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Septic Arthritis in Infancy and

Childhood

Manuel Cassiano Neves, J. L. Campagnolo, M. J. Brito, and


C. F. Gouveia

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,

G. Bentley (ed.), European Surgical Orthopaedics and Traumatology, 4469


DOI 10.1007/978-3-642-34746-7_169, # EFORT 2014
4470 M.C. Neves et al.

Fig. 1 Prevalence of septic


arthritis

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.

laboratory methods [11]. Moumile et al., using


a combination of blood-culture vials and
a DNA-amplification method for synovial fluid
specimens, found that Kingella kingae was the
most common cause of skeletal infections in
France, in children below 3 years [13]. Overall,
K. kingae seems to be responsible for musculoskel-
etal infections below the age of 5 years, with over
60 % of the episodes below the age of two [22].
Children with invasive K. kingae infections often
have a recent history of stomatitis or symptoms of
an infection of the upper respiratory tract [31].
In newborns and sexually active adolescents
who have a septic arthritis, Neisseria gonorrhea Fig. 3 Radiograph showing capsular distention and wid-
ening of the joint space on the left
should be considered [32]. Septic arthritis caused
by gram-negative bacteria is rare in children.
However Salmonella should be considered, move the affected limb (pseudoparalysis)
especially in children with sickle-cell disease [16, 38, 39]. All joints can be affected but 80 %
[33], or Pseudomonas aeruginosa when associ- of infections occur in the lower limb with the hip
ated with an infected puncture wound [34]. and the knee being the most implicated.
Brucella and Mycobacterium tuberculosis may Imaging can be very helpful in establishing
cause chronic monoarticular arthritis with a gran- a correct diagnosis. In a study by Jung et al. [40]
ulomatous reaction especially in endemic regions all the children who presented with septic arthri-
in southern Europe [35]. tis showed a displacement or blurring of the peri-
articular fat pads. Plain radiographs can reveal
subtle signs such as capsular distention and wid-
Diagnosis ening of the joint space early in the disease pro-
cess (Fig. 3). With continued swelling of the
The diagnosis of septic arthritis is based on clin- capsule of the hip joint, the femoral head is
ical findings, their correlation with laboratory displaced laterally and upward [41]. Ultrasound
results and the findings on imaging. Almost all evaluation has proved to be very useful in the
patients have fever and constitutional symptoms assessment of septic arthritis, especially in deep
within the first few days of infection. joints such as the hip, where physical examina-
The typical constitutional symptoms are the tion is difficult. It is quick and can be performed
acute onset, anorexia and irritability. There is by any Orthopaedic surgeon with minimal train-
severe pain in the involved segment, aggravated ing in the technique. It is painless and child
by any attempt to move the limb passively. Usu- friendly and imparts no ionising radiation.
ally the child refuses to use the limb and if the leg McCarthy et al. [19] found a 100 % capability
I 18s involved will limp or refuse to bear weight. of ultrasound to demonstrate a joint effusion
The affected joint is swollen, tense and is locally within a capsule-to-bone distance of > 2 mm
hot. It usually lies in flexion to release the compared with the contralateral side (Fig. 4).
intracapsular pressure from the accumulation of However, Gordon et al. [42] noted the possibility
pus. This is particularly evident in the hip with of false-negative ultrasound scans especially
the child holding the joint in a position of flexion, when performed in the first 24 h after the onset
abduction and external rotation [36, 37, 69]. of symptoms. Ultrasound can also be helpful in
However, due to the deficiency of their guiding aspiration and needle placement.
immune system, neonates may display only Technetium bone scans may show decreased
anorexia, irritability and lethargy and may not uptake (cold) early in the disease process and
Septic Arthritis in Infancy and Childhood 4473

