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Canadian Family PhysicianLe Médecin de famille canadien Vol 54:  january • janVier 2008

Letters  Correspondance

committee  to  present  identified  topics.  The  speakers  are  instructed  to  provide  full  disclosure  to  their  audi- ence, and speakers with declared competing interests  that  are  selected  must  provide  full  content  of  their  presentations beforehand, which also undergoes peer  review.  Furthermore,  sessions  evaluations  are  moni- tored for perception of bias to ensure CME that is free  from commercial influence.

The  exhibit  hall  is  entirely  separate  from  our  CME  sessions. In our exhibit hall, only 30% of the booths are  sold  to  the  pharmaceutical  industry.  Recruiters,  resi- dency programs, medical associations, and not-for-profit  exhibitors make up most of the booths. There are strict  rules  in  place  preventing  sampling  or  giveaways,  and  exhibitors are allowed to distribute educational material  only.  Attendance  at  these  booths  is  not  part  of  accred- ited CME.

Again, I believe that the situation regarding industry- biased  CME  has  changed  dramatically  in  recent  years  and differs between Canada and the United States. The  guidelines  and  review  processes  that  we  have  in  place  at the College ensure that our accredited CME programs  are not abused for commercial interests.

 —Bernard Marlow MD CCFP FCFP Director of Continuing Professional Development College of Family Physicians of Canada

Correction

I

t  has  come  to  my  attention  that Figure 3  in  our  article  “Urinary  incontinence  in  Canada.  National  survey  of  family  physicians’  knowledge,  attitudes,  and  practices”  (Can Fam Physician  2002;48:86-92)  contained an error. The correct figure appears below. 

I apologize for any confusion that might have arisen  from this error.

—Graham Swanson MD MSc FCFP Burlington, Ont

by e-mail

Labour pains

I 

read with interest the article by Minty et al describing  the  challenges  of  providing  high-quality  analgesia  to  women in labour in small community hospitals.1

The  recommended  combination  of  intrathecal  (IT)  opioids  and  local  anesthetic  is  said  to  have  a  lasting  effect of about 4 hours. Hence, if the duration of remain- ing  labour  exceeds  this,  then  a  period  of  untreated  labour  pain  will  follow.  The  doses  of  opioid  and  local  anesthetic  recommended  in  the  article  are  conven- tional  and  are  limited  by  side  effects  such  as  nausea  and hypotension. 

Whereas  multiple  adjuvant  agents  to  prolong  anal- gesia  have  been  investigated  (from  IT  opioids  to  local  anesthetics), none have become widely used owing to  side effects.2 However, IT midazolam is unique among  these.  This  agent  has  been  in  use  for  more  than  20  years  as  part  of  either  a  single-shot  or  continuous  spi- nal-infusion  technique.  It  increases  the  duration  and  quality  of  IT  opioid-mediated  analgesia  in  the  labour- pain model, with no reported increase in side effects.3  Intrathecal  midazolam  has  been  used  in  the  cesarean  section model, where it not only increased the duration  of analgesia as compared with IT bupivacaine, but also  appeared to prevent nausea.4 In the surgical model, IT  midazolam  shows  a  dose-sparing  effect  on  local  anes- thetic agents.5

It  is  unfortunate  that  precise  data  on  the  duration  of  action  of  IT  midazolam  are  hard  to  obtain.  This  is  probably  because  when  administered  alone  it  has  minimal  (or  no)  detectable  effects.  Our  knowledge  is  derived  from  other  agents’  increase  in  duration  of  analgesia.  From  my  own  experience  and  from  the  available  literature,  6  hours  of  effects  from  a  single  dose  is  a  conservative  estimate.  I  have  always  had  access to an epidural (as opposed to a single-shot spi- nal) for labour-pain relief service, and have only used  spinal  analgesia  as  part  of  a  combined  spinal-epidu- ral  technique  or  to  obtain  rapid  pain  control  to  facili- tate  siting  an  epidural  catheter.  Having  tried  many  combinations  of  IT  drugs,  however,  my  spi- nal  anesthetic  of  choice  for  cesarean  section  is  heavy  bupivacaine  (9  to  10  mg),  with  mor- phine  (75  μg),  and  midazolam  (2  mg).  I  have  not  had  the  opportunity  to  test  this  in  a  trial  setting  but  have  found  that  this  combination  produces  rapid  onset  spinal  anesthesia,  with  minimal nausea and pruritus. I have found no  need to include a drug from the fentanyl fam- ily,  suggesting  that  the  onset  of  action  and  prolongation  of  the  effects  of  morphine  are  accelerated  by  the  presence  of  midazolam.  If  this were true, in the drug combination recom- mended in the review article1 sufentanil could  be  replaced  by  midazolam  in  spinal  anesthe- sia for labour pain. 

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Vol 54:  january • janVier 2008 Canadian Family PhysicianLe Médecin de famille canadien

29

It is difficult to explain why the use of IT midazolam  is  not  more  widespread  given  the  ongoing  interest  in  adjuvant  agents  and  it’s  unique  beneficial  side-effect  profile.  Concerns  over  neurotoxicity  are  often  raised.6  There  has  never  been  a  reported  case  of  neurotox- icity  in  humans,  however,  and  animal  studies  show  very  inconsistent  results.  The  largest  reported  series  of patients receiving IT midazolam to date is 547 in a  safety  study.7  Further  work  on  continuous  spinal  infu- sion  of  midazolam-containing  solutions  in  periopera- tive analgesia is ongoing.   

If  IT  midazolam  were  to  be  included  in  single-shot  spinal  analgesia  for  labour  pain,  I  believe  that  the  quality  of  analgesia  would  be  greatly  improved  at  no  extra  risk  and  negligible  cost  (studies  to  demonstrate  whether this does hold true would be relatively easy to  conduct). It should be possible to reduce the dose of IT  opioid,  and  sufentanil  could  probably  be  omitted.  The  need  for  reinstrumentation  and  alternative  analgesic  techniques (with their attendant costs and risks) would  surely be reduced. 

—Michael Andrew Duncan Bath, UK by e-mail references

1. Minty RG, Kelly L, Minty A, Hammett DC. Single-dose intrathecal analgesia to  control labour pain: is it a useful alternative to epidural analgesia? Can Fam Physician 2007;53(3):437-42.

2. Roelants F. The use of neuraxial adjuvant drugs (neostigmine, clonidine) in  obstetrics. Curr Opin Anaesthesiol 2006;19(3):233-7.

3. Tucker AP, Mezzatesta J, Nadeson R, Goodchild CS. Intrathecal midazolam  II: Combination with intrathecal fentanyl for labor pain. Anesth Analg  2004;98:1521-7.

4. Prakash S, Joshi N, Gogia AR, Prakash S, Singh R.  Analgesic efficacy of two  doses of intrathecal midazolam with bupivacaine in patients undergoing  cesarean delivery. Reg Anesth Pain Med 2006;31(3):221-6. 

5. Wu YW, Shiau JM, Hong CC, Hung CP, Lu HF, Tseng CC. Intrathecal midazolam  combined with low-dose bupivacaine improves postoperative recovery in dia- betic mellitus patients undergoing foot debridement. Acta Anaesthesiol Taiwan  2005;43(3):129-34. 

6. Yaksh TL, Allen JW. The use of intrathecal midazolam in humans: a case  study of process. Anesth Analg 2004;98(6):1536-45.

7. Tucker AP, Lai C, Nadeson R, Goodchild CS. Intrathecal midazolam I: a cohort  study investigating safety. Anesth Analg 2004;98(6):1512-20.

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