Pilot Study of Intraperitoneal Administration of Triamcinolone Acetonide for Cancerous Ascites in Patients With End-Stage Gynecological Cancer
OBJECTIVEPatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein. PAT...
Saved in:
Published in | International journal of gynecological cancer Vol. 24; no. 6; pp. 1093 - 1097 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology
01.07.2014
Elsevier Limited |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | OBJECTIVEPatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein.
PATIENTS AND METHODSWe enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use.
RESULTSTriamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation.
CONCLUSIONSIntraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites. |
---|---|
AbstractList | OBJECTIVEPatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein.
PATIENTS AND METHODSWe enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use.
RESULTSTriamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation.
CONCLUSIONSIntraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites. Patients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein. We enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use. Triamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation. Intraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites. ObjectivePatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein.Patients and MethodsWe enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use.ResultsTriamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation.ConclusionsIntraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites. Patients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein.OBJECTIVEPatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone acetonide (TA) to patients with end-stage gynecological cancer as a pilot study, and our treatment results are reported herein.We enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use.PATIENTS AND METHODSWe enrolled 26 patients with end-stage gynecological cancer requiring frequent abdominal paracentesis for ascites drainage between April 2010 and September 2012. The volume of ascites drainage was 2000 to 3000 mL per drainage session, and TA at 10 mg/kg was intraperitoneally administered after drainage. We compared abdominal paracentesis intervals, performance status (PS), total protein level, albumin level, white blood cell count, changes in C-reactive protein (CRP) level, and adverse events before and after TA use.Triamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation.RESULTSTriamcinolone acetonide was administered to 26 patients for a total of 59 times. The abdominal paracentesis intervals, PS, and mean (SD) of C-reactive protein before and after TA use were 13.2 (12.6) days and 21.9 (23.6) days (P = 0.0117), 2.4 (0.7) and 1.6 (1.1) (P < 0.0001), and 7.5 (5.2) mg/dL and 5.5 (5.0) mg/dL (P = 0.007), respectively. With regard to adverse events, abdominal pain of grade 2 was observed once (1.7%), but there were no other acute adverse events. Four subjects (15.4%) had intestinal perforation.Intraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites.CONCLUSIONSIntraperitoneal administration of TA after drainage was considered to be a useful treatment, as it seems to extend paracentesis intervals and improve PS while maintaining quality of life for end-stage gynecological cancer patients with massive ascites. |
