Free
Clinical Science  |   October 1998
Combined Intravenous Lidocaine and Inhaled Salbutamol Protect against Bronchial Hyperreactivity More Effectively than Lidocaine or Salbutamol Alone 
Author Notes
  • (Groeben) Oberarzt, Department of Anesthesiology and Critical Care Medicine.
  • (Silvanus) Funktionsoberarztin, Department of Anesthesiology and Critical Care Medicine.
  • (Beste) Technician, Department of Gastroenterology.
  • (Peters) Professor and Chairman, Abteilung fur Anasthesiologie und Intensivmedizin.
Article Information
Clinical Science
Clinical Science   |   October 1998
Combined Intravenous Lidocaine and Inhaled Salbutamol Protect against Bronchial Hyperreactivity More Effectively than Lidocaine or Salbutamol Alone 
Anesthesiology 10 1998, Vol.89, 862-868. doi:
Anesthesiology 10 1998, Vol.89, 862-868. doi:
This article is featured in “This Month in Anesthesiology.” Please see this issue of Anesthesiology, page 7A.
INSTRUMENTATION of the airway, such as tracheal intubation or bronchoscopy, can cause life-threatening bronchospasm. The closed-claim study of the American Society of Anesthesiologists revealed that 2% of the claims were related to bronchospasm and resulted in death or brain damage in more than 90% of these patients. In 69% of these patients, severe reflex bronchoconstriction occurred during induction of general anesthesia. [1] 
[Greek small letter beta]-Adrenergic aerosols, such as salbutamol, and the intravenous administration of lidocaine have been recommended to prevent bronchospasm in patients with bronchial hyperreactivity who undergo airway instrumentation. [2,3] Although [Greek small letter beta]-adrenergic aerosols are recommended as a first-line treatment for acute bronchoconstriction, the cardiac side effects (i.e., tachycardia and arrhythmia) still are a matter of concern. [4,5] Therefore, an adjunct or alternative treatment with fewer cardiac side effects would be beneficial in patients at risk for myocardial ischemia, particularly when the drugs are used to prevent a potential risk and not to treat acute life-threatening bronchospasm.
The sodium channel blockers lidocaine and mexiletine significantly attenuate reflex bronchoconstriction after intravenous and oral administration, as tested by an inhalational histamine challenge. [6] However, although lidocaine has been used to attenuate cardiac and cough reflexes for more than 20 yr, [7,8] its effects have never been compared with standard treatment and prophylaxis with [Greek small letter beta]-adrenergic aerosols. Furthermore, it has not been determined whether combined treatment with these drugs, which probably exert effects via different mechanisms, may be advantageous.
Accordingly, we assessed and compared in volunteers with bronchial hyperreactivity the effects of intravenously administered lidocaine, of inhalation of salbutamol, and of combined treatment on an inhalational challenge with histamine. We will show that lidocaine and salbutamol significantly attenuate bronchial hyperreactivity and that combined treatment even further decreases airway reactivity.
Methods
Participants
After we received approval from the local ethics committee and informed written consent, we enrolled 15 persons (age, 34.9 +/− 6.4 yr; mean +/− SD) in this randomized, double-blind, placebo-controlled study. Eight of the volunteers were women and seven were men. All had either active asthma (n = 9), childhood asthma (n = 1), severe hay fever (n = 3), or chronic obstructive pulmonary disease (n = 2) and showed symptoms consistent with airway hyperreactivity. Two of the volunteers smoked tobacco. Eight used an inhaler with [Greek small letter beta]-adrenergic drugs-three regularly, five as needed-and two used inhaled corticosteroids. None of the volunteers used a [Greek small letter beta]-adrenergic medication within at least the last 12 h before the measurement were obtained.
