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Table 1. 
Characteristics of the 2989 Study Patients*
Characteristics of the 2989 Study Patients*
Table 2. 
Serum Albumin Level, Cholesterol Levels, and Risk of All-Site Nosocomial Infection*
Serum Albumin Level, Cholesterol Levels, and Risk of All-Site Nosocomial Infection*
Table 3. 
Serum Albumin Level, Cholesterol Levels, and Risk of Surgical Site Nosocomial Infection*
Serum Albumin Level, Cholesterol Levels, and Risk of Surgical Site Nosocomial Infection*
Table 4. 
Serum Albumin Level, Cholesterol Levels, and Risk of Respiratory Tract Nosocomial Infection*
Serum Albumin Level, Cholesterol Levels, and Risk of Respiratory Tract Nosocomial Infection*
Table 5. 
Serum Albumin Level, Cholesterol Levels, and Risk of In-Hospital Death*
Serum Albumin Level, Cholesterol Levels, and Risk of In-Hospital Death*
Table 6. 
Serum Albumin Level, Cholesterol Levels, and LOS*
Serum Albumin Level, Cholesterol Levels, and LOS*
1.
Philips  AShaper  AGWhincup  PH Association between serum albumin and mortality from cardiovascular disease, cancer, and other causes.  Lancet. 1989;21434- 1436Google ScholarCrossref
2.
Shibata  HHaga  HUeno  MNagai  HYasumura  SKoyano  W Longitudinal changes of serum albumin in elderly people living in the community.  Age Ageing. 1991;20417- 420Google ScholarCrossref
3.
Klonoff-Cohen  HBarrett-Connor  ELEdelstein  SL Albumin levels as a predictor of mortality in the healthy elderly.  J Clin Epidemiol. 1992;45207- 212Google ScholarCrossref
4.
Corti  M-CGuralnik  JMSalive  MESorkin  JD Serum albumin level and physical disability as predictors of mortality in older persons.  JAMA. 1994;2721036- 1042Google ScholarCrossref
5.
Gibbs  JCull  WHenderson  WDaley  JHur  KKhuri  SF Preoperative serum albumin level as a predictor of operative mortality and morbidity: results from the National VA Surgical Risk Study.  Arch Surg. 1999;13436- 42Google ScholarCrossref
6.
Sacks  GSDearman  KReplogle  WHCora  VLMeeks  MCanada  T Use of subjective global assessment to identify nutrition-associated complications and death in geriatric long-term care facility residents.  J Am Coll Nutr. 2000;19570- 577Google ScholarCrossref
7.
Longo  WEVirgo  KSJohnson  FE  et al.  Risk factors for morbidity and mortality after colectomy for colon cancer.  Dis Colon Rectum. 2000;4383- 91Google ScholarCrossref
8.
Obialo  CIOkonofua  ECNzerue  MCTayade  ASRiley  LJ Role of hypoalbuminemia and hypocholesterolemia as copredictors of mortality in acute renal failure.  Kidney Int. 1999;561058- 1063Google ScholarCrossref
9.
Engelman  DTAdams  DHByrne  JG  et al.  Impact of body mass index and albumin on morbidity and mortality after cardiac surgery.  J Thorac Cardiovasc Surg. 1999;118866- 873Google ScholarCrossref
10.
Ryan  TARady  MYBashour  CALeventhal  MLytle  BStarr  NJ Predictors of outcome in cardiac surgical patients with prolonged intensive care stay.  Chest. 1997;1121035- 1042Google ScholarCrossref
11.
Chima  CSBarco  KDewitt  MLMaeda  MTeran  JCMullen  KD Relationship of nutritional status to length of stay, hospital costs, and discharge status of patients hospitalized in the medicine service.  J Am Diet Assoc. 1997;97975- 978Google ScholarCrossref
12.
Medina-Cuadros  MSillero-Arenas  MMartínez Gallego  GDelgado-Rodríguez  M Surgical wound infections diagnosed after discharge from hospital: epidemiological differences with in-hospital infections.  Am J Infect Control. 1996;24421- 428Google ScholarCrossref
13.
Deschenes  MVilleneuve  JP Risk factors for the development of bacterial infections in hospitalized patients with cirrhosis.  Am J Gastroenterol. 1999;942193- 2197Google ScholarCrossref
14.
Gol  MKKarahan  MUlus  AT  et al.  Bloodstream, respiratory, and deep surgical wound infections after open heart surgery.  J Card Surg. 1998;13252- 259Google ScholarCrossref
15.
Fariñas-Alvarez  CFariñas  MCFernandez-Mazarrasa  CLlorca  JCasanova  DDelgado-Rodríguez  M Analysis of risk factors for nosocomial sepsis in surgical patients.  Br J Surg. 2000;871076- 1081Google ScholarCrossref
16.
George  DLFalk  PSWunderink  RG  et al.  Epidemiology of ventilator-acquired pneumonia based on protected bronchoscopic sampling.  Am J Respir Crit Care Med. 1998;1581839- 1847Google ScholarCrossref
17.
Delgado-Rodríguez  MGómez-Ortega  ASillero-Arenas  MLlorca  J Epidemiology of surgical site infections diagnosed after discharge: a prospective cohort study.  Infect Control Hosp Epidemiol. 2001;2224- 30Google ScholarCrossref
18.
Chyou  PHEaker  ED Serum cholesterol concentrations and all-cause mortality in older people.  Age Ageing. 2000;2969- 74Google ScholarCrossref
19.
