Professional Documents
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Childhood
Contents Keywords
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4469
Aetiology Antibiotic treatment Children :
Septic Arthritis Complications Diagnosis
Pathophysiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4470
Epidemiology Pathophysiology Surgical
Aetiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4471 Treatment
Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4472
Differential Diagnosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4474
Introduction
Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4475
Prognosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4478 Most bacterial infections in childhood are easily
Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4479 diagnosed, readily treated, and have good out-
comes. By contrast suppurative infections of the
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4480
skeletal system still present challenges, since
these illnesses are often difficult to manage med-
ically and surgically. In spite of our best efforts,
a substantial portion of those treated are left with
disabling sequelae [1]. Although physicians are
getting better at diagnosis and treatment, septic
arthritis can still be a challenge in terms of the
diagnosis and management, especially in infants,
due to the lack of clinical symptoms.
According to Nelson [1], in the USA one in
5,000 children under the age of 13 years will have
osteomyelitis, and about twice as many will have
a septic arthritis (Fig. 1). Although pyogenic
M.C. Neves (*) arthritis occurs in all age groups the peak inci-
Orthopaedic Department, Hospital Cuf Descobertas, dence of the disease is in children under 3 years of
Parque das Nacoes, Lisboa, Portugal age [2] and boys are more likely to be affected
e-mail: Cassianoneves.manuel@gmail.com
than girls [3]. The incidence of septic arthritis in
J.L. Campagnolo children has been estimated as 5.5 to 12 cases per
Orthopaedic Department, Hospital Dona Estefania,
Lisbon, Portugal 100,000 individuals [4].
Although most children have no underlying
M.J. Brito C.F. Gouveia
Infectious Disease Department, Hospital Dona Estefania, disorder, risk factors for pyogenic arthritis
Lisbon, Portugal include immunodeficiency, haemoglobinopathy,
400
No Patients
300
200
100
<2 2 to 5 6 to 10 11 to 16
Age in years
diabetes, intravenous drug abuse and rheumatoid common. Penetrating injuries, especially in the
arthritis [57]. knee joint and foot, can be responsible for septic
The outcome is poor in 27 % of patients with arthritis. Metaphyseal osteomyelitis may result in
septic arthritis and in nearly 40 % of those with involvement of the adjacent joint. In infants and
involvement of the hip [1]. The clinical picture until 18 months of age, small vessels cross the
has not changed, but more recently we have seen proximal growth-plates, particularly in the non-
a change in the incidence and in the type of ossified epiphysis, leading to an extension of the
bacteria responsible for this particular condition metaphyseal abscess into the joint [15, 16]
[8]. The best example is in the virtual elimination (Fig. 2). This is more evident in the proximal
of septic arthritis caused by Haemophilus femur and may cause devastating consequences
influenzae type b in immunised patients after the in the young child if not promptly treated. After
introduction of the vaccine [9]. At the same time this age the vascular channels disappear and the
diagnostic tools such as ultrasound or the use of growth-plate starts to act as a barrier to the ter-
polymerase chain reaction for the detection of minal vessels of the metaphysis. In certain joints
bacterial pathogens have been improving the like the hip, knee, shoulder and elbow, the cap-
accuracy in the diagnosis [10, 11]. These have sular attachments are at the level of the
led to an increase in the diagnosis of metaphysis [17]. There is then a high possibility
osteoarticular infections caused by Kingella of direct spread of the metaphyseal abscess into
kingae in toddlers [12, 13]. The modern Orthope- the joint after perforation of the thin cortex by the
dic paediatric surgeon should be alerted to these abscess. Perlman et al. [18] found a 33 % inci-
new trends in order to improve his ability to dence of concomitant septic arthritis in their
diagnose and to better treat this condition. patients who had osteomyelitis, one third of
them located at the knee joint (Fig. 2).
