Objective, To assess the outcome of fibromyalgia syndrome (FM) in a 30
-month followup study of children with FM. Methods, In the original st
udy to assess the prevalence of FM in healthy Schoolchildren, we found
21 children with FM and an additional 7 fulfilling the point count cr
iterion only (11 of 18). Fifteen of the 21 and all 7 were recruited fo
r a 2nd assessment in our present study. In all children, a count of 1
8 tender points (TP) was conducted by thumb palpation. Tenderness of 9
of the TP sites as well as 4 control point sites was further assessed
using a Chatillon dolorimeter. All children were questioned concernin
g the presence of widespread pain or aching. Children were considered
to have FM if they met the American College of Rheumatology criteria f
or diagnosis. Results, After 30 months, 11 of the 15 children with FM
(73%) were no longer fibromyalgic. The mean point count of the 15 chil
dren significantly decreased from 12.5 to 4.6 (p < 0.001). The mean te
nderness threshold of the 9 tender sites increased from 2.4 to 3.4 kg
(p < 0.01), and the mean tenderness threshold of the 4 control sites i
ncreased from 4.1 to 5.6 kg (p < 0.05). Of the 7 children initially fu
lfilling the point count criterion only, none had developed FM. Their
mean point count decreased from 11.4 to 3.4 (p = 0.001), and their mea
n tenderness thresholds increased from 2.7 kg to 3.9 kg (p = 0.001) at
tender sites and from 4.3 kg to 6.8 kg (p < 0.001) at control sites.
Conclusion. We suggest that the outcome of FM in children is more favo
rable than in adults. More followup studies are needed to clarify the
longterm outcomes of FM in children and adults.