Affiliations
Department of Biostatistics, University of Wisconsin, Madison, Wisconsin
Given name(s)
Simone L.
Family name
Glinberg
Degrees
MD

DM Screening in Preoperative Patients

Article Type
Changed
Mon, 05/22/2017 - 18:33
Display Headline
Preoperative “NPO” as an opportunity for diabetes screening

In the era of Accountable Care Organizations (ACO) and need to improve transitions of care, diagnosis and management of diseases across the continuum from ambulatory to inpatient care remains of paramount importance.1, 2 Opportunities for screening have typically been viewed as the responsibility of the ambulatory primary care provider (PCP), yet in an ACO model, patients who present more frequently to a hospital as opposed to a clinic are still the responsibility of the ACO, and therefore opportunistic screening for certain diseases by hospitalists and other inpatient providers is a possibility that may merit further investigation. This opportunistic rationale has already been used to advocate for pneumococcal and influenza vaccination prior to discharge in hospitalized patients, but has not been well investigated in chronic disease screening.35

Diabetes mellitus is a disease that has reached epidemic proportions. National Health and Nutrition Examination Survey (NHANES) data documented the ambulatory prevalence of diabetes mellitus (DM) in adults 20 years of age in the United States to be 12.9%.6 However, the most significant health crisis may be that 40% of these adult patients with diabetes are unaware of their diagnosis.6 In other words, 5.1% of all adults 20 years of age or older in this country have undiagnosed diabetes.6, 7 As diabetes is a disease where clinical manifestations are often preceded by a prolonged asymptomatic period, screening with either of the preferred diagnostic tests, fasting blood glucose (FBG) or hemoglobin A1C (Hgb A1C), is required to make a new diagnosis.79

Diagnosis of hyperglycemia is important so that appropriate glycemic control can be achieved, and preventive care and risk factor modification can be initiated, including screening and treatment of hypertension, hyperlipidemia, retinopathy, nephropathy, and other comorbid conditions.7, 9 As glycemic control cannot be achieved in patients who remain undiagnosed, screening may play a role in preventing long‐term complications of diabetes.7 Awareness of the prediabetic states impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) is also important because lifestyle modification may delay or prevent the progression to diabetes and its associated complications, such as cardiovascular disease, retinopathy, and nephropathy.10, 11 In the inpatient setting, undiagnosed elevation of Hgb A1C in the diabetes or prediabetes range has been shown to increase cost and length of stay in some spine surgery patients compared to patients with known diabetes.12

Virtually every inpatient has at least 1 glucose value drawn during hospitalization as part of a chemistry panel, many of which are fasting, or NPO (nil per os, meaning nothing by mouth), by virtue of clinical condition or anticipated procedure. Provided the preoperative state in an elective surgery patient is not taxing enough to induce stress hyperglycemia,1315 this typically fasting time may provide an easy and excellent diabetes screening opportunity to not only risk stratify for the inpatient stay, but to diagnose diabetes that will initiate lifelong care and prevention, provided information learned during hospitalization is conveyed to the PCP at discharge. While prior studies1618 have measured preoperative glucose as a means to risk stratify and predict undiagnosed diabetes, none of these analyses have obtained a second glycemic test (either FBG or Hgb A1C) as required by the American Diabetes Association (ADA) to make a diagnosis of diabetes. Lack of a confirmatory glycemic test in the existing literature also leaves uncertainty in reproducibility and validity of the preoperative glucose as a risk‐stratification tool, as it is not certain that it is truly unstressed. Finally, studies to date have not evaluated or controlled for factors that could contribute to undiagnosed diabetes, such as health insurance and access to primary care.

To investigate the prevalence of undiagnosed diabetes and prediabetes in a hospitalized population, and to pilot the concept of screening in the inpatient preoperative setting, we performed a prospective analysis of adult orthopedic patients presenting for elective hip, knee, and spine surgery at a large Midwestern academic medical center from December 1, 2007 to November 30, 2008. Our primary objective was to determine the feasibility of preoperative testing in finding the prevalence of undiagnosed diabetes and prediabetes in an insured, inpatient population with access to prior preventive care. In addition, we investigated systems issues related to the general concept of inpatient screening, including assessment of whether providers recognized hyperglycemic patients in the hospital once tested, or conveyed test information to PCPs at discharge.

METHODS

The University of Wisconsin Institutional Review Board approved this prospective observational cohort study. All patients aged 18 years scheduled for elective total knee or hip arthroplasty, or elective lumbar decompression and/or fusion, presenting for preoperative appointment from December 1, 2007 to November 30, 2008, were invited to participate. Pregnant patients, and patients unable to give consent were excluded. Patients with hemolytic processes or on new regimens of oral or intravenous steroids within 7 days of surgery were also excluded. Patients on chronic oral, inhaled, intranasal, or topical steroids were included.

Preoperative Clinic Visit (Visit 1)

Patients who consented to participate had basic measures recorded, including height, weight, age, ethnicity, sex, date of surgery, and type of surgery. Patients then completed a questionnaire regarding previous history of diabetes and prediabetes (IFG or IGT), and personal history of other ADA‐designated risk factors9 to prompt diabetes screening, including gestational diabetes, hypertension, hyperlipidemia, vascular disease, and physical inactivity, as measured by the University of California, Los Angeles (UCLA) score.19 Patient self‐reported diagnosis of DM or prediabetes was compared to anesthesia preoperative assessment for confirmation. Finally, insurance status and most recent visit to a PCP were recorded (Figure 1).

Figure 1
Study protocol for Visits 1, 2, 3. Abbreviations: FBG, fasting blood glucose; Hgb A1C, hemoglobin A1C; PCP, primary care provider.

Preoperative Day of Surgery (Visit 2)

On the morning of surgery, the study coordinator met with patients in the preoperative unit to confirm fasting status (nothing to eat for 8 or more hours), no new intravenous or oral steroids, and that intravenous fluids were dextrose free. Fasting blood glucose was collected as whole blood and centrifuged in the central laboratory, after which plasma glucose was measured using the hexokinase method (Siemens Dimension Vista 3000T, Siemens Healthcare Diagnostics, Inc, Newark, DE). Hemoglobin A1C (Tosoh G7 HPLC, Tosoh Bioscience, Tokyo, Japan) was also obtained. Patients with preoperative FBG 100 mg/dL were notified and scheduled to return for another FBG measurement at their 68 week orthopedic ambulatory clinic follow‐up visit.

Postoperative Clinic Visit (Visit 3)

At 68 week follow‐up, patients with preoperative FBG 100 mg/dL had an additional FBG performed. Those who also had a follow‐up FBG 100 mg/dL at Visit 3 were determined to have DM or IFG, identified as New Diabetes/Prediabetes. Patients with glucose 100 mg/dL prior to surgery that was <100 mg/dL in follow‐up, as well as patients with blood glucose <100 mg/dL at preoperative Visit 2 (and therefore did not require a follow‐up glucose measurement) were designated Normoglycemia. Patients with preexisting DM or IFG were labeled Known Diabetes/Prediabetes.

Statistical Methods

Categorical variables were summarized using percents. Continuous variables were summarized using means and standard deviations. Chi‐square tests were conducted for categorical variables and Student t tests were used for continuous variables to compare differences between patients with newly diagnosed IFG or DM (New Diabetes/Prediabetes) and patients without diabetes (Normoglycemia), and to compare differences between patients with New Diabetes/Prediabetes and patients with known DM or IFG (Known Diabetes/Prediabetes). Sample size was determined by number of adult elective spine and total joint orthopedic patients presenting to clinic during the prespecified 1‐year period of time. All tests were considered significant if P value < 0.05.

RESULTS

A total of 302 patients met inclusion criteria and enrolled in the study. Of these patients, 27 (8.9%) were not included in final analysis due to incomplete preoperative labs (7 patients, 2.3%), lack of follow‐up (11 patients, 3.6%), withdrawal of consent (5 patients, 1.7%), or not having surgery (4 patients, 1.3%). Of the remaining 275, 54% were female. The mean patient age was 60.3 years, and 88% (243/275) of patients had a body mass index (BMI) 25 kg/m2, indicating overweight or obese. All of the patients (100%) had healthcare insurance; 97% reported having a primary care provider, with 96.6% of patients stating that they had seen a primary provider within the year prior to surgery (Table 1).

Baseline Characteristics (N = 275)
 No. (%)
  • Abbreviations: BMI, body mass index; DM, diabetes mellitus; IFG, impaired fasting glucose; IGT, impaired glucose tolerance; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles.

  • One patient omitted answer.

  • Four patients omitted answer.

Demographics 
Female148 (54)
Age, mean (SD)60.3 (11.3)
BMI, mean (SD)31.16 (5.93)
Surgery type 
Hip99 (36)
Knee147 (53)
Spine29 (11)
Socioeconomic status/healthcare access 
Have healthcare insurance*274 (100)
Have regular PCP267 (97)
Last PCP visit 
Never2 (0.7)
>3 y1 (0.4)
13 y6 (2.2)
6 mo1 y18 (6.6)
<6 mo244 (90)
Medical history 
Diabetes history 
No history of dysglycemia225 (82)
Prior IFG17 (6)
Prior DM33 (12)
American Diabetes Association risk factors 
BMI 25243 (88)
Physical inactivity (UCLA score 3)40 (18)
High risk ethnicity3 (1)
Gestational DM2 (1)
First degree family history91 (33)
Cardiac disease35 (13)
Hypertension127 (46)
Hypercholesterolemia114 (42)
Prior IFG/IGT19 (7)
Age 45 y249 (91)

Of the 275 patients, 50 (18%) had Known Diabetes/Prediabetes, 67 (24%) were given a new diagnosis of DM or IFG (New Diabetes/Prediabetes), and the remaining 158 (58%) were classified as Normoglycemia (Table 2). The sum of Known Diabetes/Prediabetes (50) and New Diabetes/Prediabetes (67) equaled the true inpatient prevalence of DM and IFG (117/275, 43%). Of the Known Diabetes/Prediabetes patients, 33/50 (66%) had DM and 17/50 (34%) had IFG. Of those with New Diabetes/Prediabetes, 8/67 (12%) had DM range values, with the remaining 59/67 (88%) in IFG range.

