Perioperative tight glycemic control using artificial pancreas decreases infectious complications via suppression of inflammatory cytokines in patients who underwent pancreaticoduodenectomy: A prospective, non-randomized clinical trial
We sought to investigate the efficacy of perioperative tight glycemic control (TGC) in reducing of postoperative infectious complications (POICs) and study its impact on early inflammatory mediators in patients who underwent pancreaticoduodenectomy. In this non-randomized trial, the artificial pancr...
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creator | Akabori, Hiroya Tani, Masaji Kitamura, Naomi Maehira, Hiromitsu Imashuku, Yasuhiko Tsujita, Yasuyuki Shimizu, Tomoharu Kitagawa, Hirotoshi Eguchi, Yutaka |
description | We sought to investigate the efficacy of perioperative tight glycemic control (TGC) in reducing of postoperative infectious complications (POICs) and study its impact on early inflammatory mediators in patients who underwent pancreaticoduodenectomy.
In this non-randomized trial, the artificial pancreas (AP) group received TGC (target glucose range of 80–110 mg/dL; n = 14), while the control group received conventional glycemic control (range of 80–180 mg/dL; n = 15). The primary endpoint was POICs.
The AP group had a markedly decreased POIC rate (28.6% vs. 73.3%; P = 0.027), mean glycemic variability (13.5 ± 3.5% vs. 16.4 ± 5.9%; P = 0.038), and plasma interleukin-6 level (26.3 ± 33.8 vs 98.3 ± 89.1 pg/ml; P = 0.036) compared to the control group, but insulin dosage (27.0 ± 13.4 vs. 10.2 ± 16.2 U; P = 0.002) and the adiponectin ratio (i.e., postoperative/preoperative adiponectin; 0.8 ± 0.2 vs. 0.6 ± 0.3; P = 0.021) were markedly higher in the AP group.
Among patients undergoing PD with impaired glucose tolerance, AP facilitated strict glycemic control and resulted in a reduction of anti-inflammatory mediators and POICs.
Perioperative hyperglycemia increases postoperative infectious complications; however, tight glycemic control using artificial pancreas can reduce them via a dual effect. Artificial pancreas facilitates strict and safe glycemic control while reducing anti-inflammatory mediators, including adiponectin, following pancreaticoduodenectomy.
•Artificial pancreas facilitates strict glycemic control after pancreatic surgery.•Tight glycemic control reduces infectious complications in patients with diabetes.•Postoperative glycemic variability is important in perioperative glycemic control.•Adipose tissue inflammation is associated with postoperative infectious complication. . |
doi_str_mv | 10.1016/j.amjsurg.2019.12.008 |
format | Article |
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In this non-randomized trial, the artificial pancreas (AP) group received TGC (target glucose range of 80–110 mg/dL; n = 14), while the control group received conventional glycemic control (range of 80–180 mg/dL; n = 15). The primary endpoint was POICs.
The AP group had a markedly decreased POIC rate (28.6% vs. 73.3%; P = 0.027), mean glycemic variability (13.5 ± 3.5% vs. 16.4 ± 5.9%; P = 0.038), and plasma interleukin-6 level (26.3 ± 33.8 vs 98.3 ± 89.1 pg/ml; P = 0.036) compared to the control group, but insulin dosage (27.0 ± 13.4 vs. 10.2 ± 16.2 U; P = 0.002) and the adiponectin ratio (i.e., postoperative/preoperative adiponectin; 0.8 ± 0.2 vs. 0.6 ± 0.3; P = 0.021) were markedly higher in the AP group.
Among patients undergoing PD with impaired glucose tolerance, AP facilitated strict glycemic control and resulted in a reduction of anti-inflammatory mediators and POICs.
Perioperative hyperglycemia increases postoperative infectious complications; however, tight glycemic control using artificial pancreas can reduce them via a dual effect. Artificial pancreas facilitates strict and safe glycemic control while reducing anti-inflammatory mediators, including adiponectin, following pancreaticoduodenectomy.
