key: cord-0006050-1zpcijm0 authors: Ebbeling, L.; Grabo, D. J.; Shashaty, M.; Dua, R.; Sonnad, S. S.; Sims, C. A.; Pascual, J. L.; Schwab, C. W.; Holena, D. N. title: Psoas:lumbar vertebra index: central sarcopenia independently predicts morbidity in elderly trauma patients date: 2013-07-24 journal: Eur J Trauma Emerg Surg DOI: 10.1007/s00068-013-0313-3 sha: ec42715038943aca896c000a88fea53d72fa00a8 doc_id: 6050 cord_uid: 1zpcijm0 INTRODUCTION: Central sarcopenia as a surrogate for frailty has recently been studied as a predictor of outcome in elderly medical patients, but less is known about how this metric relates to outcomes after trauma. We hypothesized that psoas:lumbar vertebral index (PLVI), a measure of central sarcopenia, is associated with increased morbidity and mortality in elderly trauma patients. METHODS: A query of our institutional trauma registry from 2005 to 2010 was performed. Data was collected prospectively for the Pennsylvania Trauma Outcomes Study (PTOS). Inclusion criteria: age >55 years, ISS >15, and ICU LOS >48 h. Using admission CT scans, psoas:vertebral index was computed as the ratio between the mean cross-sectional areas of the psoas muscles and the L4 vertebral body at the level of the L4 pedicles. The 50th percentile of the psoas:L4 vertebral index value was determined, and patients were grouped into high (>0.84) and low (≤0.83) categories based on their relation to the cohort median. Primary endpoints were mortality and morbidity (as a combined endpoint for PTOS-defined complications). Univariate logistic regression was used to test the association between patient factors and mortality. Factors found to be associated with mortality at p < 0.1 were entered into a multivariable model. RESULTS: A total of 180 patients met the study criteria. Median age was 74 years (IQR 63–82), median ISS was 24 (IQR 18–29). Patients were 58 % male and 66 % Caucasian. Mean PLVI was 0.86 (SD 0.25) and was higher in male patients than female patients (0.91 ± 0.26 vs. 0.77 ± 0.21, p < 0.001). PLVI was not associated with mortality in univariate or multivariable modeling. After controlling for comorbidities, ISS, and admission SBP, low PLVI was found to be strongly associated with morbidity (OR 4.91, 95 % CI 2.28–10.60). CONCLUSIONS: Psoas:lumbar vertebral index is independently and negatively associated with posttraumatic morbidity but not mortality in elderly, severely injured trauma patients. PLVI can be calculated quickly and easily and may help identify patients at increased risk of complications. mortality after traumatic injury [1, 2] but it is clear that other factors such as medical comorbidities also contribute strongly to outcomes [3, 4] . Recently, attention has been focused on the concept of frailty as a driver of outcomes across a wide range of disease states in the elderly, including chronic kidney disease, malignancy, and aortic valve disease [5] [6] [7] . The original description of frailty includes difficulty with activities of daily living, reduced speed of ambulation, subjective feelings of exhaustion, unintentional weight loss, and weakness as measured by grip strength [8] . The association of frailty with outcomes after trauma is not well characterized, perhaps in part because frailty evaluation using conventional metrics in the trauma population is not practicable. Trauma is by its nature unpredictable, and for this reason most injured patients will present without baseline measurements of frailty. Attempts to measure frailty after injury using conventional metrics may be limited by altered mental status or inability to participate in physical activity. An attractive solution to this problem is to measure a surrogate for frailty that does not rely upon active patient participation, such as radiographically determined central sarcopenia [9] . Central sarcopenia, as measured by psoas cross-sectional area, has been associated with poor outcomes after liver transplantation [10] and open repair of ruptured aortic aneurysms [11] , but the impact of central sarcopenia has not yet been well characterized in the elderly trauma population. We sought to evaluate whether central sarcopenia, as measured by psoas cross-sectional area on admission imaging, is associated with outcomes in elderly trauma patients. We hypothesized that lower psoas cross-sectional area would be associated with increased morbidity and mortality in a cohort of elderly, severely injured trauma patients. After obtaining