Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure
Background Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug di...
Gespeichert in:
Veröffentlicht in: | Brain tumor research and treatment 2022-10, Vol.10 (4), p.237 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | kor |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 4 |
container_start_page | 237 |
container_title | Brain tumor research and treatment |
container_volume | 10 |
creator | Byungjun Woo Ho-shin Gwak Ji-woong Kwon Sang-hoon Shin Heon Yoo |
description | Background Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug distribution to the extra-ventricular CSF space. This study examined the feasibility of combining a lumboperitoneal (LP) shunt with an Ommaya reservoir to both control intracranial pressure and allow for intraventricular chemotherapy.
Methods We identified 16 patients with LM who received both an Ommaya reservoir and an LP shunt, either concurrently or sequentially, and subsequently received intraventricular chemotherapy. The feasibility of this combination for intraventricular chemotherapy was evaluated by assessing 1) the distribution of intraventricularly injected drugs in CSF samples collected 0, 6, and 12 h post-injection and 2) adverse events associated with the procedure and drug administration.
Results Patients received a median of seven rounds (range 1-37) of intraventricular chemotherapy during a median follow-up period of 5.2 months after LP shunt insertion. Pharmacokinetic data were obtained from six patients. Baseline methotrexate (MTX) levels from Ommaya reservoirs varied from 339.9 μM to 1,523.5 μM. CSF sampled from LP shunt reservoirs revealed an elimination halflife (t1/2) of 2.63 h, and the mean ratio of MTX concentration at 12 h to that at baseline was 0.05±0.05, ensuring drug distribution from the ventricle to the spinal canal. Nine patients (56%) underwent revision surgery due to catheter migration, malfunction, or infection. Among these patients, CSF infections attributable to intraventricular chemotherapy (n=3) occurred, but no infections occurred in later cases after we began to employ a complete aseptic technique.
Conclusion LP shunt combined with Ommaya reservoir insertion is a feasible option for achieving both intracranial pressure control and the continuation of intraventricular chemotherapy in patients with LM. |
format | Article |
fullrecord | <record><control><sourceid>kiss</sourceid><recordid>TN_cdi_kiss_primary_4003289</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><kiss_id>4003289</kiss_id><sourcerecordid>4003289</sourcerecordid><originalsourceid>FETCH-kiss_primary_40032893</originalsourceid><addsrcrecordid>eNp9jcFKA0EQRPegkKD5glzmBwLjJMuu5yViIKKo4DH0rh23dadn6Z4J7Bf5m46oV6GoOtSj6qyYO1fXK7ex5axYqL5ba69cWVZVNS8-98m3YUShGBhhME994mia4FtifDUvFHtz7z1MYB5RUU6BxGwZ2gE1YxyJU-Z2HAVOmJ26NICYpkcfYo8C42SOQcwexxg8MvHb988dRtAs0p-PHXeCoH9TnQBTxh4EVZPgZXF-hEFx8ZsXxfJm-9zcrj5I9TAKeZDpsLF27err9f_tF9ReW2k</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure</title><source>PubMed Central Open Access</source><source>KoreaMed Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Byungjun Woo ; Ho-shin Gwak ; Ji-woong Kwon ; Sang-hoon Shin ; Heon Yoo</creator><creatorcontrib>Byungjun Woo ; Ho-shin Gwak ; Ji-woong Kwon ; Sang-hoon Shin ; Heon Yoo</creatorcontrib><description>Background Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug distribution to the extra-ventricular CSF space. This study examined the feasibility of combining a lumboperitoneal (LP) shunt with an Ommaya reservoir to both control intracranial pressure and allow for intraventricular chemotherapy.
Methods We identified 16 patients with LM who received both an Ommaya reservoir and an LP shunt, either concurrently or sequentially, and subsequently received intraventricular chemotherapy. The feasibility of this combination for intraventricular chemotherapy was evaluated by assessing 1) the distribution of intraventricularly injected drugs in CSF samples collected 0, 6, and 12 h post-injection and 2) adverse events associated with the procedure and drug administration.
Results Patients received a median of seven rounds (range 1-37) of intraventricular chemotherapy during a median follow-up period of 5.2 months after LP shunt insertion. Pharmacokinetic data were obtained from six patients. Baseline methotrexate (MTX) levels from Ommaya reservoirs varied from 339.9 μM to 1,523.5 μM. CSF sampled from LP shunt reservoirs revealed an elimination halflife (t1/2) of 2.63 h, and the mean ratio of MTX concentration at 12 h to that at baseline was 0.05±0.05, ensuring drug distribution from the ventricle to the spinal canal. Nine patients (56%) underwent revision surgery due to catheter migration, malfunction, or infection. Among these patients, CSF infections attributable to intraventricular chemotherapy (n=3) occurred, but no infections occurred in later cases after we began to employ a complete aseptic technique.
