Journal Information
Vol. 18. Issue 1.
Pages 28-33 (January - February 2014)
Share
Share
Download PDF
More article options
Visits
4562
Vol. 18. Issue 1.
Pages 28-33 (January - February 2014)
Original article
Open Access
Epidemiology of septic arthritis of the knee at Hospital das Clínicas, Universidade de São Paulo
Visits
4562
Camilo Partezani Helito
Corresponding author
camilo_helito@yahoo.com.br

Corresponding author at: Rua Dr. Ovídio Pires de Campos, 333, Cerqueira Cesar, São Paulo, SP 05403-010, Brazil.
, Guilherme Guelfi Noffs, Jose Ricardo Pecora, Riccardo Gomes Gobbi, Luis Eduardo Passarelli Tirico, Ana Lucia Munhoz Lima, Priscila Rosalba de Oliveira, Gilberto Luis Camanho
Instituto de Ortopedia e Traumatologia, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo (IOT-HCFMUSP), São Paulo, SP, Brazil
This item has received

Under a Creative Commons license
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (2)
Tables (1)
Table 1. Epidemiological summary of study results.
Abstract
Background

Septic arthritis is an infrequent disease although very important due to the possibility of disastrous outcomes if treatment is not adequately established. Adequate information concerning the epidemiology of septic arthritis is still lacking due to the uncommon nature of the disease as well as the struggle to establish a correct case-definition.

Objective

To epidemiologically characterize the population seen at Hospital das Clínicas, University of São Paulo with a diagnosis of septic arthritis between 2006 and 2011.

Methods

Sixty-one patients diagnosed with septic arthritis of the knee between 2006 and 2011 were retrospectively evaluated. The patients’ clinical and epidemiological characteristics, the microorganisms that caused the infection and the patients’ treatment and evolution were analyzed.

Results

Septic arthritis of the knee was more common among men, with distribution across a variety of age ranges. Most diagnoses were made through positive synovial fluid cultures. The most prevalent clinical comorbidities were systemic arterial hypertension and diabetes mellitus, and the most commonly reported joint disease was osteoarthritis. Staphylococcus aureus was the prevailing pathogen. Fever was present in 36% of the cases. All patients presented elevation in inflammatory tests. Gram staining was positive in only 50.8% of the synovial fluid samples analyzed. Six patients presented complications and unfavorable evolution of their condition.

Conclusion

S. aureus is still the most common pathogen in acute knee infections in our environment. Gram staining, absence of fever and normal leukocyte count cannot be used to rule out septic arthritis.

Keywords:
Knee
Infection
Septic arthritis
Epidemiology
Full Text
Introduction

Septic arthritis of the knee is an infrequent orthopedic disease, but it is extremely important.1,2 The age group of incidence ranges from newborns to more elderly individuals. In adults, the knee is the most affected site.3–5 Even with the advances in drainage techniques and antibiotic therapy, complications such as osteomyelitis, bone erosion, joint stiffness, fibrous ankylosis, sepsis, and even death can occur.6–8 Its treatment consists of early antibiotic therapy and surgical drainage, and the common factors limiting successful treatment are lack of suspicion of the pathological condition in the initial phases of the symptoms, delayed aspiration of synovial fluid, and unsuccessful joint drainage.9–12 With increasing reports of bacteria that are resistant to antibiotics in many centers, as well as increased frequency of bacteria that were not previously associated with septic arthritis, knowledge of the epidemiological characteristics of patients in each region is fundamental for adequate therapeutic planning.13–16

Objective

The objective of the present study was to epidemiologically characterize the patients with a diagnosis of septic arthritis seen at Hospital das Clínicas, Universidade de São Paulo (USP), between 2006 and 2011.

Materials and methods

This was a retrospective study on patients with diagnosis of septic arthritis of the knee seen at the Hospital das Clínicas, Faculty of Medicine of University of São Paulo, between 2006 and 2011. All septic arthritis cases diagnosed inside the complex are referred for treatment at the Institute of Orthopedics.