Author | Sugiyama, Toru Miura, Yuki Omi, Hideo Shoji, Tadahiro Kagabu, Masahiro Honda, Tatsuya Miura, Fumiharu Takeuchi, Satoshi Takatori, Eriko Takada, Anna |
AuthorAffiliation | Department of Obstetrics and Gynecology, Iwate Medical University School of Medicine, Iwate, Japan |
AuthorAffiliation_xml | – name: Department of Obstetrics and Gynecology, Iwate Medical University School of Medicine, Iwate, Japan |
Author_xml | – sequence: 1 givenname: Tadahiro surname: Shoji fullname: Shoji, Tadahiro organization: Department of Obstetrics and Gynecology, Iwate Medical University School of Medicine, Iwate, Japan – sequence: 2 givenname: Eriko surname: Takatori fullname: Takatori, Eriko – sequence: 3 givenname: Yuki surname: Miura fullname: Miura, Yuki – sequence: 4 givenname: Anna surname: Takada fullname: Takada, Anna – sequence: 5 givenname: Hideo surname: Omi fullname: Omi, Hideo – sequence: 6 givenname: Masahiro surname: Kagabu fullname: Kagabu, Masahiro – sequence: 7 givenname: Tatsuya surname: Honda fullname: Honda, Tatsuya – sequence: 8 givenname: Fumiharu surname: Miura fullname: Miura, Fumiharu – sequence: 9 givenname: Satoshi surname: Takeuchi fullname: Takeuchi, Satoshi – sequence: 10 givenname: Toru surname: Sugiyama fullname: Sugiyama, Toru |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24978712$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkdtqGzEQhkVJaQ7tG5Qi6E1uNtVptaveGZO6hkADSWnvFq2kjZWuJVfSEvwSfeaOY7cU31QgNBq-f2aY_xydhBgcQm8puaJENR-Wi_kV-fdQRV-gM1qzuqKCtycQE9FWraLfT9F5zo_AKEbUK3TKhGrahrIz9OvWj7HguzLZLY4DXoaS9MYlX6CbHvHMrn3wGZLFx7Aj7pPXa-NDHIHAM-OA9NbhISY818G4FKeMZ9n44jL2Ad-C1IWS8TdfVvg62Oqu6AeHF9vgDFR58AYa7aWv0ctBj9m9ObwX6Oun6_v55-rmy2I5n91UhreEVUrogfeCcclkb7WkVBNpua0lbayUWgsCuVYNAxGEGclaKgVpRc9r2zPJ-AW63NfdpPhzcrl0a5-NG0cdHIzf0VowplpZ79D3R-hjnFKA6TpW16zlXBEK1LsDNfVrZ7tN8mudtt2fTQMg9oBJMefkhr8IJd3O0A4M7Y4NBdnHIxns9dkLsMSP_xMfej7FsbiUf4zTk0vdCowtq2dc1U1TMUIFaeBXwWWM_wYSD7Nz |
CitedBy_id | crossref_primary_10_1111_jocs_15244 crossref_primary_10_1177_08968608231205851 crossref_primary_10_1097_MD_0000000000031464 crossref_primary_10_1016_j_jpainsymman_2021_04_010 crossref_primary_10_1016_j_rccan_2017_01_001 |
Cites_doi | 10.1165/ajrcmb.16.4.9115750 10.1016/0885-3924(94)00129-9 10.1191/026921600676345896 10.1006/gyno.1998.5215 10.1007/BF00309046 10.1016/j.jpainsymman.2008.07.002 10.1016/S0885-3924(00)00106-8 10.1111/j.1365-2133.1997.tb03783.x 10.1002/bjs.1800690802 10.1016/j.ejca.2005.11.018 10.1023/A:1018865516168 10.1016/S0002-9610(06)80078-4 |
ContentType | Journal Article |
Copyright | 2014 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology. 2014 2014 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology. |
Copyright_xml | – notice: 2014 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology. – notice: 2014 2014 by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 3V. 7X7 7XB 8FI 8FJ 8FK ABUWG AFKRA BENPR CCPQU FYUFA GHDGH K9. M0S PQEST PQQKQ PQUKI PRINS 7X8 |
