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Dive into the research topics where James W. Suliburk is active.

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Featured researches published by James W. Suliburk.


Journal of Trauma-injury Infection and Critical Care | 2003

Vacuum-assisted wound closure achieves early fascial closure of open abdomens after severe trauma.

James W. Suliburk; Drue N. Ware; Zsolt J. Balogh; Bruce A. McKinley; Christine S. Cocanour; Rosemary A. Kozar; Frederick A. Moore

BACKGROUND This study reviews the efficacy of vacuum-assisted wound closure (VAWC) to obtain primary fascial closure of open abdomens after severe trauma. METHODS The study population included shock resuscitation patients who had open abdomens treated with VAWC. The VAWC dressing was changed at 2- to 3-day intervals and downsized as fascial closure was completed with interrupted suture. The Trauma Research Database and the medical records were reviewed for pertinent data. RESULTS Over 26 months, 35 patients with open abdomens were managed by VAWC. Six died early, leaving 29 patients who were discharged. Of these, 25 (86%) were successfully closed using VAWC at a mean of 7 +/- 1 days (range, 3-18 days). Of the four patients that failed VAWC, two developed fistulas. No patients developed evisceration, intra-abdominal abscess, or wound infection. CONCLUSION VAWC achieved early fascial closure in a high percentage of open abdomens, with an acceptable rate of complications.


Journal of Trauma-injury Infection and Critical Care | 2013

TEG-guided resuscitation is superior to standardized MTP resuscitation in massively transfused penetrating trauma patients.

Nicole M. Tapia; Alex L. Chang; Michael A. Norman; Francis J. Welsh; Bradford G. Scott; Matthew J. Wall; Kenneth L. Mattox; James W. Suliburk

BACKGROUND For nearly a decade, our center performed thromboelastograms (TEGs) to analyze coagulation profiles, allowing rapid data-driven blood component therapy. After consensus recommendations for massive transfusion protocols (MTPs), we implemented an MTP in October 2009 with 1:1:1 ratio of blood (red blood cells [RBC]), plasma (fresh-frozen plasma [FFP]), and platelets. We hypothesized that TEG-directed resuscitation is equivalent to MTP resuscitation. METHODS All patients receiving 6 units (U) or more of RBC in the first 24 hours for 21 months before and after MTP initiation in an urban Level I trauma center were examined. Demographics, mechanism of injury (MOI), Injury Severity Score (ISS), 24-hour volume of RBC, FFP, platelets, crystalloid, and 30-day mortality were compared, excluding patients with traumatic brain injuries. Variables were analyzed using Student’s t-test and &khgr;2 or Fisher’s exact test. RESULTS For the preMTP group, there were 165 patients. In the MTP group, there were 124 patients. There were no significant differences in ISS, age, or sex. PreMTP patients with 6U or more RBC had significantly more penetrating MOI (p = 0.017), whereas preMTP patients with 10U or more RBC had similar MOIs. All patients received less crystalloid after MTP adoption (p < 0.001). There was no difference in volume of blood products or mortality in patients receiving 6U or more RBC. Blunt trauma MTP patients who received 10U or more RBC received more FFP (p = 0.02), with no change in mortality. Penetrating trauma patients who received 10U or more RBC received a similar volume of FFP; however, mortality increased from 54.1% for MTP versus 33.3% preMTP (p = 0.04). CONCLUSION TEG-directed resuscitation is equivalent to standardized MTP for patients receiving 6U or more RBC and for blunt MOI patients receiving 10U or more RBC. MTP therapy worsened mortality in penetrating MOI patients receiving 10U or more RBC, indicating a continued need for TEG-directed therapy. A 1:1:1 strategy may not be adequate in all patients. LEVEL OF EVIDENCE Therapeutic study, level IV.


