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1.
Am Surg ; 86(9): 1185-1193, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32723180

ABSTRACT

BACKGROUND: Venous thromboembolism (VTE) remains a serious complication for trauma patients. While early VTE prophylaxis has gained traction, the timing of prophylaxis remains uncertain. We hypothesized that VTE prophylaxis within 24 hours of admission would have lower VTE rates and similar rates of adverse events in seriously injured patients. METHODS: Trauma patients were included from 32 American College of Surgeons verified Level 1 and 2 trauma centers over a 10-year period. Patients with injury severity score (ISS) <15, death or discharge within 48 hours of arrival, or who received no prophylaxis were excluded. RESULTS: 14 096 patients received VTE prophylaxis with an ISS of ≥15. Patients given prophylaxis at <24 hours had fewer VTE events and trended toward fewer serious in-hospital complications. Mortality and return to the operating room were similar across groups. Hospital and intensive care unit length of stay in the <24 hours prophylaxis group was significantly shorter when VTE prophylaxis was initiated earlier. CONCLUSIONS: In severely injured trauma patients with ISS >15, early VTE prophylaxis within 24 hours significantly reduced the risk of VTE as compared with delayed prophylaxis. Early chemoprophylaxis was found to be efficacious in reducing the incidence of VTE; however, the safety of this practice should be evaluated by future prospective studies.


Subject(s)
Anticoagulants/therapeutic use , Chemoprevention/methods , Intensive Care Units/statistics & numerical data , Risk Assessment/methods , Trauma Centers/statistics & numerical data , Venous Thromboembolism/prevention & control , Wounds and Injuries/complications , Female , Humans , Incidence , Male , Middle Aged , Prospective Studies , Survival Rate/trends , Time Factors , Treatment Outcome , United States/epidemiology , Venous Thromboembolism/epidemiology , Venous Thromboembolism/etiology , Wounds and Injuries/diagnosis
2.
Am J Health Syst Pharm ; 76(5): 286-292, 2019 Feb 09.
Article in English | MEDLINE | ID: mdl-30753292

ABSTRACT

PURPOSE: The study assesses the safety of high-dose intravenous (i.v.) labetalol in adults. METHODS: This is a retrospective administrative record review of 28 hospitals in one health care system, from October 2010 through October 2015. Patients were included if they received 300 mg of i.v. labetalol within a 24-hour period. Vital signs, adverse events and cumulative medication doses were obtained for up to 24 hours while on labetalol. Adverse events were defined as any systolic blood pressure measurement less than 90 mm Hg or heart rate less than 60 beats per minute. RESULTS: We analyzed the records of 188 patients who received i.v. labetalol at higher than the maximum recommended dose of 300 mg. The mean dose of labetalol was 996 mg (range 300 to 4465 mg). The cumulative labetalol dose was not associated with adverse safety outcomes (p = 0.428), although eighty-one patients (44.3%) experienced adverse events. Sixty-six patients (36.5%) developed bradycardia and 34 patients (18.6%) developed hypotension. Only five patients (2.7%) required a rescue agent for refractory adverse events. CONCLUSION: A retrospective review of high-dose i.v. labetalol hydrochloride with doses greater than 300 mg in 24 hours observed a high rate of bradycardia and hypotension, but the study found that these events rarely caused clinically significant hemodynamic compromise and was not statistically associated with adverse events.


Subject(s)
Antihypertensive Agents/administration & dosage , Blood Pressure/drug effects , Heart Rate/drug effects , Hypertension/drug therapy , Labetalol/administration & dosage , Administration, Intravenous , Adult , Aged , Antihypertensive Agents/adverse effects , Blood Pressure/physiology , Bradycardia/chemically induced , Bradycardia/diagnosis , Dose-Response Relationship, Drug , Female , Heart Rate/physiology , Humans , Hypertension/diagnosis , Hypotension/chemically induced , Hypotension/diagnosis , Labetalol/adverse effects , Male , Middle Aged , Retrospective Studies
4.
BMJ Case Rep ; 20172017 Jun 22.
Article in English | MEDLINE | ID: mdl-28645925