institutional review board approval, a query of our institutional trauma registry across a 5-year time period (2005-2010) was performed. Data for our trauma registry are collected prospectively and reported to the Pennsylvania Trauma Outcomes Study (PTOS) database by trained nurse abstractors. Study inclusion criteria were age C55 years, severe injury (Injury Severity Score (ISS) [15) , and ICU length of stay [48 h. Patients were excluded if they suffered a critical head injury (defined as a Head/Neck Abbreviated Injury Scale (AIS) score C5), did not receive admission cross-sectional imaging of the abdomen, had fractures or preexisting hardware of the 4th lumbar vertebral body, or had a retroperitoneal hematoma that distorted the cross-sectional area of the psoas at the level of the L4 vertebral body. Patient demographics (age, sex, and race), physiologic variables on presentation, mechanism of injury, Injury Severity Score, hospital length of stay (HLOS), ICU length of stay (ILOS), ventilator days, and comorbidities were abstracted from the institutional registry. Morbidity was measured by PTOS-defined occurrences (see ''Appendix 1''). Patients meeting all inclusion criteria with no exclusion criteria were then uploaded into a RED Cap database [12] . Computed tomography (CT) studies of the abdomen were obtained from the medical record and evaluated for each patient by one of three trained reviewers (DG, LE, DH). Prior to abstracting the study CTs, a sample of studies were independently abstracted by the three reviewers and results were compared in order to assess for inter-rater reliability. For each study, the right and left psoas muscle cross-sectional areas (PCSA) were measured at the level of the L4 vertebral body immediately inferior to the origin of the posterior elements. To normalize for body habitus, the cross-sectional area of the L4 vertebral body was also recorded at this level ( Fig. 1 ). Mean PSCA was calculated for each patient, and the ratio between mean PSCA and L4 vertebral body area was calculated using the following formula: The 50th percentile of psoas:L4 vertebral index (PLVI) value was determined and patients were grouped into high ([0.84) and low (B0.83) categories based on their relation to the cohort median. Univariate analyses of patient demographic variables, admission vital signs, comorbidities, and outcome measures between the two groups were performed. The primary outcomes of interest of the study were inhospital mortality and morbidity. Morbidity was defined as Fig. 1 Psoas:lumbar vertebral index was calculated as the ratio between the mean psoas cross-sectional area and the vertebral crosssectional area at the level of the L4 vertebral body just inferior to the insertion of the posterior elements a composite endpoint of any of 37 PTOS-defined complications (see ''Appendix 1'') and as subgroups of respiratory complications (acute respiratory distress syndrome, acute respiratory failure, aspiration/aspiration pneumonia, atelectasis, or pneumonia), infectious complications (sepsis, septicemia, acute sinusitis, soft tissue infection, urinary tract infection, pneumonia, wound infection, central nervous system infection, or empyema), organ failure (acute respiratory distress syndrome, coagulopathy, acute renal failure, or liver failure), thromboembolic complications (pulmonary embolism or deep venous thrombosis), and hemorrhagic complications (coagulopathy or postoperative hemorrhage). Secondary outcomes of interest were hospital length of stay (HLOS), ICU length of stay, and total ventilator days, which were examined between groups. In addition, the PLVI category was examined via mechanism of injury. The associations of baseline characteristics with morbidity and with hospital mortality were tested using t test for continuous normally distributed variables and Mann-Whitney or Kruskal-Wallis for continuous non-normally distributed variables. Categorical variables were compared using v 2 or Fischer's exact tests, as appropriate. Univariate logistic regression was used to assess the association between independent variables and the primary outcomes of interest. Multivariable logistic regression models were developed to adjust the association of PLVI with morbidity and mortality for potential confounders. Variables found to be associated with the outcome of interest in univariate analysis with a p value of .10 were included in the multivariate logistic models. All statistical analyses were