Anaesthesia management of patients with airway susceptibilities: what have we learnt from animal models?

被引:9
|
作者
Habre, Walid [1 ]
Petak, Ferenc [2 ]
机构
[1] Geneva Childrens Hosp, Paediat Anaesthesia Unit, Geneva, Switzerland
[2] Univ Szeged, Dept Med Phys & Informat, Szeged, Hungary
关键词
GUINEA-PIG AIRWAYS; ACETYLCHOLINE-INDUCED BRONCHOCONSTRICTION; METHACHOLINE-INDUCED BRONCHOCONSTRICTION; THORACIC EPIDURAL-ANESTHESIA; ADVERSE RESPIRATORY EVENTS; DEPENDENT CA2+ CHANNELS; PLASMA HISTAMINE LEVELS; LARYNGEAL MASK AIRWAY; SMOOTH-MUSCLE; PORCINE TRACHEAL;
D O I
10.1097/EJA.0b013e328361d404
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Anaesthesia management of patients with airway susceptibility remains a challenge in daily clinical practice due to the increased risk of perioperative bronchospasm. Therefore, understanding the mechanisms participating in the interaction between anaesthetic drugs and the lungs is essential in providing the optimal care for patients with chronic lung diseases. Experimental studies performed on various animal models mimicking airway susceptibility have played a key role in understanding the pathogenesis of lung diseases and have characterised the different pathways involved in the altered airway and lung tissue responses to anaesthetic agents. This narrative review highlights the progress that has been achieved by investigations in animal models and discusses the potential translation of these experimental findings to the clinical setting. The application of animal models with normal and allergically sensitised airways demonstrated that volatile and intravenous anaesthetic agents, muscle relaxants, analgesics and local anaesthetics exert their pulmonary effects via different neurosensorial pathways and through activating various receptors in the lungs. Attention is drawn to the significant differences in the pulmonary effects of anaesthetic agents between lungs with normal and those with susceptible airways. Extrapolating clear-cut conclusions from animal research to clinical practices should be made with caution, particularly for muscle relaxants, opioids and local anaesthetics wherein complex pathophysiological mechanisms are responsible for the potential respiratory effects of these agents. Animal models are of great importance in evaluating the potential interaction between anaesthetic drugs and the lungs, in identifying the pathways involved and in targeting preventive or treatment strategies to the lung compartment primarily involved.
引用
收藏
页码:519 / 528
页数:10
相关论文
共 50 条
  • [41] Omics in melanoma - what have we learnt and what is the potential impact for patient management?
    Spatz, Alan
    Eggermont, Alexander M. M.
    van den Oord, Joost
    EJC SUPPLEMENTS, 2007, 5 (05): : 423 - 424
  • [42] Rotator Cuff Tears: What have we learned from animal models?
    Edelstein, L.
    Thomas, S. J.
    Soslowsky, L. J.
    JOURNAL OF MUSCULOSKELETAL & NEURONAL INTERACTIONS, 2011, 11 (02) : 150 - 162
  • [43] Human resource management in times of crisis: what have we learnt from the recent pandemic?
    Newman, Alexander
    Ferrer, Justine
    Andresen, Maike
    Zhang, Yucheng
    INTERNATIONAL JOURNAL OF HUMAN RESOURCE MANAGEMENT, 2023, 34 (15): : 2857 - 2875
  • [44] Aplastic Anemia: What Have We Learned From Animal Models and From the Clinic
    Scheinberg, Phillip
    Chen, Jichun
    SEMINARS IN HEMATOLOGY, 2013, 50 (02) : 156 - 164
  • [45] Development effectiveness: What have we learnt?
    Collier, P
    Dollar, D
    ECONOMIC JOURNAL, 2004, 114 (496): : F244 - F271
  • [46] COPD in farmers: what have we learnt?
    Elliott, Leslie
    von Essen, Susanna
    EUROPEAN RESPIRATORY JOURNAL, 2016, 47 (01) : 16 - 18
  • [47] CUP and chemotherapy: what have we learnt?
    Massard, C.
    Fizazi, K.
    ONCOLOGIE, 2008, 10 (12) : 728 - 732
  • [48] The Wrist Series – What Have We Learnt?
    Andrew E. Ajani
    Ron Waksman
    Herz, 2002, 27 : 23 - 29
  • [49] Looking back, what have we learnt?
    Louapre, C.
    MULTIPLE SCLEROSIS JOURNAL, 2022, 28 (3_SUPPL) : 102 - 103
  • [50] CANDIDATE ASSESSMENT: WHAT HAVE WE LEARNT?
    Rae, J. M.
    ANNALS OF ONCOLOGY, 2011, 22 : 26 - 26