I read with great interest the paper by Kinsella et al on rapid sequence spinal anaesthesia [1]. I have three issues I would like to raise. Firstly, I am concerned about the potential compromise of aseptic precautions in this technique. As indicated in the article, the majority of UK anaesthetists routinely wear gown, gloves, mask and hat when performing a spinal [2], and while logic suggests that for a no-touch technique a gown is probably unnecessary, (unlike for epidural insertion, where there is a catheter that may become contaminated), the AAGBI’s 2008 publication “Infection Control in Anaesthesia” [3] specifically states: “The Working Party is aware that many anaesthetists do not employ this level of asepsis for ‘one-shot’ spinals or epidurals but believes that when central neural spaces are penetrated, full aseptic precautions are required.”
There is also the issue of preparation of the skin. I am not convinced that a single wipe of 0.5% chlorhexidine over the intended insertion site allows satisfactory decontamination of the skin, especially given that chlorhexidine is colourless. Therefore, the extent of the prepared area may not be obvious. Traditionally, two applications of alcoholic chlorhexidine have been recommended [4], although recent work has suggested that one spray of alcoholic 0.5% chlorhexidine is sufficient to completely decontaminate the skin in 100% of subjects [5]. A spray will cover a larger area than a wipe, and may be performed by another member of the theatre team. It is important to remember that the chlorhexidine-containing fluid must be allowed time to dry, both to be fully effective, and because of a possible risk of chronic adhesive arachnoiditis. I am concerned that the atmosphere of urgency that is present within the operating theatre, when a Category 1 caesarean section is announced, may result in anaesthetists performing or being pressurised to perform spinal anaesthesia, before the cleaning solution is completely dry. This may increase the risk of such rare complications. It may therefore be better to recommend that the patient’s back is given a single spray with alcoholic 0.5% chlorhexidine, which is allowed to dry while the anaesthetist prepares his equipment.
Finally, I am concerned that adoption of such techniques will furthe rdecrease the exposure of junior anaesthetists to general anaesthesia for caesarean section. Whilst it is well-recognised that regional techniques have advantages over general anaesthesia for obstetric surgery, the incidence of general anaesthesia will never be zero in this population. Indeed, Kinsella et al recommend that general anaesthesia should be the fall-back technique when spinal anaesthesia is not immediately successful. However, the widespread adoption of regional anaesthesia, coupled with a fall in the number of hours worked by junior doctors in recent years, means that the number of general anaesthetics performed for obstetric surgery may be as low asone per junior doctor per year [6]. Performing a general anaesthetic aftera failed rapid sequence spinal will not only cost time, it will also add to the stress and pressure of an already difficult situation. It strikes me that patients such as these slim women (mean approximate weight of 66kg), assuming that they present during daylight hours in a consultant-led unit, present avaluable opportunity for juniors to gain supervised experience in providing general anaesthesia for caesarean section. This opportunity should not be sacrificed for a potentially suboptimal spinal technique, simply to avoid general anaesthesia at all costs.
Roy M Williamson
Liverpool Women’s Hospital
Liverpool
References
1. Kinsella SM, Girgirah K, Scrutton MJL. Rapid sequence spina lanaesthesia for category-1 urgency caesarean section: a case series. Anaesthesia 2010; 65: 664–669.
[2] Naik M, Mannakkara C, Aravindham N. National postal survey of methods used to ensure aseptic whilst performing regional analgesia and anaesthesia in obstetrics. International Journal of Obstetric Anesthesia 2008; 17:S27.
[3] Association of Anaesthetists of Great Britain and Ireland. Infection Control in Anaesthesia. Anaesthesia
2008; 63: 1027-1036.
[4] Reynolds F. Infection as a complication of neuraxial blockade. . International Journal of Obstetric Anesthesia 2005; 14: 183-188.
[5] Malhotra S, Dharmadasa A, Phillip S, Jepson A, Siegmueller C, Yentis SM. One versus two applications of chlorhexidine/ethanol for skin disinfection before regional anaesthesia. International Journalof Obstetric Anesthesia 2010; 19: S10.
[6] Searle RD, Lyons G. Vanishing experience in training for obstetric general anaesthesia: an observational study. International Journal of Obstetric Anesthesia 2008; 17:233–237.