In the absence of early treatment, destruction
Pathophysiology of the articular cartilage takes place secondary to
the release of proteolytic enzymes from the syno-
Septic arthritis is considered to be a secondary vial cells. Interleukin-1 triggers the release of
infection from a primary focus, or due to proteases from chondrocytes and synoviocytes
a transient bacteraemia from an event like in response to polymorphonuclear leucocytes
brushing the teeth [14]. Infection may reach and bacteria. Degradation results in loss of pro-
the joint through several routes with teoglycans after 5 days and of collagen by 9 days.
haematogeneous dissemination being the most Impairment of the intracapsular vascular supply
Septic Arthritis in Infancy and Childhood 4471
Fig. 2 Mechanism of
spread of a metaphyseal
abscess into the joint
also plays a role in the articular destruction, infections caused by these S. aureus strains are
with elevation of the intracapsular pressure, now much more frequent, mostly in the United
thrombosis, and progressive displacement of the States, and are thought to be associated with
femoral head from the acetabulum [1921]. worse clinical outcomes [2325]. Risk
factors for acquisition of MRSA have been
described, such as young age or lower socio-
Aetiology economic status, however their clinical relevance
is questionable [26]. MRSA infections are
Age is the most important predictor of aetiology more aggressive than Methicillin susceptible
of pyogenic arthritis. Staphylococcus aureus, infections involving multiple bones and joints
enteric gram-negative organisms and a group and sometimes are associated with thrombosis
B Streptococcus (GBS) are the most frequent and pulmonary disease [24, 27, 28].
causes of pyogenic arthritis among neonates. Streptococci (especially group A beta-
Staphylococcus aureus, Kingella kingae, Strepto- haemolytic organisms and pneumococi) have
coccus pyogenes and Streptococcus pneumonia been responsible for the majority of other gram-
cause pyogenic arthritis in children younger than positive infections. Haemophilus influenzae type
5 years of age. Staphylococcus aureus and b used to be important in children under 2 years of
S. pyogenes are the most common causes of pyo- age but due to widespread immunization is rarely
genic arthritis in children older than 5 years seen nowadays.
[13, 22]. Staphylococcus aureus is the most com- Other organisms reported to cause pyogenic
mon agent causing septic arthritis in all ages. arthritis in children include Neisseria
In recent years methicillin-resistant S. aureus meningitidis and Kingela kingae [29, 30].
(MRSA) has emerged in the community, In recent years, Kingella kingae has emerged
frequently associated with the production of as an important cause of septic arthritis
Panton-Valentine leukocidin (PVL). Osteoarticular [12, 13] mostly due to the improvement in
4472 M.C. Neves et al.
clinical and laboratory findings of a septic joint, Table 1 Differentiation of septic arthritis from transient
including positive blood cultures [49]. synovitis of the hip
Synovial protein levels that are 40 mg/dl Number of
(400 mg/L) and are less than the serum protein predictors present
(+): predictive
levels are consistent with septic arthritis. Lactate probability of
levels are typically elevated in the joint fluid in Study Predictors analyseda septic arthritis
patients with septic arthritis, except for those with Kocher History of fever 4 + :99.8 %
a gonococcal infection/ and the glucose level in et al. Non-weight bearing 3 + :93 % to 95.2 %
[35] ESR > 40 mm/h
the aspirate is lower than in the serum. 2 + :33.8 % to
In children with hyperuricaemia it is also 62.2 %
recommended that the fluid be examined for the WBC > 12,000/mm3 1 + :2.1 % to 5.3 %
0 + :0.1 %
presence of uric acid crystals in order to rule out