a sedimentation rate higher than 50 mm/h. The


measurement of C-reactive protein (CRP) is an
indication of the inflammation but will also mon-
itor the progression of the disease. It is elevated
(mean 8.5 mg/dl) [43] in more than 90 % of
children with musculoskeletal infection at the
time of admission. It peaks 2 days after admission
and returns to normal after treatment [19, 44].
Measurements of the CRP level may also be
helpful in the identification of septic arthritis in
children with underlying acute haematogenous
b osteomyelitis [45]. According to Levine et al.
[46] it is a better negative than a positive predic-
tor of the disease with an 87 % probability of
ruling out septic arthritis if less than 1.0 mg/dl.
This view was confirmed by Brown [47].
In some cases the blood tests may be only
slightly elevated even in a proven infection,
which can then make the suspicion of septic
arthritis difficult to confirm. Blood for culture
should always be taken when there is suspicion
of septic arthritis because blood cultures may
yield the pathogen when cultures of the joint
fluid do not.
Analysis of joint aspiration is essential for
Fig. 4 Ultrasound of the hip joint showing (a) joint effu-
sion with a capsule-to-bone distance of > 2 mm compared diagnosis and helpful in differentiating bacterial
with (b) the normal side and others causes of arthritis.
The fluid must be collected in a heparinised
syringe so that the large clot which usually forms
increased uptake later (hot) as a result of in fluid from patients with septic arthritis or juve-
hyperaemic response. nile rheumatoid arthritis does not preclude enu-
Gallium and indium-labelled-leucocyte meration of leucocytes. Once aspirated joint
scans may be helpful in atypical cases but take samples are obtained, it is crucial that they be
up to 78 h to complete, making them an imprac- quickly transported to the laboratory and not be
tical tool. allowed to stand for a long time without
CT scans and MRI can be of use in difficult processing. A cell and differential count should
cases as in the diagnosis of an infection of the be performed and the aspirate Gram-stained.
sacro-iliac joint or in the differential diagnosis of A white-blood cell count > 50,000 mm with
infections around the joints. 90 % polymorphonuclear leukocytes is indicative
Laboratory evaluation of suspected septic of septic arthritis, but 34 % of the patients have
arthritis generally includes peripheral blood a white blood cell count of < 25,000 mm3
count and differential, erythrocyte sedimentation A Gram-stained smear of aspirated joint fluid
rate, C-reactive protein, blood culture and joint must be assessed because joint fluid exerts
fluid analysis. a bacteriostatic effect on micro-organisms
The peripheral blood leucocyte count which can be seen, but may not grow in culture.
usually demonstrates a white blood cell count > Gram stains of the aspirate are positive in
12,000/mm3 with 4060 % polymorphonuclear 3050 % of cases [19, 48]. Approximately 35 %
leucocytes. Most patients display an erythrocyte of joint aspirates are sterile in patients with other
4474 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

Table 2 Synovila fluid analysis in differential diagnsis


Diagnosis WBC/mm3 (typical) WBC/mm3 (range) % PMNs (typical)
Normal <150 <25
Bacterial arthritis >50,000 2,000300,000 >90
Tuberculous arthritis 10,00020,000 4036,000 >50 (1099)
Candidal arthritis 75,000150,000 >90
Viral arthritis 15,000 3,00050,000 >90
Rheumatoid arthritis 2,00050,000 >70

should be managed by observation only in an defensive flexion contracture. Analysis of the