Journal of The American College of Surgeons | 2009

Early Cytokine Production Risk Stratifies Trauma Patients for Multiple Organ Failure

Kenneth M. Jastrow; Ernest A. Gonzalez; Mary F. McGuire; James W. Suliburk; Rosemary A. Kozar; Sriram Iyengar; Deborah A. Motschall; Bruce A. McKinley; Frederick A. Moore; David W. Mercer

BACKGROUND Shock is a prime inciting event for postinjury multiple organ failure (MOF), believed to induce a state of injurious systemic inflammation. In animal models of hemorrhagic shock, early (< 24 hours) changes in cytokine production are an index of the systemic inflammatory response syndrome. However, their predictive value in trauma patients remains to be fully elucidated. STUDY DESIGN In a prospective observational pilot study of > 1 year at an urban Level I trauma center, serial (every 4 hours) serum cytokine levels were determined during a 24-hour period using multiplex suspension immunoassay in patients with major torso trauma (excluding severe brain injury) who met criteria for standardized shock resuscitation. Temporal cytokine expression was assessed during shock resuscitation in severe trauma patients to predict risk for MOF. MOF was assessed with the Denver score. RESULTS Of 48 study patients (mean age 39 +/- 3 years, 67% men, 88% blunt mechanism, mean Injury Severity Score 25 +/- 2), MOF developed in 11 (23%). MOF patients had a considerably higher mortality (64% versus 3%) and fewer ICU-free days (3.5 +/- 2 versus 17.8 +/- 1.3 days) compared with non-MOF patients. Traditional predictors of MOF, including age (45 +/- 7 versus 38 +/- 3 years; p=0.21), Injury Severity Score (26 +/- 3 versus 25 +/- 2; p=0.67), admission hemoglobin (11.4 +/- 0.9 versus 12.1 +/- 0.5 g/dL; p=0.22), international normalized ratio (1.6 +/- 0.2 versus 1.4 +/- 0.06; p=0.17), and base deficit (9.0 +/- 2 versus 7.1 +/- 0.8; p=0.19), were not significantly different between MOF and non-MOF patients. Statistical analysis identified six candidate predictors of MOF: inducible protein 10, macrophage inflammatory protein-1beta, interleukin-10, interleukin-6, interleukin-1Ra, and eotaxin. CONCLUSIONS These data provide insight into cytokine expression during traumatic shock that can enable earlier identification of patients at risk for development of MOF.


BMC Emergency Medicine | 2012

A multicenter, randomized controlled trial of immediate total-body CT scanning in trauma patients (REACT-2)

Joanne C. Sierink; Teun Peter Saltzherr; Ludo F. M. Beenen; Jan S. K. Luitse; Markus W. Hollmann; Johannes B. Reitsma; Michael Edwards; Joachim Hohmann; Benn J. A. Beuker; Peter Patka; James W. Suliburk; Marcel G. W. Dijkgraaf; J. Carel Goslings

BackgroundComputed tomography (CT) scanning has become essential in the early diagnostic phase of trauma care because of its high diagnostic accuracy. The introduction of multi-slice CT scanners and infrastructural improvements made total-body CT scanning technically feasible and its usage is currently becoming common practice in several trauma centers. However, literature provides limited evidence whether immediate total-body CT leads to better clinical outcome then conventional radiographic imaging supplemented with selective CT scanning in trauma patients. The aim of the REACT-2 trial is to determine the value of immediate total-body CT scanning in trauma patients.Methods/designThe REACT-2 trial is an international, multicenter randomized clinical trial. All participating trauma centers have a multi-slice CT scanner located in the trauma room or at the Emergency Department (ED). All adult, non-pregnant, severely injured trauma patients according to predefined criteria will be included. Patients in whom direct scanning will hamper necessary cardiopulmonary resuscitation or who require an immediate operation because of imminent death (both as judged by the trauma team leader) are excluded. Randomization will be computer assisted. The intervention group will receive a contrast-enhanced total-body CT scan (head to pelvis) during the primary survey. The control group will be evaluated according to local conventional trauma imaging protocols (based on ATLS guidelines) supplemented with selective CT scanning. Primary outcome will be in-hospital mortality. Secondary outcomes are differences in mortality and morbidity during the first year post trauma, several trauma work-up time intervals, radiation exposure, general health and quality of life at 6 and 12 months post trauma and cost-effectiveness.DiscussionThe REACT-2 trial is a multicenter randomized clinical trial that will provide evidence on the value of immediate total-body CT scanning during the primary survey of severely injured trauma patients. If immediate total-body CT scanning is found to be the best imaging strategy in severely injured trauma patients it could replace conventional imaging supplemented with CT in this specific group.Trial RegistrationClinicalTrials.gov: (NCT01523626).


