Hemoglobin A1c Is a Predictor of New Insulin Dependence After Partial Pancreatectomy: A Multi-Institutional Analysis.


Journal

Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract
ISSN: 1873-4626
Titre abrégé: J Gastrointest Surg
Pays: United States
ID NLM: 9706084

Informations de publication

Date de publication:
12 2021
Historique:
received: 04 12 2020
accepted: 12 04 2021
pubmed: 6 5 2021
medline: 30 12 2021
entrez: 5 5 2021
Statut: ppublish

Résumé

Pancreatic diseases have long been associated with impaired glucose control. This study sought to identify the incidence of new insulin-dependent diabetes mellitus (IDDM) after pancreatectomy and the predictive accuracy of hemoglobin A1c (HbA1c) or blood glucose. Patients who underwent partial pancreatectomy and had preoperative HbA1c available at two academic institutions were assessed for new IDDM on discharge in relation to complication rates and survival. Of the 267 patients analyzed, 67% had abnormal HbA1c levels prior to surgery (mean 6.8%, glucose 135 mg/dL). Two hundred eight (77.9%) were not insulin-dependent prior to surgery, and 35 (16.8%) developed new IDDM after resection. On multivariable regression, increasing HbA1c and preoperative glucose were the only significant predictors for new IDDM. Optimal predictive cutoffs (HbA1c of 6.25% and glucose of 121 mg/dL) were determined in a discovery group (n = 143) and confirmed in a validation group (n = 124) with a diagnostic sensitivity of 72.7% and specificity of 84.8%. Patients with new IDDM after resection had higher rates of severe complications (OR 3.39), increased TPN at discharge (OR 4.32), and increased rates of discharge to nursing facilities (OR 2.57) (all P < 0.05). New IDDM was also associated with a decreased cancer-specific survival. Preoperative HbA1c ≥ 6.25% and blood glucose ≥ 121 mg/dL can accurately identify patients at increased risk of IDDM. These diagnostics may help identify patients in a preoperative setting that may benefit from interventions such as diabetes education or enhanced glucose control preoperatively.

Sections du résumé

BACKGROUND
Pancreatic diseases have long been associated with impaired glucose control. This study sought to identify the incidence of new insulin-dependent diabetes mellitus (IDDM) after pancreatectomy and the predictive accuracy of hemoglobin A1c (HbA1c) or blood glucose.
METHODS
Patients who underwent partial pancreatectomy and had preoperative HbA1c available at two academic institutions were assessed for new IDDM on discharge in relation to complication rates and survival.
RESULTS
Of the 267 patients analyzed, 67% had abnormal HbA1c levels prior to surgery (mean 6.8%, glucose 135 mg/dL). Two hundred eight (77.9%) were not insulin-dependent prior to surgery, and 35 (16.8%) developed new IDDM after resection. On multivariable regression, increasing HbA1c and preoperative glucose were the only significant predictors for new IDDM. Optimal predictive cutoffs (HbA1c of 6.25% and glucose of 121 mg/dL) were determined in a discovery group (n = 143) and confirmed in a validation group (n = 124) with a diagnostic sensitivity of 72.7% and specificity of 84.8%. Patients with new IDDM after resection had higher rates of severe complications (OR 3.39), increased TPN at discharge (OR 4.32), and increased rates of discharge to nursing facilities (OR 2.57) (all P < 0.05). New IDDM was also associated with a decreased cancer-specific survival.
CONCLUSION
Preoperative HbA1c ≥ 6.25% and blood glucose ≥ 121 mg/dL can accurately identify patients at increased risk of IDDM. These diagnostics may help identify patients in a preoperative setting that may benefit from interventions such as diabetes education or enhanced glucose control preoperatively.

Identifiants

pubmed: 33948858
doi: 10.1007/s11605-021-05014-0
pii: 10.1007/s11605-021-05014-0
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Insulin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3119-3129

Informations de copyright

© 2021. The Society for Surgery of the Alimentary Tract.