DOI | 10.1097/IGC.0000000000000191 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central ProQuest One Community College Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Health & Medical Complete (Alumni) Health & Medical Collection (Alumni) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest One Academic Eastern Edition ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Central China ProQuest Hospital Collection (Alumni) ProQuest Central ProQuest Health & Medical Complete Health Research Premium Collection ProQuest One Academic UKI Edition Health and Medicine Complete (Alumni Edition) ProQuest One Academic ProQuest Central (Alumni) MEDLINE - Academic |
DatabaseTitleList | MEDLINE ProQuest One Academic Eastern Edition MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database – sequence: 3 dbid: 7X7 name: Health & Medical Collection url: https://search.proquest.com/healthcomplete sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1525-1438 |
EndPage | 1097 |
ExternalDocumentID | 24978712 10_1097_IGC_0000000000000191 00009577-201407000-00022 |
Genre | Journal Article |
GroupedDBID | --- .3N .Z2 0R~ 1OC 29J 31~ 36B 4.4 53G 5GY 5VS 7X7 8-1 8FI 8FJ AAHLL AAKAS AARTV AAXUO AAYWO ABBUW ABJNI ABUWG ABXVJ ABZAD ACDDN ACEWG ACGFO ACGFS ACWDW ACWRI ACXNZ ACXQS ADZCM AENEX AFBPY AFEBI AFKRA AFTRI AFZJQ AGINI AHEFC AIZYK AJAOE AJNYG AJYBZ ALIPV ALMA_UNASSIGNED_HOLDINGS BENPR BFHJK BQLVK CAG CCPQU CO8 COF CS3 CXRWF DC6 DCZOG E.X EBS EJD EX3 F5P FDB FL- FYUFA FZ0 HAJ HMCUK HZI HZ~ IHE IN~ KD2 L-C LH4 LW6 M41 O9- OCUKA OHYEH ORVUJ OUVQU OVD OXXIT P2P RMJ ROL S4S TEORI UDS UKHRP V2I W3M W99 WOW X3V X3W YUY AALRI AAYXX ACVFH ADCNI AEUPX AFPUW AIGII AKBMS AKYEP CITATION CGR CUY CVF ECM EIF NPM 3V. 7XB 8FK K9. PQEST PQQKQ PQUKI PRINS 7X8 |
ID | FETCH-LOGICAL-c3802-94af3b423626bda611a06d3d5617d66aa4061189ff0402c628164084b35db2623 |
IEDL.DBID | 7X7 |
ISSN | 1048-891X 1525-1438 |
IngestDate | Thu Jul 10 20:05:09 EDT 2025 Mon Jun 30 13:24:24 EDT 2025 Mon Jul 21 06:04:10 EDT 2025 Thu Jul 31 00:18:24 EDT 2025 Thu Apr 24 22:57:29 EDT 2025 Fri May 16 03:44:11 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 6 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3802-94af3b423626bda611a06d3d5617d66aa4061189ff0402c628164084b35db2623 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
PMID | 24978712 |
PQID | 2552833901 |
PQPubID | 5161120 |
PageCount | 5 |
ParticipantIDs | proquest_miscellaneous_1542298652 proquest_journals_2552833901 pubmed_primary_24978712 crossref_primary_10_1097_IGC_0000000000000191 crossref_citationtrail_10_1097_IGC_0000000000000191 wolterskluwer_health_00009577-201407000-00022 |
PublicationCentury | 2000 |
PublicationDate | 2014-July |
PublicationDateYYYYMMDD | 2014-07-01 |
PublicationDate_xml | – month: 07 year: 2014 text: 2014-July |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Kidlington |
PublicationTitle | International journal of gynecological cancer |
PublicationTitleAlternate | Int J Gynecol Cancer |
PublicationYear | 2014 |
Publisher | by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology Elsevier Limited |