Houterman  SVerschuren  WMGiampaoli  S  et al.  Total but not high-density lipoprotein cholesterol is consistently associated with coronary heart disease mortality in elderly men in Finland, Italy, and the Netherlands.  Epidemiology. 2000;11327- 332Google ScholarCrossref
20.
Haim  MBenderly  MBrunner  D  et al.  Elevated serum triglyceride levels and long-term mortality in patients with coronary heart disease: the Bezafibrate Infarction Prevention (BIP) Registry.  Circulation. 1999;100475- 482Google ScholarCrossref
21.
Keil  ULiese  ADHense  HW  et al.  Classical risk factors and their impact on incident non-fatal and fatal myocardial infarction and all-cause mortality in southern Germany: results from the MONICA Augsburg cohort study 1984-1992: Monitoring Trends and Determinants in Cardiovascular Diseases.  Eur Heart J. 1998;191197- 1207Google ScholarCrossref
22.
Menotti  AKromhout  DNissinen  A  et al.  Short-term all-cause mortality and its determinants in elderly male populations in Finland, the Netherlands, and Italy: the FINE Study: Finland, Italy, Netherlands Elderly Study.  Prev Med. 1996;25319- 326Google ScholarCrossref
23.
Norrish  ANorth  DYee  RLJackson  R Do cardiovascular disease risk factors predict all-cause mortality?  Int J Epidemiol. 1995;24908- 914Google ScholarCrossref
24.
Delgado-Rodríguez  MMedina-Cuadros  MMartínez-Gallego  GSillero-Arenas  M Total cholesterol, HDL-cholesterol, and risk of nosocomial infection: a prospective study in surgical patients.  Infect Control Hosp Epidemiol. 1997;189- 18Google ScholarCrossref
25.
McCabe  WRJackson  GG Gram-negative bacteremia, II: clinical, laboratory and therapeutic observations.  Arch Intern Med. 1962;110856- 864Google ScholarCrossref
26.
Haley  RWCulver  DHMorgan  WMWhite  JWEmori  TGHooton  TM Identifying patients at high risk of surgical wound infection: a simple multivariate index of patient susceptibility and wound contamination.  Am J Epidemiol. 1985;121206- 215Google Scholar
27.
Culver  DHHoran  RCGaynes  RP  et al. and the National Nosocomial Infections Surveillance System, Surgical wound infection rates by wound class, operative procedure, and patient risk index.  Am J Med. 1991;91(suppl 3B)152S- 157SGoogle ScholarCrossref
28.
Garner  JSJarvis  WREmori  TGHoran  TCHughes  JM CDC definitions for nosocomial infections.  Am J Infect Control. 1988;16128- 140Google ScholarCrossref
29.
Horan  TCGaynes  RPMartone  WJJarvis  WREmori  TG CDC definitions of nosocomial surgical site infections, 1992: a modification of CDC definitions of surgical wound infections.  Infect Control Hosp Epidemiol. 1992;13606- 608Google ScholarCrossref
30.
Rothman  KJGreenland  S Modern Epidemiology. 2nd ed. Philadelphia, Pa Lippincott-Raven Publishers1997;
31.
Delgado-Rodríguez  MSillero-Arenas  MMedina-Cuadros  MMartínez-Gallego  G Nosocomial infection in surgical patients: comparison of two measures of intrinsic patient risk.  Infect Control Hosp Epidemiol. 1997;1819- 23Google ScholarCrossref
32.
Sammalkorpi  KValtonen  VKerttula  YNikkila  ETaskinen  MR Changes in serum lipoprotein pattern induced by acute infections.  Metabolism. 1988;37859- 865Google ScholarCrossref
33.
Delgado-Rodríguez  MSillero-Arenas  MMedina-Cuadros  MMartínez-Gallego  G Usefulness of intrinsic infection risk indices as predictors of in-hospital death.  Am J Infect Control. 1997;25365- 370Google ScholarCrossref
34.
Delgado-Rodríguez  MGómez-Ortega  ALecuona  M  et al.  Nosocomial infection, indices of intrinsic infection risk, and in-hospital death.  J Hosp Infect. 1999;41203- 211Google ScholarCrossref
35.
Yeun  JYKaysen  GA Factors influencing serum albumin in dialysis patients.  Am J Kidney Dis. 1998;32(suppl 4)S118- S125Google ScholarCrossref
36.
Kuller  LHEichner  JEOrchard  TJGrandits  GAMcCallum  LTracy  RPfor the Multiple Risk Factor Intervention Trial Research Group, The relation between serum albumin levels and risk of coronary heart disease in the Multiple Risk Factor Intervention Trial.  Am J Epidemiol. 1991;1341266- 1277Google Scholar
37.
Stevens  RGBlumberg  BS Serum albumin and mortality [letter].  Lancet. 1990;335351Google ScholarCrossref
38.
Gosling  PBeevers  DGGoode  GE  et al.  Serum albumin and mortality [letter].  Lancet. 1990;335349- 350Google Scholar
39.
Grimble  R Serum albumin and mortality [letter].  Lancet. 1990;335350Google Scholar
40.
Piccoli  GBQuarello  FSalomone  M  et al.  Are serum albumin and cholesterol reliable outcome markers in elderly dialysis patients?  Nephrol Dial Transplant. 1995;10 Suppl 672- 77Google ScholarCrossref
41.
Zimmermann  JHerrlinger  SPruy  AMetzger  TWanner  C Inflammation enhances cardiovascular risk and mortality in hemodialysis patients.  Kidney Int. 1999;55648- 658Google ScholarCrossref
42.
Criqui  MHGolomb  BA Epidemiologic aspects of lipid abnormalities.  Am J Med. 1998;105(suppl 1A)48S- 57SGoogle ScholarCrossref
Original Article
July 2002