Measurements
The same air-conditioned room was used throughout the study; therefore, the humidity was kept constant, and the room temperature (22 [degree sign]C) varied only by +/− 1 [degree sign]C. All measurements were performed for each participant at the same time of day (+/−1 h). Lung function was measured using a body plethysmograph with an integrated spirometer (Jaeger, Wurzburg, Germany). At the initial screening visit, baseline vital capacity (VC), forced expiratory volume in 1 s (FEV1), and airway resistance were assessed (Table 1), and bronchial hyperreactivity was confirmed in each volunteer using an inhalational provocation with histamine. [6] Lidocaine plasma concentrations were determined by immunofluorescence assay (Abbott TDx System, Wiesbaden, Germany). The lower level of detection is 0.1 [micro sign]g/ml, and the coefficient of variation is less than 3%. [9] The blood samples were processed from 13 of 15 volunteers. During interventions, heart rate (electrocardiographic lead II) and arterial pressure (oscillometry) were also measured.
Table 1. Demographic Data and Baseline Pulmonary Function of 15 Subjects with Bronchial Hyperreactivity at the Time of the Screening Visit
Image not available
Table 1. Demographic Data and Baseline Pulmonary Function of 15 Subjects with Bronchial Hyperreactivity at the Time of the Screening Visit
×
Aerosol Challenge. Aerosol inhalation was performed using a nebulizer (model 646, DeVilbiss, Somerset, PA) driven by compressed air at 30 psi using a mouth piece and a nose clip. The start of nebulization was triggered by integration of flow (Spira elektro 2 flow meter; Respiratory Care Center, Hameenlinna, Finland) after inspiration of 500 - 750 ml and maintained for 0.6 s. The beginning of nebulization was set to 500 ml for volunteers with a VC less than 4 1, to 600 ml for those with a VC of 4 to 5.5 1, and to 750 ml for those with a VC of more than 5.5 1. The volunteers were instructed to inspire from functional residual capacity to inspiratory capacity at an inspiratory flow rate less than 0.6 1/s. At end-inspiration the volunteers were advised to hold their breath for 5 s. This maneuver was repeated five times. One or two minutes after inhalation of each aerosol dose, FEV1and VC were measured at least three times and the largest FEV (1) and VC were accepted.
Initially the volunteers were challenged with aerosolized saline, followed by increasing doses of histamine diphosphate (Sigma-Aldrich GmbH, Deisenhofen, Germany) diluted in saline. The starting concentration of histamine diphosphate was 0.074 mg/ml, which was trebled to 0.223, 0.67, 2, and 6 on each subsequent challenge up to a maximal concentration of 18 mg/ml. The time interval between increasing histamine concentrations was kept constant between 5 and 7 min.
Challenges were discontinued if the volunteers showed symptoms of chest tightness or difficulty in breathing, a decrease in FEV1of at least 20% from pre-challenge baseline, or had received the maximal concentration of histamine diphosphate (18 mg/ml). The histamine threshold concentration necessary for a 20% decrease in FEV1was calculated for each volunteer by linear regression over the challenge steps performed. [10] Fifteen volunteer who had a decrease of 20% in FEV1within the range of histamine diphosphate concentrations tested were enrolled in the study. Five additional volunteers responded with a decrease in FEV1of less than 20%(range, 13 - 17%) to the histamine screening challenge, so consequently they were not enrolled.
In a given volunteer the starting concentration for all subsequent challenges was chosen two concentration steps lower than the concentration of histamine diphosphate that had caused a 20% decrease in FEV1(PC20) in the screening visit. If a volunteer, because of one of the interventions, did not reach a 20% decrease in FEV1during the study days, the threshold was calculated by extrapolation. [10] 
For consistency, all lung function measurements were made by a single investigator (H.G.) who was blinded to the drugs administered.
Study Protocol. Two 18-gauge cannulas were inserted into right and left antecubital veins to infuse lidocaine or placebo and withdraw blood to measure lidocaine plasma concentrations, respectively. On each study day, baseline lung function was assessed, and further measurements were postponed if the actual FEV1differed by more than 7% from the baseline value measured during the screening visit. This was necessary on 2 of the 60 study days.
At four visits, in random order, and in a double-blinded manner, the volunteers received (1) salbutamol aerosol, (2) lidocaine intravenously, (3) salbutamol and lidocaine in sequence, or (4) placebo. This was accomplished as follows.
1. Salbutamol aerosol: The participants inhaled 1.5 mg salbutamol diluted in 1.5 ml saline followed by intravenous administration of saline (0.15 ml/kg over 20 min, followed by 0.3 ml [middle dot] kg-1[middle dot] h-1until the end of the histamine challenge).
