Hindawi Publishing Corporation ISRN Anesthesiology Volume 2013, Article ID 103289, 6 pages http://dx.doi.org/10.1155/2013/103289 Clinical Study Pharmacoeconomics and Pharmacodynamic Interactions of Rocuronium and Pancuronium HariSrinivas Shyam Kumar, 1 Padmaja Durga, 2 Rama Mohan Pathapati, 3 Sujith Tumkur Rajashekar, 4 Pothula Narasimha Reddy, 5 and Gopinath Ramachandran 2 1 Department of Anesthesiology and Intensive Care, Narayana Hrudayalaya Malla Reddy Hospital, No. 1-1-216, Suraram “X” Road, Jeedimetla, Hyderabad 500055, India 2 Department of Anesthesiology and Intensive Care, Nizam’s Institute of Medical Sciences, Panjagutta, Hyderabad 500082, India 3 Departments of Clinical Pharmacology and Medical Research, Narayana Medical College and Super Specialty Hospital, Chinthareddypalem, Nellore 524002, Andhra Pradesh, India 4 Department of Clinical Pharmacology, Narayana Medical College and Super Specialty Hospital, Chinthareddypalem, Nellore 524002, Andhra Pradesh, India 5 Department of Anesthesiology and Intensive Care, Narayana Medical College and Super Specialty Hospital, Chinthareddypalem, Nellore 524002, Andhra Pradesh, India Correspondence should be addressed to Rama Mohan Pathapati; pill4ill@yahoo.co.in Received 17 December 2012; Accepted 3 January 2013 Academic Editors: E. Freye and C. H. Wong Copyright © 2013 HariSrinivas Shyam Kumar et al. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Background. We evaluated the pharmacodynamic interaction of the combination of pancuronium and Rocuronium by analyzing time-response relationship, quality of intubating conditions, changes in the hemodynamics, and cost effectiveness as compared to individual drugs. Methods. Sixty patients in the ASA-I category received either 10 ml of 0.9 mg/kg rocuronium (R) plus 10 ml of saline or 10 ml of 0.1 mg/kg pancuronium (P) plus 10 ml of saline or a combination (C) of 10 ml of 0.45 mg/kg R plus 10 ml of 0.05 mg/kg P according to randomization list. Neuromuscular function was measured up to maximal suppression of twitch height. Results. e mean times (sec) taken for twitch height to decrease to 50% of baseline in R, P, and C were 36.84 ± 2.54, 74.60 ± 4.94, and 40.81 ± 2.34, respectively. e mean cost of intubation per patient was 316.71 ± 83.61 INR in group R, 52.30 ± 14.94 INR in group P, and 93.33 ± 20.65 INR in group C. Conclusions. e combination of P and R provides rapid and smooth intubation with minimal hemodynamic changes at a reasonably priced cost. 1. Introduction Over the last few decades the focus of research has been on the development of muscle relaxants with a short onset of action that can be used for rapid sequence intubation. It has been shown that speed of onset is inversely related to molar potency [1, 2]. e major disadvantage of use of less potent drugs is pharmacoeconomics burden of intubation [3, 4]. So far, it has been very di�cult to �nd the optimal compromise between potency and rapid onset of action. e pharma- cokinetic options to achieve rapid onset of action are use of supramaximal doses, priming, and cocktails of relaxants. Many experimental combinations of amino steroid relaxants and benzo-isoquinolinium relaxants failed to demonstrate either synergism or pharmacoeconomics advantage [5]. Pancuronium is one of the most potent and least expen- sive nondepolarizing neuromuscular blocking drugs avail- able. However, its onset of action is slow. Pancuronium has predominant postsynaptic mechanism of action, whereas rocuronium, a monoquaternary analogue of Pancuronium has a predominant presynaptic action [6]. It has been hypothesized that combination of these drugs with different pharmacodynamic characteristics might confer advantage of synergism resulting in rapid onset of action at a lesser cost. To this purpose we evaluated the pharmacodynamic interaction by analyzing time-response relationship, quality