Publisher_xml | – name: by the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology – name: Elsevier Limited |
References | Jenkin (10.1097/IGC.0000000000000191_bb0070) 2008; 36 McNamara (10.1097/IGC.0000000000000191_bb0010) 2000; 14 Mackey (10.1097/IGC.0000000000000191_bb0045) 2000; 19 Nauck (10.1097/IGC.0000000000000191_bb0065) 1997; 16 Graziotto (10.1097/IGC.0000000000000191_bb0040) 1997; 42 Gotlieb (10.1097/IGC.0000000000000191_bb0005) 1998; 71 Gilly (10.1097/IGC.0000000000000191_bb0035) 1994; 41 Greenway (10.1097/IGC.0000000000000191_bb0015) 1982; 69 Becker (10.1097/IGC.0000000000000191_bb0050) 2006; 42 Palacio (10.1097/IGC.0000000000000191_bb0060) 1997; 137 Sharma (10.1097/IGC.0000000000000191_bb0020) 1995; 10 Zervos (10.1097/IGC.0000000000000191_bb0030) 1997; 63 Weaver (10.1097/IGC.0000000000000191_bb0025) 1990; 159 Furukawa (10.1097/IGC.0000000000000191_bb0075) 1993; 23 Yeo (10.1097/IGC.0000000000000191_bb0055) 1993; 53 |
References_xml | – volume: 16 start-page: 398 year: 1997 ident: 10.1097/IGC.0000000000000191_bb0065 article-title: Induction of vascular endothelial growth factor by platelet-activating factor and platelet-derived growth factor is downregulated by corticosteroids publication-title: Am J Respir Cell Mol Biol. doi: 10.1165/ajrcmb.16.4.9115750 – volume: 10 start-page: 237 year: 1995 ident: 10.1097/IGC.0000000000000191_bb0020 article-title: Management of symptomatic malignant ascites with diuretics: two case reports and a review of the literature publication-title: J Pain Symptom Manage. doi: 10.1016/0885-3924(94)00129-9 – volume: 41 start-page: 124 year: 1994 ident: 10.1097/IGC.0000000000000191_bb0035 article-title: Regional chemotherapy (with mitomycin C) and intra-operative hyperthermia for digestive cancers with peritoneal carcinomatosis publication-title: Hepatogastroenterology. – volume: 14 start-page: 62 year: 2000 ident: 10.1097/IGC.0000000000000191_bb0010 article-title: ParacentesisVan effective method of symptom control in the palliative care setting? publication-title: Palliat Med. doi: 10.1191/026921600676345896 – volume: 71 start-page: 381 year: 1998 ident: 10.1097/IGC.0000000000000191_bb0005 article-title: Intraperitoneal pressures and clinical parameters of total paracentesis for palliation of symptomatic ascites in ovarian cancer publication-title: Gynecol Oncol. doi: 10.1006/gyno.1998.5215 – volume: 23 start-page: 298 year: 1993 ident: 10.1097/IGC.0000000000000191_bb0075 article-title: Experimental and clinical studies on the intraperitoneal administration of cis-diamminedichloroplatinum (II) for peritoneal carcinomatosis caused by gastric cancers publication-title: Surg Today. doi: 10.1007/BF00309046 – volume: 63 start-page: 157 year: 1997 ident: 10.1097/IGC.0000000000000191_bb0030 article-title: Peritoneovenous shunts in patients with intractable ascites: palliation at what price? publication-title: Am Surg. – volume: 36 start-page: e4 year: 2008 ident: 10.1097/IGC.0000000000000191_bb0070 article-title: The use of intraperitoneal triamcinolone acetonide for the management of recurrent malignant ascites in a patient with non-Hodgkin’s lymphoma