Cholesterol and Serum Albumin Levels as Predictors of Cross Infection, Death, and Length of Hospital Stay

Author Affiliations

From the Division of Preventive Medicine and Public Health, University of Ja[[eacute]]n (Drs Delgado-Rodr[[iacute]]guez and Mariscal-Ortiz), the Service of General Surgery, Hospital General Ciudad de Ja[[eacute]]n (Drs Medina-Cuadros, G[[oacute]]mez-Ortega, and Mart[[iacute]]nez-Gallego), and the Service of Health Programs, Provincial Office for Health (Dr Sillero-Arenas), Ja[[eacute]]n, Spain; and the Division of Preventive Medicine and Public Health, University of Navarra, Navarra, Spain (Drs Delgado-Rodr[[iacute]]guez and Martinez-Gonzalez).

Arch Surg. 2002;137(7):805-812. doi:10.1001/archsurg.137.7.805
Abstract

Hypothesis  The levels of cholesterol, its fractions (high-density lipoprotein cholesterol [HDL-C] and low-density lipoprotein cholesterol [LDL-C]), and serum albumin reflect nutritional status and are related to in-hospital death, nosocomial infection, and length of stay in the hospital.

Design  A prospective cohort study of hospitalized patients.

Setting  The Service of General Surgery of a tertiary hospital.

Patients  A consecutive series of 2989 patients admitted for more than 1 day.

Main Outcome Measures  Nosocomial infection, in-hospital death, and length of stay.

Results  During follow-up, 62 (2%) of the patients died, 382 (13%) developed a nosocomial infection, and 257 (9%) developed a surgical site infection. Serum albumin (lowest quintile vs highest quintile: adjusted odds ratio [OR], 1.9; 95% confidence interval, 1.2-2.9) and HDL-C (lowest quintile vs highest quintile: OR, 2.0; 95% confidence interval, 1.3-3.0) levels showed an inverse and highly significant relationship with nosocomial infection (mainly due to surgical site infection) in crude and multivariate analyses (controlling for the Study on the Efficacy of Nosocomial Infection Control [SENIC] index, the American Society of Anesthesiologists' score, cancer, and age). Regarding total and LDL-C levels, only their lowest quintiles increased the risk of nosocomial infection. Serum albumin and HDL-C levels showed an inverse trend (P<.001) with mortality, with high multivariate-adjusted ORs in the lowest quintile (serum albumin: OR, 5.8; 95% confidence interval, 0.8-44.6; HDL-C: OR, 7.2; 95% confidence interval, 0.9-55.0), whereas no trend was appreciated with other cholesterol fractions or ratios. Serum albumin, HDL-C, and LDL-C levels showed independent, significant (P<.001), and inverse relationships with length of stay.

Conclusion  The levels of serum albumin and cholesterol fractions, mainly HDL-C, which are routinely measured at hospital admission, are predictors of in-hospital death, nosocomial infection, and length of stay.

SEVERAL COMMUNITY studies1-4 have reported a relationship between a low serum albumin level and an increased risk of death. In the hospital setting, many reports have related serum albumin level to in-hospital mortality,5-9 length of stay (LOS),9-11 and nosocomial infection.5,12-17 These reports suggest that the routine measurement of serum albumin level at hospital admission is a risk marker for a bad prognosis for hospital stay. Total cholesterol (TC) and its fractions, like serum albumin, are markers of nutritional status6 and are universally used as cardiovascular disease–related epidemiological features; nevertheless, their role as markers of bad prognosis in surgical patients has been less frequently studied.