appropriate clinical setting, whereas patients fluid aspirated from the joint will help differentiate
with high probability (4 or 5) are candidates for the diagnosis (Table 2).
aspiration in the operating room since they may Reactive arthritis refers to a sterile joint effu-
require surgical drainage. sion associated with an extra-articular infection,
Peripelvic infections mimicking septic arthri- noted particularly following episodes of diar-
tis of the hip in children can be very challenging rhoea caused by Shigella, Salmonella,
in diagnosis and treatment. These conditions Campylobacteria or Yersinia species [58].
often present a similar clinical picture to septic All hip diseases related to development such
arthritis with fever and limitation of the range as Perthes disease or slipped capital femoral
of movement of the involved hip [44]. epiphysis should be considered in the differential
A psoas abscess, although a rare entity, has a diagnosis of septic arthritis although the clinical
predisposition for children [42, 54, 55] and usu- course will run without fever.
ally presents with a positive psoas sign, with the Septic suppurative bursitis, though a rare
pain aggravated by extension of the hip and event in children, can be difficult to distinguish
relieved by flexion, leading to the mis-diagnosis from septic arthritis. It is mostly associated with
of hip arthritis. Imaging can be very helpful since trauma and can present with a similar clinical
in most of these cases the ultrasound does not picture. Ultrasound can be helpful in differentiat-
show an intra-articular abscess but may indicate ing the diagnosis.
a psoas abscess, better identifiable either by a CT
scan or MRI [54].
Pyomyositis although a rare condition, has been Treatment
rising in temperate countries, associated with the
recent emergency of MRSA, PVL positive strains Septic arthritis is a true emergency that can lead to
[56]. It can lead to misdiagnosis, particularly when devastating effects if not properly treated, with
it involves the muscles around the hip [57]. Once serious compromise of the musculoskeletal system
again the physical signs complemented by thor- (Fig. 5). The cornerstone when dealing with septic
ough imaging studies will allow for the differential arthritis is fast identification of the condition,
diagnosis. Most of these conditions will be treated emergency drainage of the joint and appropriate
by antibiotics and needle aspiration guided either antibiotics [46]. The outcome is mostly related to
by ultrasound or CT scan. Juvenile idiopathic the time spent between the beginning of the symp-
arthritis (JRA) may be acute in onset. In particular toms and the initiation of therapy. The presence of
cases, besides the inflammatory local signs, the osteomyelitis associated with septic arthritis can
child can present with fever mimicking septic be an aggravating factor, and when it is suspected
arthritis, when the knee is involved this is particu- aspiration of the bone should be considered at the
larly evident, making the differential diagnosis same time as drainage of the joint [19].
difficult. The child is usually less sick and the Identification of the responsible organism is
pain is moderate although the joint adopts the fundamental for correct antibiotic treatment.
4476 M.C. Neves et al.

a ultrasound-guided aspirations [59] or arthro-


scopic treatment [60, 61]. Treatment of septic
arthritis of the hip joint by repeated ultrasound-
guided aspirations done under sedation was
described by Givon et al. [59]. This treatment
was successful in 24 of 28 patients. In four
cases the patients did not improve and an
arthrotomy was necessary with resolution of the
symptoms. The mean number of aspirations was
3.6 (35) and 75 % of the patients resumed walk-
ing after 24 h. With a mean follow-up of 7.4 years
they report no complications. This method must
be undertaken with care with close follow-up. An
b arthrotomy is indicated if the symptoms do not
resolve. It is best used when symptoms have been
present for less than 24 h and when the joint fluid
is rich in fibrin. This should allow a proper wash-
out. The advantages of this method are to avoid
the complications of surgery and general
anaesthesia.
Since the advent of arthroscopy, there have
been several reports on surgical drainage by
arthroscopy in adults. Only recently has arthros-
copy been advocated for septic arthritis in children
[60, 61]. Although it has a learning curve, arthros-
copy allows for decompression of the joint, reduc-
tion of the bacterial load and debridement under
direct vision. It also makes it easier to wash out the
joint and allows placing a drain with a minimal
scar. However, particularly at the hip joint, it is
not an entirely benign procedure and should only
be performed by surgeons experienced in this
Fig. 5 Radiographs showing (a) serious compromise of particular technique [60].
the left hip joint secondary to late diagnosis of septic Independent of the type of surgical approach,
arthritis complicated by osteomyelitis of the proximal children should be followed with care. If surgery
femur and (b) a newborn with septic arthritis at a follow-
up of 2.5 years with complete necrosis of the femoral head
is not followed by a rapid reversal of the clinical
symptoms and normalisation of the vital signs
and the CRP, re-exploration should be consid-
ered, bearing in mind the possibility of associated
Drainage by arthrotomy is still the treatment of osteomyelitis.
choice for a joint effusion with emphasis on Draining the joint fluid is only one part of the
removing a capsular window in order to allow treatment.
continued drainage. A drain should be left in Antimicrobial agents play a major role in
place until the volume of the drainage decreases the management of septic arthritis and every
(Fig. 6ad). department should have an algorithm for the
There have been several recent reports in treatment of this condition. The antibiotic regi-
the literature supporting either repeated men should be started immediately after
Septic Arthritis in Infancy and Childhood 4477

