Craniofacial Trauma: An Assessment of Risk
Related to Timing of Surgery
C. Derdyn, M.D., J. A. Persing, M.D., W. C. Broadus, M.D., Ph.D.,
|. B, Delashaw, M.D.,
J. Jane, M.D., Ph.D., P. A. Levine, M.D., and J. Torner, Ph.D.
Charloweseilte, Va
Following the retrospective analysis of approximately
4000 head-injury patients, 49 were identified with a
combination of displaced facial fractures and significant
cerebral trauma. ‘The purpose ofthis study was to define
clinical and radiographic features in these patients that
te asvocited witha poor progmosis, which in tum might
influence the timing of facial fracture repair. The pres-
ence of an upper-level facial fracture, low Glasgow coma
Score, intracranial hemorrhage, displacement of nor-
mally midline cerebral structures, and. multisystem
trauma was associated with a. statistically significant
poorer prognosis. Additionally, in demographically sim
ilar groups of patients (age, sex, concomitant injury)
preselected for intracranial pressures of less than 15
InmtTg at the time of surgery, no significant difference
in survival was appreciated in patients who underwent
early (0 to 8 days), middle (4 10 7 days), or late (>7 days)
surgical repair. Early surgical repair of facial fractures in
these circumstances does not appear to have a negative
impact on recovery.
Facial fractures are commonly associated with
cerebral injury. Approximately 52 percent of
patients with facial fractures have an associated
closed head injury (CHI),' with the greater the
energy at impact (j.e., motor vehicle accidents
versus falls or assault), the greater the likelihood
of a closed head injury. Life-threatening cerebral
injury may be associated with facial fractures in
as much as 36 percent of high-velocity trauma.
Recently, great emphasis has been placed on
the immediate and full correction of facial frac-
tures, because of the obviously improved aes-
thetic and functional results obtained by this
treatment approach compared with that of de-
layed surgery.“ Despite the obvious benefits of
From the Departments of Pati Sung
early facial fracture reduction, it is clear that
some individuals with combined facial bone and
cerebral injuries may be placed at risk for further
cerebral injury by early surgery. Supine position-
ing, intraoperative fluid shifts, and cerebrovas-
cular dilating anesthetics all may exacerbate cer-
ebral edema and negatively affect outcome. This
study seeks to identify factors that might be used
at the time of initial evaluation to recognize those
individuals who might be adversely affected by
early surgical reduction of facial fractures.
PATIENTS AND METHODS
Patient Population
Approximately 4000 patients were admitted
to the University of Virginia Health Sciences
Center between January of 1980 and July of
1987 with a history of, at a minimum, a loss of
consciousness (concussion). Each patient was
evaluated by the trauma and neurosurgical serv-
ices and, on an alternating weekly schedule, the
plastic surgery or otolaryngology surgery serv-
ices. These patients’ case histories were retro-
spectively analyzed to identify those patients with
displaced facial fractures plus cerebral injury se-
vere enough to require, at least, intracranial pres-
sure (ICP) monitoring (ie., significant cerebral
contusions or intracranial hemorrhage requiring
operative intervention). Excluded were patients
with isolated cerebral or cranial vault injury,
patients with isolated facial fractures, patients
with cerebral concussions (mild cerebral injury)
combined with facial fractures, and patients with
ry, Neurological Surgery. and Otolaryngology-Head and Neck Surgery atthe University of Virginia
Health Sciences Cente. Received for publication Apri 10, 1980; revised July 26, 1080
38Vol. 86, No. 2 / CRANIOFACIAL TRAUMA
any severity of cerebral injury associated with
nondisplaced facial fractures.
Data Collection
Admission data collected included the mode
and time of injury, the age and sex of the patient,
the admission neurologic examination, and the
Glasgow coma scale (GCS) score” as a standard-
ized measure of neurologic injury (Table 1). A
high postinjury GCS score is associated with a
lesser degree of cerebral injury and greater like-
lihood of good neurologic recovery, while a low
score predicts a low probability of good neu
logic outcome. Notation was made as well of the
location and type of associated injuries to other
body systems (pulmonary, gastrointestinal, and
so on).