Références

2017. Classification and Diagnosis of Diabetes. Diabetes Care. Jan, 40 (Supplement 1), S11–S24. https://doi.org/10.2337/dc17-S005 .
Bassi, C. et al. 2017. The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 Years After. Surgery. 161, 3: 584–591. https://doi.org/10.1016/j.surg.2016.11.014 .
doi: 10.1016/j.surg.2016.11.014 pubmed: 28040257
Bilimoria, K.Y., Bentrem, D.J., Ko, C.Y., Stewart, A.K., Winchester, D.P. and Talamonti, M.S. 2007. National failure to operate on early stage pancreatic cancer. Annals of Surgery. 246, 2, 173–180. https://doi.org/10.1097/SLA.0b013e3180691579 .
doi: 10.1097/SLA.0b013e3180691579 pubmed: 17667493
Burkhart, R.A. et al. 2015. Incidence and Severity of Pancreatogenic Diabetes After Pancreatic Resection. Journal of Gastrointestinal Surgery. 19, (2015), 217–225. https://doi.org/10.1007/s11605-014-2669-z .
doi: 10.1007/s11605-014-2669-z pubmed: 25316483
Cameron, J.L. and He, J. 2015. Two thousand consecutive pancreaticoduodenectomies. Journal of the American College of Surgeons. 220, 4, 530–536. https://doi.org/10.1016/j.jamcollsurg.2014.12.031 .
doi: 10.1016/j.jamcollsurg.2014.12.031 pubmed: 25724606
Cannon, R.M. et al. 2012. Multi-institutional analysis of pancreatic adenocarcinoma demonstrating the effect of diabetes status on survival after resection. HPB. 14, (2012), 228–235. https://doi.org/10.1111/j.1477-2574.2011.00432.x .
doi: 10.1111/j.1477-2574.2011.00432.x pubmed: 22404260
Chagpar, R.B. et al. 2011. Medically Managed Hypercholesterolemia and Insulin-Dependent Diabetes Mellitus Preoperatively Predicts Poor Survival after Surgery for Pancreatic Cancer. Journal of Gastrointestinal Surgery. 15, 4, 551–557. https://doi.org/10.1007/s11605-011-1448-3 .
doi: 10.1007/s11605-011-1448-3 pubmed: 21327533
Chu, C.K., Mazo, A.E., Sarmiento, J.M., Staley, C.A., Adsay, N.V., Umpierrez, G.E. and Kooby, D.A. 2010. Impact of Diabetes Mellitus on Perioperative Outcomes after Resection for Pancreatic Adenocarcinoma. Journal of the American College of Surgeons. 210, 4, 463–473. https://doi.org/10.1016/j.jamcollsurg.2009.12.029 .
doi: 10.1016/j.jamcollsurg.2009.12.029 pubmed: 20347739
De Bruijn, K.M.J. and Van Eijck, C.H.J. 2015. New-onset Diabetes after Distal Pancreatectomy: A Systematic Review. Annals of Surgery. 261, 5, 854–861. https://doi.org/10.1097/SLA.0000000000000819 .
doi: 10.1097/SLA.0000000000000819 pubmed: 24983994
Dindo, D., Demartines, N. and Clavien, P.A. 2004. Classification of surgical complications: A new proposal with evaluation in a cohort of 6336 patients and results of a survey. Annals of Surgery. 240, 2, 205–213. https://doi.org/10.1097/01.sla.0000133083.54934.ae .
doi: 10.1097/01.sla.0000133083.54934.ae pubmed: 15273542
Ehehalt, F., Sturm, D., Rösler, M., Distler, M., Weitz, J., Kersting, S., Ludwig, B., Schwanebeck, U., Saeger, H.D., Solimena, M. and Grützmann, R. 2015. Blood glucose homeostasis in the course of partial pancreatectomy - Evidence for surgically reversible diabetes induced by cholestasis. PLoS ONE. 10, 8, e0134140. https://doi.org/10.1371/journal.pone.0134140 .
doi: 10.1371/journal.pone.0134140 pubmed: 26248027
Fan, K.Y. et al. 2014. Baseline hemoglobin-A1c impacts clinical outcomes in patients with pancreatic cancer. JNCCN Journal of the National Comprehensive Cancer Network. 12, 1, 50–57. https://doi.org/10.6004/jnccn.2014.0006 .
doi: 10.6004/jnccn.2014.0006 pubmed: 24453292
Gaujoux, S., Brennan, M.F., Gonen, M., D’Angelica, M.I., DeMatteo, R., Fong, Y., Schattner, M., DiMaio, C., Janakos, M., Jarnagin, W.R. and Allen, P.J. 2011. Cystic lesions of the pancreas: Changes in the presentation and management of 1,424 patients at a single institution over a 15-year time period. Journal of the American College of Surgeons. 212, 4, 590–600. https://doi.org/10.1016/j.jamcollsurg.2011.01.016 .
doi: 10.1016/j.jamcollsurg.2011.01.016 pubmed: 21463795
Hart, P.A. and Chari, S.T. 2013. Diabetes mellitus and pancreatic cancer: Why the association matters? Pancreas.