a b Lateral femoral cutancous nerve

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

utilizing greater trochanteric arthroplasty or pel-


vic support osteotomy (Fig. 7ad). Summary
Appropriately timed epiphysiodesis of the con-
tralateral limb is easy to perform and more suitable Septic arthritis in children is common and can be
than lengthening the affected limb with all the devastating if not properly diagnosed and rapidly
risks of increasing pressure around a non-healthy treated. The aetiology can be diverse and the
joint. Ipsilateral epiphysiodesis of the greater tro- presentation changes according to the age of the
chanter, to establish a more normal anatomy of the child and the organism present, making diagnosis
proximal femur, or around the knee to correct difficult. Long term follow-up is needed in order
a mal-alignment are simple procedures with very to prevent late complications.
satisfactory results if performed at the appropriate It is necessary to make an accurate diagnosis
time. Arthrodesis or arthroplasty may be indicated and to undertake prompt treatment with antibi-
for a painful joint with severe osteoarthritis in later otics and surgical drainage to prevent potential
stages [67, 68, 74]. hazards.
4480 M.C. Neves et al.

osteomyelitis in pediatric patients. J Pediatr Orthop.


References 2000;20:403.
19. McCarthy JJ, Dormans JP, Kozin SH, Pizzutillo PD.
Musculoskeletal infections in children: basic treat-
1. Nelson JD. Skeletal infections in children. Adv Pediatr ment principles and recent advancement. J Bone
Infect Dis. 1991;6:5978. Joint Surg Am. 2005;54-A:51528.
2. Welkon CJ, Long SS, Fisher MC, et al. Pyogenic 20. Dingle JT. The role of lysosomal enzymes in skeletal
arthritis in infants and children: a review of 95 cases. tissues. J Bone Joint Surg Br. 1973;55-B:8795.
Pediatr Infect Dis J. 1986;5:669. 21. Paterson D. Septic arthritis of the hip joint. Orthop
3. Gutierrez K. Bone and joint infections in children. Clin North Am. 1978;9:13542.
Pediatr Clin North Am. 2005;52:77994. 22. Yagupsky P. Kingella kingae: from medical rarity to
4. Gillespie WJ. Infection in total joint replacement. an emerging paediatric pathogen. Lancet Infect Dis.
Infect Dis Clin N Am. 1990;4:46584. 2004;4:35867.
5. Goldenberg D, Cohen AS. Acute infectious arthritis. 23. Lina G, Piemont Y, et al. Involvement of Panton-
Am J Med. 1976;60:369. Valentine leukocidin-producing Staphylococcus
6. Goldin RH, Chow AW, Edwards JE, et al. aureus in primary skin infections and pneumonia.
Sternoarticular septic arthritis in heroin users. N Engl Clin Infect Dis. 1999;29(5):112832.
J Med. 1993;289:616. 24. Martinez-Aguilar G, Avalos-Mishaan A, Hulten K.
7. Vassilopoulos D, Chalasani P, Jurado RL, et al. Community-acquired, methicillin-resistant and meth-
Musculoskeletal infections in patients with human icillin-susceptible Staphylococcus aureus musculo-
immunodeficiency virus infection. Medicine. skeletal infections in children. Pediatr Infect Dis J.
1997;76:284. 2004;23:701.
8. Deshpande SS, Taral N, Modi N, Singrakhia M. 25. Dohin B, Gillet Y, et al. Pediatric bone and joint
Changing epidemiology of neonatal septic arthritis. infections caused by Panton-Valentine leukocidin-