The only inclusion criterion was a confirmed diagnosis of septic arthritis of the knee. The patients were selected through review of the medical records. All records of patients with IDC-10 of septic arthritis were identified and epidemiological, clinical and laboratory data were abstracted by detailed charge review, with information recorded on a standardized form. Cases of infection that occurred less than one year after any knee surgery were excluded, because these were considered post-surgical infection. Cases of multifocal septic arthritis were also excluded.

Septic arthritis was defined based on the criteria described by Newman.17 Cases were considered to be confirmed if they presented:

  • -

    positive synovial fluid cultures (group A);

  • -

    positive blood cultures with negative synovial fluid cultures (group B);

  • -

    negative cultures due to previous use of antibiotics, but purulent drainage of the knee joint (group C); or

  • -

    definite radiological or postmortem diagnosis of septic arthritis (group D).

After inclusion, the following data were gathered from the medical records: sex, age, cause of infection, origin of the patient in order to characterize the infection as community or health service-related,18 leukocyte count, defining leukocytosis as a leukocyte count greater than 11,000, C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) of the blood in the initial evaluation, Gram staining, synovial fluid culturing, antibiogram, number of drainages, surgical procedures used for drainage, comorbidities, patient's immunosuppression, time elapsed between the beginning of the symptoms and drainage, previous joint disease, empirical antibiotic therapy, systemic and joint complications, and length of hospital stay.

Results

After analyzing the medical records we identified 61 patients who met the inclusion criteria.

The majority were male (60% versus 40%); the mean age was 41.6 years, ranging from six months to 85 years (Fig. 1).

Fig. 1.

Age distribution of septic arthritis cases.

(0.07MB).

Out of the 61 septic arthritis cases studied, 56 had positive synovial cultures (Newman A), regardless of blood culture result. Two cases had positive blood cultures and negative synovial cultures (Newman B), and three had purulent secretion without isolation of any bacteria (Newman C). No cases were framed as Newman D.

Among the patients analyzed, 55 had hematogenous infection, two had infection after knee joint aspiration (direct inoculation) and four patients were infected through soft-tissue infection around the knee (contiguity) (Fig. 2).

Fig. 2.

Causal distribution of septic arthritis cases.

(0.19MB).

Previous joint disease was observed in 28 patients (45.4%), of which osteoarthritis was the most prevalent (19 cases). At least one clinical comorbidity was observed in 37 patients (60.6%), of whom 16 (26.2%) presented systemic arterial hypertension (SAH) and 12 (19.6%) diabetes mellitus (DM). In 21 patients (34.4%), immunosuppression of varying causes was observed, among which neoplasia and chronic use of corticoids were the commonest.

Leukocytosis was observed in 32 (52.4%) patients, and all patients presented altered ESR and CRP when admitted to the hospital. Temperatures above 37.8°C were observed only in 22 patients (36%). The most common complaints were pain (88.5%) and joint effusion (72.3%). The mean time elapsed between the appearance of symptoms and the clinical diagnosis was eight days. Four patients had their symptoms for more than 30 days before hospital admission.

Among the 61 patients studied, 56 had positive synovial fluid cultures (91.8%), with or without positive blood cultures. Two patients had negative cultures while bacteria were identified in blood cultures, and no bacteria were identified in three patients due to previous use of antibiotics. Gram stained bacteria were observed in only 50.8% of the cases.

Staphylococcus aureus was isolated in 44 cases (72.1%), of which 42 were from synovial cultures and two from blood cultures, and was the most prevalent bacteria. Staphylococcus epidermidis, Streptococcus spp. and Escherichia coli were the next most prevalent bacteria, with three cases each (4.9%). Salmonella spp. was found in two cases (3.2%) and Enterococcus spp., Pseudomonas aeruginosa and Neisseria gonorrhoeae in one case each (1.6%). Among the patients infected by Gram-positive bacteria, strains of oxacillin-resistant Staphylococcus spp. were isolated in 16 cases. According to the Centers for Disease Control and Prevention (CDC) criteria for oxacillin-resistant Staphylococcus spp.,19 no case was classified as community-acquired. There were no documented cases of fungi and mycobacteria.