Diagnosis by Glucose Value (N = 275)
DiagnosisNo. (%)Hemoglobin A1C (Mean, SD)Preoperative Glucose (Mean, SD)Follow‐up Glucose (Mean, SD)Days Between (Mean, SD)
  • NOTE: Patients with known history of diabetes or impaired fasting glucose, or normal preoperative glucose did not have follow‐up glucose testing. Abbreviations: SD, standard deviation.

  • Preoperative glucose 100, follow‐up ambulatory value also 100.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Normoglycemia.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Preop glucose 100, follow‐up <100.

  • Days Between represents days elapsed between preoperative and follow‐up glucose draws.

Known diabetes/prediabetes50 (18)6.53 (0.99)129.02 (33.85)  
New diabetes/prediabetes*67 (24)5.80 (0.39)110.79 (8.69)107.91 (7.47)51.67 (13.73)
Normoglycemia158 (58)5.45 (0.36)96.04 (9.10)  
Preop glucose 100, follow‐up <10038 (14)5.54 (0.35)107.26 (8.69)93.68 (5.16)49.21 (12.11)
Preop glucose <100120 (44)5.42 (0.36)92.49 (5.73)  

Patients with New Diabetes/Prediabetes had a higher preoperative Visit 2 glucose (mean [standard deviation], 110.79 [8.69] and 96.04 [9.10], P < 0.0001) and Hgb A1C (5.80 [0.39] and 5.45 [0.36], P < 0.0001) compared to Normoglycemia. A subset of the Normoglycemia patients (38/158, 24%), had an elevated preoperative Visit 2 glucose, but a normal (<100 mg/dL) second confirmatory Visit 3 glucose, and therefore did not have New Diabetes/Prediabetes. New Diabetes/Prediabetes was also significantly different from this particular Normoglycemia subset in both FBG (110.79 [8.69] and 107.26 [8.69], P = 0.048) and Hgb A1C (5.80 [0.39] and 5.54 [0.35], P = 0.001) (Table 2). Preoperative Visit 2 FBG of 100 mg/dL predicted Visit 3 FBG 100 mg/dL 64% of the time. Having both preoperative Visit 2 FBG 100 mg/dL and Hgb A1C 5.7 (the ADA‐determined level for prediabetes),3 predicted Visit 3 FBG 100 mg/dL 72% of the time.

Patients with New Diabetes/Prediabetes were slightly older than Normoglycemia patients (62.37 [9.70] vs 58.08 [12.01], P = 0.0054), meeting the ADA diabetes screening age of 45 significantly more often than Normoglycemia patients (100% [67] vs 84% [132], P < 0.001). The groups otherwise did not differ in the incidence of other ADA‐defined risk factors9 (Table 3). Patients with New Diabetes/Prediabetes were less likely to report having seen their PCP within 6 months prior to surgery compared to their Normoglycemia counterparts (82% [54] vs 91% [141], P = 0.046), although this difference disappeared by 1 year (94% vs 96%). Finally, there was no increase in the number of point‐of‐care (POC) glucose tests ordered, or mention of hyperglycemia on discharge summaries in the New Diabetes/Prediabetes group (Table 3).

Patient Characteristics by Diagnosis
DemographicsNormoglycemia (N = 158)New Diabetes/ Prediabetes (N = 67)Known Diabetes/ Prediabetes (N = 50)
  • NOTE: All values are No. (%) unless otherwise specified. Abbreviations: BMI, body mass index; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles. *P < 0.05 for Normoglycemia vs New Diabetes/Prediabetes. P < 0.05 for New Diabetes/Prediabetes vs Known Diabetes/Prediabetes.

Female90 (57)33 (49)25 (50)
Age, mean (SD)58.08 (12.01)*62.37 (9.70)64.60 (9.02)
BMI, mean (SD)30.13 (5.76)31.65 (5.76)33.74 (5.92)
Surgery type   
Hip62 (39)21 (31)16 (32)
Knee76 (48)41 (61)30 (60)
Spine20 (13)5 (7)4 (8)
Socioeconomic status/healthcare access
Have healthcare insurance158 (100)66 (100)50 (100)
Have regular PCP153 (97)65 (98)49 (98)
Last PCP Visit   
Never2 (1)0 (0)0 (0)
>3 y1 (1)0 (0)0 (0)
13 y1 (1)4 (6)1 (2)
6 mo1 y10 (6)8 (12)0 (0)
In last 6 mo141 (91)*54 (82)49 (98)
Medical history   
American Diabetes Association risk factors
BMI 25133 (84)62 (93)48 (96)
Physical inactivity (UCLA score 3)16 (13)10 (18)14 (35)
High‐risk ethnicity2 (1)1 (1)1 (2)
Gestational diabetes1 (1)1 (1)0 (0)
First degree family history45 (28)19 (28)27 (55)
Cardiac disease14 (9)7 (10)14 (28)
Hypertension62 (39)31 (46)34 (68)
Hyperlipidemia54 (34)28 (42)32 (64)
Age 45132 (84)*67 (100)50 (100)
Follow‐up
Point‐of‐care glucose ordered1 (1)0 (0)31 (62)
Dysglycemia mentioned on discharge summary0 (0)0 (0)28 (56)

DISCUSSION AND CONCLUSION

The main finding of this study is that in an insured, elective orthopedic population with access to primary care, 24% of patients had unrecognized IFG or DM on the basis of 2 fasting blood glucose values. Remarkably, this statistic likely represents a best‐case scenario, as the percent of undiagnosed patients is likely higher in uninsured patients,20 those without primary care visits, and those hospitalized for emergent or urgent reasons who, by definition, did not have an ambulatory preoperative evaluation, and who may also have greater severity of illness at baseline. With over 1,053,000 total knee and hip operations done in the United States each year, opportunistic screening of this population alone could identify 252,720 patients with prediabetes or diabetes who might otherwise remain undiagnosed.21 Even more significant, with at least 70 million patients undergoing ambulatory or inpatient procedures each year, if even a quarter of these procedures were elective adult lower acuity surgeries allowing for easy preoperative testing, over 4 million cases of DM and IFG could be found each year using this process.21, 22 These numbers demonstrate the need to investigate new and novel screening opportunities, such as in hospitalized patients. These statistics also demonstrate the need for all inpatient providers to be aware of undiagnosed diabetes and prediabetes in their patients, and confirm recommendations of the Endocrine Society to obtain a blood glucose for all patients on admission, and measure Hgb A1C in all hyperglycemic or diabetic inpatients if not performed in the preceding 23 months.23

Diagnosis of DM has historically been difficult to make in the hospital setting. The primary diagnostic test, FBG, may be elevated in the setting of counter‐regulatory hormone surge and inflammatory stress response, and its use has been discouraged in the acute care setting.14, 15, 24 While not affected by stress, Hgb A1C, endorsed in 2010 by the ADA for diagnosis of DM,8 may still be unreliable in the setting of blood loss, transfusion, hemolysis, and other factors common during surgery and hospitalization.9, 25 However, we found that 64% of patients with elevated (100 mg/dL) blood glucose at the time of pre‐anesthesia evaluation did have persistently elevated blood glucose at 68 week follow‐up. This suggests that the preoperative glucose is unstressed, and may be a rapid, reasonably reliable indicator of patients needing ambulatory follow‐up to confirm DM or prediabetes. This may also provide perioperative risk stratification if glycemic history is unknown. As many fasting, preoperative patients have routine chemistry panels ordered already, the simple glucose included in such panels may prove to be the most useful diabetes test for anesthesiologists, surgeons, hospitalists, and other inpatient providers. Our data suggests that Hgb A1C 5.7, the ADA‐suggested IFG/prediabetes cut point,9 can also be used in combination with FBG 100 to predict persistent hyperglycemia.

This study also revealed several significant systems issues that merit attention if opportunistic inpatient screening or preventive care is to be successful in a shared responsibility ACO system. Most importantly, none of our patients with elevated preoperative blood glucose had these results conveyed to their primary care provider at discharge, revealing both a need for improved transitions in care and development of formal ACO structure if inpatient or preoperative screening is to be successful. Second, our study also showed that providers did not change plan of care for patients without known DM or IFG and preoperative elevated glucose. None of these patients had point‐of‐care glucose checks ordered while in the hospital, demonstrating that previously undiagnosed dysglycemic patients receive different in‐hospital care compared to patients with known DM. While it is possible that providers consciously decided not to monitor patients with mild hyperglycemia, consistent with inpatient guidelines recommending glycemic targets of <180 mg/dL for general care patients,20 it is more likely that there was lack of recognition of hyperglycemia in these patients without prior DM or IFG, as has been demonstrated previously.26 Inpatient providers should be informed of, and encouraged to, follow Endocrine Society recommendations to monitor POC glucose in patients with hyperglycemia (>140 mg/dL) for at least 2448 hours.23

It is important to state that controversy exists regarding which patients should be screened for diabetes. The United States Preventive Services Task Force (USPSTF) recommends screening adult patients only if they have hypertension.27 The ADA recommends screening all patients 45 years of age and older, and younger, overweight patients with at least 1 additional risk factor.9 We have previously shown that using USPSTF guidelines misses 33.1% of cases of DM compared to the ADA standard.28 As such, our institution and the Wisconsin State Diabetes Screening Guidelines mirror the ADA guidelines.29, 30 In the present study, 91% were aged 45 and older, and 88% were overweight, so nearly everyone in our study met our state and institution guidelines for diabetes screening. However, this might not be the case at all institutions if USPSTF guidelines were instead followed.

A limitation of the present study was that a selection bias of subjects could have occurred by both patients and providers, as less healthy patients with higher surgical risk may not have been candidates for surgery as often as lower‐risk patients. While entirely appropriate to maximize safety for elective surgery patients, this may in part explain the lower Hgb A1C (6.53 [0.14]) in our Known Diabetes/Prediabetes group, and lower range of blood glucose values in our New Diabetes/Prediabetes patients, with the majority being in the prediabetes range. However, this limitation also allows for the conclusion that any patient, regardless of perceived good health and primary care visits, may still have undiagnosed DM or IFG.