In community studies,18-20 a low high-density lipoprotein cholesterol (HDL-C) level, a high low-density lipoprotein cholesterol (LDL-C) level, and TC were independent predictors of cardiovascular disease–related mortality. A low HDL-C level was also reported as a predictor of all-cause mortality in several countries.21-23 Serum cholesterol level and its fractions have not been frequently studied in hospitalized patients. Hypocholesterolemia is a predictor of death in geriatric patients6 and in patients with acute renal failure.8 To our knowledge, only 1 previous study24 has reported a relationship between a low HDL-C level and nosocomial infection in surgical patients. The available information on surgical patients is not enough to recommend or to discard the routine use of HDL-C and/or TC level at hospital admission. We assessed prospectively their value in predicting the postoperative course (death, LOS, and nosocomial infection) in a consecutive series of 2989 patients undergoing various general surgery procedures.

Patients and methods
Study population

Our study was performed at the Ciudad de Jaén General Hospital, a 680-bed tertiary center with a referral population of 650 000 (in the province of Jaén, Andalusia, southern Spain). The study population was recruited from the patients attending the Service of General Surgery during 2 periods (from November 1, 1992, to June 30, 1994, and from December 1, 1995, to January 30, 1997). Those patients who were admitted to the service for short observation and transferred or discharged in less than 1 day were excluded. Informed consent was obtained from every eligible subject, and none refused to participate. A total of 2989 patients were enrolled.

Data collection

Patients were interviewed at the outpatient office or within the first 24 hours after hospital admission. The following data were gathered before surgical intervention: smoking status, alcohol consumption, height (to the nearest centimeter), weight (without shoes and dressed in light clothes), the levels of TC and its fractions (HDL-C and LDL-C), the serum creatinine level, liver failure, immunodeficiency, the American Society of Anesthesiologists' preoperative assessment score, neoplasms, the serum albumin level, diabetes mellitus status, and glucose intolerance. The serum albumin level could not be measured at hospital admission in 46 patients, whereas the levels of cholesterol and its fractions were missed in 65 patients. The severity of illness was classified according to the criteria proposed by McCabe and Jackson25 as rapidly fatal (death anticipated during hospitalization), ultimately fatal (death anticipated within 5 years), and nonfatal (disease unlikely to be fatal within 5 years).

During the hospital stay, information on the following diagnostic and therapeutic procedures was recorded (including starting and ending dates): peripheral catheters, central catheters, mechanical ventilation, parenteral nutrition, histamine2 receptor antagonists, antibiotics, and other medications. Information on variables associated with surgery (type of surgical wound and duration of surgery) was also gathered. The Study on the Efficacy of Nosocomial Infection Control (SENIC) index26 and the National Nosocomial Infections Surveillance (NNIS) index27 for assessing intrinsic patient risk of nosocomial infection were computed. The SENIC index was computed by scoring 1 point to each 1 of these 4 risk factors: abdominal operation, operation longer than 2 hours, contaminated or dirt-infected operation, and patient has more than 2 diagnoses. The NNIS index was calculated by assessing 3 risk factors (each receiving 1 point): contaminated or dirt-infected operation, American Society of Anesthesiologists' score higher than 2, and operation longer than T hours (varying with the surgical procedure).

Patients with hospital infections were prospectively identified. Three of us (M.M.-C., A.G.-O., and G.M.-G.) visited patients admitted to the Service of General Surgery daily to collect all pertinent data. Data were recorded on a standardized data collection form. Hospital infections were diagnosed according to the Centers for Disease Control and Prevention criteria.28,29 Surveillance was extended to 30 days after hospital discharge, to detect hospital infections that clinically developed at home. Postdischarge infections are not considered in this report because their risk factors are different from in-hospital infections and the serum albumin level was unrelated to them.12,17

Blood sampling and laboratory methods

Serum samples were obtained from whole blood samples collected in Vacutainer tubes (Becton, Dickinson and Company, Rutherford, NJ) without anticoagulant. Samples were collected after 12 to 14 hours of fasting. Serum samples were analyzed immediately or stored at 4°C and analyzed within 12 hours of collection. All samples were analyzed in the same laboratory.

The serum albumin level was determined by electrophoresis of serum proteins with an automated system (HITE System 600; Olympus Optical Co, Tokyo, Japan), on cellulose acetate, with a buffer of Tris, barbital, and sodium barbitate (pH 8.6-9.0), staining with ponceau 3D, and automated densitometry of the protein fractions. Calibration was performed using control and pathologic serum samples (Normal Validate and Pathologic Validate; Organon Inc, West Orange, NJ). The normal range for albumin is 3.4 to 5.0 g/dL.