Regional Anesthesia and Pain Medicine | 2012

Bilateral Transversus Abdominis Plane Block Does Not Decrease Postoperative Pain After Laparoscopic Cholecystectomy When Compared With Local Anesthetic Infiltration of Trocar Insertion Sites

Jaime Ortiz; James W. Suliburk; Kenneth Wu; Neil S. Bailard; Chawla Mason; Charles G. Minard; Raja R. Palvadi

Background and Objectives Transversus abdominis plane (TAP) block has been shown to reduce pain and analgesic requirements after abdominal surgery. Our hypothesis was that bilateral TAP blocks decrease pain after laparoscopic cholecystectomy when compared with local anesthetic infiltration of trocar insertion sites. Methods Eighty patients undergoing laparoscopic cholecystectomy were randomized to receive either bilateral TAP blocks or local anesthetic infiltration of trocar insertion sites with ropivacaine 0.5%. Postoperative pain scores and analgesic use for the first 24 hrs were recorded. Results Eighty patients were enrolled in the study. After exclusions, data were analyzed on 39 patients in group T (bilateral TAP block) and 35 patients in group I (infiltration). There was no statistically significant difference in pain scores on the numeric analog scale (0–10) between the groups at 4 hrs after surgery (P = 0.18) or during the 24 hrs after surgery (P = 0.23). The time interval from anesthesia start to surgery start was greater in group T than group I (48 vs 35 mins, P < 0.001). There was no significant difference found in analgesic use during the first 24 hrs after surgery. Conclusions Bilateral ultrasound-guided TAP block is equivalent to local anesthetic infiltration of trocar insertion sites for overall postoperative pain in a heterogeneous group of patients undergoing laparoscopic cholecystectomy.


Annals of Surgery | 2008

Training future surgical scientists: realities and recommendations.

James W. Suliburk; Lillian S. Kao; Rosemary A. Kozar; David W. Mercer

Objective:To examine factors influencing surgical research and assess the current state of training future surgical scientists. Summary Background Data:The number of surgeons actively engaged in research seems to be decreasing. Training future surgical scientists to increase these numbers depends on a variety of factors that are constantly changing. Current trends at the National Institutes of Health (NIH) and changes in graduate medical education make the training of the next generation of surgical scientists more challenging than ever. Methods:Recent literature in surgical education, surgical research, and funding patterns at the NIH were reviewed. Results:Quantitative and qualitative deficiencies exist in surgical research. Although an increasing number of students are becoming interested in surgery, the burden of debt from medical school may preclude them from pursuing research during or after residency. Research training is complicated by the fact that no formal curriculum exists for training in research and oversight is lacking. Junior faculty face increased demands for clinical revenue, which decreases time for research. In addition, surgeons are less successful at obtaining NIH funding when compared with nonsurgeons and seem to be at a disadvantage. Conclusions:Development of the next generation of surgical scientists begins by attracting the best students into surgery and by providing a structured research curriculum with appropriate oversight. Senior surgical faculty need to become more active at the NIH and provide appropriate financial support and mentorship for residents and junior faculty engaged in research.


European Surgical Research | 2008

The gut in systemic inflammatory response syndrome and sepsis. Enzyme systems fighting multiple organ failure.

James W. Suliburk; Kenneth S. Helmer; Frederick A. Moore; David W. Mercer

The prognosis and care of critically ill ICU patients has improved over recent years, but the development of multiple organ failure (MOF) continues to cause significant morbidity and mortality. Shock, with resultant organ ischemia, appears to play a critical role in the development of MOF. It is our global hypothesis that MOF is a gut-derived phenomenon and that novel interventions can improve outcome in shock-induced gut inflammation and dysfunction in critically ill patients. We have found that the anesthetic agent ketamine has a profound impact on the response to endotoxic shock. This review summarizes our findings on the mechanisms of action by which ketamine is able to modulate the nitric oxide, cyclo-oxygenase and heme-oxygenase enzyme systems to attenuate endotoxin-induced organ dysfunction.


AIDS | 2015

Human adipose tissue as a reservoir for memory CD4+ T cells and HIV

Jacob Couturier; James W. Suliburk; Jeremy M. Brown; David J. Luke; Neeti Agarwal; Xiaoying Yu; Chi Nguyen; Dinakar Iyer; Claudia A. Kozinetz; Paul A. Overbeek; Michael L. Metzker; Ashok Balasubramanyam; Dorothy E. Lewis

Objective:The objective of this study is to determine whether adipose tissue functions as a reservoir for HIV-1. Design:We examined memory CD4+ T cells and HIV DNA in adipose tissue–stromal vascular fraction (AT-SVF) of five patients [four antiretroviral therapy (ART)-treated and one untreated]. To determine whether adipocytes stimulate CD4+ T cells and regulate HIV production, primary human adipose cells were cocultured with HIV-infected CD4+ T cells. Methods:AT-SVF T cells were studied by flow cytometry, and AT-SVF HIV DNA (Gag and Env) was examined by nested PCR and sequence analyses. CD4+ T-cell activation and HIV production were measured by flow cytometry and ELISA. Results:AT-SVF CD3+ T cells were activated (>60% CD69+) memory CD4+ and CD8+ T cells in uninfected and HIV-infected persons, but the AT-SVF CD4+/CD8+ ratio was lower in HIV patients. HIV DNA (Gag and Env) was detected in AT-SVF of all five patients examined by nested PCR, comparably to other tissues [peripheral blood mononuclear cell (PBMC), lymph node or thymus]. In coculture experiments, adipocytes increased CD4+ T-cell activation and HIV production approximately two to three-fold in synergy with gamma-chain cytokines interleukin (IL)-2, IL7 or IL15. These effects were mitigated by neutralizing antibodies against IL6 and integrin-&agr;1&bgr;1. Adipocytes also enhanced T-cell viability. Conclusion:Adipose tissues of ART-treated patients harbour activated memory CD4+ T cells and HIV DNA. Adipocytes promote CD4+ T-cell activation and HIV production in concert with intrinsic adipose factors. Adipose tissue may be an important reservoir for HIV.


Anz Journal of Surgery | 2011

Sutureless total thyroidectomy: a safe and cost-effective alternative

Ling-Yun Chang; Christine J. O'Neill; James W. Suliburk; Stan B. Sidhu; Leigh Delbridge; Mark S. Sywak

Background:  Advanced vessel sealing devices provide an alternative to conventional ligation techniques for thyroidectomy. To date, most studies have been inadequately powered to explore differences in the infrequent post‐operative complications following thyroidectomy. This study is designed to compare the outcomes of sutureless thyroidectomy and conventional thyroidectomy for recurrent laryngeal nerve (RLN) injury, permanent hypoparathyroidism, and haematoma formation.


Digestive Diseases and Sciences | 2006

Ketamine-Induced Gastroprotection During Endotoxemia: Role of Heme-Oxygenase-1

Kenneth S. Helmer; James W. Suliburk; David W. Mercer

Inducible nitric oxide synthase contributes to lipopolysacharide-induced gastric injury. In contrast, heme-oxygenase-1 has anti-inflammatory effects and is protective against oxidative tissue injury. Ketamine attenuates injury from lipopolysacharide and is associated with changes in oxidative stress proteins, but its effects on the stomach remain to be fully elucidated. We hypothesized that ketamine would diminish gastric injury from lipopolysacharide via down-regulation of nuclear factor-κß, activator protein-1, and inducible nitric oxide synthase, as well as up-regulation of heme-oxygenase-1. Ketamine up-regulated heme-oxygenase-1 and attenuated lipopolysacharide-induced changes in gastric nuclear factor-κß, activator protein-1, and inducible nitric oxide synthase. Ketamine negated LPS-induced gastric injury from acidified ethanol, an effect reversed by tin protoporphorin IX. Ketamine diminishes the susceptibility of gastric mucosa to damage from luminal irritants during endotoxemia, which is mediated in part by down-regulation of iNOS and up-regulation of HO-1.

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David W. Mercer

University of Nebraska Medical Center

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Ernest A. Gonzalez

University of Texas Health Science Center at Houston

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Nicole M. Tapia

Baylor College of Medicine

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Aaron Scott

Baylor College of Medicine

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Emily K. Robinson

University of Texas Health Science Center at Houston

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Lillian S. Kao

University of Texas Health Science Center at Houston

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