All patients underwent open surgical drainage of the knee with access to the joint via the medial parapatellar route immediately after confirmation of the diagnosis. Forty-nine patients underwent only one surgical procedure, while 12 needed more than one drainage.

All patients received empirical antibiotic therapy for treatment until the final result from the intraoperative cultures, followed by a specific antibiotic for the bacteria identified in these cultures. Forty-two patients received oxacillin and gentamicin, 14 patients received oxacillin and ceftriaxone and five patients who were hospitalized for more than 72h due to other pathological conditions received vancomycin and cefepime. Out of the 61 patients, the causative agent was not adequately treated by empirical drugs due to resistance of the strains in 11 cases.

The mean length of hospital stay was 21 days, ranging from five to 78 days. Four patients needed care in an intensive care unit (ICU), of whom two progressed with septic shock and died while still in hospital. The other two patients went to the ICU just because of advanced age and comorbidities. One patient underwent knee disarticulation due to uncontrollable infection and soft-tissue necrosis, two patients evolved with significant stiffness of the knee (range of motion between 30 and 90°) and one patient developed chronic osteomyelitis.

Among the six patients who developed complications, five were infected by S. aureus and one by E. coli. With the exception of one of them who was HIV-positive and did not undergo the appropriate treatment, all these patients presented at least two clinical comorbidities. No previously healthy patient developed complications (Table 1).

Table 1.

Epidemiological summary of study results.

  Number  Percentage  Observations 
Sex
Male  37  60.60%   
Female  24  39.30%   
Age
  41.6 (6 months–85 years)     
Diagnostic
Leukocytosis  32  52.40%  >11,000 leukocytes 
ESR and PCR raise  61  100%   
Fever  22  36%  T>37.8°C 
Pain  54  88.52%   
Joint effusion  44  72.13%   
Time to diagnosis (days)    Between beginning of symptoms to confirmed diagnosis 
Gram staining  31  50.80%  Gram positive=28; Gram negative=
Positive synovial fluid culture  56  91.80%   
Positive blood culture  11.40%   
Classification
Newman A  56  91.80%   
Newman B  3.20%   
Newman C  4.90%   
Etiology
Hematogenic
Distant site infection  11.40%  Pneumonia; UTI; meningitis; encephalitis 
Drug user  6.50%   
Unknown site  44  72.13%   
Direct inoculation  3.20%   
Contiguity  6.50%   
Previous articular disease  28  45.90%   
Osteoarthritis  19  31.10%   
Rheumatoid arthritis  4.90%   
Osteonecrosis  4.90%   
Ligamentous lesion  3.20%   
Charcot  3.20%   
Blount  1.60%   
Comorbidities  37  60.60%   
Hypertension  16  26.20%   
Diabetes  12  19.60%   
Imunossupression  21  34.40%   
Corticoid  11.40%   
Neoplasias  11.40%   
HIV  3.20%   
Alcoholism  3.20%   
Chronic renal disease  3.20%   
Falciform anemia  1.60%   
Isolated bacteria  58  95.00%   
S. aureus  44  72.10%  MRSA: 16; MSSA: 28 
S. epidermidis  4.90%   
Streptococcus spp.  4.90%   
E. coli  4.90%   
Salmonella spp.  3.20%   
Enterococcus spp.  1.60%   
Pseudomonas aeruginosa  1.60%   
Neisseria spp.  1.60%   
Treatment
Number of procedures per patients (average)  1.45 (1–8)     
Need to change empirical antibiotic  11  18.00%   
Hospitalization days per patient (average)  21 (5–78)     
Intensive care unit admission  6.50%  2 Evolved to septic shock 
Septic shock  3.20%  All died 
Death  3.20%   
Amputation  1.60%   
Knee stiffness  3.20%   
Chronic osteomyelitis  1.60%   
Discussion

Although septic arthritis is not a common disease, approximately 10 cases per year are identified at the studied hospital. Considering that these cases relate only to the knee joint, it can be said that this disease has a significant importance in our environment, in terms of incidence in relation to other joints and other regions of the world.16,20,21

The presence of patients classified as Newman type C may have caused selection bias in this study, as the evaluation of purulent secretion is arbitrary, and can sometimes be mistaken for inflammatory fluid of rheumatological diseases. However, only three patients fitted into this category.22