2. Lidocaine intravenously: The participants inhaled 1.5 ml normal saline followed by intravenous administration of lidocaine (1.5 mg/kg lidocaine over 20 min followed by infusion of 3 mg [middle dot] kg-1[middle dot] h-1lidocaine of a lidocaine solution, 1%, to maintain lidocaine plasma concentrations until the end of the histamine challenge.
3. Combined lidocaine and salbutamol treatment: The participants received inhaled salbutamol and intravenous lidocaine in sequence with the same dosages and timing as described previously.
4. Placebo control: The participants inhaled saline and received saline intravenously according to the same infusion regimen and timing as described previously.
To determine lidocaine plasma concentrations, venous blood was drawn before the start of the lidocaine or saline infusions and, subsequently, at 5-min intervals for 90 min.
Data Analysis
Data were presented as mean +/− SD. The following a priori null hypotheses were tested:(1) Intravenously administered lidocaine, salbutamol, or lidocaine and salbutamol combined do not change the histamine threshold compared with placebo. (2) The effects of combined treatment with salbutamol and lidocaine are not different than the effects of treatment with either salbutamol or lidocaine alone. Comparisons were made using the Friedman test followed by Wilcoxon's signed rank test with Bonferroni correction for multiple comparisons. The null hypotheses were rejected, and significant differences were assumed with an [Greek small letter alpha] error of less than 0.05.
Results
(Table 1) shows the anthropometric data, the baseline lung function, and the PC20at the initial visit.
Baseline FEV1and VC on each study day also were compared with the FEV1and VC after treatment with lidocaine, salbutamol, lidocaine and salbutamol, and placebo. The FEV1significantly increased after the administration of salbutamol and salbutamol combined with lidocaine, whereas placebo and lidocaine alone did not significantly change baseline FEV1or VC (Table 2).
Table 2. FEV1and VC on Each Study Day and Posttreatment with Lidocaine, Salbutamol, Combined Lidocaine and Salbutamol, or Placebo (n = 15)
Image not available
Table 2. FEV1and VC on Each Study Day and Posttreatment with Lidocaine, Salbutamol, Combined Lidocaine and Salbutamol, or Placebo (n = 15)
×
(Figure 1) shows lidocaine plasma concentrations after intravenous administration. Peak plasma concentrations at the end of the administration of the initial lidocaine infusion averaged 2.4 +/− 0.6 [micro sign]g/ml when lidocaine was administered alone and was 2.2 +/− 0.6 [micro sign]g/ml after salbutamol inhalation. These concentrations did not differ significantly from the concentrations at the end of the inhalational challenge (2.2 +/− 0.5 [micro sign]g/ml and 2.1 +/− 0.6 [micro sign]g/ml, respectively). As shown in Figure 1, lidocaine plasma concentrations were maintained at a nearly constant concentration during the inhalation challenge.
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
×
The histamine threshold (PC20) after intravenous and inhalational administration of placebo (6.4 +/− 4.3 mg/ml histamine) did not differ significantly from the threshold obtained at the screening visit (7.2 +/− 5 mg/ml).
Intravenous administration of lidocaine and inhalation of salbutamol each significantly increased the histamine threshold by more than 100% to 14.2 +/− 9.5 mg/ml and to 16.8 +/− 10.9 mg/ml, respectively. The combination of intravenous lidocaine and salbutamol aerosol increased the histamine threshold even further to 30.7 +/− 15.7 mg/ml when compared with placebo. This threshold was significantly higher than the thresholds observed after treatment with lidocaine or salbutamol alone. Figure 2shows the thresholds for each volunteer on each study day.
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
×
Heart rate and arterial blood pressure were not affected significantly by lidocaine infusion (data not shown). However, one volunteer responded with a reproducible increase in heart rate (by 11 - 15 beats/min) after each salbutamol inhalation compared with the salbutamol-free study days.
Three of 15 volunteers noted mild symptoms such as light-headedness and slight vertigo during the intravenous administration of lidocaine, and one volunteer mentioned these symptoms during placebo administration.