In summary, this study strongly supports the practice of screening obligate fasting patients to reduce the prevalence of undiagnosed diabetes. Despite the fact that our patients had insurance and recent primary care visits, nearly one‐quarter of individuals had previously unrecognized dysglycemia. This study also revealed systems issues, including the need for improved care transitions and development of a structure for shared responsibility in an ACO system, that need to be addressed if screening initiatives are to be effective in the hospital setting. Future studies will be needed to determine if other opportunistic screening tests have case‐finding potential, and further, how transitions processes can be improved to ensure that knowledge gained in the hospital is conveyed to the ambulatory setting.

Acknowledgements

The authors thank the orthopedic midlevel providers and nurses who assisted with patient recruitment, and the Clinical Trials staff, particularly Lori Wollet, for their assistance throughout the study. All authors disclose no relevant or financial conflicts of interest.

Files
References
  1. Centers for Medicare and Medicaid Services. Accountable Care Organizations: What providers need to know. Available at: https://www.cms.gov/MLNProducts/downloads/ACO_Providers_Factsheet_ICN907406.pdf. Accessed February 20,2012.
  2. Cibulskis C,Giardino A,Moyer V.Care transitions from inpatient to outpatient settings: ongoing challenges and emerging best practices.Hosp Pract (Minneapolis).2001;39:128139.
  3. Ellerbeck E,Totten B,Markello S,Patterson K,Sipe T,Tilden C.Quality improvement in critical access hospitals: addressing immunizations prior to discharge.J Rural Health.2003;19:433438.
  4. IDSA Guidelines. Immunization Programs for Infants, Children, Adolescents, and Adults: Clinical Practice Guidelines by the Infectious Diseases Society of America. Available at: http://www.idsociety.org/uploadedFiles/IDSA/Guidelines‐Patient_Care/PDF_Library/Immunization.pdf. Accessed February 23,2012.
  5. Agency for Healthcare Research and Quality: Pneumococcal Vaccination Prior to Hospital Discharge. Available at: http://www/ahrq.gov/clinic/ptsafety/chap36.htm. Accessed February 23,2012.
  6. Cowie C,Rust K,Ford E, et al.Full accounting of diabetes and pre‐diabetes in the U.S. population in 1988–1994 and 2005–2006.Diabetes Care.2009;32:287294.
  7. Sheehy A,Coursin D,Gabbay R.Back to Wilson and Jungner: 10 good reasons to screen for type 2 diabetes mellitus.Mayo Clin Proc.2009;84:3842.
  8. American Diabetes Association.Standards of medical care in diabetes—2010.Diabetes Care.2010;33:S11S61.
  9. American Diabetes Association.Standards of medical care in diabetes—2012.Diabetes Care.2012;35:s11s63.
  10. National Diabetes Information Clearinghouse NIDDK National Diabetes Statistics 2011. Available at: http://diabetes.niddk.nih.gov/dm/pubs/statistics/index.htm#people. Accessed February 23,2012.
  11. Nathan D,Davidson M,DeFronzo R, et al.Impaired fasting glucose and impaired glucose tolerance: implications for care.Diabetes Care.2007;30:753759.
  12. Walid M,Newman B,Yelverton J,Nutter J,Ajjan M,Robinson J.Prevalence of previously unknown elevation of glycosylated hemoglobin in spine surgery patients and impact on length of stay and total cost.J Hosp Med.2010;5:E10E14.
  13. Dungan K,Braithwaite S,Preiser J.Stress hyperglycemia.Lancet.2009;373:17981807.
  14. Clement S,Braithwaite S,Magee M, et al.Management of diabetes and hyperglycemia in hospitals.Diabetes Care.2004;27:553591.
  15. Sheehy A,Gabbay R.An overview of preoperative glucose evaluation, management, and perioperative impact.J Diabetes Sci Technol.2009;3:12611269.
  16. Grek S,Gravenstein N,Morey T,Rice M.A cost‐effective screening method for preoperative hyperglycemia.Anesth Analg.2009;109:16221624.
  17. Hatzakorian R,Bui H,Carvalho G,Shan WLP,Sidhu S,Schricker T.Fasting blood glucose levels in patients presenting for elective surgery.Nutrition.2011;27:298301.
  18. Abdelmalak B,Abdelmalak J,Knittel J, et al.The prevalence of undiagnosed diabetes in non‐cardiac surgery patients, an observational study.Can J Anesth.2010;57:10581064.
  19. Beaule P,Dorey F,Hoke R,LeDuff M,Amstutz H.The value of patient activity level in the outcome of total hip arthroplasty.J Arthroplasty.2006;21:547552.
  20. Sheehy A,Flood G,Tuan W,Liou J,Coursin D,Smith M.Analysis of guidelines for screening diabetes mellitus in an ambulatory population.Mayo Clin Proc.2010;85:2735.
  21. Centers for Disease Control and Prevention National Center for Health Statistics Inpatient Surgery Statistics, 2007. Available at: http://www.cdc.gov/nchs/fastats/insurg.htm. Accessed February 23,2012.
  22. Centers for Disease Control and Prevention National Health Statistics Reports Ambulatory Surgery Statistics, 2006. Available at: http://www.cdc.gov/nchs/data/nhsr/nhsr011.pdf. Accessed February 23,2012.
  23. Umpierrez G,Hellman R,Korytkowski M, et al.Management of hyperglycemia in hospitalized patients in non‐critical care setting: an Endocrine Society Clinical Practice Guideline.J Clin Endocrinol Metab.2012;97:1638.
  24. Alberti KG,Zimmet PZ.Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation.Diabet Med.1998;15:539553.
  25. National Glycohemoglobin Standardization Program (NGSP). Available at: http://www.ngsp.org. Accessed February 23,2012.
  26. Moghissi E,Korytkowski M,DiNardo M, et al.American Association of Clinical Endocrinologists and American Diabetes Association consensus statement on inpatient glycemic control.Diabetes Care.2009;32:11191131.
  27. Umpierrez G,Isaacs S,Bazargan N,You X,Thaler L,Kitabchi A.Hyperglycemia: an independent marker of in‐hospital mortality in patients with undiagnosed diabetes.J Clin Endocrinol Metab.2002;87:978982.
  28. United States Preventive Services Task Force Diabetes Screening Guideline. Available at: http://www.uspreventiveservicestaskforce.org/uspstf/uspsdiab.htm. Accessed February 22,2012.
  29. University of Wisconsin and UW Health Preventive Care Guidelines. Available at: https://ghcscw.com/media/2011_ph_Preventive_Care_Guidelines_2010.pdf. Accessed February 22,2012.
  30. Wisconsin Diabetes Mellitus Essential Care Guidelines 2011. Available at: http://www.dhs.wisconsin.gov/health/diabetes/PDFs/GL13.pdf. Accessed February 22,2012.
Article PDF
Issue
Journal of Hospital Medicine - 7(8)
Publications
Page Number
611-616
Sections
Files
Files
Article PDF
Article PDF

In the era of Accountable Care Organizations (ACO) and need to improve transitions of care, diagnosis and management of diseases across the continuum from ambulatory to inpatient care remains of paramount importance.1, 2 Opportunities for screening have typically been viewed as the responsibility of the ambulatory primary care provider (PCP), yet in an ACO model, patients who present more frequently to a hospital as opposed to a clinic are still the responsibility of the ACO, and therefore opportunistic screening for certain diseases by hospitalists and other inpatient providers is a possibility that may merit further investigation. This opportunistic rationale has already been used to advocate for pneumococcal and influenza vaccination prior to discharge in hospitalized patients, but has not been well investigated in chronic disease screening.35

Diabetes mellitus is a disease that has reached epidemic proportions. National Health and Nutrition Examination Survey (NHANES) data documented the ambulatory prevalence of diabetes mellitus (DM) in adults 20 years of age in the United States to be 12.9%.6 However, the most significant health crisis may be that 40% of these adult patients with diabetes are unaware of their diagnosis.6 In other words, 5.1% of all adults 20 years of age or older in this country have undiagnosed diabetes.6, 7 As diabetes is a disease where clinical manifestations are often preceded by a prolonged asymptomatic period, screening with either of the preferred diagnostic tests, fasting blood glucose (FBG) or hemoglobin A1C (Hgb A1C), is required to make a new diagnosis.79

Diagnosis of hyperglycemia is important so that appropriate glycemic control can be achieved, and preventive care and risk factor modification can be initiated, including screening and treatment of hypertension, hyperlipidemia, retinopathy, nephropathy, and other comorbid conditions.7, 9 As glycemic control cannot be achieved in patients who remain undiagnosed, screening may play a role in preventing long‐term complications of diabetes.7 Awareness of the prediabetic states impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) is also important because lifestyle modification may delay or prevent the progression to diabetes and its associated complications, such as cardiovascular disease, retinopathy, and nephropathy.10, 11 In the inpatient setting, undiagnosed elevation of Hgb A1C in the diabetes or prediabetes range has been shown to increase cost and length of stay in some spine surgery patients compared to patients with known diabetes.12

Virtually every inpatient has at least 1 glucose value drawn during hospitalization as part of a chemistry panel, many of which are fasting, or NPO (nil per os, meaning nothing by mouth), by virtue of clinical condition or anticipated procedure. Provided the preoperative state in an elective surgery patient is not taxing enough to induce stress hyperglycemia,1315 this typically fasting time may provide an easy and excellent diabetes screening opportunity to not only risk stratify for the inpatient stay, but to diagnose diabetes that will initiate lifelong care and prevention, provided information learned during hospitalization is conveyed to the PCP at discharge. While prior studies1618 have measured preoperative glucose as a means to risk stratify and predict undiagnosed diabetes, none of these analyses have obtained a second glycemic test (either FBG or Hgb A1C) as required by the American Diabetes Association (ADA) to make a diagnosis of diabetes. Lack of a confirmatory glycemic test in the existing literature also leaves uncertainty in reproducibility and validity of the preoperative glucose as a risk‐stratification tool, as it is not certain that it is truly unstressed. Finally, studies to date have not evaluated or controlled for factors that could contribute to undiagnosed diabetes, such as health insurance and access to primary care.

