Abstract
Postoperative adhesion development remains a very frequent occurrence, which is often unrecognized by surgeons because of limited ability to conduct early second-look laparoscopies. The consequences include infertility, pelvic pain, bowel obstruction, and difficult reoperative procedures. To date, approaches to limit adhesions primarily have involved barriers to separate tissue during reepithelization. Future progress in regulating adhesion development and tissue fibrosis likely will require an improved understanding of the molecular processes involved in normal peritoneal repair and its aberrations leading to adhesion development. We hypothesize that tissue hypoxia (in part resulting from tissue incision, fulguration, suture ligation, etc.) is the major inciting event, which leads to a coordinated series of molecular events that promote an inflammatory response leading to enhanced tissue fibrosis. These events are reduced plasminogen activator activity, extracellular matrix deposition, increased cytokine production, increased angiogenesis, and reduced apoptosis (programmed cell death). Improved understanding of these events and their regulation will provide the opportunity to regulate better postoperative adhesion development and tissue fibrosis, thereby reducing the morbidity and mortality they cause.
Original language | English (US) |
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Pages (from-to) | 307-314 |
Number of pages | 8 |
Journal | Journal of the American Association of Gynecologic Laparoscopists |
Volume | 11 |
Issue number | 3 |
DOIs | |
State | Published - Jan 1 2004 |
Externally published | Yes |
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ASJC Scopus subject areas
- Obstetrics and Gynecology
Cite this
Molecular characterization of postoperative adhesions : The adhesion phenotype. / Saed, Ghassan M.; Diamond, Michael Peter.
In: Journal of the American Association of Gynecologic Laparoscopists, Vol. 11, No. 3, 01.01.2004, p. 307-314.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Molecular characterization of postoperative adhesions
T2 - The adhesion phenotype
AU - Saed, Ghassan M.
AU - Diamond, Michael Peter
PY - 2004/1/1
Y1 - 2004/1/1
N2 - Postoperative adhesion development remains a very frequent occurrence, which is often unrecognized by surgeons because of limited ability to conduct early second-look laparoscopies. The consequences include infertility, pelvic pain, bowel obstruction, and difficult reoperative procedures. To date, approaches to limit adhesions primarily have involved barriers to separate tissue during reepithelization. Future progress in regulating adhesion development and tissue fibrosis likely will require an improved understanding of the molecular processes involved in normal peritoneal repair and its aberrations leading to adhesion development. We hypothesize that tissue hypoxia (in part resulting from tissue incision, fulguration, suture ligation, etc.) is the major inciting event, which leads to a coordinated series of molecular events that promote an inflammatory response leading to enhanced tissue fibrosis. These events are reduced plasminogen activator activity, extracellular matrix deposition, increased cytokine production, increased angiogenesis, and reduced apoptosis (programmed cell death). Improved understanding of these events and their regulation will provide the opportunity to regulate better postoperative adhesion development and tissue fibrosis, thereby reducing the morbidity and mortality they cause.
AB - Postoperative adhesion development remains a very frequent occurrence, which is often unrecognized by surgeons because of limited ability to conduct early second-look laparoscopies. The consequences include infertility, pelvic pain, bowel obstruction, and difficult reoperative procedures. To date, approaches to limit adhesions primarily have involved barriers to separate tissue during reepithelization. Future progress in regulating adhesion development and tissue fibrosis likely will require an improved understanding of the molecular processes involved in normal peritoneal repair and its aberrations leading to adhesion development. We hypothesize that tissue hypoxia (in part resulting from tissue incision, fulguration, suture ligation, etc.) is the major inciting event, which leads to a coordinated series of molecular events that promote an inflammatory response leading to enhanced tissue fibrosis. These events are reduced plasminogen activator activity, extracellular matrix deposition, increased cytokine production, increased angiogenesis, and reduced apoptosis (programmed cell death). Improved understanding of these events and their regulation will provide the opportunity to regulate better postoperative adhesion development and tissue fibrosis, thereby reducing the morbidity and mortality they cause.
UR - http://www.scopus.com/inward/record.url?scp=4444343130&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=4444343130&partnerID=8YFLogxK
U2 - 10.1016/S1074-3804(05)60041-2
DO - 10.1016/S1074-3804(05)60041-2
M3 - Article
C2 - 15559339
AN - SCOPUS:4444343130
VL - 11
SP - 307
EP - 314
JO - Journal of Minimally Invasive Gynecology
JF - Journal of Minimally Invasive Gynecology
SN - 1553-4650
IS - 3
ER -