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Métodos Terapêuticos e Terapias MTCI
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1.
Am J Emerg Med ; 70: 19-29, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-37196592

RESUMO

PURPOSE: Rapid-sequence intubation (RSI) is the process of administering a sedative and neuromuscular blocking agent (NMBA) in rapid succession to facilitate endotracheal intubation. It is the most common and preferred method for intubation of patients presenting to the emergency department (ED). The selection and use of medications to facilitate RSI is critical for success. The purpose of this review is to describe pharmacotherapies used during the RSI process, discuss current clinical controversies in RSI medication selection, and review pharmacotherapy considerations for alternative intubation methods. SUMMARY: There are several steps to the intubation process requiring medication considerations, including pretreatment, induction, paralysis, and post-intubation sedation and analgesia. Pretreatment medications include atropine, lidocaine, and fentanyl; but use of these agents in clinical practice has fallen out of favor as there is limited evidence for their use outside of select clinical scenarios. There are several options for induction agents, though etomidate and ketamine are the most used due to their more favorable hemodynamic profiles. Currently there is retrospective evidence that etomidate may produce less hypotension than ketamine in patients presenting with shock or sepsis. Succinylcholine and rocuronium are the preferred neuromuscular blocking agents, and the literature suggests minimal differences between succinylcholine and high dose rocuronium in first-pass success rates. Selection between the two is based on patient specific factors, half-life and adverse effect profiles. Finally, medication-assisted preoxygenation and awake intubation are less common methods for intubation in the ED but require different considerations for medication use. AREAS FOR FUTURE RESEARCH: The optimal selection, dosing, and administration of RSI medications is complicated, and further research is needed in several areas. Additional prospective studies are needed to determine optimal induction agent selection and dosing in patients presenting with shock or sepsis. Controversy exists over optimal medication administration order (paralytic first vs induction first) and medication dosing in obese patients, but there is insufficient evidence to significantly alter current practices regarding medication dosing and administration. Further research examining awareness with paralysis during RSI is needed before definitive and widespread practice changes to medication use during RSI can be made.


Assuntos
Etomidato , Ketamina , Bloqueadores Neuromusculares , Humanos , Succinilcolina , Etomidato/uso terapêutico , Rocurônio , Indução e Intubação de Sequência Rápida , Ketamina/uso terapêutico , Estudos Retrospectivos , Hipnóticos e Sedativos/uso terapêutico , Serviço Hospitalar de Emergência , Bloqueadores Neuromusculares/uso terapêutico , Intubação Intratraqueal/métodos
2.
J Pharm Pract ; 36(3): 716-718, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35109718

RESUMO

D-cycloserine (DCS) is an anti-tuberculosis medication that has been utilized for years for drug-resistant tuberculosis. DCS works via a centrally acting mechanism which can cause neurotoxic adverse effects which has limited its use. This centrally acting mechanism also allows for DCS to be utilized for various neuropsychiatric purposes. Our patient was on high-dose DCS for autism spectrum disorder and presented to the emergency department (ED) with a seizure. The seizure episode was managed with both anti-epileptics and pyridoxine. With increasing novel use of this older medication, it is imperative for ED clinicians to be aware of the different management strategies that may be required when a patient presents with a neurotoxic effect, specifically seizures, secondary to DCS.


Assuntos
Transtorno do Espectro Autista , Ciclosserina , Humanos , Ciclosserina/efeitos adversos , Transtorno do Espectro Autista/tratamento farmacológico , Anticonvulsivantes/uso terapêutico , Convulsões/induzido quimicamente , Serviço Hospitalar de Emergência
4.
Am J Emerg Med ; 38(9): 1984.e1-1984.e3, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32505475