performed using SPSS version 19.0 (IBM, Chicago IL). Secondary outcomes of interest were hospital length of stay (HLOS), ICU length of stay, and total ventilator days. In addition, mechanism injury by PLVI category was examined. At total of 234 patients met the inclusion criteria, of whom 54 were excluded (Fig. 2) , leaving 180 patients for analysis. Median age in the cohort was 74 years (IQR 63-82), and median ISS was 24 (IQR 18-29). Patients were 58 % male and 66 % Caucasian. There was no correlation between L4 vertebral body CSA and age, but psoas CSA did have a weak negative relationship with age (R 2 = 0.15). The correlation between right and left psoas CSA was high but not complete (R 2 = 0.75), so mean psoas CSA was used to calculate the PLVI. PLVI values were found to be normally distributed within the study population, with a mean value of 0.85 ± 0.25. PLVI values were higher in male patients than in female patients (0.91 ± 0.26 vs. 0.77 ± 0.21, p \ 0.001). Lumbar-psoas vertebral index rating reliability was found to be good between raters, with a maximum deviation of 23 %, which resulted in no misclassifications based on groups. Compared to patients in the high-PLVI group, patients in the low-PLVI group were older (median age 79 (IQR 72-85) vs. 70 (IQR 60-77), p \ 00.1), less likely to be male (43 vs. 71 %, p \ 0.001), and less likely to be Caucasian (63 vs. 69 %, p = 0.04). No significant differences were seen between the two groups in terms of number of baseline comorbidities, mechanism of injury, ISS, or admission vitals (Table 1 ). In unadjusted analysis, patients in the low-PLVI group had higher morbidity (83 vs. 58 %, p \ 0.001), but no difference was seen in mortality (16 vs. 10 %, p = 0.26) or any of the secondary endpoints of hospital length of stay, ICU length of stay, or ventilator days. In univariate analysis (Table 2) , PLVI category was not significantly associated with mortality. Only age in years (OR 1.05, 95 % CI 1.01-1.10), comorbidities (OR 1.30, 95 % CI 1.01-1.60), and AIS head (OR 1.44, 95 % CI 1.02-2.02) were found to be associated with mortality. In contrast, low PLVI was strongly associated with development of morbidity (OR 3.66, 95 % CI 1.83-7.32), as was ISS (OR 1.05, 95 % CI 1.01-1.10). Multivariable logistic regression analysis (Table 3 ) did not demonstrate an association between PLVI and mortality, but even after controlling for baseline comorbidities, ISS, and admission SBP, low PLVI was found to be strongly associated with morbidity (OR 4.91, 95 % CI 2.28-10.60). In the unadjusted analysis of morbidity subcategories of complications (Table 4 ), we found that infectious complications were statistically more likely to occur in the low PLVI group (60 vs. 39 %, p = 0.03). Mechanism of injury also differed between the two groups (Table 5) , with patients in the low PLVI category more likely to have sustained a fall (59 vs. 43 %, p \ 0.05) and less likely to have sustained an MVC (20 vs. 33 %, p \ 0.05). With an increasing elderly population living with greater numbers of chronic medical conditions and decreased physiologic reserve, the concept of frailty is emerging as a significant syndrome in the elderly patient population. Frailty further diminishes the older patient's ability to compensate when stressed. Fried and colleagues [8] described frailty as a phenotype that includes three of the following five characteristics: unintentional weight loss, slow walking speed, self-reported exhaustion, low physical activity, and weakness as measured by grip strength. The physiology of aging or an inherent decline in various organ systems accounts for this phenotype, and includes increased levels of inflammatory markers (CRP, IL-6), diminution in bone density (osteoporosis), cognitive changes (delirium and dementia), and sarcopenia [13] . In this cohort of elderly, severely injured trauma patients, we found that central sarcopenia as measured by PLVI was associated with morbidity but not mortality. The PLVI has several advantages over other metrics of frailty available for use in the trauma population. Because the majority of blunt trauma patients will undergo cross-sectional imaging upon admission [14] , the ability to measure PLVI is present early on for most elderly trauma patients. Since imaging occurs extremely early in the hospital course of trauma patient, admission PLVI is unlikely to be greatly affected by injuries, interventions undertaken to treat injuries, or complications