J Orthop Surg (Hong Kong). 2004;12:103. positive Staphylococcus aureus. Pediatr Infect Dis J.
9. Howard AW, Viskontas D, Sabbagh C. Reduction in 2007;26(11):10428.
osteomyelitis and septic arthritis related to Haemophilus 26. Miller LG, Quan C, et al. A prospective investigation
influenzae Type B vaccination. J Pediatric Orthop. of outcomes after hospital discharge for endemic,
1999;1(9):7059. community-acquired methicillin-resistant and -
10. Butbul-Aviel Y, Koren A, Halevy R, Sakran W. susceptible Staphylococcus aureus skin infection.
Procalcitonin as a diagnostic aid in osteomyelitis Clin Infect Dis. 2007;44(4):48392.
and septic arthritis. Pediatr Emerg Care. 27. Gonzalez BE, Martinez-Aguilar G, Hulten KG,
2005;21:82832. et al. Severe staphylococcal sepsis in adolescents
11. Verdier I, Gayet-Ageron A, Ploton C, et al. Contribu- in the era of community-acquired methicillin-
tion of a broad range polymerase chain reaction to the resistant Staphylococcus aureus. Pediatrics.
diagnosis of osteoarticular infections caused by 2005;115:642.
Kingella kingae: description of twenty-four recent 28. Teruya J, Gonzalez BE, Mahoney Jr DH, et al. Venous
pediatric diagnoses. Pediatr Infect Dis J. thrombosis associated with staphylococcal osteomye-
2005;24:6926. litis in children. Pediatrics. 2006;117:1673.
12. Kiang KM, Dgunmodede F, Juni BA, et al. Outbreak 29. Rompalo AM, Hook EW, Roberts PG, et al. The acute
of osteomyelitis/septic arthritis caused by Kingella arthritis dermatitis syndrome. The changing impor-
kingae among child care center attendees. Pediatrics. tance of Neisseria gonorrhoeae and Neisseria
2005;116:e206-13. Epub 2005 Ju11 5. meningitidis. Arch Intern Med. 1987;147:281. 37a.
13. Moumile K, Merckx J, Glorion C, et al. Bacterial 30. Zevit N, Yarden-Bilavsky H, Bilavsky E, et al.
etiology of acute osteoarticular infections in children. Primary meningococccal arthritis in a child: case
Acta Paediatr. 2005;94:41922. report and literature review. Scand J Infect Dis.
14. Everett ED, Hirschmann JV. Transient bacteremia and 2006;38:396.
endocarditis prophylaxis: a review. Medicine (Balti- 31. Yagupsky P, Dagan R, Howard CB, et al. Clinical
more). 1977;56:6177. features and epidemiology of invasive Kingella kingae
15. Alderson M, Speers D, Emslie K, Nade S. Acute infections in Southem Israel. Pediatrics.
haematogenous osteomyelitis and septic arthritis: 1993;92:8004.
a single disease: an hypothesis based upon the pres- 32. Folland DS, Burke RE, Hinman AR, Schaffner W.
ence of transphyseal blood vessels. J Bone Joint Surg Gonorrhea in preadolescent children: an inquiry into
Br. 1986;68-B:26874. source of infection and mode of transmission. Pediat-
16. Ogden JA, Lister G. The pathology of neonatal osteo- rics. 1997;60:1536.
myelitis. Pediatrics. 1975;55:4748. 33. Almeida A, Roberts I. Bone involvement in sickle cell
17. De Boeck H. Osteomyelitis and septic arthritis in disease: an hypothesis based upon the presence of
children. Acta Orthop Belg. 2005;71:50515. transphyseal blood vessels. Br J Haematol.
18. Perlman MH, Patzakis MJ, Kumar PJ, Holtom P. The 2005;129:48290.
incidence of joint involvement with adjacent
Septic Arthritis in Infancy and Childhood 4481