Hart, P.A. and Chari, S.T. 2015. Pancreapedia: The Exocrine Pancreas Knowledge Base. Pancreapedia: Exocrine Pancreas Knowledge Base. https://doi.org/10.3998/panc.2015.34 .
He, X.Y., Li, J.F., Yao, W.Y. and Yuan, Y.Z. 2013. Resolution of new-onset diabetes after radical pancreatic resection predicts long-term survival in patients with pancreatic ductal cell adenocarcinoma. Annals of Surgical Oncology. 20, 12, 3809–3816. https://doi.org/10.1245/s10434-013-3095-2 .
doi: 10.1245/s10434-013-3095-2 pubmed: 23943021
He, J., Ahuja, N., Makary, M.A., Cameron, J.L., Eckhauser, F.E., Choti, M.A., Hruban, R.H., Pawlik, T.M. and Wolfgang, C.L. 2014. 2564 resected periampullary adenocarcinomas at a single institution: Trends over three decades. HPB. 16, 1, 83–90. https://doi.org/10.1111/hpb.12078 .
doi: 10.1111/hpb.12078 pubmed: 23472829
Kang, J.S., Jang, J.Y., Kang, M.J., Kim, E., Jung, W., Chang, J., Shin, Y., Han, Y. and Kim, S.W. 2016. Endocrine Function Impairment after Distal Pancreatectomy: Incidence and Related Factors. World Journal of Surgery. 40, (2016), 440–446. https://doi.org/10.1007/s00268-015-3228-9 .
doi: 10.1007/s00268-015-3228-9 pubmed: 26330237
Kleeff, J. et al. 2016. The impact of diabetes mellitus on survival following resection and adjuvant chemotherapy for pancreatic cancer. British Journal of Cancer. 115, 7, 887–894. https://doi.org/10.1038/bjc.2016.277 .
doi: 10.1038/bjc.2016.277 pubmed: 27584663
Leal, J.N., Kingham, T.P., D’Angelica, M.I., DeMatteo, R.P., Jarnagin, W.R., Kalin, M.F. and Allen, P.J. 2015. Intraductal Papillary Mucinous Neoplasms and the Risk of Diabetes Mellitus in Patients Undergoing Resection Versus Observation. Journal of Gastrointestinal Surgery. 19, (2015), 1974–1981. https://doi.org/10.1007/s11605-015-2885-1 .
doi: 10.1007/s11605-015-2885-1 pubmed: 26160323
Lee, W., Yoon, Y.S., Han, H.S., Cho, J.Y., Choi, Y., Jang, J.Y. and Choi, H. 2016. Prognostic relevance of preoperative diabetes mellitus and the degree of hyperglycemia on the outcomes of resected pancreatic ductal adenocarcinoma. Journal of Surgical Oncology. 113, (2016), 203–208. https://doi.org/10.1002/jso.24133 .
doi: 10.1002/jso.24133 pubmed: 26799261
Malleo, G., Mazzarella, F., Malpaga, A., Marchegiani, G., Salvia, R., Bassi, C. and Butturini, G. 2013. Diabetes mellitus does not impact on clinically relevant pancreatic fistula after partial pancreatic resection for ductal adenocarcinoma. Surgery. 153, 5, 641–650. https://doi.org/10.1016/j.surg.2012.10.015 .
doi: 10.1016/j.surg.2012.10.015 pubmed: 23276391
Maxwell, D.W., Jajja, M.R., Tariq, M., Mahmooth, Z., Galindo, R.J., Sweeney, J.F. and Sarmiento, J.M. 2019. Development of Diabetes after Pancreaticoduodenectomy : Results of a 10-Year Series Using Prospective Endocrine Evaluation. Journal of the American College of Surgeons. 228, 4, 400–414.
doi: 10.1016/j.jamcollsurg.2018.12.042
Maxwell, D.W., Jajja, M.R., Galindo, R.J., Nadeem, S.O., Sweeney, J.F., Blair, C.M. and Sarmiento, J.M. 2020. Post-Pancreatectomy Diabetes Index : A Validated Score Predicting Diabetes Development after Major Pancreatectomy. Journal of the American College of Surgeons. 230, 4, 393–404.
doi: 10.1016/j.jamcollsurg.2019.12.016
Mayo, S.C., Herman, J.M., Cosgrove, D., Bhagat, N., Kamel, I., Geschwind, J.F.H. and Pawlik, T.M. 2013. Emerging approaches in the management of patients with neuroendocrine liver metastasis: Role of liver-directed and systemic therapies. Journal of the American College of Surgeons. 216, 1, 123–134. https://doi.org/10.1016/j.jamcollsurg.2012.08.027 .
doi: 10.1016/j.jamcollsurg.2012.08.027 pubmed: 23063263
McAuliffe, J.C. and Christein, J.D. 2013. Type 2 Diabetes Mellitus and Pancreatic Cancer. Surgical Clinics of North America. 93, 3, 619–627. https://doi.org/10.1016/j.suc.2013.02.003 .
doi: 10.1016/j.suc.2013.02.003
McMillan, M.T. et al. 2016. Risk-adjusted Outcomes of Clinically Relevant Pancreatic Fistula Following Pancreatoduodenectomy: A Model for Performance Evaluation. Annals of Surgery. 264, 2, 344–352. https://doi.org/10.1097/SLA.0000000000001537 .
doi: 10.1097/SLA.0000000000001537 pubmed: 26727086