Discussion
Prevention of bronchospasm in persons with bronchial hyperreactivity is desirable when airway instrumentation for general anesthesia or bronchoscopy is necessary. We found that lidocaine significantly attenuated bronchial hyperreactivity in awake volunteers with bronchial hyperreactivity as much as did an inhaled dose of 1.5 mg salbutamol. Furthermore, the combination of lidocaine and salbutamol attenuates bronchial hyperreactivity to a much greater extent than does pretreatment with either drug alone.
These results emerged from studies in 15 volunteers with moderate bronchial hyperreactivity. All were in a stable clinical condition during current medication period or during a symptom-free interval and were not exposed to their seasonal allergens. Volunteers with moderate bronchial hyperreactivity were selected because persons with more severe hyperreactivity would have been at greater risk during the challenges and might have shown a greater daily variability of lung function in response to a histamine challenge. [11] 
A histamine challenge was chosen because it is well standardized, and the results obtained are comparable to our previous study. [6] Histamine inhalation not only directly stimulates smooth muscle cells, as does methacholine, but also involves neural pathways. [12,13] It has been shown by direct, single nerve fiber recordings from lung-irritant receptors that histamine causes irritation of the airways that is similar to that caused by pharmacologically inert carbon dust or cigarette smoke. [12] 
Therefore, a challenge with histamine is, to some extent, comparable to the stimulation evoked by tracheal intubation.
To minimize uneven distribution by turbulent air flow, the challenge was performed with control of inspiratory flow, a 5-s breath hold at the end of inspiration, a defined time of nebulization during inspiration, [14] and a fixed number of breaths to ensure high reproducibility of the challenges during each of the four study days. Maximal reproducibility of the challenge also was the reason to use the FEV1(that is associated with a low daily variability) as the variable to analyze the responses to histamine. [15-17] 
The dose of lidocaine we chose was somewhat less than the dose used in a previous study in which we observed more severe side effects. [6] In this way, we decreased lidocaine peak plasma concentrations and observed fewer volunteers with mild side effects than with the previous study. Frequent determinations of lidocaine plasma concentration indicated that lidocaine administration resulted in an initial increase but, of greater methodological importance, an almost constant lidocaine concentration throughout the challenge series (Figure 2).
Salbutamol led to a statistically significant increase in baseline FEV1by 5%. Although the change in baseline was significant in healthy persons, a shift of 5 - 10% is necessary to be clinically significant. In persons with asthma or chronic obstructive pulmonary disease, the change must be even greater to be clinically relevant. [15-17] Therefore, it is unlikely that the baseline shift that was observed has a significant effect on the subsequent challenge.
In elderly patients, cardiac side effects are the main concern and limit the use of [Greek small letter beta]-mimetic bronchodilators, as outlined recently in an editorial and an original article. [4,5] Therefore, a moderate dose of salbutamol with a low risk for the occurrence of tachycardia or dysrhythmia was chosen. With this dose, no significant increase in heart rate with salbutamol inhalation was observed, although one volunteer showed a reproducible mild increase in heart rate after salbutamol inhalation. With a further increase in the dose of salbutamol, a higher incidence of cardiac side effects would have been possible. Thus, the dose of salbutamol chosen for pretreatment was protective against the histamine challenge but carried a low risk for cardiac complications. Similarly, the dose of lidocaine was chosen below the threshold for central nervous side effects. The mechanisms by which lidocaine attenuates bronchoconstriction may include direct effects on smooth muscle cells and neural blockade of vagal reflex pathways. [18-20] 
A direct relaxing effect of lidocaine on airway smooth muscle has been shown in vitro in which topical lidocaine (104to 103M) significantly attenuated the contractile response of pig tracheal muscle strips to direct stimulation by acetylcholine and by hyperkalemia. [19] However, lidocaine concentrations used in these experiments far exceed (10- to 100-fold) the lidocaine plasma concentrations observed during clinical use. Therefore, although it cannot be completely ruled out that direct effects on smooth muscle contribute to attenuation of bronchial hyperreactivity, this mechanism does not seem to be a likely explanation for attenuation of bronchial hyperreactivity by intravenous lidocaine observed in our volunteers.