ABSTRACT

Strangulated gastric prolapse through a percutaneous endoscopic gastrostomy tract is a rare and potentially life-threatening complication that requires surgical intervention. We describe a case of a 74-year-old woman who was debilitated and ventilator-dependent and who presented with acute gastric prolapse with resultant ischaemic necrosis. The patient underwent an emergent exploratory laparotomy, partial gastrectomy, repair of gastrostomy defect and placement of a gastrojejunostomy feeding tube remote to the previous location. Literature on gastric prolapse in adult patients is sparse, and therefore treatment is not standardised. In this patient with strangulated tissue, the principles of management included the assessment of gastric mucosa viability, resection of ischaemic tissue and closure of the gastrostomy defect.


Subject(s)
Enteral Nutrition/adverse effects , Gastrectomy , Gastric Mucosa , Gastrostomy/adverse effects , Intubation, Gastrointestinal/adverse effects , Visceral Prolapse/etiology , Aged , Equipment Failure , Female , Humans , Ischemia/etiology , Jejunostomy , Necrosis/etiology , Surgical Stomas , Visceral Prolapse/pathology , Visceral Prolapse/surgery
6.
J Crit Care ; 28(6): 1111.e1-5, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24011754

ABSTRACT

PURPOSE: Peripheral tissue oxygen saturation (Sto2) has shown promise as an early indicator of tissue hypoperfusion and as a risk stratification tool in various forms of shock. The purpose of this study was to determine if Sto2 would predict admission to an intensive (ICU) or progressive care unit in patients with early signs of sepsis. METHODS: In this prospective observational study, a rapid response team measured Sto2 levels in patients screening positive for sepsis. Using a logistic regression model, the value of Sto2 as a predictor for ICU admission within 72 hours of the initial assessment was determined. RESULTS: The 31 (47%) of 66 patients who required ICU admission within 72 hours of evaluation had a significantly lower Sto2 value (median, 78% vs 81%; P = .05). All patients with Sto2 less than 70% required ICU admission. A 1-point increase in Sto2 was associated with a 7% decrease in the odds of requiring ICU admission, and the area under the curve for Sto2 was 0.64 (0.51-0.77, P = .01). CONCLUSIONS: Low Sto2 levels in patients screening positive for sepsis are associated with an increased risk of ICU admission, but their reliability as a predictor is rather low. An Sto2 below 70% might be an interesting cutoff value for further study.


Subject(s)
Intensive Care Units/statistics & numerical data , Oxygen/metabolism , Risk Assessment/methods , Sepsis/metabolism , Sepsis/physiopathology , Aged , Algorithms , Disease Progression , Female , Hospital Rapid Response Team , Humans , Male , Middle Aged , Monitoring, Physiologic , Predictive Value of Tests , Prospective Studies
7.
J Trauma Acute Care Surg ; 73(3): 612-7, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22929492

ABSTRACT

PURPOSE: We think that general surgeons are underprepared to respond to mass casualty disasters. Preparedness education is required in emergency medicine (EM) residencies, yet such requirements are not mandated for general surgery (GS) training programs. We hypothesize that EM residents receive more training, consider themselves better prepared, and are more comfortable responding to disaster events than are GS residents. METHODS: From February to May 2009, the Eastern Association for the Surgery of Trauma-Committee on Disaster Preparedness conducted a Web-based survey cataloging training and preparedness levels in both GS and EM residents. Approximately 3000 surveys were sent. Chi-squared, logistic regression, and basic statistical analyses were performed with SAS. RESULTS: Eight hindered forty-eight responses were obtained, GS residents represented 60.6% of respondents with 39% EM residents, and four residents did not respond with their specialty (0.4%). We found significant disparities in formal training, perceived preparedness, and comfort levels between resident groups. Experience in real-life disaster response had a significant positive effect on comfort level in all injury categories in both groups (odds ratio, 1.3-4.3, p < 0.005). CONCLUSION: This survey confirms that EM residents have more disaster-related training than GS residents. The data suggest that for both groups, comfort and confidence in treating victims were not associated with training but seemed related to previous real-life disaster experience. Given wide variations in the relationship between training and comfort levels and the constraints imposed by the 80-hour workweek, it is critical that we identify and implement the most effective means of training for all residents.