Total cholesterol, HDL-C, LDL-C, glucose, and serum creatinine determinations were performed with an autoanalyzer (Hitachi 717; Boehringer Mannheim Diagnostics, Mannheim, Germany). Daily calibration was done using precinorm U y precipath U (Boehringer Mannheim Diagnostics).

Statistical analyses

For every serum albumin level and cholesterol fraction (distributed in quintiles), the incidence of nosocomial infection and mortality was calculated by dividing the number of events by the number of patients within that category. The univariate relationships between biochemical variables and in-hospital death and nosocomial infection were tested using the relative risk and its 95% confidence interval. Logistic regression analysis was used to adjust for potential confounders.30 For nosocomial infection, the SENIC index was used for adjustment because it is one of the best predictors of nosocomial infection in patients undergoing surgery26,31; estimates were also adjusted for infection existing at hospital admission because infection alters serum lipid levels, decreasing the levels of TC and HDL-C.32 The mortality results were adjusted for the NNIS index because it is an independent predictor of death in patients undergoing general surgery.33,34 To assess the statistical significance of a trend in multivariate analyses, quintiles of each biochemical variable were introduced in the logistic regression model as a continuous variable.30

The LOS distribution was normalized by a natural logarithmic transformation. A stepwise linear regression analysis was developed to detect independent predictors of LOS. The relationships between serum albumin and cholesterol fractions (in quintiles) and LOS were assessed by an analysis of variance. To estimate the adjusted LOS for each quintile, the variables included in the linear regression analysis were controlled for using an analysis of covariance.

Results

The baseline characteristics of the study population are summarized in Table 1. The mean ± SD age of the patients was 53.1 ± 18.1 years (range, 10-92 years); 53% were females, 2% died during the hospital stay, and 13% developed a nosocomial infection. The geometric average LOS was 7.1 days (median, 7 days; interquartile range, 4-10 days).

The results for all-site nosocomial infection are summarized in Table 2. Serum albumin level showed in the crude analysis a clear and significant trend with nosocomial infection risk: as albumin level decreased, the rate of infection increased. The same trend was observed after adjusting for the SENIC index, the American Society of Anesthesiologists' score, age, and HDL-C level. Adjustment for additional risk factors of nosocomial infection did not change the output. The same happened with HDL-C level: it was inversely related to all-site nosocomial infection. The levels of TC and LDL-C showed a U relationship with mortality, with a clear increased risk of nosocomial infection in their lowest quintiles, which was responsible for the significance of the trend, although in the middle quintiles the variation of the risk was scarce. Ratios of TC/HDL-C and LDL-C/HDL-C did not show any relationship in multivariate analyses.

For specific sites of infection, clear relationships were appreciated with surgical site infection (Table 3) in crude and multivariate analyses with serum albumin and HDL-C levels. With TC and LDL-C levels, borderline trends were observed, although significance was not achieved in any quintile. Given the few respiratory tract infections, we compared extreme quintiles (Table 4). Those with the lowest quintile of serum albumin, TC, HDL-C, and LDL-C levels exhibited a higher risk of respiratory tract infections. After adjusting for several variables (the NNIS index, age, mechanical ventilation, upper abdominal surgery, and chronic obstructive lung disease), all the associations disappeared, apart from that of LDL-C level, which remained statistically significant (the confidence interval excluded the null value). There was no association with urinary tract infection, and the number of patients with sepsis is too small to allow any reliable analysis (results not shown).

The relationship with in-hospital death is detailed in Table 5. Serum albumin and HDL-C levels exhibited an inverse relationship with the risk of dying: mortality augmented when these variables diminished. Patients in the lowest quintiles showed the highest risk of dying. The trend was attenuated, albeit statistically significantly, after controlling for the NNIS index and age. The inclusion in the multivariate model of other predictors of death (severity of illness, stay at the intensive care unit, and cancer) did not change the results. No relationship was observed with any other cholesterol variable or ratio.

To study the relationship with LOS, a stepwise linear regression model was developed. The variables included in the model were serum albumin level, HDL-C level, LDL-C level, American Society of Anesthesiologists' score, nosocomial infection, age, antibiotic prophylaxis, preoperative stay, cancer, duration of the operation, type of surgical wound, glycemia, community-acquired infection, and stay at the intensive care unit. With these variables, an adjusted r2 = 0.61 was obtained. The associations between LOS and quintiles of serum albumin and cholesterol fractions are displayed in Table 6. An inverse trend can be easily appreciated in the table in crude and multivariate analyses (adjusting for the variables included in the linear regression model). Patients in the lowest quintiles of serum albumin, HDL-C, and LDL-C levels showed a clearly higher LOS.

