RSS-Feed abonnieren
DOI: 10.1055/s-0034-1394188
Prealbumin as a Serum Biomarker of Impaired Perioperative Nutritional Status and Risk for Surgical Site Infection after Spine Surgery
Publikationsverlauf
28. August 2013
23. Mai 2014
Publikationsdatum:
16. Januar 2015 (online)
Abstract
Introduction Impaired perioperative nutritional status has been shown to be an important predictor of surgical morbidity and is the earliest marker of nutritional deficiency. No study, however, has examined serum prealbumin as a surrogate marker of nutritional status in patients undergoing spine surgery.
Methods We performed a retrospective review of all patients who developed a postoperative deep wound infection after undergoing spine surgery at the University of Pittsburgh Medical Center from January 2008 through December 2011. Demographics, preoperative diagnosis, type of surgery, perioperative serum prealbumin level, time to infection, number and type of debridement procedures, and length of hospital stay were recorded.
Results A total of 83 patients had prealbumin levels available at the time of presentation of infection. Mean patient age was 56 years, and 71% were women. Surgical treatment for the infection required between 1 and 13 debridements, and 21 (25%) of the 83 patients who had instrumentation placed at the time of the initial surgery required removal of their instrumentation. Inpatient hospitalizations were extended by an average of 13 days. Prealbumin levels were below normal in 82 (99%) of the 83 patients; levels were < 7 mg/dL in 24 patients, between 7 and 11 mg/dL in 32 patients, and between 11 and 19 mg/dL in 26 patients.
Conclusions All patients except one who developed postoperative deep wound infection after spine surgery had serum prealbumin levels in the malnutrition range at the time of presentation. The current study suggests serum prealbumin levels may be an inexpensive screening biomarker for nutritional status and risk stratification for postoperative infection after spine surgery.
-
References
- 1 The Veterans Affairs Total Parenteral Nutrition Cooperative Study Group. Perioperative total parenteral nutrition in surgical patients. N Engl J Med 1991; 325 (8) 525-532
- 2 Bower RH, Cerra FB, Bershadsky B , et al. Early enteral administration of a formula (Impact) supplemented with arginine, nucleotides, and fish oil in intensive care unit patients: results of a multicenter, prospective, randomized, clinical trial. Crit Care Med 1995; 23 (3) 436-449
- 3 Braga M, Gianotti L, Nespoli L, Radaelli G, Di Carlo V. Nutritional approach in malnourished surgical patients: a prospective randomized study. Arch Surg 2002; 137 (2) 174-180
- 4 Brandstrup B, Tønnesen H, Beier-Holgersen R , et al; Danish Study Group on Perioperative Fluid Therapy. Effects of intravenous fluid restriction on postoperative complications: comparison of two perioperative fluid regimens: a randomized assessor-blinded multicenter trial. Ann Surg 2003; 238 (5) 641-648
- 5 Daly JM, Weintraub FN, Shou J, Rosato EF, Lucia M. Enteral nutrition during multimodality therapy in upper gastrointestinal cancer patients. Ann Surg 1995; 221 (4) 327-338
- 6 Gianotti L, Braga M, Nespoli L, Radaelli G, Beneduce A, Di Carlo V. A randomized controlled trial of preoperative oral supplementation with a specialized diet in patients with gastrointestinal cancer. Gastroenterology 2002; 122 (7) 1763-1770
- 7 Sungurtekin H, Sungurtekin U, Balci C, Zencir M, Erdem E. The influence of nutritional status on complications after major intraabdominal surgery. J Am Coll Nutr 2004; 23 (3) 227-232
- 8 Bansal V, Ochoa JB. Arginine availability, arginase, and the immune response. Curr Opin Clin Nutr Metab Care 2003; 6 (2) 223-228
- 9 Efron DT, Barbul A. Modulation of inflammation and immunity by arginine supplements. Curr Opin Clin Nutr Metab Care 1998; 1 (6) 531-538
- 10 Ochoa JB, Bernard AC, Mistry SK , et al. Trauma increases extrahepatic arginase activity. Surgery 2000; 127 (4) 419-426