developing thereafter. The admission PLVI can therefore be thought of as a baseline ''snapshot'' that represents the patient's condition at the time of injury. Because this metric is objective, does not require patient cooperation or recall, and does not require the ability to ambulate, it may be far easier to assess in patients suffering traumatic injury. The use of central sarcopenia as a proxy for frailty and predictor of outcomes has been studied in other groups of surgical patients in recent years. Decreased psoas crosssectional area has been shown to be associated with mortality after liver transplantation [10] , elective abdominal aortic aneurysm repair [15] , and esophagectomy [16] . In a cohort of patients undergoing hepatic resection for colorectal metastases, Peng et al. [17] found that a total psoas cross-sectional area of \500 mm was associated with increased risk of postoperative complications and hospital length of stay, but not mortality. Of note, our methodology differs from the above-referenced studies in that, rather than reporting the combined cross-sectional area of the psoas muscles at the L4 vertebra (or ''total psoas area'', TPA), we report the ratio of psoas CSA to the L4 vertebral body CSA. The intent of this methodology is to provide a PSCA value that is normalized to individual patient body habitus, but further research will be necessary to determine the optimal measurement of central sarcopenia. Injury Severity Score is one of the best known predictors of mortality in trauma patients, and so it may seem surprising that this failed to predict mortality in our models. However, the distribution of ISS in our cohort is relatively tightly distributed around the median of 24 (range 16-59), with 80 % of our cohort having an ISS between 16 and 32. Given that the predicted mortality in this range of ISS for patients greater than 55 years of age would be expected to be between *5 and 13 %, it is not entirely surprising, considering the relatively small sample size, that no difference is seen in our model. In the subgroup analysis, the only category of complications to reach statistical significance between the two groups was infectious complications. Frailty has been associated with alterations in both the innate and adaptive immune system [18] [19] [20] , and it is thus possible that in the presence of frailty as reflected by low PLVI, host immune responses may be compromised. Alternatively, it may be that the frailty phenotype necessitates interventions which result in increased risk of infections. For instance, patients who are unable to be mobilized from bed may be subjected to prolonged use of indwelling urinary catheters, resulting in increased risk of urinary tract infection. Despite our findings, this study has some important limitations. The utility of using ''any complication'' as a combined primary endpoint may be questioned, as different complications have different risk factors which may not be equally distributed between our two groups. Given our relatively small sample size and the degree of complexity that would be introduced in order to control for all of the risk factors for each individual complication, we have chosen to look at an aggregate measure instead. However, the use of morbidity as a combined endpoint may be more meaningful than rates of specific complications, as the aggregate reflects the overall baseline condition and host response to trauma. Additionally, as no specific treatments are available to protect frail patients from posttraumatic morbidity, the therapeutic benefit of a frailty index is currently very limited. However, the addition of central sarcopenia to the traditional predictors of outcome may help inform clinicians when discussing likely outcomes with family patients and their families. Future prospective studies may identify specific opportunities for improvement in this cohort. Finally, this study represents a singleinstitution experience with a limited number of patients, and as such may not be applicable to other centers. Specifically, the LPVI median of 0.84 from which we derive our cut-point to divide the cohort into ''high'' and ''low'' PLVI groups may not be valid in other populations. Further work with larger cohorts may help clarify this issue. In conclusion, the PLVI is an easily-obtained metric which may help physicians caring for trauma patients to identify a subpopulation of elderly patients at increased risk of morbidity, independent