Subject(s)
Clinical Competence , Disaster Planning/organization & administration , Emergency Medicine/education , General Surgery/education , Internet , Internship and Residency/organization & administration , Adult , Chi-Square Distribution , Confidence Intervals , Cross-Sectional Studies , Curriculum , Disasters , Education, Medical, Graduate/methods , Female , Humans , Logistic Models , Male , Program Evaluation , Societies, Medical , Surveys and Questionnaires , United States
8.
Am J Surg ; 201(3): 320-3; discussion 323, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21367371

ABSTRACT

BACKGROUND: Our institution initiated the implementation of the Surviving Sepsis Campaign guidelines in 2006. We hypothesize that the addition of a surgical intensivist improved results more than the implementation of the guidelines alone. METHODS: We collected data on 273 patients who were admitted to the surgical intensive care unit for sepsis. The groups were divided into pre-bundle, n = 19; bundle, n = 186; and bundle-plus, n = 68, to denote the method by which the patients were treated for sepsis. RESULTS: There was no difference in age or sex between groups. There was a statistically significant decrease in length of stay (LOS) between the 3 groups, and in mortality between the bundle and bundle-plus treatment groups (P < .01). In addition, there was an average cost savings between each group. CONCLUSIONS: Implementation of evidence-based guidelines decreased LOS and decreased cost in our surgical intensive care unit. By adding the expertise of a surgical intensivist, we reduced LOS, cost, and relative risk of death even further than using the guidelines alone.


Subject(s)
Critical Care/methods , Critical Care/standards , Patient Care Team/organization & administration , Sepsis/therapy , Adult , Aged , Aged, 80 and over , Evidence-Based Medicine , Health Care Costs , Humans , Leadership , Middle Aged , Patient Care Team/trends , Practice Guidelines as Topic , Retrospective Studies , Sepsis/economics , Sepsis/mortality , Shock, Septic/therapy , Survival Analysis , Time Factors
9.
J Intensive Care Med ; 26(5): 304-13, 2011.
Article in English | MEDLINE | ID: mdl-21220270

ABSTRACT

UNLABELLED: While clinicians' management of severe sepsis and septic shock has been positively influenced by a number of clinical research studies in the last decade, challenges remain regarding early hemodynamic optimization as envisioned in the Surviving Sepsis Campaign's (SSC) resuscitation bundle (RB). We examined the impact of a hospital-wide continuous quality improvement (CQI) initiative on patients presenting with severe sepsis and septic shock, and the impact of the sepsis RB on patient outcomes when completed beyond the 6-hour recommendation period. The study was an 18-month, prospective cohort study enrolling patients who met the definition of severe sepsis or septic shock. Compliance with the hemodynamic components of the sepsis RB was defined as achieving goal mean arterial pressure (MAP) ≥ 65 mm Hg, central venous pressure (CVP) ≥ 8 mm Hg, and central venous oxygen saturation (ScvO2) ≥ 70%. Compliance was assessed at 6 hours and 18 hours after diagnosis of severe sepsis or septic shock. In all, 498 patients with severe sepsis and/or septic shock were evaluated to determine the upper limit of the range of hours that compliance with the RB would still improve outcomes. Using 18 hours as a marker, Compliers at 18 hrs and Non-Compliers at 18 hrs were compared. There were 202 patients who had the RB completed in less than or equal to 18 hours. There were 296 patients who did not complete the RB at 18 hours. The Compliers at 18 hrs had a significant 10.2% lower hospital mortality 37.1% (22% relative reduction) compared to the Non-Compliers at 18 hrs hospital mortality of 47.3% (P < .03). When the two groups were adjusted for differences in baseline illness severity, the Compliers at 18 hrs had a greater reduction in predicted mortality of 26.8% versus 9.4%, P < 0.01. CONCLUSIONS: Initiating the sepsis RB for patients with severe sepsis and/or septic shock decreased mortality. A CQI initiative that monitored the implementation in real-time allowed for improvement in compliance and efficacy of the bundle on outcomes. Multiple studies have shown that compliance to the RB within 6 hours lowers hospital mortality. This study uniquely shows that when bundle completion is extended to 18 hours, the mortality reduction remains significant.