To investigate the prevalence of undiagnosed diabetes and prediabetes in a hospitalized population, and to pilot the concept of screening in the inpatient preoperative setting, we performed a prospective analysis of adult orthopedic patients presenting for elective hip, knee, and spine surgery at a large Midwestern academic medical center from December 1, 2007 to November 30, 2008. Our primary objective was to determine the feasibility of preoperative testing in finding the prevalence of undiagnosed diabetes and prediabetes in an insured, inpatient population with access to prior preventive care. In addition, we investigated systems issues related to the general concept of inpatient screening, including assessment of whether providers recognized hyperglycemic patients in the hospital once tested, or conveyed test information to PCPs at discharge.

METHODS

The University of Wisconsin Institutional Review Board approved this prospective observational cohort study. All patients aged 18 years scheduled for elective total knee or hip arthroplasty, or elective lumbar decompression and/or fusion, presenting for preoperative appointment from December 1, 2007 to November 30, 2008, were invited to participate. Pregnant patients, and patients unable to give consent were excluded. Patients with hemolytic processes or on new regimens of oral or intravenous steroids within 7 days of surgery were also excluded. Patients on chronic oral, inhaled, intranasal, or topical steroids were included.

Preoperative Clinic Visit (Visit 1)

Patients who consented to participate had basic measures recorded, including height, weight, age, ethnicity, sex, date of surgery, and type of surgery. Patients then completed a questionnaire regarding previous history of diabetes and prediabetes (IFG or IGT), and personal history of other ADA‐designated risk factors9 to prompt diabetes screening, including gestational diabetes, hypertension, hyperlipidemia, vascular disease, and physical inactivity, as measured by the University of California, Los Angeles (UCLA) score.19 Patient self‐reported diagnosis of DM or prediabetes was compared to anesthesia preoperative assessment for confirmation. Finally, insurance status and most recent visit to a PCP were recorded (Figure 1).

Figure 1
Study protocol for Visits 1, 2, 3. Abbreviations: FBG, fasting blood glucose; Hgb A1C, hemoglobin A1C; PCP, primary care provider.

Preoperative Day of Surgery (Visit 2)

On the morning of surgery, the study coordinator met with patients in the preoperative unit to confirm fasting status (nothing to eat for 8 or more hours), no new intravenous or oral steroids, and that intravenous fluids were dextrose free. Fasting blood glucose was collected as whole blood and centrifuged in the central laboratory, after which plasma glucose was measured using the hexokinase method (Siemens Dimension Vista 3000T, Siemens Healthcare Diagnostics, Inc, Newark, DE). Hemoglobin A1C (Tosoh G7 HPLC, Tosoh Bioscience, Tokyo, Japan) was also obtained. Patients with preoperative FBG 100 mg/dL were notified and scheduled to return for another FBG measurement at their 68 week orthopedic ambulatory clinic follow‐up visit.

Postoperative Clinic Visit (Visit 3)

At 68 week follow‐up, patients with preoperative FBG 100 mg/dL had an additional FBG performed. Those who also had a follow‐up FBG 100 mg/dL at Visit 3 were determined to have DM or IFG, identified as New Diabetes/Prediabetes. Patients with glucose 100 mg/dL prior to surgery that was <100 mg/dL in follow‐up, as well as patients with blood glucose <100 mg/dL at preoperative Visit 2 (and therefore did not require a follow‐up glucose measurement) were designated Normoglycemia. Patients with preexisting DM or IFG were labeled Known Diabetes/Prediabetes.

Statistical Methods

Categorical variables were summarized using percents. Continuous variables were summarized using means and standard deviations. Chi‐square tests were conducted for categorical variables and Student t tests were used for continuous variables to compare differences between patients with newly diagnosed IFG or DM (New Diabetes/Prediabetes) and patients without diabetes (Normoglycemia), and to compare differences between patients with New Diabetes/Prediabetes and patients with known DM or IFG (Known Diabetes/Prediabetes). Sample size was determined by number of adult elective spine and total joint orthopedic patients presenting to clinic during the prespecified 1‐year period of time. All tests were considered significant if P value < 0.05.

RESULTS

A total of 302 patients met inclusion criteria and enrolled in the study. Of these patients, 27 (8.9%) were not included in final analysis due to incomplete preoperative labs (7 patients, 2.3%), lack of follow‐up (11 patients, 3.6%), withdrawal of consent (5 patients, 1.7%), or not having surgery (4 patients, 1.3%). Of the remaining 275, 54% were female. The mean patient age was 60.3 years, and 88% (243/275) of patients had a body mass index (BMI) 25 kg/m2, indicating overweight or obese. All of the patients (100%) had healthcare insurance; 97% reported having a primary care provider, with 96.6% of patients stating that they had seen a primary provider within the year prior to surgery (Table 1).

Baseline Characteristics (N = 275)
 No. (%)
  • Abbreviations: BMI, body mass index; DM, diabetes mellitus; IFG, impaired fasting glucose; IGT, impaired glucose tolerance; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles.

  • One patient omitted answer.

  • Four patients omitted answer.

Demographics 
Female148 (54)
Age, mean (SD)60.3 (11.3)
BMI, mean (SD)31.16 (5.93)
Surgery type 
Hip99 (36)
Knee147 (53)
Spine29 (11)
Socioeconomic status/healthcare access 
Have healthcare insurance*274 (100)
Have regular PCP267 (97)
Last PCP visit 
Never2 (0.7)
>3 y1 (0.4)
13 y6 (2.2)
6 mo1 y18 (6.6)
<6 mo244 (90)
Medical history 
Diabetes history 
No history of dysglycemia225 (82)
Prior IFG17 (6)
Prior DM33 (12)
American Diabetes Association risk factors 
BMI 25243 (88)
Physical inactivity (UCLA score 3)40 (18)
High risk ethnicity3 (1)
Gestational DM2 (1)
First degree family history91 (33)
Cardiac disease35 (13)
Hypertension127 (46)
Hypercholesterolemia114 (42)
Prior IFG/IGT19 (7)
Age 45 y249 (91)

Of the 275 patients, 50 (18%) had Known Diabetes/Prediabetes, 67 (24%) were given a new diagnosis of DM or IFG (New Diabetes/Prediabetes), and the remaining 158 (58%) were classified as Normoglycemia (Table 2). The sum of Known Diabetes/Prediabetes (50) and New Diabetes/Prediabetes (67) equaled the true inpatient prevalence of DM and IFG (117/275, 43%). Of the Known Diabetes/Prediabetes patients, 33/50 (66%) had DM and 17/50 (34%) had IFG. Of those with New Diabetes/Prediabetes, 8/67 (12%) had DM range values, with the remaining 59/67 (88%) in IFG range.

Diagnosis by Glucose Value (N = 275)
DiagnosisNo. (%)Hemoglobin A1C (Mean, SD)Preoperative Glucose (Mean, SD)Follow‐up Glucose (Mean, SD)Days Between (Mean, SD)
  • NOTE: Patients with known history of diabetes or impaired fasting glucose, or normal preoperative glucose did not have follow‐up glucose testing. Abbreviations: SD, standard deviation.

  • Preoperative glucose 100, follow‐up ambulatory value also 100.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Normoglycemia.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Preop glucose 100, follow‐up <100.

  • Days Between represents days elapsed between preoperative and follow‐up glucose draws.

Known diabetes/prediabetes50 (18)6.53 (0.99)129.02 (33.85)  
New diabetes/prediabetes*67 (24)5.80 (0.39)110.79 (8.69)107.91 (7.47)51.67 (13.73)
Normoglycemia158 (58)5.45 (0.36)96.04 (9.10)  
Preop glucose 100, follow‐up <10038 (14)5.54 (0.35)107.26 (8.69)93.68 (5.16)49.21 (12.11)
Preop glucose <100120 (44)5.42 (0.36)92.49 (5.73)  

Patients with New Diabetes/Prediabetes had a higher preoperative Visit 2 glucose (mean [standard deviation], 110.79 [8.69] and 96.04 [9.10], P < 0.0001) and Hgb A1C (5.80 [0.39] and 5.45 [0.36], P < 0.0001) compared to Normoglycemia. A subset of the Normoglycemia patients (38/158, 24%), had an elevated preoperative Visit 2 glucose, but a normal (<100 mg/dL) second confirmatory Visit 3 glucose, and therefore did not have New Diabetes/Prediabetes. New Diabetes/Prediabetes was also significantly different from this particular Normoglycemia subset in both FBG (110.79 [8.69] and 107.26 [8.69], P = 0.048) and Hgb A1C (5.80 [0.39] and 5.54 [0.35], P = 0.001) (Table 2). Preoperative Visit 2 FBG of 100 mg/dL predicted Visit 3 FBG 100 mg/dL 64% of the time. Having both preoperative Visit 2 FBG 100 mg/dL and Hgb A1C 5.7 (the ADA‐determined level for prediabetes),3 predicted Visit 3 FBG 100 mg/dL 72% of the time.

Patients with New Diabetes/Prediabetes were slightly older than Normoglycemia patients (62.37 [9.70] vs 58.08 [12.01], P = 0.0054), meeting the ADA diabetes screening age of 45 significantly more often than Normoglycemia patients (100% [67] vs 84% [132], P < 0.001). The groups otherwise did not differ in the incidence of other ADA‐defined risk factors9 (Table 3). Patients with New Diabetes/Prediabetes were less likely to report having seen their PCP within 6 months prior to surgery compared to their Normoglycemia counterparts (82% [54] vs 91% [141], P = 0.046), although this difference disappeared by 1 year (94% vs 96%). Finally, there was no increase in the number of point‐of‐care (POC) glucose tests ordered, or mention of hyperglycemia on discharge summaries in the New Diabetes/Prediabetes group (Table 3).

Patient Characteristics by Diagnosis
DemographicsNormoglycemia (N = 158)New Diabetes/ Prediabetes (N = 67)Known Diabetes/ Prediabetes (N = 50)
  • NOTE: All values are No. (%) unless otherwise specified. Abbreviations: BMI, body mass index; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles. *P < 0.05 for Normoglycemia vs New Diabetes/Prediabetes. P < 0.05 for New Diabetes/Prediabetes vs Known Diabetes/Prediabetes.

