Management of Periprosthetic Joint Infections (PJIs) ( Woodhead Publishing Series in Biomaterials )

Publication series :Woodhead Publishing Series in Biomaterials

Author: Arts   J. J. Chris;Geurts   Jan  

Publisher: Elsevier Science‎

Publication year: 2016

E-ISBN: 9780081002421

P-ISBN(Paperback): 9780081002056

Subject: R619 Pre - and Post - surgical complications.

Keyword: 基础医学,整形外科学(修复外科学),外科学

Language: ENG

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Description

Management of Periprosthetic Joint Infections (PJIs): Management of PJIs discusses periprosthetic joint infection (PJI), a fairly rare occurrence that is nonetheless one of the most serious complications in joint replacement surgery. Intricate interactions between the pathogen, the host, and the implant can result in PJIs which are not only physically devastating for the patient, but also financially crippling for health authorities and insurance companies.

Actions taken to minimize the risk of PJIs can be extremely challenging for the orthopaedic community. Consequently, new research, which is detailed in this comprehensive book, is being undertaken to minimize and manage these challenging infections.

  • Provides essential background knowledge on the mechanisms and identification of PJIs
  • Dedicated chapters focus on the complex, but vital eccentricities between PJIs in different areas of the body
  • Contains contributions from a mixture of clinical and academic experts in the field, thus ensuring balanced coverage