Subject(s)
Fluid Therapy/methods , Resuscitation/methods , Sepsis/therapy , Shock, Septic/therapy , Vasoconstrictor Agents/therapeutic use , APACHE , Acidosis, Lactic/etiology , Acidosis, Lactic/therapy , Aged, 80 and over , Cohort Studies , Female , Guideline Adherence/standards , Guideline Adherence/statistics & numerical data , Hospital Mortality , Humans , Hypotension/etiology , Hypotension/therapy , Male , Middle Aged , Outcome Assessment, Health Care , Oximetry , Prospective Studies , Quality Improvement , Risk Assessment , Sepsis/complications , Sepsis/diagnosis , Sepsis/mortality , Shock, Septic/diagnosis , Shock, Septic/etiology , Shock, Septic/mortality , Time-to-Treatment , United States/epidemiology
10.
J Trauma ; 68(2): 289-93, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20154539

ABSTRACT

BACKGROUND: Youth violence is a significant problem in the United States with high recidivism rates. Considering these high recidivism rates in youths after an initial injury, we hypothesized a hospital-based violence prevention program aimed at increasing awareness, empowering positive conflict resolution, and promoting future vocational goals would benefit at-risk youth before they are injured. METHODS: A feasibility study was completed on our Violence and Injury Prevention (VIP) tour program at our urban Level I trauma center. Participants were at-risk youth, aged 11 years to 17 years. Anonymous data were collected using an Audience Response System. RESULTS: One hundred eighty-five students participated from January 2007 to August 2008. Sixty-three percent were 6th to 8th graders, 70% were boys. Seventy-nine percent stated that they knew someone who had been injured or killed because of violence, with significantly more boys than girls (p = 0.05). More boys than girls stated that they have access to a gun (p < 0.05). Almost 60% of the participants stated that they had engaged in violence within the past 6 months, with no difference by gender (p = 0.085). Of the respondents, 84.2% reported an increase in their awareness on the consequences of violence. This was more significant for girls than boys (p < 0.05). Of the participants, 86.3% reported increased understanding of hospital care for a trauma patient. Participants stated that they would recommend VIP to others. CONCLUSION: VIP educated local urban youth about violence and increased their awareness of the injuries resulting from violence. In addition, at-risk youths were exposed to career opportunities in health care.


Subject(s)
Power, Psychological , Violence/prevention & control , Adolescent , Child , Feasibility Studies , Female , Hospitals , Humans , Imagery, Psychotherapy , Male , Self Efficacy , Urban Population , Violence/psychology
11.
Jt Comm J Qual Patient Saf ; 36(7): 291-300, 2010 Jul.
Article in English | MEDLINE | ID: mdl-21226382

ABSTRACT

BACKGROUND: In 2002, tight glycemic control (TGC) was mandated at Henry Ford Hospital (Detroit) to reduce surgical site infections (SSIs). THE FIVE STEPS FOR IMPROVEMENT: The TGC initiative was developed in terms of the five primary steps of the Institute for Healthcare Improvement (IHI) framework for leadership for improvement to drive practice change and maintain continuous improvement. In terms of Steps 1-3 (set direction, establish the foundation, and build will), in April 2002 the chief executive officer of the Henry Ford Hospital (Detroit) announced a hospitalwide initiative to reduce SSIs. For steps 4 and 5 (generate ideas and execute change), the 40-bed surgical intensive care unit (SICU) was designated the practice-change setting. TGC protocols were implemented in cardiothoracic patients, followed by all SICU patients, with target glucose ranges moving from the initial < 150 mg/dL to 80-110 mg/dL. Results showed decreases in SSIs and mortality. The project's success led initiation of hospitalwide TGC in the next two years. RESPONDING TO A CHANGING EVIDENCE BASE: In 2009, as studies began to show that the recommended glucose target of 80-110 mg/dL was not associated with clinical improvement in ICU patients and perhaps may cause harm (increased mortality), the target ranges were modified. LESSONS LEARNED: Barriers to adoption of new practice change must be integrated into the planning process. Leadership champions are required across multiple levels of the organization to drive change to the bedside for effective and lasting improvement. CONCLUSIONS: A universal TGC protocol continues to be used throughout the hospital, with modifications and next-generation improvements occurring as evidence arises.