Jung Body temperature 5 + :99.1 %
crystalline joint disease. et al. > 37 C
Fluid aspirated from the joint must be cul- [25] ESR > 20 mm/h 4 + :84.8 % to
tured both aerobically and under anaerobic con- 97.3 %
ditions. The use of blood culture vials enhance CRP > 1 mg/dl 3 + :24.3 % to
the recovery of Kingella kingae and other organ- 77.2 %
isms [11, 13]. WBC > 11,000/mm3 2 + :4.3 % to
22.7 %
Actually, attempts to isolate this organism on
Increased hip joint 1 + :0.3 % to 9.9 %
routine solid media have failed, whereas inocula- space > 2 mm 0 + :0.1 %
tion into aerobic blood vials recovered the organ- a
ESR erythrocyte sedimentation rate; WBC white blood
ism. It has been postulated that the dilution of cell, CRP c-reactive protein
exudates in a large bottle volume decreases the
concentration of destructive factors improving constitutes the first differential diagnosis of septic
recovery of the organism [22]. The use of DNA- arthritis [50]. In both cases the children can pre-
amplification methods for synovial fluid speci- sent with severe limitation of movement, with the
mens, although still investigational, is likely to hip lying in flexion, abduction and external rota-
become a valuable add-on the diagnosis of cul- tion. The pain is severe and the child will cry on
ture negative disease, mostly for K. kingae any attempt to move the limb. The differential
infections. diagnosis between these two conditions is
extremely important since treatment varies dra-
matically, with simple observation and nonsteroi-
Differential Diagnosis dal anti-inflammatory drugs for transient
synovitis to open arthrotomy and prolonged anti-
In the presence of a typical clinical picture of biotic therapy for septic arthritis.
fever associated with inflammatory signs of the In recent years Kocher, Zurakowski and Kasse
joint and a positive culture of the joint fluid, it is [51] and Jung et al. [40] have published algo-
easy to make a diagnosis of septic arthritis. How- rithms to help differentiate septic arthritis from
ever, this is not the situation in almost 50 % of the transient synovitis of the hip (Table 1). In these
cases seen in our clinics. In these children, Ortho- studies when all the four or five criteria were met
paedic surgeons must be aware of other potential respectively, there was a 99 % chance of the
diagnoses that can resemble septic arthritis. Most child having a septic arthritis. More recent data
of the children will be afebrile and have a normal [50, 52, 53] called attention to the difficulty in
erythrocyte sedimentation rate. evaluating these specific findings. Nevertheless
The most common problems are around the the Orthopaedic surgeon must be aware that clin-
hip, because of the difficulty in observing a joint ical judgment is still necessary in the further
covered by large muscles. Transient synovitis of management of these patients. However patients
the hip is very common in children, and with minimal probability (0 predictive score)
Septic Arthritis in Infancy and Childhood 4475
Sartorius
muscle
Tensor
fasciae
muscle
Incise
and
enter
here
c d
Reflected head of rectus femoris is devided
Reflected head of rectus for improved access to hip capsule
Rectus femoris
femoris muscle
muscle
straight head Kerrison
rongeur
Tensor Tensor
fasciae fasciae
muscle
Fat over
Anterior
joint capsule
hip
capsula
Sartorius Sartorius
Rectus
muscle
femoris
Fig. 6 (a) Skin incision for drainage of the hip. over hip capsule. (d) Division of reflected head of rectus
(b) Exposure of hip between tensor fascia lata and femoris to expose hip capsule adequately prior to
sartorius. (c) Muscle retraction exposing fatty tissue arthrotomy
aspiration of joint fluid. It should be based on There are several therapeutic antibiotic pro-
the most common pathogens and rely on local tocols published in the literature [11, 18, 19, 62].