Chapter

Chapter 1: Prevention of joint infections

1.1 Introduction

1.2 Preoperative considerations

1.2.1 Preoperative patient selection and risk factors for infection

1.2.2 Nonmodifiable comorbidities

1.2.3 Modifiable comorbidities

1.2.3.1 Active pyogenic infections

1.2.3.2 Colonization with Staphylococcus aureus

1.2.3.3 Hyperglycemia and diabetes

1.2.3.4 Dental disease

1.2.3.5 Immunosuppression and autoimmune/rheumatologic disease

1.2.3.6 Human immunodeficiency virus (HIV)

1.2.3.7 Obesity and malnutrition

1.2.3.8 Integumentary alterations

1.2.3.9 Tobacco, Ethanol, and intravenous drug use

1.2.3.10 Preoperative urinary screening and management of bacteriuria

1.3 Prevention of infection in the perioperative period

1.3.1 Body cleansing at home in anticipation of surgery

1.3.2 Preoperative hair management

1.3.3 Perioperative antibiotics

1.3.4 Surgical skin preparation

1.3.5 Antibiotic-loaded bone cement (ALBC) prophylaxis in primary and revision arthroplasty

1.3.6 The role of laminar air flow and body suits in operating rooms during arthroplasty

1.4 Prevention of infection after arthroplasty

1.4.1 Early postoperative period

1.4.1.1 Wound issues

1.4.1.2 Cellulitis and superficial wound infection

1.4.1.3 Postoperative fever

1.4.2 Late considerations

1.5 Conclusions and future trends

References

Chapter 2: Biofilm formation and the biological response

2.1 Introduction

2.2 Biofilm formation

2.2.1 Matrix proteins

2.2.1.1 Biofilm-associated protein (Bap)

2.2.1.2 Outer membrane vesicles (OMVs)

2.2.1.3 Bacterial nucleoid-binding proteins

2.3 Resistance to antimicrobial agents

2.3.1 Delayed penetration of the antimicrobial agent

2.3.2 Altered growth rate of biofilm organisms

2.4 Host response against biofilm

2.4.1 How biofilm evades host' defenses

2.5 Clinical significance of biofilm

2.6 Therapeutic strategies against biofilm

2.6.1 Biofilm matrix-degrading enzymes

2.6.2 Ultrasonic treatment

2.6.3 Bacteriophages

2.6.4 Quorum sensing inhibitors

2.6.5 Silver nanoparticles

2.7 Future trends

References

Chapter 3: Biomaterials in treatment of orthopedic infections

3.1 Orthopedic implant-related infections

3.2 Biomaterials

3.2.1 Local antibiotic delivery

3.2.2 Bone defect filling

3.2.3 Materials for local antimicrobial treatment

3.2.3.1 Polymers

Collagen

3.2.3.2 Ceramics, composites, and bioactive glasses

Calcium sulfates

Calcium phosphates

Bioactive glasses

3.3 Latest clinical evidence treatment osteomyelitis

3.3.1 Collagen fleeces

3.3.2 Antibiotic-loaded bone graft substitutes (ceramics)

3.3.3 Bioactive glass

3.4 Summary

References

Chapter 4: S53P4 bioactive glass

4.1 Introduction

4.2 Working mechanism

4.2.1 Surface reactions

4.2.2 Bond to bone

4.2.3 Osteostimulation

4.2.4 Bone proliferation in a BAG graft layer

4.2.5 BAG degradation

4.3 Antibacterial effects

4.4 Effect on angiogenesis

4.5 Current clinical applications

References

Chapter 5: Experimental models in orthopedic infection research

5.1 Osteomyelitis

5.2 Prostheses, osteosynthesis, and infection

5.3 Treatment

5.4 Infection development and prevention

5.5 Experimental models for orthopedic infections

5.6 Scoring of orthopedic infections in experimental models—(semi) systemic parameters

5.7 Scoring of orthopedic infections in experimental models—imaging and histology

5.8 Concluding remarks

References

Part Two: Types of periprosthetic joint infections

Chapter 6: Periprosthetic infection in the hip joint

6.1 Introduction

6.2 Definition

6.3 Classification

6.4 Causative organisms

6.4.1 Biofilm formation

6.5 Diagnosis

6.5.1 History and clinical examination

6.5.2 Laboratory blood tests

6.5.3 Joint aspiration (synovial fluid tests)

6.5.4 Radiological investigations

6.5.5 Intraoperative tissue specimens

6.6 Other new diagnostic tools

6.6.1 Microcalorimetry

6.6.2 Mass spectrometry

6.6.3 Fluorescence in situ hybridization

6.6.4 Sonication of explanted prosthesis

6.7 Management

6.7.1 Multidisciplinary team working

6.7.2 Preoperative planning and decision making

6.7.3 Debridement and implant retention (with or without exchange of mobile parts)

6.7.4 Single-stage revision (direct exchange)

6.7.5 Two-stage revision and implantation of a cement spacer

6.7.6 Long-term suppressive antibiotics

6.7.7 Salvage procedures (amputation/arthrodesis/excisional arthroplasty-girdlestones procedures)

6.8 Management of periprosthetic fracture in the presence of chronic PJI

6.9 The eradication of biofilm: Goals for the future

6.10 Conclusion

References

Chapter 7: Infection in total knee arthroplasty

7.1 Total knee arthroplasty today

7.2 Infection risks and prevention

7.2.1 Antibiotic prophylaxis in TKA

7.3 Diagnosis

7.3.1 Acute hematogenous infections of a TKA

7.4 Chronic TKA infection

7.5 Management of the infected TKA

7.6 One-stage revision

7.7 Two-stage revision

7.7.1 Postoperative course of antibiotics after first stage in two-stage revision

7.7.2 Second stage in the two-stage revision

7.8 Outcomes

7.9 Knee arthrodesis

7.10 Complications

References

Chapter 8: Periprosthetic infection in shoulder and elbow joints

8.1 Introduction

8.2 Clinical presentation

8.3 Diagnostic testing

8.3.1 General

8.3.2 Shoulder specific

8.3.3 Propionibacterium acnes

8.3.4 Elbow specific

8.4 Treatment and outcomes—Shoulder

8.5 Treatment and outcomes—Elbow

8.6 Conclusion and future directions

References

Part Three: Managing and treating periprosthetic joint infections

Chapter 9: Practice and guidelines for treating periprosthetic joint infections: Single- and two-stage revision

9.1 Introduction

9.2 Patient preparation, implant removal, and surgical debridement

9.2.1 One-stage technique

9.2.2 Two-stage technique

9.2.3 Indications and patient information

9.3 Analysis of results

9.3.1 Hip

9.3.2 Knee

9.4 Conclusions and future trends

References

Chapter 10: PMMA beads and spacers for local antibiotic administration

10.1 History

10.2 Rationale and pharmacokinetics of antibiotic-loaded PMMA

10.3 Beads

10.4 Spacers

10.4.1 Static vs mobile spacer in the knee [ 20–23 ]

References

Chapter 11: Pathogen-directed antibiotic therapy

11.1 Introduction

11.2 Cultures and diagnosis

11.3 Prophylaxis and empirical therapy

11.4 The pathogens in PJI

11.5 The antibiotics

11.5.1 General principles

11.5.2 Resistance induction and combination therapy

11.5.3 Duration of treatment and tolerability of antibiotics

11.5.4 Intravenous to oral switch

11.5.5 Suppressive antibiotic therapy

11.5.6 Clinical monitoring of patients receiving long-term antibiotic therapy

11.6 Pathogen-directed choice

11.6.1 Staphylococcus aureus (MSSA (methicillin-sensitive S. aureus .) and MRSA)

11.6.2 Coagulase-negative Staphylococci (CoNS)

11.6.3 Enterococci: Enterococcus faecalis and Enterococcus faecium

11.6.4 Streptococci

11.6.5 Gram-negative bacilli

11.6.6 Anaerobic microorganisms

11.6.7 Polymicrobial infections

11.6.8 Fungi

11.6.9 Other microorganisms

11.7 Conclusion and areas for further research

References

Part Four: Case studies

Chapter 12: Imaging of prosthetic joint infections

12.1 Introduction

12.2 Conventional imaging

12.2.1 Plain radiographs

12.2.2 Ultrasound

12.2.3 Computed tomography and magnetic resonance imaging

12.3 Nuclear imaging

12.3.1 Bone scintigraphy

12.3.2 Gallium scintigraphy

12.3.3 Leukocyte scintigraphy

12.3.4 Antigranulocyte scintigraphy

12.3.5 Fluorodeoxyglucose positron emission tomography

12.4 Imaging in the assessment of PJI

12.4.1 Hybrid imaging and new infection-specific agents

12.4.2 Multimodality diagnostic work-up of PJI

References

Index

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