Subject(s)
Blood Glucose , Intensive Care Units/organization & administration , Postoperative Care/methods , Quality Assurance, Health Care/organization & administration , Clinical Protocols , Humans , Leadership , Patient Care Team/organization & administration , Process Assessment, Health Care/organization & administration
12.
Am J Surg ; 197(3): 279-83, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19245901

ABSTRACT

BACKGROUND: In 2000, we implemented an evidence-based guideline in the surgical intensive care unit (SICU) using a transfusion threshold of hemoglobin <8 g/dL. We hypothesized that continual education on the transfusion protocol would decrease transfusions. METHODS: We analyzed 2-month samples of admissions in even-numbered years from 1998 to 2006. Any infusion of packed red blood cells (PRBCs) was included. RESULTS: We analyzed data from 2,138 patients resulting in 5,130 transfusions. Thirty-six patients received >20 U of blood. The only difference between groups occurred in 2006 when renal failure increased. Transfusions decreased from 3.2 +/- 0.34 (SE) to 1.7 +/- 0.2. The number of patients who received blood also decreased. Mortality and length of stay (LOS) were not different among the groups. Every unit of blood transfused increased the mortality risk by 14%. CONCLUSIONS: Implementation of an evidence-based transfusion guideline reduced the number of infused units and patients transfused without an increase in mortality.


Subject(s)
Erythrocyte Transfusion , Professional Practice , Adult , Aged , Anemia/therapy , Critical Care , Erythrocyte Transfusion/mortality , Female , Hemoglobins , Humans , Male , Middle Aged , Practice Guidelines as Topic , Retrospective Studies
13.
Am J Surg ; 196(3): 379-83, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18513693

ABSTRACT

BACKGROUND: Universal agreement on criteria for acute renal failure (ARF) is lacking. The purpose of the current study was to determine which of 6 definitions for ARF best predicted clinical outcomes in postoperative cardiothoracic surgery (CTS) patients. METHODS: Criteria for ARF were retrospectively applied to 1,085 CTS patients. General linear models analyzed length of stay (LOS) and ventilator days with logistic regression for mortality. RESULTS: Thirty-seven percent of patients met at least 1 of 6 definitions of ARF. For each 1-mg/dL increase from the initial creatinine, LOS increased by 6.96 days, ventilator days increased by 3.58 days, and mortality increased by 2.23 times (P < .0001). CONCLUSIONS: One definition that best predicted ARF was not found. ARF was a significant independent predictor of increased mortality, LOS, and ventilator days. Even small increases in creatinine correlate with clinically significant worsening of expected outcomes.


Subject(s)
Acute Kidney Injury/diagnosis , Cardiopulmonary Bypass/adverse effects , Acute Kidney Injury/blood , Acute Kidney Injury/epidemiology , Acute Kidney Injury/etiology , Adolescent , Adult , Aged , Aged, 80 and over , Cardiopulmonary Bypass/statistics & numerical data , Creatinine/blood , Female , Humans , Incidence , Length of Stay , Linear Models , Male , Middle Aged , Morbidity , Mortality , Prognosis , Respiration, Artificial , Retrospective Studies
14.
Am J Surg ; 195(3): 304-6; discussion 306-7, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18206848