RESUMO

INTRODUCTION: Systemic reactions from local tetracaine use are often an anomaly - not only is tetracaine short-acting and quickly metabolized by the pseudocholinesterase system leading to very limited systemic uptake, but most adverse reactions are usually associated with dental or spinal anesthesia. Furthermore, reactions to local anesthetics manifest in standard allergy-type reactions. When local anesthetics lead to nervous or cardiac system abnormalities, it is termed a local anesthetic systemic toxicity - an event with an incidence currently estimated to be 0.03%. CASE PRESENTATION: We present a case of a 56-year-old female who experienced a systemic reaction to tetracaine 1% while undergoing a fine needle biopsy of a thyroid nodule. The patient had previous allergic reactions to lidocaine. Upon conclusion of the procedure, the patient began convulsing and became rigid and non-verbal. She was able to move all extremities, had no respiratory distress, no swelling, hives, or redness, and was swallowing without difficulty. After about 5 min, the patient began to improve and experienced reversal of all previous symptoms. Her physical exam and labs were otherwise normal, she returned to her baseline functioning, and was discharged without any medical interventions. DISCUSSION: This case illustrates a case of LAST in a patient with previous Lidocaine allergy without any other obvious risk factors. There have been no cases of cross-reaction between lidocaine and tetracaine so it explores the possibility of patients having cross reaction to those two different kinds of local anesthetic.


Assuntos
Anestésicos Locais/toxicidade , Convulsões/induzido quimicamente , Tetracaína/toxicidade , Anestesia Local/efeitos adversos , Anestesia Local/métodos , Biópsia por Agulha/efeitos adversos , Feminino , Humanos , Pessoa de Meia-Idade , Nódulo da Glândula Tireoide/patologia
5.
Am J Emerg Med ; 38(4): 853.e1-853.e3, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31831341

RESUMO

INTRODUCTION: Heat stroke occurs when the body's core temperature becomes elevated above 40 °C, which may impact multiple organ systems. We present a case of heat stroke resulting in acute liver injury (ALI) successfully treated with intravenous N-acetylcysteine (NAC). CASE PRESENTATION: A 24-year-old unresponsive male without significant past medical history presented to the emergency department with heat stroke; his initial temperature was 107.4 °F. During his hospital course, he developed ALI with significant elevation in aspartate aminotransferase, alanine aminotransferase, and total bilirubin. These laboratory findings peaked by hospital day two, but improved prior to discharge on hospital day five and throughout his follow up clinic visits. His treatment course included cooling measures, supportive care, supplemental oxygen and airway management, seizure control, and intravenous NAC therapy. CONCLUSION: Hepatocellular injury is one of the most serious complications of heat stroke. We discuss the incidence and outcomes for patients who develop acute liver injury secondary to heat stroke and the use of NAC as an early potential therapeutic option.


Assuntos
Acetilcisteína/uso terapêutico , Golpe de Calor/complicações , Falência Hepática Aguda/etiologia , Acetilcisteína/administração & dosagem , Serviço Hospitalar de Emergência , Humanos , Infusões Intravenosas , Falência Hepática Aguda/tratamento farmacológico , Falência Hepática Aguda/terapia , Masculino , Adulto Jovem
6.
Burns ; 45(1): 32-41, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-29776863

RESUMO

Recently, many studies have demonstrated pleotropic effects of vitamin D, including immune modulation and cardiovascular system activity. Sufficient vitamin D concentrations and supplementation of vitamin D may be of benefit in burn-injured patients. Low 25(OH)D has been observed in nearly all pediatric and most adult burn patients. Vitamin D has primarily been studied in pediatric burn patients, focusing on bone marker measurements and the incidence of fractures. The preferred vitamin D dose, formulation, and route of administration remain unknown, and there is limited data on the impact of vitamin D status on clinical outcomes. Further research should focus on determining optimal monitoring strategies, supplementation regimens and clinical outcomes like mortality, length of stay and incidence of sepsis.


Assuntos
Osso e Ossos/metabolismo , Queimaduras/metabolismo , Cálcio/metabolismo , Deficiência de Vitamina D/metabolismo , Vitamina D/metabolismo , Vitaminas/uso terapêutico , Adulto , Queimaduras/imunologia , Criança , Estado Terminal , Suplementos Nutricionais , Humanos , Vitamina D/análogos & derivados , Vitamina D/imunologia , Vitamina D/uso terapêutico , Deficiência de Vitamina D/imunologia , Deficiência de Vitamina D/terapia , Proteína de Ligação a Vitamina D/metabolismo
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