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Vergleich der peroralen endoskopischen Myotomie (POEM) und der laparoskopischen Heller Myotomie (LHM) in der Therapie der primär idiopathischen Achalasie und anderer Ösophagusmotilitätsstörungen / Comparison of peroral endoscopic myotomy (POEM) and laparoscopic Heller myotomy (LHM) in the therapy of primary idiopathic achalasia and other esophageal motility disordersAl-Nasser, Mohammed Mohammed Ali January 2020 (has links) (PDF)
Hier wird über den objektiven Vergleich der Kurz- und Langzeitergebnisse, die mit der laparoskopischen Heller-Myotomie plus Dor-Fundoplikatio (LHM + Dor) und der per-oralen endoskopischen Myotomie (POEM) an einer einzigen Institution erzielt wurden und über die Entwicklung eines "maßgeschneiderten Ansatzes" berichtet. Die laparosko-pischen Heller Myotomie (LHM) gilt aktuell als das Standardverfahren zur Therapie der Achalasie. Die perorale endoskopische Myotomie (POEM) bietet eine neue Alternative zur Durchführung der Heller-Myotomie auf endoskopischem und natural orifice translu-minal endoscopic surgery (NOTES) Wege.
Wir berichten über unsere unselektierte konsekutive Patientenserien (n = 238), die zwi-schen 2009 und 2017 entweder einer LHM + Dor Prozedur (n = 100) oder einer POEM Operation (n = 138) unterzogen wurden.
Es gab keine Unterschiede hinsichtlich des Behandlungserfolgs (Eckardt-Score ≤ 3) nach 3 - 6 Monaten (LHM: 90,1% vs. POEM: 90,5%; p = 0,735), 12 Monate (LHM 84,4% vs. POEM 84,0%; p = 0,766 und> 2 Jahre (LHM 81,1% vs. POEM 79,2%; p = 0,432). Die Verbesserung der Lebensqualität (GIQLI-Score) und die Patientenzufriedenheit waren in beiden Gruppen ebenfalls ver-gleichbar gut (~ 90%) und zu jedem Zeitpunkt der Nachbeobachtung. Refluxraten sind ebenfalls ähnlich (Sodbrennen LHM: 32,9% vs. POEM: 30,1%; Ösophagitis LHM: 16,3% vs. POEM: 14,6%; PPI-Aufnahme 21,2% vs. 32,5%, pathologischer pH-Wert -Meter-LHM: 8,8% vs. POEM: 23,3%) ohne Signifikanz der Unterschiede.
Die „maßgeschneiderte Verfahrenswahl POEM vs. LHM“ könnte geeignet sein und sollte in weiteren Studien weiter untersucht werden. / This article reports on the objective comparison of the short and long-term results obtained with the laparoscopic Heller myotomy plus Dor fundoplication (LHM + Dor) and per-oral endoscopic myotomy (POEM) at a single institution and on the development of a " tailored approach". The laparoscopic Heller Myotomy (LHM) is currently considered the standard procedure for the treatment of achalasia. Peroral endoscopic myotomy (POEM) offers a new alternative to Heller myotomy by endoscopic and natural orifice transluminal endoscopic surgery (NOTES).
We report on our unselected consecutive patient series (n = 238) who underwent either an LHM + Dor procedure (n = 100) or POEM surgery (n = 138) between 2009 and 2017.
There were no differences in treatment success (Eckardt-Score ≤ 3) after 3 - 6 months (LHM: 90.1% vs. POEM: 90.5%; p = 0.735), 12 months (LHM 84.4% vs.POEM 84.0%; p = 0.766 and> 2 years (LHM 81.1% vs. POEM 79.2%; p = 0.432). The improvement of quality of life (GIQLI-Score) and patient satisfaction were also comparably good (~ 90%) in both groups and at all times of follow-up. Reflux rates are also similar (heartburn LHM: 32.9% vs. POEM: 30.1%; esophagitis LHM: 16.3% vs. POEM: 14.6%; PPI uptake 21.2% vs. 32.5%, pathological pH meter-LHM: 8.8% vs. POEM: 23.3%) without significance of the differences.
The "tailored approach for choosing the procedure POEM vs. LHM" might be appropriate and should be further investigated in further studies.
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Triple A syndrome with a novel indel mutation in the AAAS gene and delayed puberty: Patient reportBustanji, Haidar, Sahar, Bashar, Hübner, Angela, Ajlouni, Kamel, Landgraf, Dana, Hamamy, Hanan, Koehler, Katrin 23 June 2020 (has links)
Triple A syndrome, formerly known as Allgrove syndrome, is an autosomal recessive disorder characterized clinically by adrenal insufficiency, alacrima, achalasia, and neurological abnormalities. We report a 17-year-old boy presented to the endocrine clinic with delayed puberty and a 4-year’s history of fatigue and muscle weakness. He had achalasia, alacrima, and skin and mucosal hyperpigmentation. Hormonal assessment revealed isolated glucocorticoid deficiency. Clinical diagnosis of triple A syndrome was confirmed by sequencing the entire coding region including exon-intron boundaries of the AAAS gene. Analysis revealed a homozygous novel indel mutation encompassing intron 7 to intron 10 of the gene (g.16166_17813delinsTGAGGCCTGCTG; NG_016775). This is the first report of triple A syndrome in Jordan with a novel indel mutation and presenting with delayed puberty.
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Retrospektive Analyse über die Therapie mit Botulinumtoxin bei verschiedenen Dysphagieformen am Beispiel des oberen und unteren Ösophagussphinkters / Retrospective analysis of the therapy with botulinumtoxin on different modes of dysphagia using the example of the upper and lower esophageal sphincterBartsch, Katharina 15 December 2009 (has links)
No description available.
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