Comparison of 120-200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate.
Identifieur interne : 000380 ( PubMed/Checkpoint ); précédent : 000379; suivant : 000381Comparison of 120-200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate.
Auteurs : Christopher Netsch [Allemagne] ; Thorsten Bach ; Laura Pohlmann ; Thomas Herrmann ; Andreas J. GrossSource :
- Journal of endourology / Endourological Society [ 1557-900X ] ; 2012.
Descripteurs français
- KwdFr :
- MESH :
- effets indésirables : Thérapie laser.
- usage thérapeutique : Aluminium, Thulium, Yttrium.
- étiologie : Complications postopératoires.
- Adulte d'âge moyen, Humains, Mâle, Prostate, Sujet âgé, Sujet âgé de 80 ans ou plus, Thérapie laser, Études de suivi.
English descriptors
- KwdEn :
- MESH :
- chemical , therapeutic use : Aluminum, Thulium, Yttrium.
- adverse effects : Laser Therapy.
- etiology : Postoperative Complications.
- methods : Laser Therapy.
- surgery : Prostate.
- Aged, Aged, 80 and over, Follow-Up Studies, Humans, Male, Middle Aged.
Abstract
To evaluate efficacy and safety of 200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate (ThuVEP) for patients with benign prostatic obstruction (BPO).
DOI: 10.1089/end.2011.0173
PubMed: 22191688
Affiliations:
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pubmed:22191688Le document en format XML
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<author><name sortKey="Netsch, Christopher" sort="Netsch, Christopher" uniqKey="Netsch C" first="Christopher" last="Netsch">Christopher Netsch</name>
<affiliation wicri:level="3"><nlm:affiliation>Department of Urology, Asklepios Hospital Barmbek, Hamburg, Germany. c.netsch@asklepios.com</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Department of Urology, Asklepios Hospital Barmbek, Hamburg</wicri:regionArea>
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<author><name sortKey="Pohlmann, Laura" sort="Pohlmann, Laura" uniqKey="Pohlmann L" first="Laura" last="Pohlmann">Laura Pohlmann</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Aged, 80 and over</term>
<term>Aluminum (therapeutic use)</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Laser Therapy (adverse effects)</term>
<term>Laser Therapy (methods)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Postoperative Complications (etiology)</term>
<term>Prostate (surgery)</term>
<term>Thulium (therapeutic use)</term>
<term>Yttrium (therapeutic use)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Aluminium (usage thérapeutique)</term>
<term>Complications postopératoires (étiologie)</term>
<term>Humains</term>
<term>Mâle</term>
<term>Prostate ()</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Thulium (usage thérapeutique)</term>
<term>Thérapie laser ()</term>
<term>Thérapie laser (effets indésirables)</term>
<term>Yttrium (usage thérapeutique)</term>
<term>Études de suivi</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Aluminum</term>
<term>Thulium</term>
<term>Yttrium</term>
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<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Laser Therapy</term>
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<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Thérapie laser</term>
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<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Laser Therapy</term>
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<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Prostate</term>
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<keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Aluminium</term>
<term>Thulium</term>
<term>Yttrium</term>
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<term>Aged, 80 and over</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Humains</term>
<term>Mâle</term>
<term>Prostate</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Thérapie laser</term>
<term>Études de suivi</term>
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<front><div type="abstract" xml:lang="en">To evaluate efficacy and safety of 200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate (ThuVEP) for patients with benign prostatic obstruction (BPO).</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">22191688</PMID>
<DateCreated><Year>2012</Year>
<Month>03</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted><Year>2012</Year>
<Month>08</Month>
<Day>06</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1557-900X</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>26</Volume>
<Issue>3</Issue>
<PubDate><Year>2012</Year>
<Month>Mar</Month>
</PubDate>
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<Title>Journal of endourology / Endourological Society</Title>
<ISOAbbreviation>J. Endourol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Comparison of 120-200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate.</ArticleTitle>
<Pagination><MedlinePgn>224-9</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1089/end.2011.0173</ELocationID>
<Abstract><AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">To evaluate efficacy and safety of 200 W 2 μm thulium:yttrium-aluminum-garnet vapoenucleation of the prostate (ThuVEP) for patients with benign prostatic obstruction (BPO).</AbstractText>
<AbstractText Label="PATIENTS AND METHODS" NlmCategory="METHODS">Twenty-eight consecutive patients with symptomatic BPO were treated with 200 W ThuVEP. Patients were matched for age and preoperative prostate volume with 28 patients from our 120 W ThuVEP database. Patient data and postoperative outcome at 12-month follow-up were compared.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Mean prostate volume (65.39 vs 68.62 cc) and resected weight (40.72 vs 53.18 g) differed not significantly between 200 and 120 W ThuVEP. The percentage of resected tissue was lower with 200 W compared with 120 W (58.48 vs 72.93%, P=0.047) because of the higher rate of ablated tissue. There were no differences in mean operative (69.21 vs 78.67 min), laser (45.43 vs 48.58 min), morcellation (16.52 vs 20.48 min), and catheter (2.2 vs 2.1 d) time between the devices. Three patients needed immediate re-treatment (hemorrhage necessitating coagulation 1=200 W, secondary apical resection 2 120/200 W). One (1.79%) patient (120 W) needed a blood transfusion postoperatively. Fifty-one (91%) patients completed 12-month follow-up. Quality of life, International Prostate Symptom Score, peak urinary flow rate, postvoid residual urine, prostate-specific antigen level, and prostate volume improved significantly (P≤0.019) and were not different between the devices. At follow-up, two (3.57%) patients (120/200 W) had a bladder neck contracture.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">ThuVEP is a safe and efficacious procedure for patients with symptomatic BPO. 120 and 200 W ThuVEP had an equivalent clinical outcome at 12-month follow-up.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Netsch</LastName>
<ForeName>Christopher</ForeName>
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<NameOfSubstance UI="C503779">yttrium-aluminum-garnet</NameOfSubstance>
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<name sortKey="Gross, Andreas J" sort="Gross, Andreas J" uniqKey="Gross A" first="Andreas J" last="Gross">Andreas J. Gross</name>
<name sortKey="Herrmann, Thomas" sort="Herrmann, Thomas" uniqKey="Herrmann T" first="Thomas" last="Herrmann">Thomas Herrmann</name>
<name sortKey="Pohlmann, Laura" sort="Pohlmann, Laura" uniqKey="Pohlmann L" first="Laura" last="Pohlmann">Laura Pohlmann</name>
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<country name="Allemagne"><region name="Hambourg"><name sortKey="Netsch, Christopher" sort="Netsch, Christopher" uniqKey="Netsch C" first="Christopher" last="Netsch">Christopher Netsch</name>
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