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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Non-Doppler hemorrhoidal artery ligation and hemorrhoidopexy combined with pudendal nerve block for the treatment of hemorrhoidal disease: a non-inferiority randomized controlled trial

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Author
Perivoliotis K., Spyridakis M., Zintzaras E., Arnaoutoglou E., Pramateftakis M.-G., Tepetes K.
Date
2021
Language
en
DOI
10.1007/s00384-020-03768-8
Keyword
adult
Article
clinical article
clinical effectiveness
comparative effectiveness
controlled study
Doppler ultrasonography
female
food intake
gastrointestinal surgery
hemorrhoid
hemorrhoidal artery ligation
hemorrhoidectomy
human
male
middle aged
mobilization
morbidity
nerve block
operation duration
outcome assessment
outpatient care
patient satisfaction
priority journal
prospective study
pudendal nerve
randomized controlled trial
recurrent disease
remission
Short Form 36
spinal anesthesia
validation process
adverse event
artery
ligation
treatment outcome
Arteries
Hemorrhoidectomy
Hemorrhoids
Humans
Ligation
Pudendal Nerve
Treatment Outcome
Springer Science and Business Media Deutschland GmbH
Metadata display
Abstract
Background: In this study, we proposed a combined outpatient treatment modality for hemorrhoidal disease. Methods: This study was a prospective non-inferiority randomized controlled trial (RCT). The experimental group included the dearterialization and hemorrhoidopexy under pudendal nerve block, whereas the comparator consisted of the standard Doppler guided hemorrhoidal artery ligation and hemorrhoidopexy, under spinal anesthesia. As primary hypothesis, we considered the non-inferiority of the proposed modality in terms of the presenting symptom remission rate (non-inferiority margin: 10%). Randomization was based on a 1:1 ratio. Blinding was confined to the patient and the investigator. Results: Overall, 60 patients were enrolled. The primary hypothesis of this RCT (96.7% vs 73.3%) was validated. The experimental group was associated with a lower operation duration and an expedited onset of mobilization and feeding. Moreover, a favorable profile regarding short-term morbidity and analgesia was identified. The control group displayed a higher pile recurrence rate and a suboptimal patient satisfaction. A significant effect of the treatment modality in most of the SF-36 components was confirmed. Conclusions: The proposed treatment modality was associated with favorable short and long-term outcomes. Due to specific limitations, further RCTs, with a larger sample size, are required. Trial Registration ClinicalTrials.gov: NCT03298997. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
URI
http://hdl.handle.net/11615/78074
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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