Comment

The main limitation of this study is the low number of some effects. It may imply lack of statistical power to draw significant conclusions on mortality and other nosocomial infection sites apart from surgical site. Nevertheless, despite the few deaths, clear and significant trends were observed for HDL-C and serum albumin levels. Regarding lower respiratory tract infections, the number was small and may be responsible for the lack of association in multivariate analysis found in larger studies.5

We would like to emphasize the prospective design of our study. Serum albumin and cholesterol levels were not measured in a selected series of patients in whom physicians believed that these variables would add relevant clinical information, but the study was planned to measure serum albumin and cholesterol fractions at hospital admission in all participants.

Our results on the relationship between serum albumin level and mortality agree with those of most reports.5-9 Serum albumin level is considered an objective measure of nutritional status.6 Malnutrition and inflammation suppress albumin synthesis.35 In patients undergoing dialysis, it is believed that inflammation plays a more important role because it produces a switch of protein synthesis in the liver from albumin to acute phase proteins (C-reactive protein and cytokines [interleukins 1 and 2 and tumor necrosis factor]), which are elevated in these patients.36,37 The proportion of patients with renal failure in our sample was small (32 patients, 6 deaths, and a mean ± SD serum albumin level of 3.6 ± 0.8 vs 4.4 ± 0.1 g/dL for the remaining patients). Thus, this mechanism is unlikely to explain all the deaths in patients with a low serum albumin level. Other potential mechanisms may be involved: (a) the ability of serum albumin to adsorb small molecules, thus suppressing the effects of mediators released from activated or damaged cells38; (b) a generalized increase in vascular permeability due to underlying disease39; and (c) the antioxidant capacity of serum albumin.39

The results on the association between a low serum albumin level and an increased risk of nosocomial infection, mainly surgical site infection, also agree with those of previous reports.5,12-17 If nosocomial infection lengthens the duration of hospitalization, it is expected that serum albumin level shows an association with LOS. Even after taking the effect of nosocomial infection into account in multivariate analysis, serum albumin level was still a predictor of LOS, in agreement with other studies.9-11

To our knowledge, no previous report assessed the use of cholesterol level as a marker of poor prognosis in surgical patients. Only 1 report,24 using the first 1207 patients from this study, has related cholesterol fractions to nosocomial infection risk. With more than twice the number of patients of that report, we observed similar results: a low HDL-C level behaves as a risk factor for nosocomial infection, mainly surgical site infection. In the previous report,24 the few lower respiratory tract infections did not allow relating them with cholesterol and its fractions. Now, with more than 40 infections, HDL-C level was unrelated to this infection site in multivariate analysis, although patients in the lowest quintile show a 3-fold raw incidence vs patients with higher levels. The LDL-C level remained a significant predictor after adjusting for the most common risk factors of respiratory tract infection.

Because low HDL-C levels increase the risk of nosocomial infection, especially surgical site infection, and a low LDL-C level increases the risk of lower respiratory tract infection, it would be expected that these variables increase the LOS. Even after controlling for nosocomial infection in multivariate analysis, the 2 cholesterol fractions showed an inverse trend with LOS.

Cholesterol level is considered an objective measure of nutritional status6 and a reliable outcome marker of poor prognosis (for mortality) in patients undergoing dialysis.40 Low apolipoprotein A-I and HDL-C levels are found with an increase in C-reactive protein, a prototypical acute phase protein, which is closely related to all-cause mortality in patients undergoing long-term hemodialysis.41 Again, the number of patients with renal failure was too small to imply this mechanism as responsible for the increased risk of death observed in patients with low levels of cholesterol and its fractions. Malnutrition may be another possibility to consider.

In cardiovascular epidemiology, the single most predictive lipid factor is the TC/HDL-C ratio. This is the best predictor of outcome and treatment benefit.42 According to our results, this ratio has no predictive ability for poor prognosis in surgical patients because low HDL-C and low LDL-C levels behave in a similar way.

In conclusion, according to our results, the routine measurement of serum albumin and cholesterol fractions, mainly HDL-C, at hospital admission is recommended. By measuring them, a better prediction of nosocomial infection, in-hospital death, and LOS is achieved. An additional advantage of including these measurements in the hospital routine is the potential improvement of the control of cardiovascular diseases.

This study was supported in part by a grant from the Jaén Institute for Research, Jaén.

Corresponding author and reprints: Miguel Delgado-Rodríguez, MD, MPH, Division of Preventive Medicine and Public Health, University of Jaén, Bldg B-3, 23071 Jaén, Spain (e-mail: mdelgado@ujaen.es).