Facial fractures were categorized as upper,
middle, or lower face or any combination of the
three regions (after Gentry et al.” and Lee et
al.”), Briefly, fractures cephalad to the frontozy-
gomatic sutures laterally and the nasoethmoid
sutures medially (ie., supraorbital rim, frontal
sinus fractures) were designated upper-level,
fractures caudad to this level but cephalad to the
interocclusal plane (ie., ethmoid, maxillary, zy-
TABLE 1
Glasgow Coma Seale (GCS) Summates Responses to Three
inical Observations—Eye Opening, Verbal Response,
and Movement—to Give an Index of the Severity of
Neurologic Injury (Higher numerical score indicates less
severe neurologic injury.)
Eyes: Open Spontancously a
To verbal command 3
To pin 2
No response 1
Best motor re Toverbal Obese o
sponee ‘command
To painful Lacalizes pin 5
ssimulus®
Hexion-witdrawal 4
Hlexionabnormal (des 3
corticate rigidity)
Estension decerebrawe 2
visit)
No tesponse
Best verbal re Oriented and con
sponse ——
Disoriented and com
Inappropriate words 8
Incomprehensible 2
No response 1
TOTAL
239
gomatic, and nasal fractures) were designated
middle-level, and fractures caudad to the inter-
occlusal plane (.e., mandibular fractures) were
identified as lower-level facial fractures. Patients
with frontal bone fractures that did not involve
the frontal sinus or the supraorbital rim were
excluded from this study. Fractures such as a Le
Fort III fracture (including the nasoethmoid,
orbital floor, maxilla, and so on) were counted
singly as one fracture and not subdivided into
component parts. CT scans of the face, panra-
diography of the skull and face, and operative
notes from the repair procedure were used to
assign location, number, and nature to the frac-
tures.
‘The admission cerebral CT scan was inter-
preted by the radiology or neurological surgery
staff. Information gathered from these scans in-
cluded the degree of shift of normally midline
cerebral structures; the number, location, and
nature of high-density lesions (i.e., epidural, sub-
dural, or intracerebral hematom:
ence of compress
brospinal fluid cisterns (as an indication of intra-
cranial spatial decompensation and_ incipient
cerebral herniation). The facial CT scan was
interpreted by the plastic surgery or otolaryn-
gology-head and neck surgery staff to note the
location and degree of displacement of the facial
fractures.
Neurosurgical procedures were carried out as
indicated by the clinical findings supported by
the CT scan. Facial fractures were managed by
the plastic surgery or the otolaryngology-head
and neck surgery services on a rotating weekly
schedule. The timing of the facial fracture repair
was determined by the preference of the con-
sultant, except when contraindicated by the fol-
lowing clinical situations
1. Elevated intracranial pressure (ICP) arbi-
trarily set at 15 mmHg on admission (all
patients undergoing early facial fracture
reduction had placement of ICP monitors;
normal ICP in a supine patient may be as
high as 12 mmHg)
2. Severe associated injury (such as massive
pulmonary contusion)
3. Severe medical conditions (such as dissem-
inated intravascular coagulation)
4. Obvious poor prognosis for survival due to
cerebral injury (clinical criteria for brain
death or severe brainstem level dysfunc-
tion)240 PLASTIC AND RECONSTRUCTIVE SURGERY, August 1990
‘The timing of facial fracture repair was divided
into three groups:
1, Early (0 to 3 days)
2. Middle (4 to 7 days)
3. Late (after 7 days)
‘The operative notes from all procedures per-
formed were reviewed, and data were collected
regarding date and length of each procedure
(neurosurgical and facial fracture repair), the
type of procedures, and the total of perioperative
fluids administered. The preoperative and post-
operative GCS scores were obtained from the
hospital record.
