Evid Based Nurs 2008 Treatment 11
Evid Based Nurs 2008 Treatment 11
Evid Based Nurs 2008 Treatment 11
com
These include:
References This article cites 2 articles
http://ebn.bmj.com/content/11/1/11.full.html#ref-list-1
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Notes
Treatment
Review: vaccines against human Outcomes: high-grade cervical lesions (high-grade squamous
intraepithelial lesion or grade 2 or 3 cervical intraepithelial
papillomavirus prevent cervical cancer neoplasia [CIN]), any grade cervical lesions, persistent HPV
infection, external genital lesions, and adverse events.
precursors in young women
MAIN RESULTS
QUESTION
HPV vaccines reduced the risks of all outcomes in the
Do vaccines against human papillomavirus (HPV) prevent
modified intention-to-treat population that included 84–
cervical cancer precursors in young women?
100% of randomised women (table). Groups did not differ
for serious adverse events (table).
METHODS
Data sources: Medline and EMBASE/Excerpta Medica (to
May 2007); Medline in process (to June 2007); Cochrane CONCLUSION
Library and Cochrane Central Register of Controlled Trials Vaccines against human papillomavirus (HPV) in young
(Issue 1, 2007); conference proceedings (2004–7); clinical trial women prevent persistent infection and precancerous cervical
registers; Google Scholar; public health announcements; disease associated with vaccine-specific HPV types.
reference lists; and vaccine manufacturers.
Study selection and assessment: randomised controlled
ABSTRACTED FROM
trials (RCTs) that compared a vaccine against >1 oncogenic
Rambout L, Hopkins L, Hutton B, et al. Prophylactic
type of HPV with placebo or no HPV vaccine for prophylaxis
vaccination against human papillomavirus infection and
of oncogenic HPV-related infection and disease in women. 9
disease in women: a systematic review of randomized
reports of 6 RCTs (n = 40 323; mean age 20 y, range 15–26 y)
controlled trials. CMAJ 2007;177:469–79.
met the selection criteria. 1 RCT (n = 2392) evaluated a
monovalent HPV 16 vaccine, 2 RCTs (n = 19 757) evaluated a Correspondence to: Ms L Rambout, Ottawa Hospital, Ottawa, Ontario, Canada;
bivalent HPV 16/18 vaccine, and 3 RCTs (n = 18 174) lrambout@ottawahospital.on.ca
evaluated a quadrivalent HPV 6/11/16/18 vaccine. Quality
Source of funding: not stated.
assessment of individual trials was based on the Jadad scale
and allocation concealment; all 6 RCTs were of high c Clinical impact ratings: Family/General practice 5/7; Infectious disease 5/7;
methodological quality. Oncology 5/7; Women’s health 6/7
Vaccines against oncogenic types of human papillomavirus (HPV) v placebo or no HPV vaccine to prevent vaccine-type HPV-associated cervical cancer
precursors in young women (modified intention-to-treat population)*
Weighted event rates
Outcomes at 15–60 months Number of trials (n) Vaccine Control RRR (95% CI) NNT (CI)
Grade 2 CIN or worse 5 (36 266) 0.8% 1.5% 48% (37 to 57) 138 (116 to 179)
Any grade CIN 5 (24 613) 0.7% 1.9% 64% (55 to 71) 81 (73 to 95)
Persistent HPV infection at 6 months 3 (14 207) 0.9% 4.0% 77% (72 to 81) 33 (31 to 35)
Persistent HPV infection at 12 months 2 (7774) 0.4% 1.6% 74% (59 to 84) 86 (76 to 108)
External genital lesions 2 (5981) 1.1% 3.5% 69% (56 to 77) 41 (37 to 51)
Serious adverse events 6 (39 609) 2.2% 2.2% 0% (214 to 13) Not significant
*CIN = cervical intraepithelial neoplasia; other abbreviations defined in glossary. Weighted event rates, RRR, NNT, and CI calculated from data in article.
COMMENTARY
he systematic review by Rambout et al is a in real world populations, duration of effect, and the efficacy has not been determined. Vaccination must