It is more likely that nerve conduction blockade offers the main explanation for the effects of lidocaine. Lidocaine, in concentrations of 61 [middle dot] 106M, abolishes constriction of rat tail arteries evoked by sympathetic nerve stimulation but not constriction induced by direct stimulation of smooth muscle cells by potassium or norepinephrine. [20] Furthermore, different reflexes (the Betzold-Jarisch reflex, the cough reflex, the intestinal stretch reflexes) are attenuated or even completely abolished after intravenous administration of lidocaine and other local anesthetics in clinically relevant concentrations in animals. [21,22] Finally, in humans undergoing general anesthesia for surgery, intravenous lidocaine effectively suppressed the reflex-induced cough. [7,23] Therefore, reflex suppression is the most likely mechanism to explain the protective effect of lidocaine as assessed by a histamine challenge in persons with bronchial hyperreactivity. That lidocaine attenuated airway reflexes but did not alter baseline bronchial tone is also consistent with unaltered lung function at baseline observed in this and in our previous study, in contrast to [Greek small letter beta]-adrenergic aerosols with direct relaxing effects on smooth muscle cells. [24] The idea that both drugs attenuate the response to histamine by different mechanisms and the finding that both drugs were not administered to maximal effect (to minimize the side effects) can explain the marked effect of combined pretreatment, with lidocaine and salbutamol increasing PC20significantly more than either pretreatment alone.
In conclusion, intravenous lidocaine significantly attenuates bronchial hyperreactivity to an extent that is comparable to a moderate dose of salbutamol. Furthermore, the combination of intravenous lidocaine and inhaled salbutamol markedly increases the protective effect of either drug alone without increasing cardiac or central nervous side effects. Therefore, combined pretreatment with intravenous lidocaine and salbutamol aerosol can be recommended to protect patients with bronchial hyperreactivity from noxious stimulation of their airways (such as during tracheal intubation or bronchoscopy), particularly those with a coexisting risk for myocardial ischemia.
REFERENCES
Cheney FW, Posner KL, Caplan RA: Adverse respiratory events infrequently leading to malpractice suits. Anesthesiology 1991; 75:932-9
Kil HK, Rooke GA, Ryan-Dykes MA, Bishop MJ: Effect of prophylactic treatment on lung resistance after tracheal intubation. Anesthesiology 1994; 81:43-8
Gal TJ: Bronchial hyperresponsiveness and anesthesia: Physiologic and therapeutic perspectives. Anesth Analg 1994; 78:559-73
Leff AR: Identifying patients at risk from the use of beta-adrenergic agonists (editorial). Am J Respir Crit Care Med 1996; 154:1593
Suissa S, Hemmelgarn B, Blais L, Ernst P: Bronchodilators and acute cardiac death. Am J Respir Crit Care Med 1996; 154:1598-602
Groeben H, Foster WM, Brown RH: Intravenous lidocaine and oral mexiletine block reflex bronchoconstriction in asthmatic subjects. Am J Respir Crit Care Med 1996; 154:885-8
Steinhaus JE, Gaskin L: A study of lidocaine as a suppressant of cough reflex. Anesthesiology 1963; 24:285-90
Stoelting RK: Circulatory changes during direct laryngoscopy and tracheal intubation. Anesthesiology 1977; 47:381-3
Jolley ME: Fluorescence polarization immunoassay for the determination of therapeutic drug levels in human plasma. J Anal Toxicol 1981; 5:236-40
Manning PJ, Jones GL, O'Byrne PM: Tachyphylaxis to inhaled histamine in asthmatic subjects. J Appl Physiol 1987; 63:1572-7
Eiser NM, Kerrebijn KF, Quanjer PH: Guidelines for standardization of bronchial challenges with (nonspecific) bronchoconstricting agents. Bull Europ Physiopath Resp 1983; 19:495-514
Sellick H, Widdicombe JG: Stimulation of lung irritant receptors by cigarette smoke, carbon dust, and histamine aerosol. J Appl Physiol 1971; 31:15-9
Shore SA, Bai TR, Wang CG, Martin JG: Central and local cholinergic components of histamine-induced bronchoconstriction in dogs. J Appl Physiol 1985; 58:443-51