ABSTRACT

BACKGROUND: Hyperbilirubinemia in intensive care unit (ICU) patients is common. We hypothesized that hyperbilirubinemia in the surgical ICU predisposes patients to infection. METHODS: Patients with bilirubin < or = 3 mg/dL were compared to patients with bilirubin > 3 mg/dL. We then compared the low bilirubin patients to high bilirubin patients who developed infection after their hyperbilirubinemia. RESULTS: There were 1,620 infections in 5,712 patients with low bilirubin (28%), compared with 284 in 409 patients in the high bilirubin group (69%, P < .001). After removing the patients in whom hyperbilirubinemia developed after infection, we found infection in 156 of 281 remaining patients (56%, P < .001). This group had a 3-fold increased risk of infection compared with low bilirubin (odds ratio [OR] 3.17, 95% confidence interval [CI] 2.48-4.03, P < .001). CONCLUSIONS: There is an increased susceptibility to infection among jaundiced surgical ICU (SICU) patients that persists even when sepsis-related hyperbilirubinemia patients are excluded.


Subject(s)
Critical Care/statistics & numerical data , Hyperbilirubinemia/complications , Infections/etiology , Adolescent , Adult , Aged , Aged, 80 and over , Disease Susceptibility , Female , Humans , Male , Middle Aged , Retrospective Studies , Risk Factors
15.
Am Surg ; 73(8): 743-6; discussion 746-7, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17879677

ABSTRACT

The negative impact of mild to moderate renal dysfunction on patient outcome is often under-estimated. Any amount of renal dysfunction is deleterious in the surgical intensive care unit (SICU). We evaluated all surgery patients admitted to our SICU. We identified two groups of patients: no renal failure and acute renal failure. A total of 5152 patients were included in this study. There were 1259 patients in the acute renal failure group. The average number of ventilator days increased by 2.2 for every increase of creatinine by 1.0. Patients who required dialysis stayed an average of 11 days longer than patients who did not have any renal failure. For every increase of creatinine by 1.0, average cost increased by $23,048. Only 7 per cent of the patients with acute renal failure required dialysis (n = 85). The odds ratio for mortality compared with those patients without renal failure was 7.06 (confidence interval, 3.91-12.76) regardless of the definition of renal failure. This study demonstrates that even mild to moderate renal failure increases mortality. Moreover, we demonstrated that even a mild decline in renal function increases length of stay, ventilator days, and cost in patients in the SICU. Aggressive vigilance in the prevention of any loss of renal function is warranted in the SICU.


Subject(s)
Hospital Mortality/trends , Intensive Care Units , Postoperative Complications , Renal Insufficiency , Surgical Procedures, Operative/adverse effects , Adolescent , Adult , Aged , Aged, 80 and over , Confidence Intervals , Creatinine/blood , Female , Follow-Up Studies , Humans , Male , Michigan/epidemiology , Middle Aged , Odds Ratio , Prognosis , Renal Insufficiency/etiology , Renal Insufficiency/metabolism , Renal Insufficiency/mortality , Retrospective Studies , Risk Factors
16.
J Trauma ; 62(6): 1362-4, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17563649

ABSTRACT

BACKGROUND: Acute renal failure (ARF) is a devastating complication in critically ill patients. There is a paucity of data that describes the impact of ARF on the outcome of trauma patients admitted to the intensive care unit. METHODS: We studied trauma patients admitted to the surgical intensive care unit to determine the effect of increases in serum creatinine on the number of ventilator days, length of stay, mortality, and cost. We used the administrative database of the hospital and the trauma registry. Renal failure (RF) was defined as one or more of the following: creatinine >1.5 mg/dL, increase in creatinine of >50%, or increase of creatinine by 0.5 mg/dL. RESULTS: We obtained data on 1,033 patients. Two hundred and forty-six (23.8%) patients met at least one criterion for RF. Only 25 of these patients had one or more episodes of renal replacement therapy. The RF group had mortality of 24.4% compared with 2.3% in the no renal failure group (p < 0.0001). For each 1 mg/dL increase from the initial creatinine, length of stay increased by 2.21 days, ventilator days increased by 1.09 days, and the mortality risk increased by 1.83 times (CI, 1.47-2.29; p < 0.0001). For any diagnosis of renal dysfunction, the average cost increase was $3,088.00 and increased mortality risk was 7.19 times (CI, 4.11-12.58). CONCLUSION: Vigilance in preventing creatinine increases and ameliorating or removing potential causes should occur as soon as creatinine begins to rise to avoid worsening renal function, to reduce cost, and to improve patient outcome.