- 11 Ochoa JB, Makarenkova V, Bansal V. A rational use of immune enhancing diets: when should we use dietary arginine supplementation?. Nutr Clin Pract 2004; 19 (3) 216-225
- 12 Rodriguez PC, Quiceno DG, Ochoa AC. L-arginine availability regulates T-lymphocyte cell-cycle progression. Blood 2007; 109 (4) 1568-1573
- 13 Rodriguez PC, Quiceno DG, Zabaleta J , et al. Arginase I production in the tumor microenvironment by mature myeloid cells inhibits T-cell receptor expression and antigen-specific T-cell responses. Cancer Res 2004; 64 (16) 5839-5849
- 14 Tsuei BJ, Bernard AC, Shane MD , et al. Surgery induces human mononuclear cell arginase I expression. J Trauma 2001; 51 (3) 497-502
- 15 Beck FK, Rosenthal TC. Prealbumin: a marker for nutritional evaluation. Am Fam Physician 2002; 65 (8) 1575-1578
- 16 Klein JD, Garfin SR. Nutritional status in the patient with spinal infection. Orthop Clin North Am 1996; 27 (1) 33-36
- 17 Klein JD, Hey LA, Yu CS , et al. Perioperative nutrition and postoperative complications in patients undergoing spinal surgery. Spine 1996; 21 (22) 2676-2682
- 18 Kudsk KA, Tolley EA, DeWitt RC , et al. Preoperative albumin and surgical site identify surgical risk for major postoperative complications. JPEN J Parenter Enteral Nutr 2003; 27 (1) 1-9
- 19 Spiekerman AM. Nutritional assessment (protein nutriture). Anal Chem 1995; 67 (12) 429R-436R
- 20 Levi AD, Dickman CA, Sonntag VK. Management of postoperative infections after spinal instrumentation. J Neurosurg 1997; 86 (6) 975-980
- 21 Rechtine GR, Bono PL, Cahill D, Bolesta MJ, Chrin AM. Postoperative wound infection after instrumentation of thoracic and lumbar fractures. J Orthop Trauma 2001; 15 (8) 566-569
- 22 Rihn JA, Lee JY, Ward WT. Infection after the surgical treatment of adolescent idiopathic scoliosis: evaluation of the diagnosis, treatment, and impact on clinical outcomes. Spine 2008; 33 (3) 289-294
- 23 Veeravagu A, Patil CG, Lad SP, Boakye M. Risk factors for postoperative spinal wound infections after spinal decompression and fusion surgeries. Spine 2009; 34 (17) 1869-1872
- 24 Mok JM, Guillaume TJ, Talu U , et al. Clinical outcome of deep wound infection after instrumented posterior spinal fusion: a matched cohort analysis. Spine 2009; 34 (6) 578-583
- 25 Bernstein LH, Ingenbleek Y. Transthyretin: its response to malnutrition and stress injury. clinical usefulness and economic implications. Clin Chem Lab Med 2002; 40 (12) 1344-1348
- 26 Martindale RG, McClave SA, Vanek VW , et al; American College of Critical Care Medicine; A.S.P.E.N. Board of Directors. Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine and American Society for Parenteral and Enteral Nutrition: Executive Summary. Crit Care Med 2009; 37 (5) 1757-1761
- 27 Todd SR, Gonzalez EA, Turner K, Kozar RA. Update on postinjury nutrition. Curr Opin Crit Care 2008; 14 (6) 690-695
- 28 Schoenfeld AJ, Carey PA, Cleveland 3rd AW, Bader JO, Bono CM. Patient factors, comorbidities, and surgical characteristics that increase mortality and complication risk after spinal arthrodesis: a prognostic study based on 5,887 patients. Spine J 2013; 13 (10) 1171-1179
- 29 Lenke LG, Bridwell KH, Blanke K, Baldus C. Prospective analysis of nutritional status normalization after spinal reconstructive surgery. Spine 1995; 20 (12) 1359-1367
- 30 Ingenbleek Y, Young VR. Significance of transthyretin in protein metabolism. Clin Chem Lab Med 2002; 40 (12) 1281-1291
- 31 Férard G, Gaudias J, Bourguignat A, Ingenbleek Y. C-reactive protein to transthyretin ratio for the early diagnosis and follow-up of postoperative infection. Clin Chem Lab Med 2002; 40 (12) 1334-1338
- 32 Shenkin A. Serum prealbumin: is it a marker of nutritional status or of risk of malnutrition?. Clin Chem 2006; 52 (12) 2177-2179
- 33 Tuten MB, Wogt S, Dasse F, Leider Z. Utilization of prealbumin as a nutritional parameter. JPEN J Parenter Enteral Nutr 1985; 9 (6) 709-711