TY - JOUR
T1 - Surgery for treating femoroacetabular impingement (protocol)
AU - Wall, Peter D H
AU - Brown, Jamie S
AU - Parsons, Nick
AU - Buchbinder, Rachelle
AU - Costa, Matthew L
AU - Griffin, Damian
PY - 2013
Y1 - 2013
N2 - In the last few years there has been increasing recognition of the
syndrome of femoroacetabular impingement (FAI), sometimes
also called hip impingement, which seems to account for a large
proportion of previously undiagnosed cases of hip pain and restricted
range of motion in young adults (Lavigne 2004).
Subtle shape abnormalities of the hip (a ball and socket joint)
combine to cause impingement between the femoral neck and
head (ball) and anterior rimof the acetabulum(socket),most often
in flexion and internal rotation (Lavigne 2004). Three types of
deformities have been recognised:
1. Cam type, asphericity of the femoral head and widening of the
femoral neck (abnormalities of shape, typically bumps around the
ball of the joint);
2. Pincer type, over coverage of the antero-superior acetabularwall,
and abnormal version of the femur or acetabulum (irregularities of
shape, typically a socket that is too deep or pointing in an abnormal
direction); or
3. mixed type, a combination of the two (Ganz 2003).
Excess contact forces between the proximal femur and the acetabular
rim during the end range of motion of the hip results in soft
tissue lesions of the acetabular labrum (the soft cushion around
the socket) and the adjacent acetabular cartilage leading to pain
and restricted range of movement (Beck 2004). FAI seems to be
associated with progressive articular degeneration of the acetabulum,
usually starting from the antero-superior rim and extending
medially and posteriorly (Beck 2004).
The cause of FAI shapemalformations is likely to bemultifactorial,
but may include slipped capital femoral epipihysis (SCFE), which
is thought to lead to Cam type FAI (Leunig 2000;Mamisch 2009;
Millis 2011). However, other authors now suggest that FAI shape
malformations are actually part of a hominid evolutionary process
(Hogervorst 2011) whereby Cam type morphology, so called cox
recta, is an adaptive
AB - In the last few years there has been increasing recognition of the
syndrome of femoroacetabular impingement (FAI), sometimes
also called hip impingement, which seems to account for a large
proportion of previously undiagnosed cases of hip pain and restricted
range of motion in young adults (Lavigne 2004).
Subtle shape abnormalities of the hip (a ball and socket joint)
combine to cause impingement between the femoral neck and
head (ball) and anterior rimof the acetabulum(socket),most often
in flexion and internal rotation (Lavigne 2004). Three types of
deformities have been recognised:
1. Cam type, asphericity of the femoral head and widening of the
femoral neck (abnormalities of shape, typically bumps around the
ball of the joint);
2. Pincer type, over coverage of the antero-superior acetabularwall,
and abnormal version of the femur or acetabulum (irregularities of
shape, typically a socket that is too deep or pointing in an abnormal
direction); or
3. mixed type, a combination of the two (Ganz 2003).
Excess contact forces between the proximal femur and the acetabular
rim during the end range of motion of the hip results in soft
tissue lesions of the acetabular labrum (the soft cushion around
the socket) and the adjacent acetabular cartilage leading to pain
and restricted range of movement (Beck 2004). FAI seems to be
associated with progressive articular degeneration of the acetabulum,
usually starting from the antero-superior rim and extending
medially and posteriorly (Beck 2004).
The cause of FAI shapemalformations is likely to bemultifactorial,
but may include slipped capital femoral epipihysis (SCFE), which
is thought to lead to Cam type FAI (Leunig 2000;Mamisch 2009;
Millis 2011). However, other authors now suggest that FAI shape
malformations are actually part of a hominid evolutionary process
(Hogervorst 2011) whereby Cam type morphology, so called cox
recta, is an adaptive
UR - http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD010796/pdf
U2 - 10.1002/14651858.CD010796
DO - 10.1002/14651858.CD010796
M3 - Article
VL - 11
SP - 1
EP - 13
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
SN - 1469-493X
M1 - CD010796
ER -