Conclusion LP shunt combined with Ommaya reservoir insertion is a feasible option for achieving both intracranial pressure control and the continuation of intraventricular chemotherapy in patients with LM.</description><identifier>ISSN: 2288-2405</identifier><language>kor</language><publisher>대한뇌종양학회·대한신경종양학회·대한소아뇌종양학회</publisher><subject>Cerebrospinal fluid ; Chemotherapy ; Leptomeningeal metastasis ; Lumboperitoneal shunt ; Ommaya</subject><ispartof>Brain tumor research and treatment, 2022-10, Vol.10 (4), p.237</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Byungjun Woo</creatorcontrib><creatorcontrib>Ho-shin Gwak</creatorcontrib><creatorcontrib>Ji-woong Kwon</creatorcontrib><creatorcontrib>Sang-hoon Shin</creatorcontrib><creatorcontrib>Heon Yoo</creatorcontrib><title>Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure</title><title>Brain tumor research and treatment</title><addtitle>Brain Tumor Research and Treatment</addtitle><description>Background Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug distribution to the extra-ventricular CSF space. This study examined the feasibility of combining a lumboperitoneal (LP) shunt with an Ommaya reservoir to both control intracranial pressure and allow for intraventricular chemotherapy.
Methods We identified 16 patients with LM who received both an Ommaya reservoir and an LP shunt, either concurrently or sequentially, and subsequently received intraventricular chemotherapy. The feasibility of this combination for intraventricular chemotherapy was evaluated by assessing 1) the distribution of intraventricularly injected drugs in CSF samples collected 0, 6, and 12 h post-injection and 2) adverse events associated with the procedure and drug administration.
Results Patients received a median of seven rounds (range 1-37) of intraventricular chemotherapy during a median follow-up period of 5.2 months after LP shunt insertion. Pharmacokinetic data were obtained from six patients. Baseline methotrexate (MTX) levels from Ommaya reservoirs varied from 339.9 μM to 1,523.5 μM. CSF sampled from LP shunt reservoirs revealed an elimination halflife (t1/2) of 2.63 h, and the mean ratio of MTX concentration at 12 h to that at baseline was 0.05±0.05, ensuring drug distribution from the ventricle to the spinal canal. Nine patients (56%) underwent revision surgery due to catheter migration, malfunction, or infection. Among these patients, CSF infections attributable to intraventricular chemotherapy (n=3) occurred, but no infections occurred in later cases after we began to employ a complete aseptic technique.
Conclusion LP shunt combined with Ommaya reservoir insertion is a feasible option for achieving both intracranial pressure control and the continuation of intraventricular chemotherapy in patients with LM.</description><subject>Cerebrospinal fluid</subject><subject>Chemotherapy</subject><subject>Leptomeningeal metastasis</subject><subject>Lumboperitoneal shunt</subject><subject>Ommaya</subject><issn>2288-2405</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9jcFKA0EQRPegkKD5glzmBwLjJMuu5yViIKKo4DH0rh23dadn6Z4J7Bf5m46oV6GoOtSj6qyYO1fXK7ex5axYqL5ba69cWVZVNS8-98m3YUShGBhhME994mia4FtifDUvFHtz7z1MYB5RUU6BxGwZ2gE1YxyJU-Z2HAVOmJ26NICYpkcfYo8C42SOQcwexxg8MvHb988dRtAs0p-PHXeCoH9TnQBTxh4EVZPgZXF-hEFx8ZsXxfJm-9zcrj5I9TAKeZDpsLF27err9f_tF9ReW2k</recordid><startdate>20221030</startdate><enddate>20221030</enddate><creator>Byungjun Woo</creator><creator>Ho-shin Gwak</creator><creator>Ji-woong Kwon</creator><creator>Sang-hoon Shin</creator><creator>Heon Yoo</creator><general>대한뇌종양학회·대한신경종양학회·대한소아뇌종양학회</general><scope>HZB</scope><scope>Q5X</scope></search><sort><creationdate>20221030</creationdate><title>Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure</title><author>Byungjun Woo ; Ho-shin Gwak ; Ji-woong Kwon ; Sang-hoon Shin ; Heon Yoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kiss_primary_40032893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2022</creationdate><topic>Cerebrospinal fluid</topic><topic>Chemotherapy</topic><topic>Leptomeningeal metastasis</topic><topic>Lumboperitoneal shunt</topic><topic>Ommaya</topic><toplevel>online_resources</toplevel><creatorcontrib>Byungjun