antimicrobial susceptibilities. Subsequently In healthy neonates, group-B Streptococcus is the
should be adapted, according to the results of most common organism with S. aureus in more
the culture. prominent high-risk neonates. Gram-negative
4478 M.C. Neves et al.
bacilli should also be considered in this age Table 3 Antibiotic doses for children with septic arthritis
group. Recommended antibiotic treatment Newborn Oxacillin: varies with age
includes oxacillin plus cefotaxime or gentamicin Cefotaxime:50 mg/Kg/dosis/ 812 h
for a high-risk neonate (Table 3). Gentamicin:4 mg/Kg/day in 1 dosis
S. aureus is the most common organism in 28 days to 2 Oxacillin: 200 mg/Kg/day in 4 divided
infants and children no matter what age, and oxa- years dosis
cillin should still be considered the treatment of Cefuroxime: 150 mg/Kg/day in 3
divided dosis
choice in areas where MRSA is not a concern. In
>2 years Oxacillin: 200 mg/Kg/day in 4 divided
severe infections gentamicin can be added based dosis
on the synergic effect. Although clindamycin is MRSA Vancomycin 4060 mg/Kg/day in 4
a suitable antibiotic to treat osteoarticular infec- divided dosisa
tions (when local clindamycin resistant is below Clindamycin 40 mg/Kg/day in 3
15 %) we must discourage its use in patients with divided dosis
methicilin-susceptible or PVL negative S. aureus Neisseria Cefotaxime:100200 mg/Kg/day
gonorrheae divided in 3 to 4 dosis
infections as a beta-lactam antibiotic is a more
Ceftriaxone:100 mg/Kg/day 1 dosis
appropriate option [63]. In regions where MRSA a
Doses should be adapted to vancomycin serum
prevalence approaches 1015 %, vancomycin, concentration
or clindamycin should be included for empiric
treatment [64]. A double disk diffusion test
(D-test) can be used to determine if clindamycin-
susceptible CA-MRSA strains harbour inducible
resistance [63]. Prognosis
Infants younger than 3 months of age should be
treated with antibiotics active agains S. aureus, In septic arthritis several factors put the child at
gram-negative enteric organisms and GBS. risk of a poor result. They include age (prematu-
Children 3 months to 5 years of age should rity is associated with poor results), delay in
receive empiric therapy for S. aureus, K. kingae, treatment of more than 4 days, concurrent
S. pneumoniae and S. pyogenes. Children older osteomyelitis (especially around the hip) and
than 5 years are most likely to be infected with when associated with dislocation of the hip.
S. aureus or streptococci. In children younger The sequelae of septic arthritis are common and
than 2 years unimmunized against H. influenza around the hip such complications occur in as
type b, second or third-generation cephalosporins many as 40 % of the children [19]. Most of the
should be added to the antistaphylococcal problems are related to loss of movement related
agent. Also when Kingella kingae is a possibility to partial or total destruction of the epiphysis,
the recommended antibiotics should include osteonecrosis, growth problems with mal-
cephalosporins or penicillin [31]. alignment and progressive limb-length discrep-
For Streptococcus spp. septic arthritis penicil- ancy, unstable joints or ankylosis.
lin G or ampicillin is the treatment option. For Long-term follow-up is essential to identify
penicillin-resistant S. pneumoniae ceftriaxone or these potential outcomes. It is a challenge to the
cefotatime can be an alternative but most resistent Orthopaedic surgeon to deal with this problem.
S. pneumoniae isolates are susceptible to vanco- He must consider not only the insult to the joint
mycin and clindamycin or meropenem. Ceftriax- but also future growth disturbances. This is par-
one and cefotaxime are appropriated for the ticularly true when the hip is involved and espe-
treatment of gonococal infections [65] (Table 3). cially in neonates because of the devastating
The usual course of therapy is 2 weeks for complications such as complete necrosis of the
arthritis due to H. influenzae or Streptococcus epiphysis. Choi et al. [66, 67] developed
spp. and 3 weeks for arthritis due to S. aureus or a classification to help plan reconstructive sur-
gram-negative bacilli [65]. gery in these particular and difficult cases,
Septic Arthritis in Infancy and Childhood 4479
a b
Fig. 7 Radiographs showing (a) non-union of the femoral neck secondary to septic arthritis complicated by osteomy-
elitis of the proximal femur, (b) and (c) treatment by fixation and valgus osteotomy and (d) follow-up at 6 years
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