Outcome data collected included the date of
discharge, the discharge GCS score, and if appro-
priate, the date and time of death. Glasgow out-
come score (GOS)"” was computed from the
chart and reflects an objective measure of the
degree of impairment of patients following re-
covery from head injury (Table II).
Outcome was divided into two categories:
1. Good recovery with
(GOS 5)
2. Moderate to severe disability or death
(GOS <4)
val disability
Statistical analysis of the data was performed
using either chi-square analysis or Fisher's exact,
test
TABLE Il
Glasgow Outcome Scale (Abbreviated Scale), A Measure of
Function Following Cerebral Injury
Pan can Dead a Fall
and independent life
‘with or without min
inal neurologic def
‘GOS Moderate recovers! Patient has neurologic
‘or intellect in
Pairment but is inde-
ene
‘GOSS: Severely dimblede —__ Gonscions patent, but
{otally dependent on
others to get
{hrough the activities
forthe day
OS 8: Vegetative warvial
TABLE U1
iphies of Combined Craniofacial Trauma Patient
Population
Demogr
Percent of
1 2
5 31
27 55
5 10
1 2
‘Mate 43 88
Female 6 i
Mechanism of injury
wa 2 86
csw 2 4
‘Asc 1 2
Fall 4 8
Resutts
Population
Forty-nine patients were admitted during
1980-1987 with a combined facial fracture and
neurologic injury requiring operative interven-
tion, or approximately 1 percent of this head-
injury population. As with most head-injury se-
ries, the majority of patients injured were male,
aged 21 to 40 years, who had been involved ina
motor vehicle accident (Table II1).
‘The admission GCS score of the 49 patients
for study demonstrates a nearly even distribution
between severe (GCS 3 to 5), moderate (GCS 6
to 8), and relatively mild (GCS 9 to 14) neuro-
logic injury (Table IV),
Fractures of the craniofacial skeleton were dis-
tributed as listed in Table V. Overall, the injuries
were severe, with a majority of the patients hav-
ing an average of four to six fractures per patient.
Patients undergoing early surgery (0 to 3 days
after injury) generally had a higher GCS score
(less severe injury) (Table V1). Patients with more
severe injury tended to be delayed owing to the
initial recording of ICP being greater than 15
TABLE 1V
Admission GCS Scores of Patients with Combined
Craniofacial Trauma, Indicating Severity of Cerebral
Injury
GCS Score Frequcny
x 1%
6x 20
9-14 4Vol. 86, No. 2 / CRANIOFACIAL TRAUMA
TABLE V
Fracture Frequency and Distribution in Patients with
‘Combined Craniofacial Trauma
241
TABLE VU
Severity of Neurologic Injury (GCS Score) on Admission
Compared with Ourcome (Note that lower GCS scores are
associated with poorer prognosis.)
Upper face
roma bone *
Frat ane sinus 5
Front post sinus 7
Orbital tot 5
Orbit mea wall 0
Nasocthonoid *
Middle ace
Orbital floor 1 Levent 7
‘Zygon 9 LeFort ll 10
‘sgomatic aren S LeFort
Nasal 6
Palate 2
Manilla
Lower face
‘Mandible
mmHg. Finally, 12 patients with the most severe
head injuries were not operated on because of
evidence of severe brainstem-level dysfunction
or brain death at the time of initial evaluation.
Outcome
‘The GCS score accurately predicted outcome
(Table VI). Those patients with a GCS score of
less than 5 uniformly did poorly, all patients
cither expiring or having severe disability,
whereas the patients with a high GCS score (9 to
14) did well, 86 percent achieving a good recov-
ery statu
CT scan findings also accurately predicted sur-
vival. The presence of intracranial hemorrhage
and/or shift of midline cerebral structures was
associated with a statistically significant poorer
prognosis (Tables VIII and IX). The presence of
basal CSF cistern effacement showed a tendency
to be associated with a poor prognosis, but this
difference was not statistically significant (Table
X). There were, however, 10 CT scans that were
TABLE VI
Severity of Neurologic Injury (GCS Score) Compared with
Timing of Facial Fracture Surgery (Note that less severely
injured patients are operated on earl
than more severely
GS Score Ded Dabied Good Revoery
* 7 °
68 7 n
oa 2 2
unavailable for analysis because they were either
technically inadequate to determine obliteration
of the cistern or they were physically purged
from radiographic files. The small numbers of
available scans for review also affected our ability
to further characterize the prognostic effect of
the type (epidural, subdural, intracranial), loca
tion, and size of cranial hemorrhage.