Considering the samples studied, the mean age demonstrates that septic arthritis is no longer a disease with great predominance among children (only three patients were younger than 10 years of age) and has gained significant representation among middle-aged and elderly patients, with 15 patients (24.5%) over 60 years of age. Although most patients with this condition have not presented unfavorable outcomes, infection among elderly patients may result in more serious consequences, considering that two patients over 60 years progressed to death.23

The great majority of the infections were of hematogenous origin. However, cases in which there was an infection in the contiguity of the joint and cases in which needles were introduced in the knee were responsible for a small portion of the infections (6.5% and 3.2%, respectively). This reinforces the notion that joint infiltrations should be carried out in appropriate environments with rigorous aseptic techniques and that infectious processes around joints should be considered severe because of the intra articular complications they can cause.24 Another risk factor for joint infections is the use of illicit intravenous drugs, because this practice provides a distant entry point that can favor hematogenic dissemination.25

The 45.9% rate of joint disease in septic arthritis patients was similar to that found in the literature, as well as greater presence of osteoarthritis among these pathological conditions.20,26 Most of the patients presented some clinical comorbidities, among which SAH and DM were the most common. Because of the patients’ advanced age and the high prevalence of SAH among this population, this condition cannot be considered to be a risk factor, unlike DM, which has been widely studied and shown to be a predisposing factor for infectious joint diseases among adults.27 Greater number of comorbidities was associated with poor prognosis of the disease. There were 34.4% of patients with immunosuppression, especially related to neoplasias and chronic use of corticosteroids. This can be explained by the fact that this hospital complex is a reference center for treatment of neoplastic and rheumatological diseases, thus concentrating a greater number of patients with these diseases or comorbidities.

Similar to cases of other infections of the musculoskeletal system, systemic symptoms such as fever were of little help for the diagnosis, since less than 50% of the patients presented with high temperature initially. Furthermore, the leukocyte count must not be used to rule out joint infection, because leukocytosis was present in only approximately 50% of the cases. Unlike the elevated leukocyte counts, inflammatory tests (ESR and CRP) were positive in 100% of the cases. Results of these tests within the normal range are not indicative of the diagnosis of septic arthritis.16,26,28

The present study did not show any increase in the number of surgical procedures, or any development of systemic or joint complications through delayed indication of surgical treatment. Only one of the patients who presented more than 10 days of complaints underwent more than one surgical drainage procedure, although there is support in the literature for the belief that a delay of more than three days after the beginning of the symptoms can lead to a worse prognosis.28,29

The great majority of the cultures showed growth of Gram-positive bacteria, especially S. aureus (72.1%), which is consistent with the epidemiology found in several regions of the world. This also corroborate the findings from our service in the 1990s, when S. aureus was found in 68.8% of the cases.30–34 Only 31 initial synovial fluid sampling were positive for Gram-stained bacteria, showing that such result cannot be taken as definitive for guiding whether to drain the joint, in cases of suspected septic arthritis.

In our service, out of the 28 cases (45.9%) that have not presented positive Gram staining, only six had not undergone drainage initially and had to wait for the definitive culture, for diagnosis confirmation. The diagnostic approach needs to be based not only on Gram staining but also on the systemic and local clinical condition, on inflammatory tests such as CRP and ESR, and on the differential cell count in the synovial fluid.

Only one patient presented infection by Neisseria, which is considered in the United States to be the most common pathogen in acute joint infections among young adults. Decreased incidence of infections by this pathogen has been observed in several centers over the last few years, although it has maintained high prevalence in the United States.34,35

High incidence of oxacillin-resistant S. aureus was observed,15,36 which prompted the initial empirical antibiotic regimen to be changed for 18% of the patients.

Conclusion

It is important to characterize each population epidemiologically, so that empirical treatment based on local evidence can be implemented. From the data analysis, it was possible to conclude that S. aureus is still the most common pathogen in acute knee infections in our environment. Risk factors such as comorbidities, immunosuppression and degenerative and inflammatory diseases also constitute important associated factors. Gram staining, absence of fever and normal leukocyte count cannot be used to rule out septic arthritis.