•Artificial pancreas facilitates strict glycemic control after pancreatic surgery.•Tight glycemic control reduces infectious complications in patients with diabetes.•Postoperative glycemic variability is important in perioperative glycemic control.•Adipose tissue inflammation is associated with postoperative infectious complication. .</description><identifier>ISSN: 0002-9610</identifier><identifier>EISSN: 1879-1883</identifier><identifier>DOI: 10.1016/j.amjsurg.2019.12.008</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>Abdominal surgery ; Adiponectin ; Artificial pancreas ; Clinical trials ; Complications ; Cytokines ; Diabetes ; Glucose ; Glucose tolerance ; Hyperglycemia ; Hypoglycemia ; Infections ; Inflammation ; Insulin ; Insulin resistance ; Interleukin 6 ; Interleukins ; Laboratories ; Metabolism ; Pancreas ; Pancreaticoduodenectomy ; Patients ; Plasma ; Postoperative period ; Surgeons ; Tight glycemic control</subject><ispartof>The American journal of surgery, 2020-08, Vol.220 (2), p.365-371</ispartof><rights>2019 Elsevier Inc.</rights><rights>2019. Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-8e6bc645a803b6c317f690ede9e358be29f849e9b071c6669dfd46250e7d2c213</citedby><cites>FETCH-LOGICAL-c480t-8e6bc645a803b6c317f690ede9e358be29f849e9b071c6669dfd46250e7d2c213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2425700606?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997,64387,64389,64391,72471</link.rule.ids></links><search><creatorcontrib>Akabori, Hiroya</creatorcontrib><creatorcontrib>Tani, Masaji</creatorcontrib><creatorcontrib>Kitamura, Naomi</creatorcontrib><creatorcontrib>Maehira, Hiromitsu</creatorcontrib><creatorcontrib>Imashuku, Yasuhiko</creatorcontrib><creatorcontrib>Tsujita, Yasuyuki</creatorcontrib><creatorcontrib>Shimizu, Tomoharu</creatorcontrib><creatorcontrib>Kitagawa, Hirotoshi</creatorcontrib><creatorcontrib>Eguchi, Yutaka</creatorcontrib><title>Perioperative tight glycemic control using artificial pancreas decreases infectious complications via suppression of inflammatory cytokines in patients who underwent pancreaticoduodenectomy: A prospective, non-randomized clinical trial</title><title>The American journal of surgery</title><description>We sought to investigate the efficacy of perioperative tight glycemic control (TGC) in reducing of postoperative infectious complications (POICs) and study its impact on early inflammatory mediators in patients who underwent pancreaticoduodenectomy.
In this non-randomized trial, the artificial pancreas (AP) group received TGC (target glucose range of 80–110 mg/dL; n = 14), while the control group received conventional glycemic control (range of 80–180 mg/dL; n = 15). The primary endpoint was POICs.
The AP group had a markedly decreased POIC rate (28.6% vs. 73.3%; P = 0.027), mean glycemic variability (13.5 ± 3.5% vs. 16.4 ± 5.9%; P = 0.038), and plasma interleukin-6 level (26.3 ± 33.8 vs 98.3 ± 89.1 pg/ml; P = 0.036) compared to the control group, but insulin dosage (27.0 ± 13.4 vs. 10.2 ± 16.2 U; P = 0.002) and the adiponectin ratio (i.e., postoperative/preoperative adiponectin; 0.8 ± 0.2 vs. 0.6 ± 0.3; P = 0.021) were markedly higher in the AP group.
Among patients undergoing PD with impaired glucose tolerance, AP facilitated strict glycemic control and resulted in a reduction of anti-inflammatory mediators and POICs.
Perioperative hyperglycemia increases postoperative infectious complications; however, tight glycemic control using artificial pancreas can reduce them via a dual effect. Artificial pancreas facilitates strict and safe glycemic control while reducing anti-inflammatory mediators, including adiponectin, following pancreaticoduodenectomy.