34. Fernandes P, Neves MC, Gomes AR. Ferida 51. Kocher MS, Zurakowski O, Kasser JR. Differentiating
perfurante do pe. Rev Port Orthop Trauma. between septic arthritis and transient synovitis of the
1999;7:6972. hip in children: an evidence-based clinical prediction
35. Lopes RG, Madail C, Marques, Neves MC. Brucellic algorithm. J Bone Joint Surg Am. 1999;81-
arthritis in one infant: mothers milk transmission. A:166270.
Submitted for publication. 52. Kocher MS, Mandiga R, Zurakowski O, Barnewolt C,
36. Frank G, Mahoney HM, Eppes SC. Musculoskeletal Kasser JR. Validation of a clinical prediction rule for
infections in children. Pediatr Clin North Am. the differentiation between septic arthritis and tran-
2005;52:1083106. sient synovitis of the hip in children. J Bone Joint Surg
37. Frick SL. Evaluation of the child who has hip pain. Am. 2004;86-A:162935.
Orthop Clin North Am. 2006;37:13340. 53. Luhmann SJ, Jones A, Schootman M, et al.
38. Kabak S, Halici M, Akcakus M, Cetin N, Narin N. Differentiation between septic arthritis and tran-
Septic arthritis in patients followed-up in neonatal sient synovitis of the hip in children with clinical
intensive care unit. Pediatr Int. 2002;44:6527. prediction algorithms. J Bone Joint Surg Am.
39. Obletz BE. Acute suppurative arthritis of the hip in the 2004;86-A:95662.
neonatal period. J Bone Joint Surg Am. 1960;42- 54. Song J, Letts M, Monson R. Differentiation of psoas
A:2330. muscle abscess from septic arthritis of the hip in chil-
40. Jung ST, Rowe SM, Moon ES, et al. Significance of dren. Clin Orthop. 2001;391:25865.
laboratory and radiologic findings for differentiating 55. Williams RH, Thomas P. An unusual case of sponta-
between septic arthritis and transient synovitis of the neous bacterial myositis. Postgrad Med J.
hip. J Pediatr Orthop. 2003;23:36872. 1975;51:2557.
41. Chont L. Roentgen sign of early suppurative arthritis 56. Pannaraj PS, Hulten KG, et al. Infective pyomyositis
of the hip in infancy. Radiology. 1942;38:70814. and myositis in children in the era of community-
42. Gordon JE, Huang M, Dobbs M, et al. Causes of false- acquired, methicillin-resistant Staphylococcus
negative ultrasound scans in the diagnosis of septic aureus infection. Clin Infect Dis. 2006;43(8):
arthritis of the hip in child ren. J Pediatr Orthop. 95360.
2002;22:3126. 57. Shirtliff ME, Mader JT. Acute septic arthritis. Clin
43. Kallio MJ, Unkila-Kallio L, Aalto K, et al. Serum C- Microbial Rev. 2002;15:52744.
reactive protein, erythrocyte sedimentation rate, and 58. Wong-Chung J, Bagali M, Kaneker S. Physical signs
white blood cell count in septic arthritis of children. in pyomyositis presenting as a painful hip in children:
Pediatr Infect Dis J. 1997;16:411. a case report and review of the literature. J Pediatr
44. Song KS, Lee SM. Peri pelvic infections mimicking Orthop. 2004;13:2113.
septic arthritis of the hip in children: treatment 59. Givon U, Liberman B, Schindler A, Blankstein A,
with needle aspiration. J Pediatr Orthop B. Ganel A. Treatment of septic arthritis of the hip joint
2003;12:3546. by repeated ultrasound-guided aspirations. J Pediatr
45. Unkila-Kallio L, Kallio MJ, Peltola H. The usefulness Orthop. 2004;24:26670.
of C-reactive protein levels in the identification of 60. DeAngelis NA, Busconi BD. Hip arthroscopy in the
concurrent septic arthritis in children who have acute pediatric population. Clin Orthop 2003;406:60-3.
haematogenous osteomyelitis. A comparison with the 61. Kim SJ, Choi NH, Ko SH, Linton JA, Park HW.
usefulness of the erythrocyte sedimentation rate and Arthroscopic treatment of septic arthritis of the hip.
the white-blood cell count. J Bone Joint Surg Am. Clin Orthop. 2003;407:2114.
1994;76:84853. 62. Malhotra R, Singh KD, Bhan MS, Dave PK. Primary
46. Levine MJ, McGuire KJ, McGowan KL, Flynn JM. pyogenic abscess of the psoas muscle. J Bone Joint
Assessment of the test characteristics of C-reactive Surg Am. 1992;74-A:27884.
protein for septic arthritis in children. J Pediatr Orthop. 63. Nathwani D, Morgan M, et al. Guidelines for UK
2003;23:3737. practice for the diagnosis and management of methi-
47. Brown MD. Letter to the editor. J Pediatr Orthop. cillin-resistant Staphylococcus aureus (MRSA) infec-
2004;3:344. tions presenting in the community. J Antimicrob
48. Chang WS, Chiu NC, Chi H, Li WC, Huang FY. Chemother. 2008;61(5):97694.
Comparison of the characteristicsof culture-negative 64. Fergie J, Purcell K. The treatment of community-
versus culture-positive septic arthritis in children. acquired methicillin-resistant Staphylococcus
J Microbial Immunol Infect. 2005;38:18993. aureus infections. Pediatr Infect Dis J. 2008;
49. Barton LL, Dunkle LM, Habib FH. Septic arthritis in 27(1):678.
childhood: a 13-year review. Am J Dis Child. 65. Krogstad P. Septic arthritis. In: Feigin RD, editor.
1987;141:898900. Textbook of pediatric infectious diseases, vol. 1.
50. Caird MS, Flynn JM, Leung Y, et al. Factors Philadelphia, PA: Saunders Elservier; 2009.
distinguishing septic arthritis from transient synovitis p. 7428.
of the hip in children; a prospective study. J Bone Joint 66. Choi IH, Pizutillo PO, Bowen JR, Dragann R, Malhis
Surg Am. 2006;88-A:12517. T. Sequelae and reconstruction after aseptic arthritis of
4482 M.C. Neves et al.