Female90 (57)33 (49)25 (50)
Age, mean (SD)58.08 (12.01)*62.37 (9.70)64.60 (9.02)
BMI, mean (SD)30.13 (5.76)31.65 (5.76)33.74 (5.92)
Surgery type   
Hip62 (39)21 (31)16 (32)
Knee76 (48)41 (61)30 (60)
Spine20 (13)5 (7)4 (8)
Socioeconomic status/healthcare access
Have healthcare insurance158 (100)66 (100)50 (100)
Have regular PCP153 (97)65 (98)49 (98)
Last PCP Visit   
Never2 (1)0 (0)0 (0)
>3 y1 (1)0 (0)0 (0)
13 y1 (1)4 (6)1 (2)
6 mo1 y10 (6)8 (12)0 (0)
In last 6 mo141 (91)*54 (82)49 (98)
Medical history   
American Diabetes Association risk factors
BMI 25133 (84)62 (93)48 (96)
Physical inactivity (UCLA score 3)16 (13)10 (18)14 (35)
High‐risk ethnicity2 (1)1 (1)1 (2)
Gestational diabetes1 (1)1 (1)0 (0)
First degree family history45 (28)19 (28)27 (55)
Cardiac disease14 (9)7 (10)14 (28)
Hypertension62 (39)31 (46)34 (68)
Hyperlipidemia54 (34)28 (42)32 (64)
Age 45132 (84)*67 (100)50 (100)
Follow‐up
Point‐of‐care glucose ordered1 (1)0 (0)31 (62)
Dysglycemia mentioned on discharge summary0 (0)0 (0)28 (56)

DISCUSSION AND CONCLUSION

The main finding of this study is that in an insured, elective orthopedic population with access to primary care, 24% of patients had unrecognized IFG or DM on the basis of 2 fasting blood glucose values. Remarkably, this statistic likely represents a best‐case scenario, as the percent of undiagnosed patients is likely higher in uninsured patients,20 those without primary care visits, and those hospitalized for emergent or urgent reasons who, by definition, did not have an ambulatory preoperative evaluation, and who may also have greater severity of illness at baseline. With over 1,053,000 total knee and hip operations done in the United States each year, opportunistic screening of this population alone could identify 252,720 patients with prediabetes or diabetes who might otherwise remain undiagnosed.21 Even more significant, with at least 70 million patients undergoing ambulatory or inpatient procedures each year, if even a quarter of these procedures were elective adult lower acuity surgeries allowing for easy preoperative testing, over 4 million cases of DM and IFG could be found each year using this process.21, 22 These numbers demonstrate the need to investigate new and novel screening opportunities, such as in hospitalized patients. These statistics also demonstrate the need for all inpatient providers to be aware of undiagnosed diabetes and prediabetes in their patients, and confirm recommendations of the Endocrine Society to obtain a blood glucose for all patients on admission, and measure Hgb A1C in all hyperglycemic or diabetic inpatients if not performed in the preceding 23 months.23

Diagnosis of DM has historically been difficult to make in the hospital setting. The primary diagnostic test, FBG, may be elevated in the setting of counter‐regulatory hormone surge and inflammatory stress response, and its use has been discouraged in the acute care setting.14, 15, 24 While not affected by stress, Hgb A1C, endorsed in 2010 by the ADA for diagnosis of DM,8 may still be unreliable in the setting of blood loss, transfusion, hemolysis, and other factors common during surgery and hospitalization.9, 25 However, we found that 64% of patients with elevated (100 mg/dL) blood glucose at the time of pre‐anesthesia evaluation did have persistently elevated blood glucose at 68 week follow‐up. This suggests that the preoperative glucose is unstressed, and may be a rapid, reasonably reliable indicator of patients needing ambulatory follow‐up to confirm DM or prediabetes. This may also provide perioperative risk stratification if glycemic history is unknown. As many fasting, preoperative patients have routine chemistry panels ordered already, the simple glucose included in such panels may prove to be the most useful diabetes test for anesthesiologists, surgeons, hospitalists, and other inpatient providers. Our data suggests that Hgb A1C 5.7, the ADA‐suggested IFG/prediabetes cut point,9 can also be used in combination with FBG 100 to predict persistent hyperglycemia.

This study also revealed several significant systems issues that merit attention if opportunistic inpatient screening or preventive care is to be successful in a shared responsibility ACO system. Most importantly, none of our patients with elevated preoperative blood glucose had these results conveyed to their primary care provider at discharge, revealing both a need for improved transitions in care and development of formal ACO structure if inpatient or preoperative screening is to be successful. Second, our study also showed that providers did not change plan of care for patients without known DM or IFG and preoperative elevated glucose. None of these patients had point‐of‐care glucose checks ordered while in the hospital, demonstrating that previously undiagnosed dysglycemic patients receive different in‐hospital care compared to patients with known DM. While it is possible that providers consciously decided not to monitor patients with mild hyperglycemia, consistent with inpatient guidelines recommending glycemic targets of <180 mg/dL for general care patients,20 it is more likely that there was lack of recognition of hyperglycemia in these patients without prior DM or IFG, as has been demonstrated previously.26 Inpatient providers should be informed of, and encouraged to, follow Endocrine Society recommendations to monitor POC glucose in patients with hyperglycemia (>140 mg/dL) for at least 2448 hours.23

It is important to state that controversy exists regarding which patients should be screened for diabetes. The United States Preventive Services Task Force (USPSTF) recommends screening adult patients only if they have hypertension.27 The ADA recommends screening all patients 45 years of age and older, and younger, overweight patients with at least 1 additional risk factor.9 We have previously shown that using USPSTF guidelines misses 33.1% of cases of DM compared to the ADA standard.28 As such, our institution and the Wisconsin State Diabetes Screening Guidelines mirror the ADA guidelines.29, 30 In the present study, 91% were aged 45 and older, and 88% were overweight, so nearly everyone in our study met our state and institution guidelines for diabetes screening. However, this might not be the case at all institutions if USPSTF guidelines were instead followed.

A limitation of the present study was that a selection bias of subjects could have occurred by both patients and providers, as less healthy patients with higher surgical risk may not have been candidates for surgery as often as lower‐risk patients. While entirely appropriate to maximize safety for elective surgery patients, this may in part explain the lower Hgb A1C (6.53 [0.14]) in our Known Diabetes/Prediabetes group, and lower range of blood glucose values in our New Diabetes/Prediabetes patients, with the majority being in the prediabetes range. However, this limitation also allows for the conclusion that any patient, regardless of perceived good health and primary care visits, may still have undiagnosed DM or IFG.

In summary, this study strongly supports the practice of screening obligate fasting patients to reduce the prevalence of undiagnosed diabetes. Despite the fact that our patients had insurance and recent primary care visits, nearly one‐quarter of individuals had previously unrecognized dysglycemia. This study also revealed systems issues, including the need for improved care transitions and development of a structure for shared responsibility in an ACO system, that need to be addressed if screening initiatives are to be effective in the hospital setting. Future studies will be needed to determine if other opportunistic screening tests have case‐finding potential, and further, how transitions processes can be improved to ensure that knowledge gained in the hospital is conveyed to the ambulatory setting.

Acknowledgements

The authors thank the orthopedic midlevel providers and nurses who assisted with patient recruitment, and the Clinical Trials staff, particularly Lori Wollet, for their assistance throughout the study. All authors disclose no relevant or financial conflicts of interest.

In the era of Accountable Care Organizations (ACO) and need to improve transitions of care, diagnosis and management of diseases across the continuum from ambulatory to inpatient care remains of paramount importance.1, 2 Opportunities for screening have typically been viewed as the responsibility of the ambulatory primary care provider (PCP), yet in an ACO model, patients who present more frequently to a hospital as opposed to a clinic are still the responsibility of the ACO, and therefore opportunistic screening for certain diseases by hospitalists and other inpatient providers is a possibility that may merit further investigation. This opportunistic rationale has already been used to advocate for pneumococcal and influenza vaccination prior to discharge in hospitalized patients, but has not been well investigated in chronic disease screening.35

Diabetes mellitus is a disease that has reached epidemic proportions. National Health and Nutrition Examination Survey (NHANES) data documented the ambulatory prevalence of diabetes mellitus (DM) in adults 20 years of age in the United States to be 12.9%.6 However, the most significant health crisis may be that 40% of these adult patients with diabetes are unaware of their diagnosis.6 In other words, 5.1% of all adults 20 years of age or older in this country have undiagnosed diabetes.6, 7 As diabetes is a disease where clinical manifestations are often preceded by a prolonged asymptomatic period, screening with either of the preferred diagnostic tests, fasting blood glucose (FBG) or hemoglobin A1C (Hgb A1C), is required to make a new diagnosis.79

Diagnosis of hyperglycemia is important so that appropriate glycemic control can be achieved, and preventive care and risk factor modification can be initiated, including screening and treatment of hypertension, hyperlipidemia, retinopathy, nephropathy, and other comorbid conditions.7, 9 As glycemic control cannot be achieved in patients who remain undiagnosed, screening may play a role in preventing long‐term complications of diabetes.7 Awareness of the prediabetic states impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) is also important because lifestyle modification may delay or prevent the progression to diabetes and its associated complications, such as cardiovascular disease, retinopathy, and nephropathy.10, 11 In the inpatient setting, undiagnosed elevation of Hgb A1C in the diabetes or prediabetes range has been shown to increase cost and length of stay in some spine surgery patients compared to patients with known diabetes.12

Virtually every inpatient has at least 1 glucose value drawn during hospitalization as part of a chemistry panel, many of which are fasting, or NPO (nil per os, meaning nothing by mouth), by virtue of clinical condition or anticipated procedure. Provided the preoperative state in an elective surgery patient is not taxing enough to induce stress hyperglycemia,1315 this typically fasting time may provide an easy and excellent diabetes screening opportunity to not only risk stratify for the inpatient stay, but to diagnose diabetes that will initiate lifelong care and prevention, provided information learned during hospitalization is conveyed to the PCP at discharge. While prior studies1618 have measured preoperative glucose as a means to risk stratify and predict undiagnosed diabetes, none of these analyses have obtained a second glycemic test (either FBG or Hgb A1C) as required by the American Diabetes Association (ADA) to make a diagnosis of diabetes. Lack of a confirmatory glycemic test in the existing literature also leaves uncertainty in reproducibility and validity of the preoperative glucose as a risk‐stratification tool, as it is not certain that it is truly unstressed. Finally, studies to date have not evaluated or controlled for factors that could contribute to undiagnosed diabetes, such as health insurance and access to primary care.