The level of facial fracture affected survival,
with patients having fractures located in the up-
per level combined with patients having upper-
and middle-level facial injuries faring statistically
more poorly (p< 0.05) than patients with lower-
level lesions (Table X1). Moreover, patients ex-
hibiting an additional body system trauma (e.
pulmonary, cardiac, gastrointestinal) did statisti-
cally more poorly (p < 0.05) than patients who
did not.
Effects of Surgery
Of the 49 patients fulfilling the criteria for
combined cerebral and facial trauma, 12 died or
remained in a “vegetative” state prior to repair
of the facial fracture. All these patients had an
admission GCS score of less than 5. Thirty-seven
patients underwent repair of their facial frac-
tures. The patient groups that underwent early,
middle, and late surgery did not differ signifi-
cantly between groups with respect to age, sex,
type of neurologic procedure (i.e., cerebral in-
TABLE VIL
Frequency of CT-Demonstrated Intracranial Hemorrhage
Compared with Outcome (Note the statistically significant
less frequent hemorrhage present in patients with good
recovery.)
injured patients.)
GG sore ine Nowe ___Hemorrage __—_Dese/Diabled Goad Recovery
z 2 Absent T B
5 0 Present 6 7
9
6
peour242 PLASTIC AND RECONSTRUCTIVE SURGERY, August 1990
TABLE IX
Shift of the Normally Midline Septum Pellucidum
Compared with Outcome (Note the statistically significant
poorer outcome associated with shift of the septum
pellucidum.)
TABLE XI
Location of Facial Fracture Compared with Outcome
(Note that upper-level fractures are associated with poorer
‘Absent 15 28
Prevent 7 2
peo0s
jury), number of associated system injuries, num-
ber of facial fractures, length of operative pro-
cedure, or fluid replacement.
Likewise, the three groups of patients did not
differ statistically with respect to admission GCS
scores, though a trend toward early surgery for
patients with less severe cerebral injury was evi-
dent (Table X11). Likewise, a nonstatistically sig-
nificant trend toward improved survival was doc-
umented in the patients who had early repair of
facial fractures compared with those who under-
went late repair.
From a statistical standpoint, no patient oper-
ated on in any time period showed a decrement
in GCS score. The majority of patients’ GCS
scores were unchanged from the time of surgery
to the date of discharge approximately 1 month
later. There were individuals, particularly those
operated on in the early surgery category, dem-
onstrating improved neurologic outcome (higher
GCS scores) following surgery. This is probably
due to the fact that they were operated on during
the stage of rapid neurologic recovery, soon after
trauma, before stabilization had taken place,
rather than due to any beneficial effect of the
surgery itself (Fig. 1).
‘Two patients in the series of operated patients
died. Their numerical GCS scores were not wors-
TABLE X
Status of Cerebrospinal Fluid Cisterns Compared with
‘Outcome (Note that deformity of cisterns is more common
in patients with poor outcome, but the difference does not
achieve statistical significance.)
outcome.)
Reon Ded/Diabled Good Roney
U+UM 12 4
L+ML+ UML+M 4 Ig
7 opper Me mde Lower
ened by surgery; on admission, they already had
as low a GCS score as was possible (ie., GCS 3).
One underwent facial fracture repair 10 days
after admission (j.e., late) and died of pulmonary-
induced sepsis 107 days later. The second patient
underwent early repair (24 hours after injury),
with death occurring on the first postoperative
day. This patient, with an admission GCS score
of 8, also had a CT demonstration of basal cistern
effacement indicating incipient transtentorial
herniation. He died the day following surgery as
a result of uncontrolled ICP. Although it is dif-
ficult to implicate surgical treatment as affecting
outcome in the patient undergoing late surgery,
the patient undergoing surgery within 24 hours
of injury and subsequently dying due to in-
creased intracranial pressure most likely was neg-
atively affected.
