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11. |
Extravasation rates and complications of intraosseous needles during gravity and pressure infusion |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2023-2028
Joseph MD LaSpada,
Niranjan MBBS Kissoon,
Richard MD Melker,
Suzanne PhD Murphy,
Gary PhD Miller,
Richard MD Peterson,
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摘要:
ObjectiveTo compare the extravasation rates and insertion complications under gravity and 300 mm Hg (40 kPa) pressure infusion of threaded (SurFast Registered Trademark and Sussmane-Raszynski intraosseous needles, Cook Critical Care, Bloomington, IN); and nonthreaded needles (16-gauge disposable intraosseous needle with 45 degrees trocar Cook Critical Care, Bloomington, IN; Jamshidi bone marrow needle; Baxter Health Care Corp, Valencia, CA).DesignA prospective, randomized study.SettingAn animal laboratory at a university center.SubjectsFive healthy mix breed piglets, weighing 15 to 15.5 kg.InterventionsPiglets were anesthetized and ventilated. Tibial, femoral, and humeral osseous sites were exposed by dissection of overlying tissue. All bleeding points were cauterized and oozing was prevented by sealing with cyanoacrylate. Intraosseous access devices then were inserted one at a time in random order and rated for difficulty of insertion. Normal saline solution was infused under gravity or 300 mm Hg (40 kPa) pressure. Extravasation rates then were calculated from the increase in weight of a gauze sponge wrapped tightly at the base of the needle during infusion.Measurements and Main ResultsNo significant (p more than .05) differences in extravasation rates were noted among the different types of needles, either under gravity or pressure infusions. The Sussmane-Raszynski needle was significantly more difficult to insert than the others (rated difficult to insert and control in 16 of 34 attempts). Inadvertent penetration of both cortices occurred with nonthreaded needles only (three of 66 attempts). The Sur-Fast Registered Trademark needle provided greatest penetration control and was most resistant to accidental dislodgement.ConclusionsUnder ideal conditions, needle type does not influence extravasation rates. However, difficulty with insertion and penetration of both cortices occur commonly and may lead to extravasation during stressful emergency situations or when performed by unskilled personnel.(Crit Care Med 1995; 23:2023-2028)
ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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12. |
A canine study of cold water drowning in fresh versus salt water |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2029-2037
Alan W. MD Conn,
Katsuyuki MD Miyasaka,
Masao MD Katayama,
Michio PhD Fujita,
Hiromitsu PhD Orima,
Geoffrey MB Barker,
Desmond MB Bohn,
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摘要:
ObjectiveTo compare the pathophysiologic changes occurring during drowning in cold fresh water and cold salt water with reference to viability.DesignRandomized, prospective, controlled submersion experiments in two contrasting cold liquids.SettingA laboratory at a large university-affiliated medical institution.SubjectsThirteen healthy, anesthetized mongrel dogs. Three dogs served as controls and were immersed but not submerged. The remainder were submerged in cold fresh water or cold salt water (4 degrees C).InterventionsCatheters were placed in the femoral artery, right carotid artery and right internal jugular vein. Electrocardiogram, pneumogram, and rectal temperatures were measured continuously during submersion/immersion.Measurements and Main ResultsCold water submersion with drowning produced a large initial decrease in carotid artery temperature (approximate 7.5 degrees C in the first 2 mins) compared with a minor decrease (approximate 0.8 degrees C with immersion). No significant differences were noted in the rate of decrease of temperature between drowning in fresh water and salt water.During cold fresh water drowning, aspiration produced gross hemodilution with an average increase in body weight of 16.5%. Hematocrit values, serum sodium concentrations, and osmolality decreased while serum potassium concentrations, catecholamines, and free hemoglobin increased. All measured biochemical data (except Pao2) remained at viable levels. By contrast, during cold salt water drowning, average body weight increased by only 6%, with hemoconcentration and a shrinkage of vascular volume. Hematocrit and hemoglobin values increased by 30%, but initial plasma free hemoglobin values remained unchanged. Serum sodium concentrations, osmolality, and potassium concentrations increased rapidly to critical levels.ConclusionsOn submersion in cold water, all of the experimental animals developed tachypnea immediately, followed by aspiration with predictable effects. The biochemical and pathophysiologic changes in cold water drowning approximated those changes reported for warm water drowning for both fresh and salt water with one exception and continued aspiration of cold water produced extremely rapid core cooling as long as the circulation remained intact. This process of acute submersion hypothermia may protect the brain temporarily from lethal damage, as reported in cases of cold fresh water drowning. Concentrations of circulating catecholamines increased exponentially in both groups of test animals. Clinically, their acute effects on the circulation, compounded by significant hypothermia and extreme anoxia, must hamper the detection of residual circulation at rescue and may play a role in sudden death from cold water in the absence of drowning.(Crit Care Med 1995; 23:2029-2037)
ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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13. |
Sedation for the critically ill neurologic patient |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2038-2053
Marek A. MD Mirski,
Birgitt MD Muffelman,
John A. MD Ulatowski,
Daniel F. MD Hanley,
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摘要:
ObjectiveTo review the scientific basis for sedation of critically ill neurologic patients by summarizing the distinct neurophysiologic disturbances present in this population and presenting the central nervous system effects of sedative agents to permit optimal drug therapy.Data SourcesReview of the English language clinical and scientific literature using MEDline data search.Study SelectionLiterature references were selected through a key word search of sedative therapy, drugs used for sedation, and specific neurologic disorders and processes to provide an in-depth overview of sedative drug mechanisms of action, effects on neurophysiology and intracranial dynamics, pharmacokinetics, and toxicity profile. Special emphasis was placed on neurologic side effects.Data ExtractionClinical and scientific literature was reviewed and data relevant to neurophysiologic effects of sedative drug therapy were summarized. Recommendations for institution of sedative therapy and of particular agents were made as a result of analysis of all pooled data.Data SynthesisCritically ill patients with neurologic pathology present as a unique subset of individuals cared for in an acute care setting. Because monitoring of neurologic patients requires frequent assessment of the neurologic examination, the goal of sedative therapy should be to enhance, or to minimally perturb elicitation of the examination. Neurophysiologic disturbances introduce distinct risks for sedation and require their identification and understanding before the initiation of any sedative therapy. Sedative drugs, in particular, act to disturb central nervous system function and their effects may result in diagnostic confusion and further neurologic deterioration. The pharmacokinetic and neurophysiologic actions of the common classes of sedative agents, such as benzodiazepines, opioids, barbiturates, and neuroleptics, as well as ketamine, propofol, and clonidine are discussed. Recommendations are presented based on the specific type of sedation required and the underlying neurologic disturbance. Several specific examples, including head trauma, neuromuscular disease, and alcohol withdrawal, are provided.ConclusionsPreservation of the neurologic examination is paramount in documenting clinical improvement or deterioration in the critically ill neurologic patient. Pharmacologic sedation in this unique population of acute care patients requires careful consideration of the underlying neurophysiologic disturbances and potential adverse effects introduced by sedative drugs.(Crit Care Med 1995; 23:2038-2053)
ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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14. |
Remote communication from a mobile terminalAn adjunct for a computerized intensive care unit order management system |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2054-2057
Neil A. MD Halpern,
Gary BSEE Burnett,
Steven BMT Morgan,
Paul BS Miller,
Robert MD Greenstein,
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摘要:
ObjectivesTo develop and implement a fully mobile computer terminal that interfaces with our computerized intensive care unit (ICU) local area network and order management system. This system can provide access to the entire network and to order review and entry and during ICU bedside rounds.DesignDescriptive report.SettingSurgical ICU in Department of Veterans Affairs Medical Center.System ConfigurationA parallel local area network was configured for the remote mobile computer system. A proprietary remote transmission system (Altair II, Motorola) was used. This high-throughput system minimizes interference and errors by using licensed, nonshared, radiofrequency spectra.ConclusionThe resulting mobile system is an economical and time-efficient adjunct to an established ICU computerized network and order management system. Clinical working bedside rounds are now routinely conducted with the mobile terminal, providing immediate access to full network resources.(Crit Care Med 1995; 23:2054-2057)
ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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15. |
Use of T-Test With Nonparametric DataFentanyl Withdrawal Syndrome |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2058-2059
Robert MD Katz,
H. William PharmD Kelly,
Clifford PhD Qualls,
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ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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16. |
Death to DustWhat Happens to Dead Bodies? |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2059-2060
Karen DO O'Mara,
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ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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17. |
Metabolic Support of the Critically Ill Patient |
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Critical Care Medicine,
Volume 23,
Issue 12,
1995,
Page 2060-2060
David C. MS Frankenfield,
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ISSN:0090-3493
出版商:OVID
年代:1995
数据来源: OVID
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