Subject(s)
Wounds and Injuries/complications , Acute Kidney Injury/blood , Acute Kidney Injury/economics , Acute Kidney Injury/etiology , Adolescent , Adult , Aged , Aged, 80 and over , Biomarkers/blood , Creatinine/blood , Female , Humans , Male , Middle Aged , Treatment Outcome , Wounds and Injuries/economics
17.
Surgery ; 138(4): 742-7; discussion 747-8, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16269304

ABSTRACT

BACKGROUND: Nonoperative management (NOM) of blunt liver injuries (BLIs) is common, but little data exist on the management of complications related to NOM. Furthermore, bile leaks are emerging as frequent complications of NOM. The goal of this study was to determine which BLI patients are at greatest risk for bile leaks and how to manage this complication. METHODS: Patients treated with NOM, including angiographic embolization (AE) and observation, were compared with those undergoing operation (OR). Mortality, hospital length of stay, liver-related complications, and severity of liver injury were compared among the groups. RESULTS: Two hundred eighty-one patients sustained a BLI from 1997 through 2004. The Injury Severity Score and age of the groups were similar. The mortality rate of the OR patients was higher (P = .02). All bile leaks occurred in patients with a liver Abbreviated Injury Score (AIS) of > or = 4. For survivors of more than 4 days, 71% of OR, 50% of AE, and 17% of observed patients developed bile leaks. For the OR and AE groups, HIDA scanning detected all leaks, leading to earlier drainage procedures. Detection of a bile leak in NOM patients before 5 days of hospitalization led to shorter HLOS, P = .02. No patient with a negative HIDA scan developed a subsequent bile leak. CONCLUSIONS: NOM of BLIs is associated with lower mortality, but significant complications. Bile leaks are more common in patients with higher liver AIS, and in this study presented in only those with liver AIS > or = 4. HIDA scanning successfully diagnosed all patients with bile leaks and led to less invasive drainage procedures over time and shorter HLOS.


Subject(s)
Bile/metabolism , Biliary Tract Diseases/diagnosis , Biliary Tract Diseases/therapy , Liver/injuries , Wounds, Nonpenetrating/complications , Adult , Biliary Tract Diseases/etiology , Biliary Tract Diseases/metabolism , Embolization, Therapeutic , Female , Humans , Imino Acids , Injury Severity Score , Length of Stay , Male , Middle Aged , Mortality , Surgical Procedures, Operative , Wounds, Nonpenetrating/pathology , Wounds, Nonpenetrating/physiopathology
18.
J Burn Care Rehabil ; 26(2): 151-61, 2005.
Article in English | MEDLINE | ID: mdl-15756117

ABSTRACT

Thermal injury historically constitutes approximately 5% to 20% of conventional warfare casualties. This article reviews medical planning for burn care during war in Iraq and experience with burns during the war at the US Army Burn Center; aboard the USNS Comfort hospital ship; and at Combat Support Hospitals in Iraq and in Afghanistan. Two burn surgeons were deployed to the military hospital in Landstuhl, Germany, and to the Gulf Region to assist with triage and patient care. During March 2003 to May 2004, 109 burn casualties from the war have been hospitalized at the US Army Burn Center in San Antonio, Texas, and US Army Burn Flight Teams have moved 51 critically ill burn casualties to the Burn Center. Ten Iraqi burn patients underwent surgery and were hospitalized for up to 1 month aboard the Comfort, including six with massive wounds. Eighty-six burn casualties were hospitalized at the 28th Combat Support Hospital for up to 53 days. This experience highlights the importance of anticipating the burn care needs of both combatants and the local civilian population during war.


