Acute Management of Open Fractures: An Evidence-Based Review
Acute Management of Open Fractures: An Evidence-Based Review
Acute Management of Open Fractures: An Evidence-Based Review
An Evidence-Based Review
Mohamad J. Halawi, MD; Michael P. Morwood, MD
Department of Orthopaedic Surgery, Duke University Medical Center, Durham, North
Carolina.
Open fractures are often the result of high-energy trauma and can lead to
significant long-term morbidity and disability.1
An open fracture is defined as one with an associated break in the skin that is
capable of communicating with the fracture and/or its hematoma.2
Communication with the outside environment higher rates of infection, malunion,
and nonunion if not recognized and treated appropriately.1,3,4
1850s open fractures early amputation because sepsis and gangrene
On the 20th century aseptic technique by English Surgeon, Joseph Lister
mortality rate drop from the historic 50% down to 9%.5,6
Epidemiology
Crush injuries (the most common), falls from a standing height and road traffic
accidents.
Males : Females = 7:3 , mean age of 40.8 and 56 years
Type of fractures :
fractures of finger phalanges (incidence 14/10 per year),
fractures of the tibia (3.4/10 per year)
and distal radius (2.4/10 per year) in the general population
Etiology
The most critical first goal is saving life Advanced Trauma Life Support
(ATLS) protocol.
Knowing the mechanism of injury
A systematic inspection of each limb is critical; the dimensions, locations,
and degree of soft tissue involvement of open wounds should be noted
prior to reduction and/ or splinting.
A complete neurovascular examination should be performed, and, if
necessary, vascular studies should be obtained for those injuries with a
questionable vascular examination.
Initial Management
Gustilo and Anderson10 70% of open wounds were contaminated with bacteria and argued
that the routine use of antibiotics was a therapeutic
The authors recommended a combination of a first-generation cephalosporin and
anaminoglycoside, or a third-generation cephalosporin for type III open fractures.11
Johnson et al32 , in a prospective, randomized study comparing the first- and third-generation
cephalosporins in types II and III open fractures, found no statistical difference in the rate of
infection between the 2 treatment groups.
Surgical Debridement
Although bone and skin viability are assessed by their capacity to bleed,
muscle viability is assessed by the criteria outlined by Artz et al,37 which
consist of the 4 Cs: color, contractility, consistency, and capacity to
bleed.
Timing of Surgery
Early fracture stabilization reduces pain, facilitates bed transfers and ambulation,
prevents further soft tissue injury, and promotes healing.
This is particularly important for intra-articular fractures where early joint motion may
be advantageous.3
There are many different treatment options for open fractures depending on
hemodynamic status, fracture location and pattern, and extent of soft tissue injury.
External Fixation
Bone grafting can help in fracture repair and reconstruction of skeletal defects. 32
It can be performed at the time of closure for types I and II open fractures but should be
delayed until the wound has healed in type III fractures, owing to the extensive periosteal
stripping, soft tissue damage, and possible blood flow compromise associated with these
severe injuries.32
Bone graft : recombinant human bone morphogenetic protein-2 (rhBMP-2) can also be
used at the time of definitive wound closure to accelerate healing.
Since the BESTT study, rhBMP-2 has been approved by the US Food and Drug
Administration for use in the primary treatment of open tibial shaft fractures.
Wound Closure
Delayed wound closure may increase risk of infection with nosocomial gram negative
microorganisms, such as Pseudomonas species, Enterobacter species, and methicillin-resistant S
aureus.3,68
Benson et al69, in a double-blind, randomized trial examining open fractures with adequate soft
tissue coverage, found no increased risk of infection when wound closure was delayed for 5 days
in highly contaminated fractures provided patients received antibiotic prophylaxis and surgical
debridement.
For wounds with extensive tissue loss (type IIIB and IIIC injuries), Gopal et al70 favored early internal
fracture fixation and flap coverage (within 72 hours). Their conclusion was supported by a higher
rate of infection when flap coverage was delayed, although they cautioned that this difference
was not statistically significant.
Negative-PressureWound Therapy
Most wounds associated with type I open fractures will heal by secondary intention or can
be closed primarily without an increased risk of infection.71
However, higher-energy injuries (type II and III open fractures) may require temporary
coverage between serial debridements or until flap coverage.
Stannard et al7 ,in a prospective, randomized trial2, showed that the use of negative-
pressure wound therapy (NPWT) between surgical debridements prior to wound closure
resulted in a five fold decrease in infection rate compared with standard gauze dressing. In
contrast, Bhattacharyya et al 73 retrospectively reviewed
Conclusion
Prophylactic antibiotics (eg, a first generation cephalosporin) reduce the risk of deep
infection.
Urgent operative irrigation and debridement is the standard of care.
The goals of surgery are to achieve thorough debridement, bone stabilization, and
restoration of the soft tissue envelope.
Multiple fixation techniques are available, each with its advantages and disadvantages.
The role of adjunctive therapies, such as antibiotic-impregnated devices, rhBMP-2, and
NPWT between serial debridements, is emerging.
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