publication-title: J Pain Symptom Manage. doi: 10.1016/j.jpainsymman.2008.07.002 – volume: 19 start-page: 193 year: 2000 ident: 10.1097/IGC.0000000000000191_bb0045 article-title: A phase II trial of triamcinolone hexacetanide for symptomatic recurrent malignant ascites publication-title: J Pain Symptom Manage. doi: 10.1016/S0885-3924(00)00106-8 – volume: 137 start-page: 540 year: 1997 ident: 10.1097/IGC.0000000000000191_bb0060 article-title: Contact allergens and sodium lauryl sulphate upregulate vascular endothelial growth factor in normal keratinocytes publication-title: Br J Dermatol. doi: 10.1111/j.1365-2133.1997.tb03783.x – volume: 69 start-page: 441 year: 1982 ident: 10.1097/IGC.0000000000000191_bb0015 article-title: Control of malignant ascites with spironolactone publication-title: Br J Surg. doi: 10.1002/bjs.1800690802 – volume: 42 start-page: 589 year: 2006 ident: 10.1097/IGC.0000000000000191_bb0050 article-title: Malignant ascites: systematic review and guideline for treatment publication-title: Eur J Cancer. doi: 10.1016/j.ejca.2005.11.018 – volume: 42 start-page: 1708 year: 1997 ident: 10.1097/IGC.0000000000000191_bb0040 article-title: Reinfusion of concentrated ascetic fluid versus total paracentesis. A randomized prospective trial publication-title: Dig Dis Sci. doi: 10.1023/A:1018865516168 – volume: 53 start-page: 2912 year: 1993 ident: 10.1097/IGC.0000000000000191_bb0055 article-title: Vascular permeability factor (vascular endothelial growth factor) in guinea pig and human tumor and inflammatory effusions publication-title: Cancer Res. – volume: 159 start-page: 600 year: 1990 ident: 10.1097/IGC.0000000000000191_bb0025 article-title: Percutaneous Denver peritoneovenous shunt insertion publication-title: Am J Surg. doi: 10.1016/S0002-9610(06)80078-4 |
SSID | ssj0009209 |
Score | 2.085386 |
Snippet | OBJECTIVEPatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered... Patients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered triamcinolone... ObjectivePatients with end-stage cancer have poorly controlled ascites retention resulting due to cancerous peritonitis. We intraperitoneally administered... |
SourceID | proquest pubmed crossref wolterskluwer |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1093 |
SubjectTerms | Abdomen Adult Aged Anti-Inflammatory Agents - administration & dosage Ascites Ascites - drug therapy Ascites - etiology Cancer Drainage Female Follow-Up Studies Genital Neoplasms, Female - complications Genital Neoplasms, Female - therapy Gynecological cancer Gynecology Humans Injections, Intraperitoneal Middle Aged Neoplasm Invasiveness Neoplasm Staging Paracentesis Peritoneal Neoplasms - complications Peritoneal Neoplasms - therapy Peritonitis - drug therapy Peritonitis - etiology Pilot Projects Prognosis Proteins Quality of Life Triamcinolone Acetonide - administration & dosage |
Title | Pilot Study of Intraperitoneal Administration of Triamcinolone Acetonide for Cancerous Ascites in Patients With End-Stage Gynecological Cancer |
URI | https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00009577-201407000-00022 https://www.ncbi.nlm.nih.gov/pubmed/24978712 https://www.proquest.com/docview/2552833901 https://www.proquest.com/docview/1542298652 |