Conflicts of interest

The authors declare no conflicts of interest.

References
[1]
K.C. Donatto.
Orthopedic management of septic arthritis.
Rheum Dis Clin North Am, 24 (1998), pp. 275-286
[2]
M.H. Pioro, B.F. Mandell.
Septic arthritis.
Rheum Dis Clin North Am, 23 (1997), pp. 239-258
[3]
A.K. Shetty, A. Gedalia.
Septic arthritis in children.
Rheum Dis Clin North Am, 24 (1998), pp. 287-304
[4]
D. Bettin, B. Schul, L. Schwering.
Diagnosis and treatment of joint infections in elderly patients.
Acta Orthop Belg, 64 (1998), pp. 131-135
[5]
A. Dessì, M. Crisafulli, S. Accossu, V. Setzu, V. Fanos.
Osteo-articular infections in newborns: diagnosis and treatment.
J Chemother, 20 (2008), pp. 542-550
[6]
R.J. Williams, C.T. Laurencin, R.F. Warren.
Septic arthritis after arthroscopic anterior cruciate ligament reconstruction. Diagnosis and management.
Am J Sports Med, 25 (1997), pp. 261-267
[7]
C. Kirchhoff, V. Braunstein, J. Paul, A.B. Imhoff, S. Hinterwimmer.
Septic arthritis as a severe complication of elective arthroscopy: clinical management strategies.
Patient Saf Surg, 3 (2009), pp. 6
[8]
S. Aslam, R.O. Darouiche.
Antimicrobial therapy for bone and joint infections.
Curr Infect Dis Rep, 11 (2009), pp. 7-13
[9]
A. Molloy, A. Laing, K. O'Shea, L. Bell, K. O’Rourke.
The complications of septic arthritis in the elderly.
Aging Clin Exp Res, 22 (2010), pp. 270-273
[10]
M. Favero, F. Schiavon, L. Riato, V. Carraro, L. Punzi.
Rheumatoid arthritis is the major risk factor for septic arthritis in rheumatological settings.
Autoimmun Rev, 8 (2008), pp. 59-61
[11]
C.J. Kaandorp, P. Krijnen, H.J. Moens.
The outcome of bacterial arthritis: a prospective community-based study.
[12]
R.W. Armstrong, F. Bolding, R. Joseph.
Septic arthritis following arthroscopy: clinical syndromes and analysis of risk factors.
Arthroscopy, 8 (1992), pp. 213-223
[13]
S. Arnold, D. Elias, S.C. Buckinghan.
Changing patterns of acute hematogenous osteomyelitis and septic arthritis: emergence of community-associated methicillin-resistant staphylococcus aureus.
J Pediatr Orthop, 26 (2006), pp. 703-708
[14]
B.W. Frazee, C. Fee, L. Lambert.
How common is MRSA in adult septic arthritis?.
Ann Emerg Med, 54 (2009), pp. 695-700
[15]
S.S. Al-Nammari, P. Bobak, R. Venkatesh.
Methicillin resistant Staphylococcus aureus versus methicillin sensitive Staphylococcus aureus adult haematogenous septic arthritis.
Arch Orthop Trauma Surg, 127 (2007), pp. 537-542
[16]
L. Eder, D. Zisman, M. Rozenbaum, I. Rosner.
Clinical features and aetiology of septic arthritis in northern Israel.
Rheumatology, 44 (2005), pp. 1559-1563
[17]
J.H. Newman.
Review of septic arthritis throughout the antibiotic era.
Ann Rheum Dis, 35 (1976), pp. 198
[18]
Centers for Disease Control and Prevention.
CDC/NHSN surveillance definition of health care-associate infection and criteria for specific types of infections in the acute care setting.
Am J Infect Control, 36 (2008), pp. 309-332
[19]
Minnesota Department of Health.
Community-associated methicillin-resistant Staphylococcus aureus in Minnesota.
Dis Control Newslett, 32 (2004), pp. 61-72
[20]
C. Cooper, M.I. Cawley.