There were no significant differences in the
number of postoperative complications experi-
enced between the groups undergoing carly,
middle, and late surgery (Table XID).
Discussion
In this preliminary study, our data indicate
that low GCS score, upper-level facial fracture,
CT evidence of intracranial hemorrhage, and
shift of midline cerebral structures are associated
with a poor prognosis. Additionally, evidence for
basal CSF cistern effacement on CT scan may
TABLE XI
ing of Surgery Compared with Outcome (A trend
toward early surgery in patients with less severe neurologic
injury is seen.)
CSFCicrint —_—_Dead/Disbied Good Recovery Deed/Diabled Goad Reorery
Nan 10 7 Ean 4 2
Mild 1 1 Middle 3 5
B A Lae 8 7
: . Nondisplaced 4 5
NMI porma il il deforony del deine dori pas rn 4
ahersp= 0088: p= 0.087Vol. 86, No. 2 / CRANIOFACIAL TRAUMA
POSTOPERATIVE CHANGE IN GCS
Eon (0-3 0098)
Di Lote attr 7 0045)
dale (5-7 Days)
Number g
yi
y
Vy,
)
y
@ | @ $a 5
oes,
Fig. 1. Histogram demonstrating change in GCS score in
patients undergoing early, middle, and late period surgery
No patient demonstrated & worsening of GCS score.
MN
TABLE XII
Comparison of Different Systems Injury ($1) Frequency
with Timing of Facial Fracture Repair (No significant
differences were appreciated between groups undergoing
early, middle, late, or no surgery.)
w
° ® 5
1 4 4
2 3 3 1
> 1 6 4 2
indicate a poor prognosis, but statistical support
for this statement is lacking.
Patients who underwent early surgical reduc-
tion of their facial fractures demonstrated a non-
statistically significant improvement in survival.
‘The improvement is probably artifactual, since
this is a retrospective study with a preselection
bias inherent in the treatment of these patients:
a greater number of patients with lesser cerebral
injury (high GCS scores) were selected for early
surgery. It is interesting to note, however, that
when the early, middle, and late surgery groups
are compared relative to major prognostic fac-
tors and demographic characteristics, they are
similar with no appreciable or statistically signif-
icant differences. These data suggest that, at
least, early surgery does not appear to worsen
survival when compared to the middle and later
surgical groups if one of the selection criteria for
surgery is an ICP of less than 15 mmHg. Because
early surgical treatment of facial fractures can
243
provide a better aesthetic result and it does not
appear to worsen survival, support for the early
surgery recommendation is given by this study.
Early surgery for facial trauma, as stated pre-
viously by Manson et al.,* Gruss and Mackinnon,*
and others, is appealing because the techniques
of direct exposure of fracture fragments with
anatomic reduction and interfragment bone fix-
ation largely obviate the need for precise intra-
operative soft-tissue contour assessment, which
ordinarily is distorted due to edema. Addi-
tionally, since fracture reduction may be
achieved prior to fibroblast ingrowth into and
collagen production in the traumatized area, sec-
ondary abnormal distortion of facial structures
by scar is potentially reduced. Proponents of
delayed surgery for neurologically unstable pa-
tients rightfully do exist, however. Patients with
extensive facial fractures who are apparently “fit”
by neurologic examination criteria preopera-
tively have sustained immediate unexplained
worsening in neurologic status postoperatively.”
Although vasospasm of basal cerebral vessels is
suspected, documentation is lacking.
