scholarly journals Pharmacokinetic differences between peripheral and central drug administration during cardiopulmonary resuscitation

1985 ◽  
Vol 6 (5) ◽  
pp. 1073-1077 ◽  
Author(s):  
Uzi Talit ◽  
Shimon Braun ◽  
Hillel Halkin ◽  
Boris Shargorodsky ◽  
Shlomo Laniado
1997 ◽  
Vol 86 (6) ◽  
pp. 1375-1381 ◽  
Author(s):  
Volker Wenzel ◽  
Karl H. Lindner ◽  
Andreas W. Prengel ◽  
Keith G. Lurie ◽  
Hans U. Strohmenger

Background Intravenous administration of vasopressin during cardiopulmonary resuscitation (CPR) has been shown to be more effective than optimal doses of epinephrine. This study evaluated the effect of endobronchial vasopressin during CPR. Methods After 4 min of untreated ventricular fibrillation and 3 min of CPR, 21 pigs were randomized to be treated with 0.8 U/kg intravenous vasopressin (n = 7), 0.8 U/kg endobronchial vasopressin (n = 9), or an endobronchial placebo of normal saline (n = 5). Defibrillation was performed 5 min after drug administration to attempt return of spontaneous circulation. Results All animals in the intravenous and endobronchial vasopressin group were resuscitated successfully, but only two of five animals in the placebo group were. At 2 and 5 min after drug administration, coronary perfusion pressure in the intravenous and endobronchial vasopressin group was significantly higher than in the placebo group (50 +/- 10, 34 +/- 5 vs. 16 +/- 6 mmHg, respectively; and 35 +/- 10, 39 +/- 10 vs. 19 +/- 5 mmHg, respectively; P < 0.05). Conclusions Endobronchial vasopressin is absorbed during CPR, coronary perfusion pressure is increased significantly within a short period, and the chance of successful resuscitation is increased in this porcine model of CPR. Endobronchial vasopressin may be an alternative for vasopressor administration during CPR, when intravenous access is delayed or not available.


2019 ◽  
Author(s):  
Chao Li ◽  
Hai-Fei Gu ◽  
Xiao-Li He ◽  
Yu Zhang ◽  
Jie-Qing Min ◽  
...  

Abstract Cardiac arrest (CA) and cardiopulmonary resuscitation (CPR) have always been two research hotpots in emergency medicine. Problems such as optimizing animal CA models and promoting CPR efficiency are to be explored. Establishing animal CA models is the precondition of CPR study. Previous studies usually use electric shock or intravenous drug administration to induce CA in animals. Nevertheless, as electric shock is complicated to operate and the dosage for drug administration is difficult to control, many published animal CA models are not ideally stable and operable. In order to establish a stable and operable CA model for cardiac arrest- cardiopulmonary resuscitation (CA-CPR) research, this study established different pig CA models via intravenous administration of KCI, MgSO 4 and ketamine respectively, and subsequently performed CRP with a self-designed inspiratory impedance threshold device (SIITD). The success rate of CRP in different CA models was evaluated according to hemodynamic and biochemical parameters of pigs. Results demonstrated that in the CA model established by intravenous administration of MgSO 4 , cardiac output of pigs were significantly elevated and reached the normal range at 10-min after CPR, and other vital signs and biochemical parameters in this model exhibited recovery trends throughout CPR. This study provides a more effective CA model and new ideas in methodology of future CA-CPR research.


2019 ◽  
Author(s):  
Chao Li ◽  
Hai-Fei Gu ◽  
Xiao-Li He ◽  
Yu Zhang ◽  
Jie-Qing Min ◽  
...  

Abstract Cardiac arrest (CA) and cardiopulmonary resuscitation (CPR) have always been two research hotpots in emergency medicine. Problems such as optimizing animal CA models and promoting CPR efficiency are to be explored. Establishing animal CA models is the precondition of CPR study. Previous studies usually use electric shock or intravenous drug administration to induce CA in animals. Nevertheless, as electric shock is complicated to operate and the dosage for drug administration is difficult to control, many published animal CA models are not ideally stable and operable. In order to establish a stable and operable CA model for cardiac arrest- cardiopulmonary resuscitation (CA-CPR) research, this study established different pig CA models via intravenous administration of KCI, MgSO 4 and ketamine respectively, and subsequently performed CRP with a self-designed inspiratory impedance threshold device (SIITD). The success rate of CRP in different CA models was evaluated according to hemodynamic and biochemical parameters of pigs. Results demonstrated that in the CA model established by intravenous administration of MgSO 4 , cardiac output of pigs were significantly elevated and reached the normal range at 10-min after CPR, and other vital signs and biochemical parameters in this model exhibited recovery trends throughout CPR. This study provides a more effective CA model and new ideas in methodology of future CA-CPR research.


Author(s):  
Gianluca Sgarbi ◽  
Timna Hitrec ◽  
Roberto Amici ◽  
Alessandra Baracca ◽  
Alessia Di Cristoforo ◽  
...  

2007 ◽  
Vol 41 (10) ◽  
pp. 1679-1686 ◽  
Author(s):  
Marcia L Buck ◽  
Barbara S Wiggins ◽  
Jefferson M Sesler

Objective: To review and assess the available literature on the use of intraosseous (IO) drug administration during cardiopulmonary resuscitation, addressing the benefits and risks of using this method of drug delivery in children and adults. Data Sources: The MEDLINE (1950–July 2007) database was searched for pertinent abstracts, using the key term intraosseous infusions. Additional references were obtained from the bibliographies of the articles reviewed. Manufacturer Web sites were used to obtain information about IO insertion devices. Study Selection and Data Extraction: All available English-language clinical trials, retrospective studies, and review articles describing IO drug administration were reviewed. Studies conducted in animal models to evaluate the effectiveness and safety of IO drug administration were also included. Data Synthesis: IO access uses the highly vascularized bone marrow to deliver fluids and medications during cardiopulmonary resuscitation. This route, developed in the 1940s, has been revived In the past decade as a means of achieving rapid vascular access when intravenous access cannot be obtained. The primary advantage of IO access is the high success rate (approximately 80%). Most trained providers can place an IO line within 1–2 minutes. A number of small-scale studies and retrospective reviews have established the usefulness of this route for the delivery of many commonly used resuscitation drugs. In addition, animal models have demonstrated rapid drug delivery to the systemic circulation. While all resuscitation drugs can be given by the IO route, administration of ceftriaxone, chloramphenicol, Phenytoin, tobramycin, and vancomycin may result in lower peak serum concentrations. The most common adverse effect seen with IO use, extravasation, has been reported in 12% of patients. Compartment syndrome, osteomyelitis, and tibial fracture are rare, but have also been reported. Conclusions: IO administration is a safe and effective method for delivering drugs during cardiopulmonary resuscitation. It should be considered whenever intravenous access cannot be rapidly obtained.


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