Bacterial arthritis in an English health district: a 10 year review.
Ann Rheum Dis, 45 (1986), pp. 458-463
[21]
D.S. Morgan, D. Fisher, A. Merianos, B.J. Currie.
An 18 year clinical review of septic arthritis from tropical Australia.
Epidemiol Infect, 117 (1996), pp. 423-428
[22]
G. Holt, C. Vass, C.S. Kumar.
Acute crystal arthritis mimicking infection after total knee arthroplasty.
BMJ, 331 (2005), pp. 1322-1323
[23]
F. Gavet, A. Tournadre, M. Soubrier, J.M. Ristori, J.J. Dubost.
Septic arthritis in patients aged 80 and older: a comparison with younger adults.
J Am Geriatr Soc, 53 (2005), pp. 1210-1213
[24]
C. Albert, O. Brocq, D. Gerard, C. Roux, L. Euller-Ziegler.
Septic knee arthritis after intra-articular hyaluronate injection. Two case reports.
Joint Bone Spine, 73 (2006), pp. 205-207
[25]
D.C. Allison, P.D. Holtom, M.J. Patzakis, C.G. Zalavras.
Microbiology of bone and joint infections in injecting drug abusers.
Clin Orthop Relat Res, 468 (2010), pp. 2107-2112
[26]
Geirsson ÁJ, S. Statkevicius, A. Víkingsson.
Septic arthritis in Iceland 1990–2002: increasing incidence due to iatrogenic infections.
Ann Rheum Dis, 67 (2008), pp. 638-643
[27]
C.J. Kaandorp, D. Van Schaardenburg, P. Krijnen, J.D. Habbema, M.A. van de Laar.
Risk factors for septic arthritis in patients with joint disease. A prospective study.
Arthritis Rheum, 38 (1995), pp. 1819-1825
[28]
V.C. Weston, A.C. Jones, N. Bradbury, F. Fawthrop, M. Doherty.
Clinical features and outcome of septic arthritis in a single UK Health District 1982–1991.
Ann Rheum Dis, 58 (1999), pp. 214-219
[29]
P. Kodumuri, G. Geutjens, H.L. Kerr.
Time delay between diagnosis and arthroscopic lavage in septic arthritis. Does it matter?.
Int Orthop, 36 (2012), pp. 1727-1731
[30]
N. Gómez Rodríguez, J. Ibáñez Ruán, M. González, A. Pintado, Y. Penelas Cortés.
Peripheral septic arthritis in adults. Epidemiologic study in a Galician health area.
An Med Interna, 18 (2001), pp. 573-577
[31]
L. Le Dantec, F. Maury, R.M. Flipo, et al.
Peripheral pyogenic arthritis. A study of one hundred seventy-nine cases.
Rev Rhum Engl Ed, 63 (1996), pp. 103-110
[32]
O. Oniankitan, Y. Bagayogo, E. Fianyo, et al.
Infectious arthritis in hospital patients in Lomé.
Med Trop (Mars), 71 (2011), pp. 61-62
[33]
A.S. Al Arfaj.
A prospective study of the incidence and characteristics of septic arthritis in a teaching hospital in Riyadh, Saudi Arabia.
Clin Rheumatol, 27 (2008), pp. 1403-1410
[34]
E.A. Pereira, R.A. Masagão, A. Lucia, L.M. Lima, M.M. Amatuzzi.
Pyoarthritis of the knee–caseload of the Hospital das Clínicas da FMUSP 1990–1994 (86 cases).
Rev Hosp Clin Fac Med Sao Paulo, 50 (1995), pp. 317-319
[35]
E.W. Hook.
Septic gonococcal arthritis is much more common in the USA than in the UK.
Br J Rheumatol, 29 (1990), pp. 283
[36]
T. Okano, M. Enokida, R. Otsuki, H. Hagino, R. Teshima.
Recent trends in adult-onset septic arthritis of the knee and hip: retrospective analysis of patients treated during the past 50 years.
J Infect Chemother, 17 (2011), pp. 666-670
Copyright © 2013. Elsevier Editora Ltda.. All rights reserved
Download PDF
The Brazilian Journal of Infectious Diseases
Article options
Tools