To investigate the prevalence of undiagnosed diabetes and prediabetes in a hospitalized population, and to pilot the concept of screening in the inpatient preoperative setting, we performed a prospective analysis of adult orthopedic patients presenting for elective hip, knee, and spine surgery at a large Midwestern academic medical center from December 1, 2007 to November 30, 2008. Our primary objective was to determine the feasibility of preoperative testing in finding the prevalence of undiagnosed diabetes and prediabetes in an insured, inpatient population with access to prior preventive care. In addition, we investigated systems issues related to the general concept of inpatient screening, including assessment of whether providers recognized hyperglycemic patients in the hospital once tested, or conveyed test information to PCPs at discharge.

METHODS

The University of Wisconsin Institutional Review Board approved this prospective observational cohort study. All patients aged 18 years scheduled for elective total knee or hip arthroplasty, or elective lumbar decompression and/or fusion, presenting for preoperative appointment from December 1, 2007 to November 30, 2008, were invited to participate. Pregnant patients, and patients unable to give consent were excluded. Patients with hemolytic processes or on new regimens of oral or intravenous steroids within 7 days of surgery were also excluded. Patients on chronic oral, inhaled, intranasal, or topical steroids were included.

Preoperative Clinic Visit (Visit 1)

Patients who consented to participate had basic measures recorded, including height, weight, age, ethnicity, sex, date of surgery, and type of surgery. Patients then completed a questionnaire regarding previous history of diabetes and prediabetes (IFG or IGT), and personal history of other ADA‐designated risk factors9 to prompt diabetes screening, including gestational diabetes, hypertension, hyperlipidemia, vascular disease, and physical inactivity, as measured by the University of California, Los Angeles (UCLA) score.19 Patient self‐reported diagnosis of DM or prediabetes was compared to anesthesia preoperative assessment for confirmation. Finally, insurance status and most recent visit to a PCP were recorded (Figure 1).

Figure 1
Study protocol for Visits 1, 2, 3. Abbreviations: FBG, fasting blood glucose; Hgb A1C, hemoglobin A1C; PCP, primary care provider.

Preoperative Day of Surgery (Visit 2)

On the morning of surgery, the study coordinator met with patients in the preoperative unit to confirm fasting status (nothing to eat for 8 or more hours), no new intravenous or oral steroids, and that intravenous fluids were dextrose free. Fasting blood glucose was collected as whole blood and centrifuged in the central laboratory, after which plasma glucose was measured using the hexokinase method (Siemens Dimension Vista 3000T, Siemens Healthcare Diagnostics, Inc, Newark, DE). Hemoglobin A1C (Tosoh G7 HPLC, Tosoh Bioscience, Tokyo, Japan) was also obtained. Patients with preoperative FBG 100 mg/dL were notified and scheduled to return for another FBG measurement at their 68 week orthopedic ambulatory clinic follow‐up visit.

Postoperative Clinic Visit (Visit 3)

At 68 week follow‐up, patients with preoperative FBG 100 mg/dL had an additional FBG performed. Those who also had a follow‐up FBG 100 mg/dL at Visit 3 were determined to have DM or IFG, identified as New Diabetes/Prediabetes. Patients with glucose 100 mg/dL prior to surgery that was <100 mg/dL in follow‐up, as well as patients with blood glucose <100 mg/dL at preoperative Visit 2 (and therefore did not require a follow‐up glucose measurement) were designated Normoglycemia. Patients with preexisting DM or IFG were labeled Known Diabetes/Prediabetes.

Statistical Methods

Categorical variables were summarized using percents. Continuous variables were summarized using means and standard deviations. Chi‐square tests were conducted for categorical variables and Student t tests were used for continuous variables to compare differences between patients with newly diagnosed IFG or DM (New Diabetes/Prediabetes) and patients without diabetes (Normoglycemia), and to compare differences between patients with New Diabetes/Prediabetes and patients with known DM or IFG (Known Diabetes/Prediabetes). Sample size was determined by number of adult elective spine and total joint orthopedic patients presenting to clinic during the prespecified 1‐year period of time. All tests were considered significant if P value < 0.05.

RESULTS

A total of 302 patients met inclusion criteria and enrolled in the study. Of these patients, 27 (8.9%) were not included in final analysis due to incomplete preoperative labs (7 patients, 2.3%), lack of follow‐up (11 patients, 3.6%), withdrawal of consent (5 patients, 1.7%), or not having surgery (4 patients, 1.3%). Of the remaining 275, 54% were female. The mean patient age was 60.3 years, and 88% (243/275) of patients had a body mass index (BMI) 25 kg/m2, indicating overweight or obese. All of the patients (100%) had healthcare insurance; 97% reported having a primary care provider, with 96.6% of patients stating that they had seen a primary provider within the year prior to surgery (Table 1).

Baseline Characteristics (N = 275)
 No. (%)
  • Abbreviations: BMI, body mass index; DM, diabetes mellitus; IFG, impaired fasting glucose; IGT, impaired glucose tolerance; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles.

  • One patient omitted answer.

  • Four patients omitted answer.

Demographics 
Female148 (54)
Age, mean (SD)60.3 (11.3)
BMI, mean (SD)31.16 (5.93)
Surgery type 
Hip99 (36)
Knee147 (53)
Spine29 (11)
Socioeconomic status/healthcare access 
Have healthcare insurance*274 (100)
Have regular PCP267 (97)
Last PCP visit 
Never2 (0.7)
>3 y1 (0.4)
13 y6 (2.2)
6 mo1 y18 (6.6)
<6 mo244 (90)
Medical history 
Diabetes history 
No history of dysglycemia225 (82)
Prior IFG17 (6)
Prior DM33 (12)
American Diabetes Association risk factors 
BMI 25243 (88)
Physical inactivity (UCLA score 3)40 (18)
High risk ethnicity3 (1)
Gestational DM2 (1)
First degree family history91 (33)
Cardiac disease35 (13)
Hypertension127 (46)
Hypercholesterolemia114 (42)
Prior IFG/IGT19 (7)
Age 45 y249 (91)

Of the 275 patients, 50 (18%) had Known Diabetes/Prediabetes, 67 (24%) were given a new diagnosis of DM or IFG (New Diabetes/Prediabetes), and the remaining 158 (58%) were classified as Normoglycemia (Table 2). The sum of Known Diabetes/Prediabetes (50) and New Diabetes/Prediabetes (67) equaled the true inpatient prevalence of DM and IFG (117/275, 43%). Of the Known Diabetes/Prediabetes patients, 33/50 (66%) had DM and 17/50 (34%) had IFG. Of those with New Diabetes/Prediabetes, 8/67 (12%) had DM range values, with the remaining 59/67 (88%) in IFG range.

Diagnosis by Glucose Value (N = 275)
DiagnosisNo. (%)Hemoglobin A1C (Mean, SD)Preoperative Glucose (Mean, SD)Follow‐up Glucose (Mean, SD)Days Between (Mean, SD)
  • NOTE: Patients with known history of diabetes or impaired fasting glucose, or normal preoperative glucose did not have follow‐up glucose testing. Abbreviations: SD, standard deviation.

  • Preoperative glucose 100, follow‐up ambulatory value also 100.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Normoglycemia.

  • P values significant at <0.05 when New diabetes/prediabetes is compared to Preop glucose 100, follow‐up <100.

  • Days Between represents days elapsed between preoperative and follow‐up glucose draws.

Known diabetes/prediabetes50 (18)6.53 (0.99)129.02 (33.85)  
New diabetes/prediabetes*67 (24)5.80 (0.39)110.79 (8.69)107.91 (7.47)51.67 (13.73)
Normoglycemia158 (58)5.45 (0.36)96.04 (9.10)  
Preop glucose 100, follow‐up <10038 (14)5.54 (0.35)107.26 (8.69)93.68 (5.16)49.21 (12.11)
Preop glucose <100120 (44)5.42 (0.36)92.49 (5.73)  

Patients with New Diabetes/Prediabetes had a higher preoperative Visit 2 glucose (mean [standard deviation], 110.79 [8.69] and 96.04 [9.10], P < 0.0001) and Hgb A1C (5.80 [0.39] and 5.45 [0.36], P < 0.0001) compared to Normoglycemia. A subset of the Normoglycemia patients (38/158, 24%), had an elevated preoperative Visit 2 glucose, but a normal (<100 mg/dL) second confirmatory Visit 3 glucose, and therefore did not have New Diabetes/Prediabetes. New Diabetes/Prediabetes was also significantly different from this particular Normoglycemia subset in both FBG (110.79 [8.69] and 107.26 [8.69], P = 0.048) and Hgb A1C (5.80 [0.39] and 5.54 [0.35], P = 0.001) (Table 2). Preoperative Visit 2 FBG of 100 mg/dL predicted Visit 3 FBG 100 mg/dL 64% of the time. Having both preoperative Visit 2 FBG 100 mg/dL and Hgb A1C 5.7 (the ADA‐determined level for prediabetes),3 predicted Visit 3 FBG 100 mg/dL 72% of the time.

Patients with New Diabetes/Prediabetes were slightly older than Normoglycemia patients (62.37 [9.70] vs 58.08 [12.01], P = 0.0054), meeting the ADA diabetes screening age of 45 significantly more often than Normoglycemia patients (100% [67] vs 84% [132], P < 0.001). The groups otherwise did not differ in the incidence of other ADA‐defined risk factors9 (Table 3). Patients with New Diabetes/Prediabetes were less likely to report having seen their PCP within 6 months prior to surgery compared to their Normoglycemia counterparts (82% [54] vs 91% [141], P = 0.046), although this difference disappeared by 1 year (94% vs 96%). Finally, there was no increase in the number of point‐of‐care (POC) glucose tests ordered, or mention of hyperglycemia on discharge summaries in the New Diabetes/Prediabetes group (Table 3).