•Artificial pancreas facilitates strict glycemic control after pancreatic surgery.•Tight glycemic control reduces infectious complications in patients with diabetes.•Postoperative glycemic variability is important in perioperative glycemic control.•Adipose tissue inflammation is associated with postoperative infectious complication. .</description><subject>Abdominal surgery</subject><subject>Adiponectin</subject><subject>Artificial pancreas</subject><subject>Clinical trials</subject><subject>Complications</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Glucose</subject><subject>Glucose tolerance</subject><subject>Hyperglycemia</subject><subject>Hypoglycemia</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Interleukin 6</subject><subject>Interleukins</subject><subject>Laboratories</subject><subject>Metabolism</subject><subject>Pancreas</subject><subject>Pancreaticoduodenectomy</subject><subject>Patients</subject><subject>Plasma</subject><subject>Postoperative period</subject><subject>Surgeons</subject><subject>Tight glycemic control</subject><issn>0002-9610</issn><issn>1879-1883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFUsGO0zAQjRBIlIVPQLLEhQMptpM6Nhe0Wu0C0kpwgLPl2pPulMQOttNV-GV-Yt12uXDhNJrRm_fePE1VvWZ0zSgT7_drM-7THHdrTplaM76mVD6pVkx2qmZSNk-rFaWU10ow-rx6kdK-tIy1zar68w0ihgmiyXgAknF3l8luWCyMaIkNPscwkDmh3xETM_Zo0QxkMt5GMIk4OFVIBH0PNmOYU1kbpwFtoQw-kQMakuZpipBSGZDQH7GDGUeTQ1yIXXL4if5EUYgzgs-J3N8FMnsH8b60f_Uy2uDm4MAXqTAuH8glmWJI01H5AO-ID76Oxrsw4m9wxA7oi4-B5Fhcv6ye9WZI8OqxXlQ_bq6_X32ub79--nJ1eVvbVtJcSxBbK9qNkbTZCtuwrheKggMFzUZugatetgrUlnbMCiGU610r-IZC57jlrLmo3p55i7VfM6SsR0wWhsF4KPFo3jRCqU5SWaBv_oHuwxx9cad5yzcdpYKKgtqcUbbcmiL0eoo4mrhoRvXxBfReP76APr6AZlzTE_vH8x6Uaw8IUSdb0rXgMJbEtAv4H4YH847GQQ</recordid><startdate>20200801</startdate><enddate>20200801</enddate><creator>Akabori, Hiroya</creator><creator>Tani, Masaji</creator><creator>Kitamura, Naomi</creator><creator>Maehira, Hiromitsu</creator><creator>Imashuku, Yasuhiko</creator><creator>Tsujita, Yasuyuki</creator><creator>Shimizu, Tomoharu</creator><creator>Kitagawa, Hirotoshi</creator><creator>Eguchi, Yutaka</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20200801</creationdate><title>Perioperative tight glycemic control using artificial pancreas decreases infectious complications via suppression of inflammatory cytokines in patients who underwent pancreaticoduodenectomy: A prospective, non-randomized clinical trial</title><author>Akabori, Hiroya ; 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In this non-randomized trial, the artificial pancreas (AP) group received TGC (target glucose range of 80–110 mg/dL; n = 14), while the control group received conventional glycemic control (range of 80–180 mg/dL; n = 15). The primary endpoint was POICs.
The AP group had a markedly decreased POIC rate (28.6% vs. 73.3%; P = 0.027), mean glycemic variability (13.5 ± 3.5% vs. 16.4 ± 5.9%; P = 0.038), and plasma interleukin-6 level (26.3 ± 33.8 vs 98.3 ± 89.1 pg/ml; P = 0.036) compared to the control group, but insulin dosage (27.0 ± 13.4 vs. 10.2 ± 16.2 U; P = 0.002) and the adiponectin ratio (i.e., postoperative/preoperative adiponectin; 0.8 ± 0.2 vs. 0.6 ± 0.3; P = 0.021) were markedly higher in the AP group.
Among patients undergoing PD with impaired glucose tolerance, AP facilitated strict glycemic control and resulted in a reduction of anti-inflammatory mediators and POICs.
Perioperative hyperglycemia increases postoperative infectious complications; however, tight glycemic control using artificial pancreas can reduce them via a dual effect. Artificial pancreas facilitates strict and safe glycemic control while reducing anti-inflammatory mediators, including adiponectin, following pancreaticoduodenectomy.
•Artificial pancreas facilitates strict glycemic control after pancreatic surgery.•Tight glycemic control reduces infectious complications in patients with diabetes.•Postoperative glycemic variability is important in perioperative glycemic control.•Adipose tissue inflammation is associated with postoperative infectious complication. .</abstract><cop>New York</cop><pub>Elsevier Inc</pub><doi>10.1016/j.amjsurg.2019.12.008</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abdominal surgery Adiponectin Artificial pancreas Clinical trials Complications Cytokines Diabetes Glucose Glucose tolerance Hyperglycemia Hypoglycemia Infections Inflammation Insulin Insulin resistance Interleukin 6 Interleukins Laboratories Metabolism Pancreas Pancreaticoduodenectomy Patients Plasma Postoperative period Surgeons Tight glycemic control |
title | Perioperative tight glycemic control using artificial pancreas decreases infectious complications via suppression of inflammatory cytokines in patients who underwent pancreaticoduodenectomy: A prospective, non-randomized clinical trial |
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