Page 34 - CPG - Clinical Practice Guidelines - Management of Cancer Pain
P. 34

Management of Cancer Pain (Second Edition)
                  RI •     25          &,      WR       DQG •     25           &,
                  2.42 to 7.54). 30, level I

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                  dry mouth. There is also an increased risk of convulsion with its use.
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                  with strong opioids. 29, level III
                  A Cochrane  systematic review comparing  codeine  ± paracetamol
                  with placebo found limited evidence to indicate that codeine is more
                  effective in cancer pain. However, it had an increased risk of nausea,
                  vomiting and constipation. 31, level I  In clinical practice, oral codeine and
                  dihydrocodeine appear to be equipotent. 9
                  Weak opioids are generally more  accessible compared with strong
                  opioids. In situations where access to morphine or other strong opioids
                  may be limited or not immediate, tramadol or dihydrocodeine may be
                  an option in cancer pain management.


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                  •  Weak opioids may be used for moderate pain (step 2 of the WHO
                    analgesic ladder) in cancer pain.

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                  the appropriate  dose is the dose which  provides  pain  relief without
                  causing major or intolerable AEs. In most settings, morphine remains
                                                                  28
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                                                    32
                  listed in the WHO essential medicines list.
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                  A large  Cochrane  systematic review  of 62 studies compared  the
                  effectiveness and safety of oral morphine  with various controls in
                  relieving cancer pain. The range of oral morphine doses used varied
                  from 25 mg/day to 300 mg/day and titrated to effect. Mean daily doses
                  UDQJHG  IURP       PJ GD\  WR       PJ GD\  ZLWK  WKH  PD[LPXP  GRVH
                  UHFRUGHG DW      PJ GD\  7KH ¿QGLQJV ZHUH  33, level I
                    {  morphine was  an effective  analgesic for  moderate to  severe
                      cancer pain and >90% of  participants had ‘no worse than mild
                      pain’
                    {  adverse  events (AEs) were common and predictable  but only
                      DSSUR[LPDWHO\      RI  SDUWLFLSDQWV  GLVFRQWLQXHG  WUHDWPHQW  ZLWK
                      morphine because of intolerable AEs


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