Subject(s)
Burn Units/organization & administration , Burns/therapy , Disaster Planning/organization & administration , Hospitals, Military/organization & administration , Military Medicine/organization & administration , Warfare , Burn Units/statistics & numerical data , Burns/etiology , Hospitals, Military/statistics & numerical data , Hospitals, Packaged/organization & administration , Hospitals, Packaged/statistics & numerical data , Humans , Iraq , Military Medicine/methods , Organizational Case Studies , Patient Care Team , Patient Transfer , Ships , Time Factors , Triage , United States
19.
J Burn Care Rehabil ; 26(1): 57-61, 2005.
Article in English | MEDLINE | ID: mdl-15640736

ABSTRACT

Ventilator-associated pneumonia (VAP) remains a major cause of morbidity and mortality for patients with burns. In nonburn populations, bronchoalveolar lavage (BAL) excludes other pathology such as systemic inflammatory response syndrome. We hypothesized that BAL would decrease our false-positive VAP rate. All ventilated patients with burn injury who were admitted to our institution from July 2000 through June 2003 were included. After June 2001, BAL was used to make the diagnosis of VAP, with > or =10(4) organisms considered a positive result. Fifty patients met criteria for VAP, 21 in the pre-BAL period and 29 in the BAL period. Six patients (21%) in the BAL group had quantitative cultures <10(4) and were not treated. The outcomes for these patients were not different than those treated for VAP. There were no differences in age, TBSA size, antibiotic use, or ventilator days for the pre-BAL or BAL groups, although the pneumonia rate was lower for the BAL time period. The use of BAL eliminated the unnecessary antibiotic treatment of 21% of patients in the BAL time period and was associated with a lower rate of VAP.


Subject(s)
Bronchoalveolar Lavage , Burns/complications , Pneumonia/diagnosis , Pneumonia/etiology , Respiration, Artificial/adverse effects , Adolescent , Adult , Child , Diagnosis, Differential , False Positive Reactions , Female , Humans , Male , Middle Aged , Sensitivity and Specificity
20.
J Trauma ; 56(5): 1022-6; discussion 1026-8, 2004 May.
Article in English | MEDLINE | ID: mdl-15179241

ABSTRACT

BACKGROUND: We hypothesize that data collected from computed tomographic (CT) scans obtained for workup of chest or abdominal injuries provide data that are sufficient to screen for spinal fractures and will decrease the cost and time of spine evaluation after trauma. METHODS: We reviewed plain radiographs from 55 selected trauma patients who also underwent CT scanning of the chest, abdomen, and pelvis. We also timed the radiologic workup of 50 consecutive trauma patients to determine the time required to complete radiographic spine evaluation. RESULTS: Forty-seven patients had thoracolumbar fractures. Thirteen patients were found to have 33 thoracolumbar spine fractures identified by CT scan but not plain radiography. Fractures were found on initial trauma CT scans of the chest, abdomen, and pelvis obtained to evaluate for visceral injuries. No injuries seen on plain film were missed on CT scan. CONCLUSION: We recommend using the data acquired from CT scans to evaluate the spine, supplementing them with additional studies only when needed for further clarification.


Subject(s)
Lumbar Vertebrae/injuries , Spinal Fractures/diagnostic imaging , Thoracic Vertebrae/injuries , Tomography, Spiral Computed , Accidental Falls/statistics & numerical data , Accidents, Traffic , Adolescent , Adult , Aged , Cost Savings , Cost-Benefit Analysis , Female , Humans , Male , Michigan/epidemiology , Middle Aged , Motorcycles , Patient Selection , Prospective Studies , Retrospective Studies , Spinal Fractures/economics , Spinal Fractures/epidemiology , Spinal Fractures/etiology , Time Factors , Time and Motion Studies , Tomography, Spiral Computed/economics , Tomography, Spiral Computed/instrumentation , Tomography, Spiral Computed/standards , Trauma Centers
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