Woo</creatorcontrib><creatorcontrib>Ho-shin Gwak</creatorcontrib><creatorcontrib>Ji-woong Kwon</creatorcontrib><creatorcontrib>Sang-hoon Shin</creatorcontrib><creatorcontrib>Heon Yoo</creatorcontrib><collection>Korean Studies Information Service System (KISS)</collection><collection>Korean Studies Information Service System (KISS) B-Type</collection><jtitle>Brain tumor research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Byungjun Woo</au><au>Ho-shin Gwak</au><au>Ji-woong Kwon</au><au>Sang-hoon Shin</au><au>Heon Yoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure</atitle><jtitle>Brain tumor research and treatment</jtitle><addtitle>Brain Tumor Research and Treatment</addtitle><date>2022-10-30</date><risdate>2022</risdate><volume>10</volume><issue>4</issue><spage>237</spage><pages>237-</pages><issn>2288-2405</issn><abstract>Background Intra-cerebrospinal fluid (CSF) chemotherapy for leptomeningeal metastasis (LM) can be delivered intraventricularly via an Ommaya reservoir. However, hydrocephalus associated with LM can interfere with chemotherapeutic drug distribution, and ventriculoperitoneal shunts can prevent drug distribution to the extra-ventricular CSF space. This study examined the feasibility of combining a lumboperitoneal (LP) shunt with an Ommaya reservoir to both control intracranial pressure and allow for intraventricular chemotherapy.
Methods We identified 16 patients with LM who received both an Ommaya reservoir and an LP shunt, either concurrently or sequentially, and subsequently received intraventricular chemotherapy. The feasibility of this combination for intraventricular chemotherapy was evaluated by assessing 1) the distribution of intraventricularly injected drugs in CSF samples collected 0, 6, and 12 h post-injection and 2) adverse events associated with the procedure and drug administration.
Results Patients received a median of seven rounds (range 1-37) of intraventricular chemotherapy during a median follow-up period of 5.2 months after LP shunt insertion. Pharmacokinetic data were obtained from six patients. Baseline methotrexate (MTX) levels from Ommaya reservoirs varied from 339.9 μM to 1,523.5 μM. CSF sampled from LP shunt reservoirs revealed an elimination halflife (t1/2) of 2.63 h, and the mean ratio of MTX concentration at 12 h to that at baseline was 0.05±0.05, ensuring drug distribution from the ventricle to the spinal canal. Nine patients (56%) underwent revision surgery due to catheter migration, malfunction, or infection. Among these patients, CSF infections attributable to intraventricular chemotherapy (n=3) occurred, but no infections occurred in later cases after we began to employ a complete aseptic technique.
Conclusion LP shunt combined with Ommaya reservoir insertion is a feasible option for achieving both intracranial pressure control and the continuation of intraventricular chemotherapy in patients with LM.</abstract><pub>대한뇌종양학회·대한신경종양학회·대한소아뇌종양학회</pub><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2288-2405 |
ispartof | Brain tumor research and treatment, 2022-10, Vol.10 (4), p.237 |
issn | 2288-2405 |
language | kor |
recordid | cdi_kiss_primary_4003289 |
source | PubMed Central Open Access; KoreaMed Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Cerebrospinal fluid Chemotherapy Leptomeningeal metastasis Lumboperitoneal shunt Ommaya |
title | Lumboperitoneal Shunt Combined With Ommaya Reservoir Enables Continued Intraventricular Chemotherapy for Leptomeningeal Metastasis With Increased Intracranial Pressure |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T20%3A22%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kiss&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Lumboperitoneal%20Shunt%20Combined%20With%20Ommaya%20Reservoir%20Enables%20Continued%20Intraventricular%20Chemotherapy%20for%20Leptomeningeal%20Metastasis%20With%20Increased%20Intracranial%20Pressure&rft.jtitle=Brain%20tumor%20research%20and%20treatment&rft.au=Byungjun%20Woo&rft.date=2022-10-30&rft.volume=10&rft.issue=4&rft.spage=237&rft.pages=237-&rft.issn=2288-2405&rft_id=info:doi/&rft_dat=%3Ckiss%3E4003289%3C/kiss%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_kiss_id=4003289&rfr_iscdi=true |