Patient Characteristics by Diagnosis
DemographicsNormoglycemia (N = 158)New Diabetes/ Prediabetes (N = 67)Known Diabetes/ Prediabetes (N = 50)
  • NOTE: All values are No. (%) unless otherwise specified. Abbreviations: BMI, body mass index; PCP, primary care provider; SD, standard deviation; UCLA score, activity score of the University of California, Los Angeles. *P < 0.05 for Normoglycemia vs New Diabetes/Prediabetes. P < 0.05 for New Diabetes/Prediabetes vs Known Diabetes/Prediabetes.

Female90 (57)33 (49)25 (50)
Age, mean (SD)58.08 (12.01)*62.37 (9.70)64.60 (9.02)
BMI, mean (SD)30.13 (5.76)31.65 (5.76)33.74 (5.92)
Surgery type   
Hip62 (39)21 (31)16 (32)
Knee76 (48)41 (61)30 (60)
Spine20 (13)5 (7)4 (8)
Socioeconomic status/healthcare access
Have healthcare insurance158 (100)66 (100)50 (100)
Have regular PCP153 (97)65 (98)49 (98)
Last PCP Visit   
Never2 (1)0 (0)0 (0)
>3 y1 (1)0 (0)0 (0)
13 y1 (1)4 (6)1 (2)
6 mo1 y10 (6)8 (12)0 (0)
In last 6 mo141 (91)*54 (82)49 (98)
Medical history   
American Diabetes Association risk factors
BMI 25133 (84)62 (93)48 (96)
Physical inactivity (UCLA score 3)16 (13)10 (18)14 (35)
High‐risk ethnicity2 (1)1 (1)1 (2)
Gestational diabetes1 (1)1 (1)0 (0)
First degree family history45 (28)19 (28)27 (55)
Cardiac disease14 (9)7 (10)14 (28)
Hypertension62 (39)31 (46)34 (68)
Hyperlipidemia54 (34)28 (42)32 (64)
Age 45132 (84)*67 (100)50 (100)
Follow‐up
Point‐of‐care glucose ordered1 (1)0 (0)31 (62)
Dysglycemia mentioned on discharge summary0 (0)0 (0)28 (56)

DISCUSSION AND CONCLUSION

The main finding of this study is that in an insured, elective orthopedic population with access to primary care, 24% of patients had unrecognized IFG or DM on the basis of 2 fasting blood glucose values. Remarkably, this statistic likely represents a best‐case scenario, as the percent of undiagnosed patients is likely higher in uninsured patients,20 those without primary care visits, and those hospitalized for emergent or urgent reasons who, by definition, did not have an ambulatory preoperative evaluation, and who may also have greater severity of illness at baseline. With over 1,053,000 total knee and hip operations done in the United States each year, opportunistic screening of this population alone could identify 252,720 patients with prediabetes or diabetes who might otherwise remain undiagnosed.21 Even more significant, with at least 70 million patients undergoing ambulatory or inpatient procedures each year, if even a quarter of these procedures were elective adult lower acuity surgeries allowing for easy preoperative testing, over 4 million cases of DM and IFG could be found each year using this process.21, 22 These numbers demonstrate the need to investigate new and novel screening opportunities, such as in hospitalized patients. These statistics also demonstrate the need for all inpatient providers to be aware of undiagnosed diabetes and prediabetes in their patients, and confirm recommendations of the Endocrine Society to obtain a blood glucose for all patients on admission, and measure Hgb A1C in all hyperglycemic or diabetic inpatients if not performed in the preceding 23 months.23

Diagnosis of DM has historically been difficult to make in the hospital setting. The primary diagnostic test, FBG, may be elevated in the setting of counter‐regulatory hormone surge and inflammatory stress response, and its use has been discouraged in the acute care setting.14, 15, 24 While not affected by stress, Hgb A1C, endorsed in 2010 by the ADA for diagnosis of DM,8 may still be unreliable in the setting of blood loss, transfusion, hemolysis, and other factors common during surgery and hospitalization.9, 25 However, we found that 64% of patients with elevated (100 mg/dL) blood glucose at the time of pre‐anesthesia evaluation did have persistently elevated blood glucose at 68 week follow‐up. This suggests that the preoperative glucose is unstressed, and may be a rapid, reasonably reliable indicator of patients needing ambulatory follow‐up to confirm DM or prediabetes. This may also provide perioperative risk stratification if glycemic history is unknown. As many fasting, preoperative patients have routine chemistry panels ordered already, the simple glucose included in such panels may prove to be the most useful diabetes test for anesthesiologists, surgeons, hospitalists, and other inpatient providers. Our data suggests that Hgb A1C 5.7, the ADA‐suggested IFG/prediabetes cut point,9 can also be used in combination with FBG 100 to predict persistent hyperglycemia.

This study also revealed several significant systems issues that merit attention if opportunistic inpatient screening or preventive care is to be successful in a shared responsibility ACO system. Most importantly, none of our patients with elevated preoperative blood glucose had these results conveyed to their primary care provider at discharge, revealing both a need for improved transitions in care and development of formal ACO structure if inpatient or preoperative screening is to be successful. Second, our study also showed that providers did not change plan of care for patients without known DM or IFG and preoperative elevated glucose. None of these patients had point‐of‐care glucose checks ordered while in the hospital, demonstrating that previously undiagnosed dysglycemic patients receive different in‐hospital care compared to patients with known DM. While it is possible that providers consciously decided not to monitor patients with mild hyperglycemia, consistent with inpatient guidelines recommending glycemic targets of <180 mg/dL for general care patients,20 it is more likely that there was lack of recognition of hyperglycemia in these patients without prior DM or IFG, as has been demonstrated previously.26 Inpatient providers should be informed of, and encouraged to, follow Endocrine Society recommendations to monitor POC glucose in patients with hyperglycemia (>140 mg/dL) for at least 2448 hours.23

It is important to state that controversy exists regarding which patients should be screened for diabetes. The United States Preventive Services Task Force (USPSTF) recommends screening adult patients only if they have hypertension.27 The ADA recommends screening all patients 45 years of age and older, and younger, overweight patients with at least 1 additional risk factor.9 We have previously shown that using USPSTF guidelines misses 33.1% of cases of DM compared to the ADA standard.28 As such, our institution and the Wisconsin State Diabetes Screening Guidelines mirror the ADA guidelines.29, 30 In the present study, 91% were aged 45 and older, and 88% were overweight, so nearly everyone in our study met our state and institution guidelines for diabetes screening. However, this might not be the case at all institutions if USPSTF guidelines were instead followed.

A limitation of the present study was that a selection bias of subjects could have occurred by both patients and providers, as less healthy patients with higher surgical risk may not have been candidates for surgery as often as lower‐risk patients. While entirely appropriate to maximize safety for elective surgery patients, this may in part explain the lower Hgb A1C (6.53 [0.14]) in our Known Diabetes/Prediabetes group, and lower range of blood glucose values in our New Diabetes/Prediabetes patients, with the majority being in the prediabetes range. However, this limitation also allows for the conclusion that any patient, regardless of perceived good health and primary care visits, may still have undiagnosed DM or IFG.

In summary, this study strongly supports the practice of screening obligate fasting patients to reduce the prevalence of undiagnosed diabetes. Despite the fact that our patients had insurance and recent primary care visits, nearly one‐quarter of individuals had previously unrecognized dysglycemia. This study also revealed systems issues, including the need for improved care transitions and development of a structure for shared responsibility in an ACO system, that need to be addressed if screening initiatives are to be effective in the hospital setting. Future studies will be needed to determine if other opportunistic screening tests have case‐finding potential, and further, how transitions processes can be improved to ensure that knowledge gained in the hospital is conveyed to the ambulatory setting.

Acknowledgements

The authors thank the orthopedic midlevel providers and nurses who assisted with patient recruitment, and the Clinical Trials staff, particularly Lori Wollet, for their assistance throughout the study. All authors disclose no relevant or financial conflicts of interest.