References
1.
Philips  AShaper  AGWhincup  PH Association between serum albumin and mortality from cardiovascular disease, cancer, and other causes.  Lancet. 1989;21434- 1436Google ScholarCrossref
2.
Shibata  HHaga  HUeno  MNagai  HYasumura  SKoyano  W Longitudinal changes of serum albumin in elderly people living in the community.  Age Ageing. 1991;20417- 420Google ScholarCrossref
3.
Klonoff-Cohen  HBarrett-Connor  ELEdelstein  SL Albumin levels as a predictor of mortality in the healthy elderly.  J Clin Epidemiol. 1992;45207- 212Google ScholarCrossref
4.
Corti  M-CGuralnik  JMSalive  MESorkin  JD Serum albumin level and physical disability as predictors of mortality in older persons.  JAMA. 1994;2721036- 1042Google ScholarCrossref
5.
Gibbs  JCull  WHenderson  WDaley  JHur  KKhuri  SF Preoperative serum albumin level as a predictor of operative mortality and morbidity: results from the National VA Surgical Risk Study.  Arch Surg. 1999;13436- 42Google ScholarCrossref
6.
Sacks  GSDearman  KReplogle  WHCora  VLMeeks  MCanada  T Use of subjective global assessment to identify nutrition-associated complications and death in geriatric long-term care facility residents.  J Am Coll Nutr. 2000;19570- 577Google ScholarCrossref
7.
Longo  WEVirgo  KSJohnson  FE  et al.  Risk factors for morbidity and mortality after colectomy for colon cancer.  Dis Colon Rectum. 2000;4383- 91Google ScholarCrossref
8.
Obialo  CIOkonofua  ECNzerue  MCTayade  ASRiley  LJ Role of hypoalbuminemia and hypocholesterolemia as copredictors of mortality in acute renal failure.  Kidney Int. 1999;561058- 1063Google ScholarCrossref
9.
Engelman  DTAdams  DHByrne  JG  et al.  Impact of body mass index and albumin on morbidity and mortality after cardiac surgery.  J Thorac Cardiovasc Surg. 1999;118866- 873Google ScholarCrossref
10.
Ryan  TARady  MYBashour  CALeventhal  MLytle  BStarr  NJ Predictors of outcome in cardiac surgical patients with prolonged intensive care stay.  Chest. 1997;1121035- 1042Google ScholarCrossref
11.
Chima  CSBarco  KDewitt  MLMaeda  MTeran  JCMullen  KD Relationship of nutritional status to length of stay, hospital costs, and discharge status of patients hospitalized in the medicine service.  J Am Diet Assoc. 1997;97975- 978Google ScholarCrossref
12.
Medina-Cuadros  MSillero-Arenas  MMartínez Gallego  GDelgado-Rodríguez  M Surgical wound infections diagnosed after discharge from hospital: epidemiological differences with in-hospital infections.  Am J Infect Control. 1996;24421- 428Google ScholarCrossref
13.
Deschenes  MVilleneuve  JP Risk factors for the development of bacterial infections in hospitalized patients with cirrhosis.  Am J Gastroenterol. 1999;942193- 2197Google ScholarCrossref
14.
Gol  MKKarahan  MUlus  AT  et al.  Bloodstream, respiratory, and deep surgical wound infections after open heart surgery.  J Card Surg. 1998;13252- 259Google ScholarCrossref
15.
Fariñas-Alvarez  CFariñas  MCFernandez-Mazarrasa  CLlorca  JCasanova  DDelgado-Rodríguez  M Analysis of risk factors for nosocomial sepsis in surgical patients.  Br J Surg. 2000;871076- 1081Google ScholarCrossref
16.
George  DLFalk  PSWunderink  RG  et al.  Epidemiology of ventilator-acquired pneumonia based on protected bronchoscopic sampling.  Am J Respir Crit Care Med. 1998;1581839- 1847Google ScholarCrossref
17.
Delgado-Rodríguez  MGómez-Ortega  ASillero-Arenas  MLlorca  J Epidemiology of surgical site infections diagnosed after discharge: a prospective cohort study.  Infect Control Hosp Epidemiol. 2001;2224- 30Google ScholarCrossref
18.
Chyou  PHEaker  ED Serum cholesterol concentrations and all-cause mortality in older people.  Age Ageing. 2000;2969- 74Google ScholarCrossref
19.
Houterman  SVerschuren  WMGiampaoli  S  et al.  Total but not high-density lipoprotein cholesterol is consistently associated with coronary heart disease mortality in elderly men in Finland, Italy, and the Netherlands.  Epidemiology. 2000;11327- 332Google ScholarCrossref
20.
Haim  MBenderly  MBrunner  D  et al.  Elevated serum triglyceride levels and long-term mortality in patients with coronary heart disease: the Bezafibrate Infarction Prevention (BIP) Registry.  Circulation. 1999;100475- 482Google ScholarCrossref
21.