Laube BL, Norman PS, Adams GK: The effect of aerosol distribution on airway responsiveness to inhaled methacholine in patients with asthma. J Allergy Clin Immunol 1992; 89:510-8
Rozas CJ, Goldman AL: Daily spirometric variability: Normal subjects and subjects with chronic bronchitis with and without airflow obstruction. Arch Intern Med 1982; 142:1287-91
Nickerson BG, Lemen RJ, Gerdes CB, Wegman MJ, Robertson G: Within-subject variability and percent change for significance of spirometry in normal subjects and in patients with cystic fibrosis. Am Rev Respir Dis 1980; 122:859-66
Dawson A: Reproducibility of spirometric measurements in normal subjects. Am Rev Respir Dis 1966; 93:264-9
Weiss EB, Hargraves WA, Viswanath SG: The inhibitory action of lidocaine in anaphylaxis. Am Rev Respir Dis 1978; 117:859-69
Kai T, Nishimura J, Kobayashi S, Takahashi S, Yoshitake J, Kanaide H: Effects of lidocaine on intracellular Ca2+and tension in airway smooth muscle. Anesthesiology 1993; 78:954-65
Szocik JF, Gardner CA, Webb RC: Inhibitory effects of bupivacaine and lidocaine on adrenergic neuroeffector junctions in rat tail artery. Anesthesiology 1993; 78:911-7
Zipf HF: The pharmacology of viscero-afferent receptors with special reference to endoanaesthesia. Acta Neuroveg 1966; 29:169-96
Zipf HF, Reichertz P: Darstellung der totalen und reversiblen Endoanaesthesie der Lungendehnungsreceptoren durch Wirkung/Zeit-Kurven. Naunyn Schmiedebergs Arch Exp Pathol Pharmacol 1957; 231:96-110
Nishino T, Hiraga K, Sugimori K: Effects of i.v. lignocaine on airway reflexes elicited by irritation of the tracheal mucosa in humans anaesthetized with enflurane. Br J Anaesth 1990; 64:682-7
Ingram RH, Wellman JJ, McFadden ER, Mead J: Relative contribution of large and small airways to flow limitation in normal subjects before and after atropine and isoproterenol. J Clin Invest 1977; 59:696-703
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
Figure 1. The time course of lidocaine serum concentration with (squares) and without (circles) salbutamol pretreatment (mean +/− SD). The peak lidocaine concentrations are less than the toxic range of 5 [micro sign]g/ml. With the continuous infusion of lidocaine after the loading dose, a nearly stable lidocaine concentration was maintained during the inhalational challenge; there is no significant difference in lidocaine concentrations at the end of the loading dose and at the end of the inhalational challenge.
×
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
Figure 2. Inhaled histamine concentrations inducing a 20% decrease in the forced expiratory volume in 1 s (FEV1) before and after lidocaine (left), salbutamol (middle), and combined salbutamol and lidocaine (right) administration, respectively. Each pair of symbols represents the response of individual volunteers, whereas the mean response (+/− SD) is shown to the left and to the right of the individual responses. Data are from 60 inhalational challenges with histamine performed on four different days in 15 persons with bronchial hyperreactivity. Lidocaine and salbutamol both significantly increased the histamine threshold compared with placebo, with no statistical difference occurring between lidocaine and salbutamol. The combination of lidocaine and salbutamol also significantly increased the histamine threshold, but markedly more than lidocaine (P = 0.0007) or salbutamol (P = 0.0008) alone.
×
Table 1. Demographic Data and Baseline Pulmonary Function of 15 Subjects with Bronchial Hyperreactivity at the Time of the Screening Visit
Image not available
Table 1. Demographic Data and Baseline Pulmonary Function of 15 Subjects with Bronchial Hyperreactivity at the Time of the Screening Visit
×
Table 2. FEV1and VC on Each Study Day and Posttreatment with Lidocaine, Salbutamol, Combined Lidocaine and Salbutamol, or Placebo (n = 15)
Image not available
Table 2. FEV1and VC on Each Study Day and Posttreatment with Lidocaine, Salbutamol, Combined Lidocaine and Salbutamol, or Placebo (n = 15)
×