References
  1. Centers for Medicare and Medicaid Services. Accountable Care Organizations: What providers need to know. Available at: https://www.cms.gov/MLNProducts/downloads/ACO_Providers_Factsheet_ICN907406.pdf. Accessed February 20,2012.
  2. Cibulskis C,Giardino A,Moyer V.Care transitions from inpatient to outpatient settings: ongoing challenges and emerging best practices.Hosp Pract (Minneapolis).2001;39:128139.
  3. Ellerbeck E,Totten B,Markello S,Patterson K,Sipe T,Tilden C.Quality improvement in critical access hospitals: addressing immunizations prior to discharge.J Rural Health.2003;19:433438.
  4. IDSA Guidelines. Immunization Programs for Infants, Children, Adolescents, and Adults: Clinical Practice Guidelines by the Infectious Diseases Society of America. Available at: http://www.idsociety.org/uploadedFiles/IDSA/Guidelines‐Patient_Care/PDF_Library/Immunization.pdf. Accessed February 23,2012.
  5. Agency for Healthcare Research and Quality: Pneumococcal Vaccination Prior to Hospital Discharge. Available at: http://www/ahrq.gov/clinic/ptsafety/chap36.htm. Accessed February 23,2012.
  6. Cowie C,Rust K,Ford E, et al.Full accounting of diabetes and pre‐diabetes in the U.S. population in 1988–1994 and 2005–2006.Diabetes Care.2009;32:287294.
  7. Sheehy A,Coursin D,Gabbay R.Back to Wilson and Jungner: 10 good reasons to screen for type 2 diabetes mellitus.Mayo Clin Proc.2009;84:3842.
  8. American Diabetes Association.Standards of medical care in diabetes—2010.Diabetes Care.2010;33:S11S61.
  9. American Diabetes Association.Standards of medical care in diabetes—2012.Diabetes Care.2012;35:s11s63.
  10. National Diabetes Information Clearinghouse NIDDK National Diabetes Statistics 2011. Available at: http://diabetes.niddk.nih.gov/dm/pubs/statistics/index.htm#people. Accessed February 23,2012.
  11. Nathan D,Davidson M,DeFronzo R, et al.Impaired fasting glucose and impaired glucose tolerance: implications for care.Diabetes Care.2007;30:753759.
  12. Walid M,Newman B,Yelverton J,Nutter J,Ajjan M,Robinson J.Prevalence of previously unknown elevation of glycosylated hemoglobin in spine surgery patients and impact on length of stay and total cost.J Hosp Med.2010;5:E10E14.
  13. Dungan K,Braithwaite S,Preiser J.Stress hyperglycemia.Lancet.2009;373:17981807.
  14. Clement S,Braithwaite S,Magee M, et al.Management of diabetes and hyperglycemia in hospitals.Diabetes Care.2004;27:553591.
  15. Sheehy A,Gabbay R.An overview of preoperative glucose evaluation, management, and perioperative impact.J Diabetes Sci Technol.2009;3:12611269.
  16. Grek S,Gravenstein N,Morey T,Rice M.A cost‐effective screening method for preoperative hyperglycemia.Anesth Analg.2009;109:16221624.
  17. Hatzakorian R,Bui H,Carvalho G,Shan WLP,Sidhu S,Schricker T.Fasting blood glucose levels in patients presenting for elective surgery.Nutrition.2011;27:298301.
  18. Abdelmalak B,Abdelmalak J,Knittel J, et al.The prevalence of undiagnosed diabetes in non‐cardiac surgery patients, an observational study.Can J Anesth.2010;57:10581064.
  19. Beaule P,Dorey F,Hoke R,LeDuff M,Amstutz H.The value of patient activity level in the outcome of total hip arthroplasty.J Arthroplasty.2006;21:547552.
  20. Sheehy A,Flood G,Tuan W,Liou J,Coursin D,Smith M.Analysis of guidelines for screening diabetes mellitus in an ambulatory population.Mayo Clin Proc.2010;85:2735.
  21. Centers for Disease Control and Prevention National Center for Health Statistics Inpatient Surgery Statistics, 2007. Available at: http://www.cdc.gov/nchs/fastats/insurg.htm. Accessed February 23,2012.
  22. Centers for Disease Control and Prevention National Health Statistics Reports Ambulatory Surgery Statistics, 2006. Available at: http://www.cdc.gov/nchs/data/nhsr/nhsr011.pdf. Accessed February 23,2012.
  23. Umpierrez G,Hellman R,Korytkowski M, et al.Management of hyperglycemia in hospitalized patients in non‐critical care setting: an Endocrine Society Clinical Practice Guideline.J Clin Endocrinol Metab.2012;97:1638.
  24. Alberti KG,Zimmet PZ.Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation.Diabet Med.1998;15:539553.
  25. National Glycohemoglobin Standardization Program (NGSP). Available at: http://www.ngsp.org. Accessed February 23,2012.
  26. Moghissi E,Korytkowski M,DiNardo M, et al.American Association of Clinical Endocrinologists and American Diabetes Association consensus statement on inpatient glycemic control.Diabetes Care.2009;32:11191131.
  27. Umpierrez G,Isaacs S,Bazargan N,You X,Thaler L,Kitabchi A.Hyperglycemia: an independent marker of in‐hospital mortality in patients with undiagnosed diabetes.J Clin Endocrinol Metab.2002;87:978982.
  28. United States Preventive Services Task Force Diabetes Screening Guideline. Available at: http://www.uspreventiveservicestaskforce.org/uspstf/uspsdiab.htm. Accessed February 22,2012.
  29. University of Wisconsin and UW Health Preventive Care Guidelines. Available at: https://ghcscw.com/media/2011_ph_Preventive_Care_Guidelines_2010.pdf. Accessed February 22,2012.
  30. Wisconsin Diabetes Mellitus Essential Care Guidelines 2011. Available at: http://www.dhs.wisconsin.gov/health/diabetes/PDFs/GL13.pdf. Accessed February 22,2012.
References
  1. Centers for Medicare and Medicaid Services. Accountable Care Organizations: What providers need to know. Available at: https://www.cms.gov/MLNProducts/downloads/ACO_Providers_Factsheet_ICN907406.pdf. Accessed February 20,2012.
  2. Cibulskis C,Giardino A,Moyer V.Care transitions from inpatient to outpatient settings: ongoing challenges and emerging best practices.Hosp Pract (Minneapolis).2001;39:128139.
  3. Ellerbeck E,Totten B,Markello S,Patterson K,Sipe T,Tilden C.Quality improvement in critical access hospitals: addressing immunizations prior to discharge.J Rural Health.2003;19:433438.
  4. IDSA Guidelines. Immunization Programs for Infants, Children, Adolescents, and Adults: Clinical Practice Guidelines by the Infectious Diseases Society of America. Available at: http://www.idsociety.org/uploadedFiles/IDSA/Guidelines‐Patient_Care/PDF_Library/Immunization.pdf. Accessed February 23,2012.
  5. Agency for Healthcare Research and Quality: Pneumococcal Vaccination Prior to Hospital Discharge. Available at: http://www/ahrq.gov/clinic/ptsafety/chap36.htm. Accessed February 23,2012.
  6. Cowie C,Rust K,Ford E, et al.Full accounting of diabetes and pre‐diabetes in the U.S. population in 1988–1994 and 2005–2006.Diabetes Care.2009;32:287294.
  7. Sheehy A,Coursin D,Gabbay R.Back to Wilson and Jungner: 10 good reasons to screen for type 2 diabetes mellitus.Mayo Clin Proc.2009;84:3842.
  8. American Diabetes Association.Standards of medical care in diabetes—2010.Diabetes Care.2010;33:S11S61.
  9. American Diabetes Association.Standards of medical care in diabetes—2012.Diabetes Care.2012;35:s11s63.
  10. National Diabetes Information Clearinghouse NIDDK National Diabetes Statistics 2011. Available at: http://diabetes.niddk.nih.gov/dm/pubs/statistics/index.htm#people. Accessed February 23,2012.
  11. Nathan D,Davidson M,DeFronzo R, et al.Impaired fasting glucose and impaired glucose tolerance: implications for care.Diabetes Care.2007;30:753759.
  12. Walid M,Newman B,Yelverton J,Nutter J,Ajjan M,Robinson J.Prevalence of previously unknown elevation of glycosylated hemoglobin in spine surgery patients and impact on length of stay and total cost.J Hosp Med.2010;5:E10E14.
  13. Dungan K,Braithwaite S,Preiser J.Stress hyperglycemia.Lancet.2009;373:17981807.
  14. Clement S,Braithwaite S,Magee M, et al.Management of diabetes and hyperglycemia in hospitals.Diabetes Care.2004;27:553591.
  15. Sheehy A,Gabbay R.An overview of preoperative glucose evaluation, management, and perioperative impact.J Diabetes Sci Technol.2009;3:12611269.
  16. Grek S,Gravenstein N,Morey T,Rice M.A cost‐effective screening method for preoperative hyperglycemia.Anesth Analg.2009;109:16221624.
  17. Hatzakorian R,Bui H,Carvalho G,Shan WLP,Sidhu S,Schricker T.Fasting blood glucose levels in patients presenting for elective surgery.Nutrition.2011;27:298301.
  18. Abdelmalak B,Abdelmalak J,Knittel J, et al.The prevalence of undiagnosed diabetes in non‐cardiac surgery patients, an observational study.Can J Anesth.2010;57:10581064.
  19. Beaule P,Dorey F,Hoke R,LeDuff M,Amstutz H.The value of patient activity level in the outcome of total hip arthroplasty.J Arthroplasty.2006;21:547552.
  20. Sheehy A,Flood G,Tuan W,Liou J,Coursin D,Smith M.Analysis of guidelines for screening diabetes mellitus in an ambulatory population.Mayo Clin Proc.2010;85:2735.
  21. Centers for Disease Control and Prevention National Center for Health Statistics Inpatient Surgery Statistics, 2007. Available at: http://www.cdc.gov/nchs/fastats/insurg.htm. Accessed February 23,2012.
  22. Centers for Disease Control and Prevention National Health Statistics Reports Ambulatory Surgery Statistics, 2006. Available at: http://www.cdc.gov/nchs/data/nhsr/nhsr011.pdf. Accessed February 23,2012.
  23. Umpierrez G,Hellman R,Korytkowski M, et al.Management of hyperglycemia in hospitalized patients in non‐critical care setting: an Endocrine Society Clinical Practice Guideline.J Clin Endocrinol Metab.2012;97:1638.
  24. Alberti KG,Zimmet PZ.Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation.Diabet Med.1998;15:539553.
  25. National Glycohemoglobin Standardization Program (NGSP). Available at: http://www.ngsp.org. Accessed February 23,2012.
  26. Moghissi E,Korytkowski M,DiNardo M, et al.American Association of Clinical Endocrinologists and American Diabetes Association consensus statement on inpatient glycemic control.Diabetes Care.2009;32:11191131.
  27. Umpierrez G,Isaacs S,Bazargan N,You X,Thaler L,Kitabchi A.Hyperglycemia: an independent marker of in‐hospital mortality in patients with undiagnosed diabetes.J Clin Endocrinol Metab.2002;87:978982.
  28. United States Preventive Services Task Force Diabetes Screening Guideline. Available at: http://www.uspreventiveservicestaskforce.org/uspstf/uspsdiab.htm. Accessed February 22,2012.
  29. University of Wisconsin and UW Health Preventive Care Guidelines. Available at: https://ghcscw.com/media/2011_ph_Preventive_Care_Guidelines_2010.pdf. Accessed February 22,2012.
  30. Wisconsin Diabetes Mellitus Essential Care Guidelines 2011. Available at: http://www.dhs.wisconsin.gov/health/diabetes/PDFs/GL13.pdf. Accessed February 22,2012.
Issue
Journal of Hospital Medicine - 7(8)
Issue
Journal of Hospital Medicine - 7(8)
Page Number
611-616
Page Number
611-616
Publications
Publications
Article Type
Display Headline
Preoperative “NPO” as an opportunity for diabetes screening
Display Headline
Preoperative “NPO” as an opportunity for diabetes screening
Sections
Article Source

Copyright © 2012 Society of Hospital Medicine

Disallow All Ads
Correspondence Location
Department of Medicine, Division of Hospital Medicine, University of Wisconsin School of Medicine and Public Health, 1685 Highland Ave, MFCB 3126, Madison, WI 53705
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Article PDF Media
Media Files