Keil  ULiese  ADHense  HW  et al.  Classical risk factors and their impact on incident non-fatal and fatal myocardial infarction and all-cause mortality in southern Germany: results from the MONICA Augsburg cohort study 1984-1992: Monitoring Trends and Determinants in Cardiovascular Diseases.  Eur Heart J. 1998;191197- 1207Google ScholarCrossref
22.
Menotti  AKromhout  DNissinen  A  et al.  Short-term all-cause mortality and its determinants in elderly male populations in Finland, the Netherlands, and Italy: the FINE Study: Finland, Italy, Netherlands Elderly Study.  Prev Med. 1996;25319- 326Google ScholarCrossref
23.
Norrish  ANorth  DYee  RLJackson  R Do cardiovascular disease risk factors predict all-cause mortality?  Int J Epidemiol. 1995;24908- 914Google ScholarCrossref
24.
Delgado-Rodríguez  MMedina-Cuadros  MMartínez-Gallego  GSillero-Arenas  M Total cholesterol, HDL-cholesterol, and risk of nosocomial infection: a prospective study in surgical patients.  Infect Control Hosp Epidemiol. 1997;189- 18Google ScholarCrossref
25.
McCabe  WRJackson  GG Gram-negative bacteremia, II: clinical, laboratory and therapeutic observations.  Arch Intern Med. 1962;110856- 864Google ScholarCrossref
26.
Haley  RWCulver  DHMorgan  WMWhite  JWEmori  TGHooton  TM Identifying patients at high risk of surgical wound infection: a simple multivariate index of patient susceptibility and wound contamination.  Am J Epidemiol. 1985;121206- 215Google Scholar
27.
Culver  DHHoran  RCGaynes  RP  et al. and the National Nosocomial Infections Surveillance System, Surgical wound infection rates by wound class, operative procedure, and patient risk index.  Am J Med. 1991;91(suppl 3B)152S- 157SGoogle ScholarCrossref
28.
Garner  JSJarvis  WREmori  TGHoran  TCHughes  JM CDC definitions for nosocomial infections.  Am J Infect Control. 1988;16128- 140Google ScholarCrossref
29.
Horan  TCGaynes  RPMartone  WJJarvis  WREmori  TG CDC definitions of nosocomial surgical site infections, 1992: a modification of CDC definitions of surgical wound infections.  Infect Control Hosp Epidemiol. 1992;13606- 608Google ScholarCrossref
30.
Rothman  KJGreenland  S Modern Epidemiology. 2nd ed. Philadelphia, Pa Lippincott-Raven Publishers1997;
31.
Delgado-Rodríguez  MSillero-Arenas  MMedina-Cuadros  MMartínez-Gallego  G Nosocomial infection in surgical patients: comparison of two measures of intrinsic patient risk.  Infect Control Hosp Epidemiol. 1997;1819- 23Google ScholarCrossref
32.
Sammalkorpi  KValtonen  VKerttula  YNikkila  ETaskinen  MR Changes in serum lipoprotein pattern induced by acute infections.  Metabolism. 1988;37859- 865Google ScholarCrossref
33.
Delgado-Rodríguez  MSillero-Arenas  MMedina-Cuadros  MMartínez-Gallego  G Usefulness of intrinsic infection risk indices as predictors of in-hospital death.  Am J Infect Control. 1997;25365- 370Google ScholarCrossref
34.
Delgado-Rodríguez  MGómez-Ortega  ALecuona  M  et al.  Nosocomial infection, indices of intrinsic infection risk, and in-hospital death.  J Hosp Infect. 1999;41203- 211Google ScholarCrossref
35.
Yeun  JYKaysen  GA Factors influencing serum albumin in dialysis patients.  Am J Kidney Dis. 1998;32(suppl 4)S118- S125Google ScholarCrossref
36.
Kuller  LHEichner  JEOrchard  TJGrandits  GAMcCallum  LTracy  RPfor the Multiple Risk Factor Intervention Trial Research Group, The relation between serum albumin levels and risk of coronary heart disease in the Multiple Risk Factor Intervention Trial.  Am J Epidemiol. 1991;1341266- 1277Google Scholar
37.
Stevens  RGBlumberg  BS Serum albumin and mortality [letter].  Lancet. 1990;335351Google ScholarCrossref
38.
Gosling  PBeevers  DGGoode  GE  et al.  Serum albumin and mortality [letter].  Lancet. 1990;335349- 350Google Scholar
39.
Grimble  R Serum albumin and mortality [letter].  Lancet. 1990;335350Google Scholar
40.
Piccoli  GBQuarello  FSalomone  M  et al.  Are serum albumin and cholesterol reliable outcome markers in elderly dialysis patients?  Nephrol Dial Transplant. 1995;10 Suppl 672- 77Google ScholarCrossref
41.
Zimmermann  JHerrlinger  SPruy  AMetzger  TWanner  C Inflammation enhances cardiovascular risk and mortality in hemodialysis patients.  Kidney Int. 1999;55648- 658Google ScholarCrossref
42.
Criqui  MHGolomb  BA Epidemiologic aspects of lipid abnormalities.  Am J Med. 1998;105(suppl 1A)48S- 57SGoogle ScholarCrossref
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