of age and comorbidities. Further investigative efforts should be directed towards translating risk identification into risk reduction. Adult (Acute) respiratory distress syndrome: ARDS occurs in conjunction with catastrophic medical conditions, such as pneumonia, shock, sepsis (or severe infection throughout the body, sometimes also referred to as systemic infection, and may include or also be called a blood or blood-borne infection), and trauma. It is a form of sudden and often severe lung failure characterized by PaO 2 /FiO 2 B200, decreased compliance, and diffuse bilateral pulmonary infiltrates without associated clinical evidence of CHF. The process must persist beyond 36 hours and require mechanical ventilation. Acute respiratory failure Need for prolonged ventilatory support after a period of normal non-assisted breathing (minimum of 48 hrs) or reintubation. a.Planned-do not report (i.e., taken to OR) b.Unplanned--report 22 Aspiration/aspiration pneumonia Documented inhalation of gastric contents or other materials followed by clinical and new radiological findings of pneumonitis which requires treatment within 48 h. Fat embolus syndrome Documented diagnosis by an attending physician in a patient w/pelvic or extremity fractures and a decreased PO2. One of the following must also be present: change in mental status; petechial signs; tachypnea; fat in urine; decreased platelets. Defined as a lodging of a blood clot in a pulmonary artery with subsequent obstruction of blood supply to the lung parenchyma. The blood clots usually originate from the deep veins or the pelvic venous system. Consider the condition present if the patient has a VQ scan interpreted as high probability of pulmonary embolism or a positive pulmonary arteriogram or positive CT angiogram. Defined as a condition in which there is swelling and an increase in pressure within a limited space (a fascial compartment) that presses on and compromises blood vessels, nerves, and/or tendons that run through that compartment. Compartment syndromes usually involve the leg but can also occur in the forearm, arm, thigh, and shoulder. Deep vein thrombosis (DVT)* *(maps to NTDB definition) The formation, development, or existence of a blood clot or thrombus within the vascular system, which may be coupled with inflammation. This diagnosis may be confirmed by a venogram, ultrasound, or CT. The patient must be treated with anticoagulation therapy and/or placement of a vena cava filter or clipping of the vena cava. A patient who did not require dialysis prior to injury, and who has worsening renal dysfunction after an injury requiring hemodialysis, ultrafiltration, or peritoneal dialysis. If the patient refuses treatment (e.g., dialysis), the condition is still considered present. Liver failure Documented by a physician. Increased serum ammonium or decreased synthetic or metabolic function (e.g., PT, TTP, or fibrinogen). Clean voided or other catheter urine specimen with C100,000 organisms/ml on C/S. Wound infection (Traumatic or incisional) drainage of purulent material from wound; active treatment of wound, or administration of antibiotics for wound. *An abdominal abscess would not be considered a wound infection and is not applicable as an occurrence. Esophageal intubation Endotracheal tube in esophagus and not immediately repositioned. Esophageal location determined by physical exam, X-ray, capnography, or endoscopy. Any endotracheal intubation procedure resulting in definitive placement of the tube in either the right or left main stem bronchus. a.Recognized and treated immediately-not reportable b.Unrecognized on two successive chest xrays--reportable Gastrointestinal 83 GI bleeding Blood loss from anywhere in GI tract, grossly positive nasogastric (NG) aspirate, or grossly positive stool which requires treatment. If the patient presents to the hospital with hypothermia, the hypothermia is considered a diagnosis. If the hypothermia presents during the hospital stay and is unexpected, the hypothermia is considered an occurrence. Postoperative hemorrhage Requiring operative intervention-procedures done in angio to control hemorrhage should be considered operative interventions and the hemorrhage should be included as an occurrence. Adverse drug reaction Documented by a physician, plus one of the following: adversely affects patient care; increases length of stay; increases morbidity and mortality. 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