Pannala, R., Leirness, J.B., Bamlet, W.R., Basu, A., Petersen, G.M. and Chari, S.T. 2008. Prevalence and Clinical Profile of Pancreatic Cancer-Associated Diabetes Mellitus. Gastroenterology. 134, 4, 981–987. https://doi.org/10.1053/j.gastro.2008.01.039 .
doi: 10.1053/j.gastro.2008.01.039 pubmed: 18395079
Rahib, L., Smith, B.D., Aizenberg, R., Rosenzweig, A.B., Fleshman, J.M. and Matrisian, L.M. 2014. Projecting cancer incidence and deaths to 2030: The unexpected burden of thyroid, liver, and pancreas cancers in the united states. Cancer Research. 74, 11, 2913–2921. https://doi.org/10.1158/0008-5472.CAN-14-0155 .
doi: 10.1158/0008-5472.CAN-14-0155 pubmed: 24840647
Shirakawa, S., Matsumoto, I., Toyama, H., Shinzeki, M., Ajiki, T., Fukumoto, T. and Ku, Y. 2012. Pancreatic Volumetric Assessment as a Predictor of New-Onset Diabetes Following Distal Pancreatectomy. Journal of Gastrointestinal Surgery. 16, 12, 2212–2219. https://doi.org/10.1007/s11605-012-2039-7 .
doi: 10.1007/s11605-012-2039-7 pubmed: 23054900
Shubert, C.R., Kendrick, M.L., Habermann, E.B., Glasgow, A.E., Borah, B.J., Moriarty, J.P., Cleary, S.P., Smoot, R.L., Farnell, M.B., Nagorney, D.M., Truty, M.J. and Que, F.G. 2018. Implementation of prospective, surgeon-driven, risk-based pathway for pancreatoduodenectomy results in improved clinical outcomes and first year cost savings of $1 million. Surgery. 163, 3, 495–502. https://doi.org/10.1016/j.surg.2017.10.022 .
doi: 10.1016/j.surg.2017.10.022 pubmed: 29275974
Vin, Y., Sima, C.S., Getrajdman, G.I., Brown, K.T., Covey, A., Brennan, M.F. and Allen, P.J. 2008. Management and Outcomes of Postpancreatectomy Fistula, Leak, and Abscess: Results of 908 Patients Resected at a Single Institution Between 2000 and 2005. Journal of the American College of Surgeons. 207, 4, 490–498. https://doi.org/10.1016/j.jamcollsurg.2008.05.003 .
doi: 10.1016/j.jamcollsurg.2008.05.003 pubmed: 18926450
Walter, U., Kohlert, T., Rahbari, N.N., Weitz, J. and Welsch, T. 2014. Impact of preoperative diabetes on long-term survival after curative resection of pancreatic adenocarcinoma: A systematic review and meta-analysis. Annals of Surgical Oncology. 21, 1082–1089. https://doi.org/10.1245/s10434-013-3415-6 .
doi: 10.1245/s10434-013-3415-6 pubmed: 24322532
Wente, M.N., Bassi, C., Dervenis, C., Fingerhut, A., Gouma, D.J., Izbicki, J.R., Neoptolemos, J.P., Padbury, R.T., Sarr, M.G., Traverso, L.W., Yeo, C.J. and Büchler, M.W. 2007. Delayed gastric emptying (DGE) after pancreatic surgery: A suggested definition by the International Study Group of Pancreatic Surgery (ISGPS). Surgery. 142, 5, 761–768. https://doi.org/10.1016/j.surg.2007.05.005 .
doi: 10.1016/j.surg.2007.05.005 pubmed: 17981197

Auteurs

Jason T Wiseman (JT)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Jeffery Chakedis (J)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Eliza W Beal (EW)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Anghela Paredes (A)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Amy McElhany (A)

Department of Surgery, Baylor College of Medicine, 6620 Main Street, Suite 1450, Houston, TX, 77030, USA.

Andrew Fang (A)

Department of Surgery, Baylor College of Medicine, 6620 Main Street, Suite 1450, Houston, TX, 77030, USA.

Andrei Manilchuk (A)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Christopher Ellison (C)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

George Van Buren (G)

Department of Surgery, Baylor College of Medicine, 6620 Main Street, Suite 1450, Houston, TX, 77030, USA.

Timothy M Pawlik (TM)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

Carl R Schmidt (CR)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA.

William E Fisher (WE)

Department of Surgery, Baylor College of Medicine, 6620 Main Street, Suite 1450, Houston, TX, 77030, USA.

Mary Dillhoff (M)

Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Arthur G. James Cancer Hospital and Solove Research Institute, 395 W. 12th Avenue, Suite 670, Columbus, OH, 43210-1267, USA. Mary.Dillhoff@osumc.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH