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1.
Emerg Infect Dis ; 21(1): 23-31, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25529825

RESUMO

In 2009, a lethal case of Crimean-Congo hemorrhagic fever (CCHF), acquired by a US soldier in Afghanistan, was treated at a medical center in Germany and resulted in nosocomial transmission to 2 health care providers (HCPs). After his arrival at the medical center (day 6 of illness) by aeromedical evacuation, the patient required repetitive bronchoscopies to control severe pulmonary hemorrhage and renal and hepatic dialysis for hepatorenal failure. After showing clinical improvement, the patient died suddenly on day 11 of illness from cerebellar tonsil herniation caused by cerebral/cerebellar edema. The 2 infected HCPs were among 16 HCPs who received ribavirin postexposure prophylaxis. The infected HCPs had mild or no CCHF symptoms. Transmission may have occurred during bag-valve-mask ventilation, breaches in personal protective equipment during resuscitations, or bronchoscopies generating infectious aerosols. This case highlights the critical care and infection control challenges presented by severe CCHF cases, including the need for experience with ribavirin treatment and postexposure prophylaxis.


Assuntos
Febre Hemorrágica da Crimeia/diagnóstico , Transmissão de Doença Infecciosa do Paciente para o Profissional , Antivirais/uso terapêutico , Infecção Hospitalar , Evolução Fatal , Alemanha , Febre Hemorrágica da Crimeia/transmissão , Humanos , Masculino , Militares , Ribavirina/uso terapêutico , Estados Unidos/etnologia , Adulto Jovem
2.
J Trauma ; 71(1 Suppl): S91-7, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21795885

RESUMO

BACKGROUND: The success of US Air Force Critical Care Air Transport Teams (CCATT) in transporting critically ill and injured patients enabled changes in military medical force deployment and casualty care practice. Even so, a subset of casualties remains who exceed even CCATT capabilities for movement. These patients led to the creation of the Landstuhl Acute Lung Rescue Team (ALeRT) to close the "care in the air" capability gap. METHODS: The ALeRT Registry was queried for the period between November 1, 2005, and June 30, 2010. Additionally, Landstuhl Regional Medical Center critical care patient transfers to host nation medical centers were reviewed for cases using extracorporeal lung support systems. RESULTS: For the review period, US Central Command activated the ALeRT on 40 occasions. The ALeRT successfully evacuated patients on 24 of 27 missions launched (89%). Three patients were too unstable for ALeRT evacuation. Of the 13 remaining activations, four patients died and nine patients improved sufficiently for standard CCATT movement. The ALeRT initiated pumpless extracorporeal lung assistance six times, but only once to facilitate evacuation. Two patients were supported with full extracorporeal membrane oxygenation support after evacuation due to progressive respiratory failure. CONCLUSIONS: ALeRT successfully transported 24 casualties from the combat zones to Germany. Without the ALeRT, these patients would have remained in the combat theater as significant consumers of limited deployed medical resources. Pumpless extracorporeal lung assistance is already within the ALeRT armamentarium, but has only been used for one aeromedical evacuation. Modern extracorporeal membrane oxygenation systems hold promise as a feasible capability for aeromedical evacuation.


Assuntos
Lesão Pulmonar Aguda/terapia , Oxigenação por Membrana Extracorpórea , Medicina Militar , Transporte de Pacientes , Campanha Afegã de 2001- , Serviços Médicos de Emergência , Alemanha , Hospitais Militares , Humanos , Guerra do Iraque 2003-2011
3.
Mil Med ; 176(3): 332-5, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21456363

RESUMO

BACKGROUND: The underpinning pathophysiology, prevalence, and clinical relevance particular to hemorrhagic shock-induced liver damage have been explored only recently. Importantly, several investigators have revealed that an aberrant periportal endothelial response, characterized by the early release of oxidizing mediators, perpetuates and eventually amplifies the extent of hepatic reperfusion injury. CASE: We present a case that illustrates the clinical impact of hepatic ischemia-reperfusion injury and a potential means of ameliorating the attendant self-propagating hepatic destruction. CONCLUSION: Reversal of hemorrhagic shock may lead to the induction of a hepatic oxidation response with a resultant furthering of liver injury. Antioxidants such as N-acetylcysteine may represent a tolerable and logical means of attenuating the aberrant oxidant cascade and stabilizing or reversing ischemic-reperfusion hepatopathy.


Assuntos
Acetilcisteína/uso terapêutico , Sequestradores de Radicais Livres/uso terapêutico , Hepatopatias/tratamento farmacológico , Traumatismo por Reperfusão/tratamento farmacológico , Adulto , Humanos , Infusões Intravenosas , Hepatopatias/complicações , Masculino , Traumatismo por Reperfusão/complicações , Traumatismo por Reperfusão/fisiopatologia , Choque Hemorrágico/complicações , Choque Hemorrágico/fisiopatologia
4.
Mil Med ; 176(9): 1071-6, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21987968

RESUMO

OBJECTIVE: Fat emboli syndrome (FES) is a disorder associated with both acute lung injury and acute respiratory distress syndrome. Both FES and diffuse alveolar hemorrhage (DAH) are bronchoscopically definable entities that may share a common etiology. We conducted a chart review analysis to examine the relationship between FES and DAH. METHODS: Retrospective chart review. RESULTS: Three cases of concurrent FES and DAH were identified. Long bone fracture and/or orthopedic procedures preceded all the events and were the likely inciting source for eventual acute lung injury. Bronchoalveolar lavage-evident DAH and FES was found in all these cases in association with hemoptysis and lung-attributed blood loss. Lung-protective ventilation and standard supportive care approaches proved sufficient in attaining good outcomes. CONCLUSION: Combined FES and DAH can occur in association with orthopedic injury and repair and are likely an under-recognized entity.


Assuntos
Acidentes por Quedas , Acidentes Aeronáuticos , Traumatismos por Explosões/complicações , Hemorragia/etiologia , Pneumopatias/etiologia , Alvéolos Pulmonares , Adulto , Lavagem Broncoalveolar , Broncoscopia , Hemoglobinas/análise , Hemorragia/diagnóstico , Hemorragia/terapia , Humanos , Pulmão/diagnóstico por imagem , Pneumopatias/diagnóstico , Pneumopatias/terapia , Masculino , Militares , Respiração com Pressão Positiva , Respiração Artificial , Tomografia Computadorizada por Raios X
5.
Mil Med ; 176(8): 932-7, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21882785

RESUMO

OBJECTIVE: To review the principles of extracorporeal membrane oxygenation (ECMO) and to describe the recent advancements in ECMO technology that permit use of this rescue therapy for severe lung injury in combat casualties. METHODS/RESULTS: Lung protective ventilation has defined the state-of-the-art treatment for acute lung injury for more than a decade. Despite the benefits provided by a low tidal volume strategy, lung injury patients may experience deterioration in gas exchange to the point that other rescue interventions are needed or the patient succumbs to progressive respiratory failure. When this occurs in combat casualties, management of the patient in an austere environment and movement to definitive care become problematic. Recent advances in ECMO technology permit long-range transport of these critically ill casualties with greater physiologic reserve and potentially less mortality. CONCLUSIONS: Advances in ECMO technology now enable the stabilization and aeromedical evacuation of even the most critically ill combat casualties with severe lung injury.


Assuntos
Lesão Pulmonar Aguda/terapia , Resgate Aéreo , Medicina Militar/organização & administração , Militares , Resgate Aéreo/organização & administração , Desenho de Equipamento , Oxigenação por Membrana Extracorpórea/instrumentação , Oxigenação por Membrana Extracorpórea/métodos , Humanos
6.
Crit Care Med ; 38(10): 1970-7, 2010 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20639746

RESUMO

OBJECTIVES: In select burn intensive care units, high-frequency percussive ventilation is preferentially used to provide mechanical ventilation in support of patients with acute lung injury, acute respiratory distress syndrome, and inhalation injury. However, we found an absence of prospective studies comparing high-frequency percussive ventilation with contemporary low-tidal volume ventilation strategies. The purpose of this study was to prospectively compare the two ventilator modalities in a burn intensive care unit setting. DESIGN: Single-center, prospective, randomized, controlled clinical trial, comparing high-frequency percussive ventilation with low-tidal volume ventilation in patients admitted to our burn intensive care unit with respiratory failure. SETTING: A 16-bed burn intensive care unit at a tertiary military teaching hospital. PATIENTS: Adult patients ≥ 18 yrs of age requiring prolonged (> 24 hrs) mechanical ventilation were admitted to the burn intensive care unit. The study was conducted over a 3-yr period between April 2006 and May 2009. This trial was registered with ClinicalTrials.gov as NCT00351741. INTERVENTIONS: Subjects were randomly assigned to receive mechanical ventilation through a high-frequency percussive ventilation-based strategy (n = 31) or a low-tidal volume ventilation-based strategy (n = 31). MEASUREMENTS AND MAIN RESULTS: At baseline, both the high-frequency percussive ventilation group and the low-tidal volume ventilation group had similar demographics to include median age (interquartile range) (28 yrs [23-45] vs. 33 yrs [24-46], p = nonsignificant), percentage of total body surface area burn (34 [20-52] vs. 34 [23-50], p = nonsignificant), and clinical diagnosis of inhalation injury (39% vs. 35%, p = nonsignificant). The primary outcome was ventilator-free days in the first 28 days after randomization. Intent-to-treat analysis revealed no significant difference between the high-frequency percussive ventilation and the low-tidal volume ventilation groups in mean (± sd) ventilator-free days (12 ± 9 vs. 11 ± 9, p = nonsignificant). No significant difference was detected between groups for any of the secondary outcome measures to include mortality except the need for "rescue" mode application (p = .02). Nine (29%) in the low-tidal volume ventilation arm did not meet predetermined oxygenation or ventilation goals and required transition to a rescue mode. By contrast, two in the high-frequency percussive ventilation arm (6%) required rescue. CONCLUSIONS: A high-frequency percussive ventilation-based strategy resulted in similar clinical outcomes when compared with a low-tidal volume ventilation-based strategy in burn patients with respiratory failure. However, the low-tidal volume ventilation strategy failed to achieve ventilation and oxygenation goals in a higher percentage necessitating rescue ventilation.


Assuntos
Queimaduras/terapia , Ventilação de Alta Frequência , Respiração Artificial , Adulto , Queimaduras/imunologia , Feminino , Fator Estimulador de Colônias de Granulócitos e Macrófagos/sangue , Ventilação de Alta Frequência/métodos , Humanos , Interleucina-1beta/sangue , Interleucina-6/sangue , Interleucina-8/sangue , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Respiração Artificial/métodos , Volume de Ventilação Pulmonar , Resultado do Tratamento , Fator de Necrose Tumoral alfa/sangue , Desmame do Respirador , Adulto Jovem
7.
J Trauma ; 69 Suppl 1: S179-87, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20622615

RESUMO

BACKGROUND: The purpose of this article is to describe the clinical course and outcome of drowning cases related to current US military combat operations. METHODS: This retrospective case series spans December 2002 to January 2009 of survivors transferred to an echelon IV military trauma center in Europe serving as the primary evacuation hub for ongoing combat operations. Patient demographics and the situational and clinical findings at the initial drowning scene were reviewed. A comprehensive analysis of care as each patient transitioned through the combat theater to the echelon IV trauma center in Europe was performed. RESULTS: Overall, mortality was 37.5% mortality rate (3 of 8 patients). Advanced modes of respiratory support such as high-frequency ventilation, airway pressure release ventilation, and extracorporeal membrane oxygenation were required in a majority of the cohort (6 of 8 patients). Limited-duration vasopressor infusions (7 of 8 patients) were also required to ensure adequate end-organ perfusion. Glasgow Coma Scale (GCS) scores and the need for cardiopulmonary resuscitation (CPR) at the scene of injury were associated with eventual patient mortality (100% mortality for an initial GCS score of 3 and 75% mortality for on-scene CPR). Survivor long-term morbidity was often related to the sequelae of acute respiratory distress syndrome and hypoxic encephalopathy. CONCLUSION: Drowning associated with combat operations was associated with severe acute respiratory distress syndrome and cardiovascular shock. GCS score and the need for CPR at the scene of injury were associated with eventual mortality because of anoxic brain injury in all cases.


Assuntos
Afogamento/epidemiologia , Síndrome Respiratória Aguda Grave/etiologia , Guerra , Reanimação Cardiopulmonar/métodos , Humanos , Incidência , Masculino , Afogamento Iminente/terapia , Estudos Retrospectivos , Síndrome Respiratória Aguda Grave/epidemiologia , Síndrome Respiratória Aguda Grave/terapia , Taxa de Sobrevida/tendências , Centros de Traumatologia , Estados Unidos/epidemiologia , Adulto Jovem
8.
J Trauma ; 69 Suppl 1: S81-6, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20622625

RESUMO

BACKGROUND: Acute lung injury (ALI) is a syndrome consisting of noncardiogenic acute hypoxemic respiratory failure with the presence of bilateral pulmonary infiltrates and occurs in up to 33% of critically ill trauma patients. Retrospective and observational studies have suggested that a blood component resuscitation strategy using equal ratios of packed red blood cells (PRBCs) and fresh frozen plasma (FFP) may have a survival benefit in combat casualties. The purpose of this study was to determine whether this strategy is associated with an increased incidence of ALI. METHODS: We performed a prospective observational study of all injured patients admitted to an intensive care unit (ICU) at a combat support hospital who required >5 units of blood transfusion within the first 24 hours of admission. Baseline demographic data along with Injury Severity Score (ISS), pulmonary injury, presence of long bone fracture, blood products transfused, mechanical ventilation data, and arterial blood gas analysis were collected. The primary endpoint of the study was the development of ALI at 48 hours after injury. Those who did not survive to ICU admission were excluded from analysis. Follow-up (including mortality) longer than 48 hours was unavailable secondary to rapid transfer out of our facility. A multivariate logistic regression was performed to determine the independent effects of variables on the incidence of early ALI. RESULTS: During a 12-month period (from January 2008 to December 2008), 87 subjects were studied; of these, 66 patients met inclusion criteria, and 22 patients developed ALI at 48 hours (33%). Overall, the ratio of FFP to PRBC was 1:1.1. Those who developed ALI had a higher ISS (32 +/- 15 vs. 26 +/- 11; p = 0.04) and received more units of FFP (22 +/- 15 vs. 12 +/- 7; p < 0.001), PRBCs (22 +/- 16 vs. 13 +/- 7; p = 0.008), and platelets (5 +/- 11 vs. 1 +/- 2; p = 0.004) compared with those who did not develop ALI. Multivariate logistic regression analysis revealed that presence of pulmonary injury (odds ratio, 5.4; 95% confidence interval, 1.3-21.9) and volume of FFP transfused (odds ratio, 1.2; 95% confidence interval, 1.1-1.3) had independent effects on ALI at 48 hours. CONCLUSION: On the basis of this small, prospective, descriptive study of severely injured patients admitted to the ICU, we determined that the presence of pulmonary injury had the greatest impact on the incidence of early ALI. There was also an independent relationship between the amount of FFP transfused and the incidence of early ALI. Further studies are required to determine the effects of the development of early ALI from FFP transfusion on short- and long-term survival.


Assuntos
Lesão Pulmonar Aguda/terapia , Transfusão de Sangue/métodos , Hospitais Militares , Unidades de Terapia Intensiva , Lesão Pulmonar Aguda/epidemiologia , Lesão Pulmonar Aguda/etiologia , Adulto , Feminino , Humanos , Incidência , Masculino , Prognóstico , Estudos Prospectivos , Taxa de Sobrevida/tendências , Fatores de Tempo , Resultado do Tratamento , Estados Unidos/epidemiologia , Ferimentos e Lesões/complicações , Ferimentos e Lesões/epidemiologia
9.
Respir Care ; 55(6): 734-40, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20507657

RESUMO

INTRODUCTION: High-frequency percussive ventilation (HFPV) is an increasingly used mode of mechanical ventilation, for which there is no proven real-time means of measuring delivered tidal volume (V(T)). OBJECTIVE: To validate a pneumotachograph for HFPV and then exploit flow-sensor data to describe the behavior of both low-frequency and high-frequency breaths. METHODS: Sensor performance was gauged during changes in high-frequency (4-12 Hz) and low-frequency rate and ratio, mean airway pressure, oxygen concentration, heated or heated-humidified gas flow, and endotracheal tube diameter. Glass bottle (adiabatic V(T)) and test lung (adiabatically derived low-frequency V(T)) based adiabatic conditions provided both an initial source for analog-signal calibration and an accepted standard comparator to flow-sensor measurement of high-frequency and low-frequency (flow-sensor-derived) V(T)), respectively. RESULTS: Pneumotachography proved accurate and precise over an array of tested settings and conditions when analyzing both high-frequency (difference between mean +/- SD high-frequency V(T) and adiabatic V(T) was -0.2 +/- 1.8%, 95% confidence interval -0.5 to 0.9%) and low-frequency breaths (mean +/- SD difference between flow-sensor-derived low-frequency V(T) and adiabatically derived low-frequency V(T) was 0.6 +/- 2.4%, 95% confidence interval 0.1-1.1%). High-frequency V(T) and frequency exhibited an exponential relationship. During HFPV, flow-sensor-derived low-frequency V(T) had a mean +/- SD of 1,337 +/- 700 mL, 95% confidence interval 1,175-1,499 mL. CONCLUSIONS: Readily available pneumotachography provided accurate measurements of low-frequency and high-frequency V(T) during HFPV. In the setting of acute lung injury, typical HFPV settings may deliver injurious V(T).


Assuntos
Ventilação de Alta Frequência/instrumentação , Volume de Ventilação Pulmonar , Humanos , Manometria/métodos , Modelos Anatômicos
10.
Neurosurg Focus ; 28(5): E11, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20568927

RESUMO

Traumatic brain injury contributes significantly to military combat morbidity and mortality. No longer maintaining comprehensive medical care facilities throughout the world, the US military developed a worldwide trauma care system making the patient the moving part of the system. Life-saving interventions are performed early, and essential care is delivered at forward locations. Patients then proceed successively through increasingly capable levels of care culminating with arrival in the US. Proper patient selection and thorough mission preparation are crucial to the safe and successful intercontinental aeromedical evacuation of critical brain-injured patients during Operations Iraqi Freedom and Enduring Freedom.


Assuntos
Campanha Afegã de 2001- , Resgate Aéreo/estatística & dados numéricos , Lesões Encefálicas/terapia , Guerra do Iraque 2003-2011 , Medicina Militar/métodos , Transporte de Pacientes/métodos , Lesões Encefálicas/cirurgia , Cuidados Críticos/métodos , Humanos , Transporte de Pacientes/organização & administração , Estados Unidos
11.
Mil Med ; 175(9): 676-85, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20882931

RESUMO

Obstructive sleep apnea/hypopnea syndrome (OSAHS) is a medical condition that has received significant attention within the medical community and mainstream media due to its potentially serious physiological consequences and relatively frequent occurrence within the general population. From the military perspective, the impact on individual readiness for deployment, and the potential degradation of performance in critically important military duties, often results in tremendous expenditures of training resources, time, and expertise to replace the military member with a suitable substitute or release of the individual from active duty. This article reviews common surgical techniques for clinical management of OSAHS patients in a presentation format for primary care and sleep medicine specialists, as well as surgeons interested in the philosophies of surgical management of sleep disordered breathing. Presentation of risks and benefits of surgical treatment are discussed in a manner to facilitate communication between patient and health care provider.


Assuntos
Procedimentos Cirúrgicos Bucais/métodos , Síndromes da Apneia do Sono/cirurgia , Humanos , Medicina Militar
12.
Respir Care ; 54(9): 1175-82, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19712493

RESUMO

BACKGROUND: Individually, noninvasive ventilation (NIV) and helium-oxygen gas mixtures (heliox) diminish ventilatory workload and improve exercise tolerance in patients with chronic obstructive pulmonary disease (COPD). NIV in combination with heliox may have additive effects on exercise tolerance in severe COPD. METHODS: We assessed the safety, tolerability, and efficacy of heliox and NIV during exercise in patients with severe COPD. SETTING: Pulmonary rehabilitation facility in an academic tertiary-care medical center. PROTOCOL: Twelve patients with severe COPD were enrolled. Using a sequential randomized placebo-controlled crossover study design, the patients performed 4 separate constant-work stationary bicycle cardiopulmonary exercise studies at 80% of maximal workload during application of sham NIV, NIV, 60:40 heliox with sham NIV, and 60:40 heliox with NIV. Tolerability, safety, and exercise duration as determined by constant-work cardiopulmonary exercise test were the primary outcome measures. Secondary outcome measures at peak exercise and iso-time included rate of perceived exertion, dyspnea, leg pain, heart rate, respiratory rate, systolic and diastolic blood pressure, tympanic temperature, and oxyhemoglobin saturation. RESULTS: No adverse effects occurred during or after application of NIV, heliox, or NIV with heliox. Exercise duration using heliox with NIV was significantly longer than both heliox (P = .01) and NIV (P = .007), but not placebo (P = .09). Relative to placebo, all treatment arms permitted lower respiratory rates at peak exercise. Heliox, with or without NIV, was associated with significant improvements in oxyhemoglobin saturation at peak exercise, relative to placebo or NIV alone. CONCLUSIONS: The adjunctive use of NIV with heliox during exercise proved both safe and tolerable in patients with severe COPD. The lack of demonstrable efficacy to any of the treatment arms relative to placebo (P = .09) may be the result of the small sample size (ie, type 2 error)-a conclusion emphasized by the large standard deviations and differences in treatment group variances in exercise duration alone.


Assuntos
Terapia por Exercício , Gases/administração & dosagem , Hélio/administração & dosagem , Oxigenoterapia/métodos , Oxigênio/administração & dosagem , Respiração com Pressão Positiva/métodos , Doença Pulmonar Obstrutiva Crônica/reabilitação , Administração por Inalação , Idoso , Estudos Cross-Over , Teste de Esforço , Estudos de Viabilidade , Humanos , Resistência Física
13.
Respir Care ; 54(3): 350-8, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19245729

RESUMO

BACKGROUND: We were concerned about the risk of inadequate humidification during high-frequency percussive ventilation (HFPV). METHODS: We studied 5 humidifiers during HFPV with a lung model, at bias gas flows of 10 L/min, 30 L/min, and 50 L/min, and compared the results to those from a comparator ventilator/humidifier setup and to the minimum temperature (30 degrees C) and humidity (30 mg/L) [corrected] recommended by the American Association for Respiratory Care, at both regular room temperature and a high ambient temperature. Temperature was measured at the humidifier outflow point and at the artificial carina. Humidity was measured at the artificial carina. RESULTS: Of the 7 HFPV/humidifier combinations, 2 (the MR850 at a bias flow of 50 L/min, and the ConchaTherm Hi-Flow with VDR nebulizer) provided a carinal temperature equivalent to the comparator setup at room temperature, whereas one HFPV/humidifier combination (the ConchaTherm Hi-Flow with modified programming, at bias flows of 30 L/min and 50 L/min) provided a higher carinal temperature. At high ambient temperature, all of the setups delivered lower carinal temperature than the comparator setup. Only 2 setups (the ConchaTherm with modified programming at a bias flow of 50 L/min, and the ConchaTherm Hi-Flow with VDR nebulizer) provided carinal humidification equivalent to the comparator setup, without regard to ambient temperature; the other humidifiers were less effective. The ConchaTherm with modified programming, and the ConchaTherm with the VDR nebulizer provided the most consistent humidification. CONCLUSION: HFPV's distinctive gas-flow mechanism may impair gas heating and humidification, so all humidification systems should be tested with HFPV prior to clinical use.


Assuntos
Ventilação de Alta Frequência/instrumentação , Umidade , Desenho de Equipamento , Modelos Lineares , Temperatura
14.
Mil Med ; 174(11): 1177-82, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19960826

RESUMO

BACKGROUND: Cardiopulmonary exercise testing (CPET) is one method to diagnose unexplained dyspnea in young adults, yet few normal reference values exist in this population. This study evaluated interpretation of maximal CPET in a young adult cohort with known pulmonary disorders using published reference values compared to age-matched normal controls. METHODS: A control population of 69 healthy military volunteers with normal chest radiographs, pulmonary function testing, and bronchoprovocation testing were compared to 105 patients with exertional dyspnea. Both groups underwent a standardized evaluation including CPET on a graded exercise treadmill to maximal exercise with expired gas analysis. RESULTS: Measurements from CPET in the dyspnea group were interpreted using published reference values compared to control population results (mean +/- 1.65 x SD). Statistical comparison of predicted normals (reference vs. control) of maximal oxygen consumption (> 83% vs. 82%), ventilatory anaerobic threshold (> 40% vs. 53%), respiratory rate (< 60 vs. 56 breaths/min), tidal volume to inspiratory capacity (< 80% vs. 111%), ventilatory equivalent for carbon dioxide production (< 40 vs. 38), and maximal voluntary ventilation minus minute ventilation (> 11 vs. -1 L/min) was performed. The overall specificity for tidal volume to inspiratory capacity improved using age-matched controls but sensitivity was decreased. Other parameters were not significantly different. CONCLUSIONS: The use of age-matched controls for CPET results in an increase in specificity and decrease in sensitivity for respiratory limitations to exercise, when compared to reference values. The study findings suggest that CPET may be insensitive in detecting mild disease in young healthy adults.


Assuntos
Dispneia/diagnóstico , Teste de Esforço , Tolerância ao Exercício , Militares , Adulto , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Dispneia/fisiopatologia , Feminino , Humanos , Masculino , Valores de Referência , Análise de Regressão , Testes de Função Respiratória
15.
Crit Care Med ; 36(7 Suppl): S383-7, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18594267

RESUMO

BACKGROUND: Landstuhl Regional Medical Center is the largest U.S. medical facility outside the United States, and it is the first permanently positioned hospital outside the combat zone providing care to the wartime sick and wounded. As of November 2007, Landstuhl Regional Medical Center personnel have treated over 45,000 patients from Operations Enduring Freedom and Iraqi Freedom. The current trauma/critical care service is a multidisciplinary, intensivist-directed team caring for a diverse range of clinical diagnoses to include battle injuries, diseases, and nonbattle injuries. Admissions arise from an at-risk population of 500,000 widely distributed over a geographic area encompassing three continents. DISCUSSION: When compared with 2001, the average daily intensive care unit census has tripled and the patient acuity level has doubled. Combat casualties account for 85% of service admissions. The clinical practice at this critical care hub continues to evolve as a result of wartime damage control trauma care, robust critical care air transport capabilities, length of stay, and other unique factors. The service's focus is to optimize patients for an uneventful evacuation to the United States for definitive care and family support. SUMMARY: Successful verification in 2007 as an American College of Surgeons level II trauma center reflects a continuing institutional commitment to providing the best possible care to the men and women serving our nation in the global war on terror.


Assuntos
Cuidados Críticos/organização & administração , Hospitais Militares/organização & administração , Unidades de Terapia Intensiva/organização & administração , Medicina Militar/organização & administração , Transporte de Pacientes/organização & administração , Centros de Traumatologia/organização & administração , Afeganistão , Nutrição Enteral , Alemanha , Humanos , Controle de Infecções , Iraque , Guerra do Iraque 2003-2011 , Tempo de Internação/estatística & dados numéricos , Medicina Militar/educação , Inovação Organizacional , Avaliação de Processos e Resultados em Cuidados de Saúde , Admissão do Paciente/estatística & dados numéricos , Equipe de Assistência ao Paciente/organização & administração , Traumatismos da Coluna Vertebral/prevenção & controle , Terrorismo , Tromboembolia/diagnóstico , Tromboembolia/etiologia , Tromboembolia/prevenção & controle , Gestão da Qualidade Total , Estados Unidos
16.
Arch Intern Med ; 167(6): 551-61, 2007 Mar 26.
Artigo em Inglês | MEDLINE | ID: mdl-17389286

RESUMO

BACKGROUND: Implementation of the chronic care model (CCM) has been shown to be an effective preventative strategy to improve outcomes in diabetes mellitus, depression, and congestive heart failure, but data are lacking regarding the effectiveness of this model in preventing complications in patients with chronic obstructive pulmonary disease. METHODS: We searched the MEDLINE, CINAHL, and Cochrane databases from inception to August 2005 and included English-language articles that enrolled adults with chronic obstructive pulmonary disease and (1) contained intervention(s) with CCM component(s), (2) included a comparison group or measures at 2 points (before/after), and (3) had relevant outcomes. Two reviewers independently extracted data. RESULTS: Symptoms, quality of life, lung function, and functional status were not significantly different between the intervention and control groups. However, pooled relative risks (95% confidence intervals) for emergency/unscheduled visits and hospitalizations for the group that received at least 2 CCM components were 0.58 (0.42-0.79) and 0.78 (0.66-0.94), respectively. The weighted mean difference (95% confidence interval) for hospital stay was -2.51 (-3.40 to -1.61) days shorter for the group that received 2 or more components. There were no significant differences for those receiving only 1 CCM component. CONCLUSIONS: Limited published data exist evaluating the efficacy of CCM components in chronic obstructive pulmonary disease management. However, pooled data demonstrated that patients with chronic obstructive pulmonary disease who received interventions with 2 or more CCM components had lower rates of hospitalizations and emergency/unscheduled visits and a shorter length of stay compared with control groups. The results of this review highlight the need for well-designed trials in this population.


Assuntos
Gerenciamento Clínico , Doença Pulmonar Obstrutiva Crônica/terapia , Dispneia/terapia , Serviço Hospitalar de Emergência/estatística & dados numéricos , Teste de Esforço , Conhecimentos, Atitudes e Prática em Saúde , Hospitalização/estatística & dados numéricos , Humanos , Doença Pulmonar Obstrutiva Crônica/mortalidade , Garantia da Qualidade dos Cuidados de Saúde , Qualidade de Vida , Projetos de Pesquisa , Testes de Função Respiratória
17.
Respir Med ; 137: 123-128, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29605194

RESUMO

RATIONALE: Acute eosinophilic pneumonia (AEP) is a rare but important cause of severe respiratory failure most typically caused by cigarette smoking, but can also be caused by medications, illicit drugs, infections and environmental exposures. There is growing evidence that disease severity varies and not all patients require mechanical ventilation or even supplemental oxygen. OBJECTIVES: To compare patients with AEP treated at Landstuhl Regional Medical Center (LRMC) to those in other published series, and to provide recommendations regarding diagnosis and treatment of AEP. METHODS: A retrospective chart review was completed on forty-three cases of AEP which were identified from March 2003 through March 2010 at LRMC, Germany. RESULTS: Tobacco smoking was reported by 91% of our patients. Only 33% of patients in our series had a fever (temperature > 100.4 °F) at presentation. Peripheral eosinophilia (>5%) was present in 35% on initial CBC, but was seen in 72% of patients during their hospital course. Hypoxemia, as measured by PaO2/FiO2 ratio, seemed to be less severe in patients with higher levels of bronchoalveolar (BAL) eosinophilia percentage. CONCLUSIONS: Based on our experience and literature review, we recommend adjustments to the diagnostic criteria which may increase consideration of this etiology for acute respiratory illnesses as well as provide clinical clues we have found particularly helpful. Similar to recent reports of initial peripheral eosinophilia correlating with less severe presentation we found that higher BAL eosinophilia correlated with less severe hypoxemia.


Assuntos
Corticosteroides/uso terapêutico , Militares/estatística & dados numéricos , Eosinofilia Pulmonar/epidemiologia , Respiração Artificial/métodos , Doença Aguda , Corticosteroides/administração & dosagem , Adulto , Líquido da Lavagem Broncoalveolar/imunologia , Broncoscopia/instrumentação , Eosinofilia/diagnóstico , Eosinofilia/metabolismo , Feminino , Alemanha , Humanos , Hipóxia/fisiopatologia , Masculino , Pessoa de Meia-Idade , Eosinofilia Pulmonar/diagnóstico por imagem , Eosinofilia Pulmonar/terapia , Respiração Artificial/estatística & dados numéricos , Insuficiência Respiratória/etiologia , Estudos Retrospectivos , Índice de Gravidade de Doença , Fumar Tabaco/epidemiologia , Estados Unidos/epidemiologia
18.
Respir Care ; 52(3): 271-7, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17328825

RESUMO

OBJECTIVE: To determine the effect of endotracheal-tube cuff deflation on airflow and F(IO2) during high-frequency percussive ventilation (HFPV), and explore methods of correcting the cuff-deflation-associated decrease in mean airway pressure and F(IO2) at the carina. METHODS: Using a mechanical lung model in our respiratory research laboratory, we measured circuit pressure near the connection to the endotracheal tube (P(vent)), mean airway pressure (P(aw)), pulsatile tidal volume (V(T)), and F(IO2) at the artificial carina. During cuff deflation we manipulated the pulsatile frequency, pulsatile flow, and the HFPV integral nebulizer. We then assessed 4 methods of correcting the decreased F(IO2) and airway pressure during cuff deflation: (1) oxygen delivery at the inspiratory fail-safe valve, (2) oxygen delivery at the T-piece between the HFPV and the endotracheal tube, (3) continuous activation of the HFPV's integral nebulizer, and (4) oxygen insufflation into the suction channel of the endotracheal tube. RESULTS: Cuff deflation reduced P(vent), P(aw), pulsatile V(T), and F(IO2). Increasing the pulsatile flow and decreasing the pulsatile frequency further reduced F(IO2) during cuff deflation. Injecting supplemental oxygen at the inspiratory fail-safe valve provided the best F(IO2) increase. Injecting oxygen at the T-piece provided the second best F(IO2) increase. Continuous activation of the integral nebulizer provided the third best F(IO2) increase. Oxygen insufflation to the suction channel was least effective in correcting the F(IO2) decrease caused by cuff deflation. CONCLUSION: Cuff-deflation-associated F(IO2), P(aw), and pulsatile V(T) compromise can be partially corrected by any of the 4 methods we studied. Injecting supplemental oxygen at the inspiratory fail-safe valve is the most effective method.


Assuntos
Ventilação de Alta Frequência/normas , Hipóxia , Intubação Intratraqueal/instrumentação , Falha de Equipamento , Estados Unidos
19.
Respir Care ; 52(1): 45-9, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17194317

RESUMO

OBJECTIVE: With a high-frequency percussive ventilator and a mechanical lung model, to measure tidal volume (V(T)), pulsatile pressure amplitude (difference between peak and nadir pulsatile pressure [DeltaP];), and mean airway pressure (P (aw)) at various pulsatile frequencies, pulsatile inspiratory-expiratory ratios (I:E(p)), and pressures (measured at the interface between the pulse-generator and the endotracheal tube [P(vent)]). METHODS: With the endotracheal tube inside an artificial trachea, we manipulated the high-frequency percussive ventilation settings and adjuncts, including pulsatile frequency, I:E(p), and P(vent) by manipulating pulsatile flow. We also studied the effects of partially deflating the endotracheal tube cuff. We measured P (aw), pulsatile pressure amplitude at the carina (DeltaP(c)), and pulsatile V(T) at the carina. With the cuff partly deflated, we measured the fraction of inspired oxygen (F(IO(2))) in the gas efflux above and below the cuff. RESULTS: Increasing the pulsatile frequency from 300 cycles/min to 600 cycles/min and changing the I:E(p) from 1:3 to 1:1 significantly reduced V(T) (p < 0.001). P (aw) and DeltaP(c) were unaffected by the change in pulsatile frequency or I:E(p), except when we did not preserve the pulsatile flow. The measured V(T) range was from 19.1 mL (at 600 cycles/min) to 47.3 mL (at 300 cycles/min). Partial cuff deflation did not significantly reduce P (aw) or DeltaP(c), but it did significantly reduce V(T) and F(IO(2)). CONCLUSION: During high-frequency percussive ventilation, the pulsatile frequency is inversely related to V(T). Partial cuff deflation reduces the delivered F(IO(2)).


Assuntos
Pressão do Ar , Ventilação em Jatos de Alta Frequência/instrumentação , Intubação Intratraqueal/instrumentação , Modelos Anatômicos , Fluxo Pulsátil/fisiologia , Volume de Ventilação Pulmonar/fisiologia , Resistência das Vias Respiratórias/fisiologia , Desenho de Equipamento , Humanos , Técnicas In Vitro , Traqueia/fisiologia
20.
J Voice ; 20(2): 291-6, 2006 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16293397

RESUMO

Chlorine gas inhalation, similar to other toxic gas exposures, can impart a variety of effects to the entire airway ranging from mucous membrane irritation to acute respiratory distress syndrome. The extent and location of damage is determined by numerous situational factors such as the duration of exposure, quantity of gas released, environmental factors, and instituted chemical defense measures. Reactive airways dysfunction and nonspecific bronchial hyperresponsiveness are commonly reported as sequelae to chlorine exposure. This article constitutes the first case of a single antecedent chlorine exposure inducing progressive vocal cord dysfunction.


Assuntos
Cloro/efeitos adversos , Doenças Profissionais/induzido quimicamente , Exposição Ocupacional/efeitos adversos , Prega Vocal/efeitos dos fármacos , Distúrbios da Voz/induzido quimicamente , Administração por Inalação , Cloro/administração & dosagem , Progressão da Doença , Dispneia/induzido quimicamente , Humanos , Masculino , Pessoa de Meia-Idade , Testes de Função Respiratória , Prega Vocal/fisiopatologia
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