Volume | 24 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1taxQxEB60BVFEfPe0lgh-Db3N7ublk5zH9UVoOaTF-7bsJlk9rLu1e0X6J_zNzmyyV09B92sybEgmk2cyk2cA3hKFkkD_nwttK545K3mZe81dqpX1mfB1X2Pp-EQenmUfFvkiXrh1Ma1ysIm9oXatpTvyPYS-eBKSh_7u4junqlEUXY0lNG7DNlGXkVarhboh3Q0pHuhxaK5Nshiezhm1d3QwDdSFw5eYZPNo-gtv3oP7P1oKYXdf-wz2386h_YfwIAJINgkr_ghu-eYx3DmOIfIn8HO-PG9XjPIDr1lbsyO6vSU6Y2LdJsENtlzqcYo6-A2F0Qw2nk2sx55L5xnCWTYlpbhsrzo2wbMSYSlbNmweuFg79mm5-sJmjeMIWT97dnDdeDsY0yj6FM72Z6fTQx6LLnCbarSOJivrtEKQhZ5O5UqZJOVYutQhzlJOyrIkBJBoU9e4_YWVQqPDNdZZleauEgimnsFWg8N9AUwK43Vqjaszn6EA9sxLX1cIoiwCk2wE6TDfhY2M5FQY47wYIuO4SsWfqzQCvpa6CIwc_-m_MyxlEfdnV9xo0wjerJtxZ1G4pGw8zmuB4FIIo2UuRvA8qMD6h4IK86kEW_iGThTh9Wo_CJMrhUYIPVg1Ds_3hXj578G8grskENKBd2BrdXnlXyPoWVW7vWbvwvb72cn84y9i1Prx |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1fb9MwED9NQ-KPEOI_hQFGgkdrjZM49gNCVdnWsnXaQyf6FhLbgYqRjKXT1C_BR-EzchcnHQUJntbX-FQrd777Xe78O4DXRKEkMP_nQpmcR9ZInsVOcRuqxLhIuKKZsTQ5lKPj6MMsnm3Az-4uDLVVdj6xcdS2MvSNfBuhL0ZCytDfnX7nNDWKqqvdCA1vFvtueYEpW_12_B71-0aI3Z3pcMTbqQLchAqPv46yIswRRSCUz20mgyDrSxtaBBKJlTLLKMQFShcF2rcwUijMKPoqysPY5kIS0QG6_GsYePuU7CWz5JLk17eUYIajuNLBrLuqp5Pt8d7QUyV2v0AH66HwL3x7C25fVFQyr782HfO_xb3du3CnBaxs4C3sHmy48j5cn7Ql-Qfw42h-Ui0Y9SMuWVWwMX0tJvpkYvkmwTV2XloxRZv_hsLodkvHBsbhyrl1DOEzG5IRnlXnNRtgbEYYzOYlO_LcrzX7OF98YTul5QiRPzu2tyyd6Zx3K_oQjq9EHY9gs8TtPgEmhXYqNNoWkYtQAFfGmStyBG0GgVDUg7B736lpGdBpEMdJ2lXiUUvpn1rqAV9JnXoGkP-s3-pUmbb-oE4vrbcHr1aP8SRTeSYrHb7XFMGsEFrJWPTgsTeB1R8KGgSYBPiEr9lE6m_LNpvQcZKg08OMOel7ugAhnv57My_hxmg6OUgPxof7z-AmCftW5C3YXJydu-cIuBb5i8bKGXy66mP1C-H-Mwc |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1fb9MwED9NnTSBEOI_hQFGgkerjZM4zgNCpWu3MlZVaBN9yxLbYdVGMpZOU78EH4hPx12ddBQkeFpf41Ot3Pnud7nz7wDeEIWSwPyfC6UzHhgteRpaxY2vIm0DYfPljKWDsdw7Cj5Ow-kG_GzuwlBbZeMTl47alJq-kXcQ-mIkpAy9k9dtEZOd4fvz75wmSFGltRmn4Uxk3y6uMH2r3o12UNdvhRgODvt7vJ4wwLWv0BXEQZr7GSIKhPWZSaXnpV1pfIOgIjJSpimFO0_FeY62LrQUCrOLrgoyPzSZkER6gO5_M6KsqAWbHwbjyedryl_XYIL5juIq9qbNxb046ox2-444sfl5sbceGP9Cu7fhzlVJBfTqdNk__1sUHN6DuzV8ZT1nb_dhwxYPYOugLtA_hB-T2Vk5Z9SduGBlzkb07ZjIlInzmwTXuHppxSGegG8ojE64sKynLa6cGcsQTLM-meRFeVmxHkZqBMVsVrCJY4Kt2JfZ_IQNCsMRMH-1bHdRWN248lr0ERzdiEIeQ6vA7T4FJkVsla9jkwc2QAFcGaY2zxDCaYRFQRv85n0nuuZDp7EcZ0lTl0ctJX9qqQ18JXXu-ED-s367UWVSe4cqubblNrxePcZzTcWatLD4XhOEtkLESoaiDU-cCaz-UNBYwMjDJ3zNJhJ3d3a5iTiMInSBmD9HXUceIMSzf2_mFWzhkUo-jcb7z-EWybq-5G1ozS8u7QtEX_PsZW3mDI5v-mT9AvyjOKI |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Pilot+study+of+intraperitoneal+administration+of+triamcinolone+acetonide+for+cancerous+ascites+in+patients+with+end-stage+gynecological+cancer&rft.jtitle=International+journal+of+gynecological+cancer&rft.au=Shoji%2C+Tadahiro&rft.au=Takatori%2C+Eriko&rft.au=Miura%2C+Yuki&rft.au=Takada%2C+Anna&rft.date=2014-07-01&rft.issn=1525-1438&rft.eissn=1525-1438&rft.volume=24&rft.issue=6&rft.spage=1093&rft_id=info:doi/10.1097%2FIGC.0000000000000191&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1048-891X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1048-891X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1048-891X&client=summon |