the hip in infants. J Bone Joint Surg Am. 1990;72- of septic arthritis in children. J Pediatr Orthop B.
A1:15065. 2005;14:1014.
67. Choi IH, Shin YW, Chung CY, et al. Surgical treat- 71. Lyon RM, Evanich JB. Culture-negative septic
ment of the severe sequelae of infantile septic arthritis arthritis in children. J Pediatr Orthop. 1999;19:
of the hip. Clin Orthop. 2005;434:1029. 65562.
68. Campagnaro JG, Donzelli O, Urso R, Valdiserri L. 72. Forward DP, Hunter JB. Arthroscopic washout of the
Treatment of the sequelae of septic osteoarthritis of shoulder for septic arthritis in infants, A new tech-
the hip during pediatric age. Chir Organi Mov. nique. J Bone Joint Surg Br. 2002;84:11735.
1992;77:22345. 73. Choi IH, Yoo WJ, Cho TJ, Chung CY. Operative
69. Kocher MS, Lee B, Dolan M, Weinberg J, Shulman reconstruction for septic arthritis of the hip. Orthop
ST. Pediatric orthopedic infections: early detection Clin North Am. 2006;37:17383.
and treatment. Pediatr Ann. 2006;35:112. 74. Dobbs MB, Sheridan JJ, Gordon JE, et al. Septic
70. Gordon JE, Wolff A, Luhmann SJ, et al. Primary and arthritis of the hip in infancy: long-term follow-up.
delayed closure after open irrigation and debridement J Pediatr Orthop. 2003;23:1628.

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