , 72 , 73 ]). Sixteen studies used a cross-sectional design (Group 1: n = 6 [ 74 , 75 , 76 , 77 , 78 , 79 ]; Group 2: n = 10 [ 80 , 81 , 82 , 83 , 84 , 85 , 86 ,…”
Section: Resultsmentioning
confidence: 99%
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“…Out of the 59 studies, 36 studies applied a pre-post design (baseline measurements provided) (Group 1: n = 23 [ 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 , 51 , 52 , 53 , 54 , 55 , 56 , 57 , 58 , 59 ]; Group 2: n = 10 [ 60 , 61 , 62 , 63 , 64 , 65 , 66 , 67 , 68 , 69 ]; Group 3: n = 4 [ 70 , 71 , 72 , 73 ]). Sixteen studies used a cross-sectional design (Group 1: n = 6 [ 74 , 75 , 76 , 77 , 78 , 79 ]; Group 2: n = 10 [ 80 , 81 , 82 , 83 , 84 , 85 , 86 ,…”
Section: Resultsmentioning
confidence: 99%
“…For Groups 1 and 2, outcome results including microbiota diversity and taxonomy changes are available in detail in Supporting Table S2 . The outcomes for Group 3 included clinical, anthropometric and/or metabolic parameters [ 70 , 72 , 73 ] and Quality of Life (QoL) [ 71 ] and are detailed in Supporting Table S3 . Analysis of microbiota samples were completed predominantly via next generation sequencing of 16S rRNA gene amplicons (Group 1: n = 23; Group 2: n = 22; Group 3: n = 1), with largely the hypervariable regions V3 and V4 targeted (detailed across studies below in the risk of bias section and for individual studies in Supporting Table S1 ).…”
Section: Resultsmentioning
confidence: 99%
“…Only one report [22] performed a single-blind trial on patients without blinding the researchers and study personnel; thus, it was considered as "high risk" in performance bias. Two trials conducted by Kazzi [22] and Chen [25] did not specify whether the outcome measurer was blinded and were categorized with an "unclear risk" in detection bias. One trial described patient age, sex, and BMI and lacked baseline comparability [25].…”
Section: Assessment Of Risk Of Bias Figures 2 and 3 Show The Qualitymentioning
confidence: 99%
“…e quality of three studies [19][20][21] was grade A, and probability of bias was low. e remaining three studies [22,25,28] were grade B with a moderate probability of bias.…”
Section: Assessment Of Risk Of Bias Figures 2 and 3 Show The Qualitymentioning
confidence: 99%
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