In the present study, the finding of a poorer
prognosis with upper facial fractures is coin
dent with previously published data by Lee et
al.’ They found upper-level facial injury most
frequently associated with closed head injury
(CHD), contrasted with isolated mandible frac-
tures with a low association with closed head
injury. Midfacial fractures with mandible frac-
ture (i.c., multiple fractures) in their data analysis
were associated with a low incidence of associated
closed head injury, invoking the idea of a protec-
tive cushioning effect of the facial fracture for
the brain, Data analysis in this study was unable
to substantiate this, although the trend was in
the same direction.
The predictive value of the GCS score is well
established by previous investigations.°""'* In
the present study, further support comes in the
finding of no “good recovery” in patients with a
GCS score of less than 5, whereas 61 percent of
those with GCS score of 6 to 8 recovered with
nal disability and 85 percent of those with
a GCS score of greater than 9 made a good
recovery.
The CT scan data have proved invaluable, as
noted by previous authors, in that the presence
of intracranial hemorrhage is recognized as a
poor prognostic sign.'” Likewise in this study, the
presence of a shift of intracranial midline struc-
tures is associated with a poor prognosis. Lipper244 PLASTIC AND RECONSTRUCTIVE SURGERY, August 1990
etal."® previously noted that a shift of intracranial
midline structures of more than 3.8 mm correctly
predicted poor outcome in 63 percent of severely
head-injured patients. Others have shown an in-
verse relationship between the degree of basal
cistern effacement and survival.!7
Intracranial hemorrhage in this study was as-
sociated with a poorer survival rate. However,
questions regarding the size and location of hem-
orthage affecting survival are left unanswered.
Previous data in patients with isolated cerebral
and cranial vault injury indicate that the larger
the hemorrhage, the worse is the prognosis, by
indirect measures such as shift of midline cere-
bral structures.
Delayed intracranial hemorrhage was not seen
in the present study but should be considered in
the overall treatment plans of patients with se-
vere head injury.'® These hemorrhages by defi-
nition are not present on initial CT scan study
but develop 1 to 24 days following trauma, the
greatest number being diagnosed as an abrupt
ge in ICP 24 to 48 hours after injury. De-
layed hemorrhages are more likely to be seen in
more severe head injuries and lower
GCS scores. Special consideration should be
given in the severely brain-injured patient (low
GCS score) with facial fractures to ICP monitor-
ing intraoperatively during facial fracture reduc-
tion at least in the early treatment phase to be
able to diagnose and treat this possi
promptly as possible.
Monitoring of intracranial pressure has been
shown to be an effective adjunct in determining
the severity and treatment of cerebral injury.
Because of this, in the present study, no patient
with an ICP of more than 15 mmElg on initial
reading underwent early surgical reduction of
facial fractures. It is believed that the relative
supine head position intraoperatively, the ex-
pected blood loss and fluid replacement, and the
need for cerebral vasodilating inhalation anes-
thetics contribute to the possibility of increasing
cerebral edema. In these cases, we recommend
surgery be delayed. Additionally, the observation
of an ICP of less than 15 mmHg on admission
should not be the sole guide to determining the
feasibility of early surgery. Fracture of the ante-
rior cranial base may result in dural tears and
CSF leaks, falsely lowering the ICP and masking
the degree of cerebral edema present.
The best treatment regimen for the combined
facial fracture and cerebral injury patient is yet
to be defined, and the relatively small number of
patients in this study disallows implementation of
rigid guidelines. These data should be consid-
ered preliminary pending completion of a larger-
scale multicenter study of this issue. However,
because of the relative frequency of these pa-
tients needing care nationwide, we offer these
early recommendations: enlist the early consul-
tation of the neurologic and trauma surgeon,
obtain appropriate radiologic studies to include
CT scans of the craniofacial skeleton, and record
the ICP to help determine the appropriate timing
of facial fracture reduction surgery. We believe
that the patient with a GCS score of 6 or higher,
no evidence of intracranial hemorrhage, midline
cranial shift, or basal cistern effacement, and an
ICP of less than 15 mmHg without an obvious
CSF leak is a good candidate for early facial
fracture reduction. Alternatively, the patient
with a GCS score of 5 or lower, evidence of
intracranial hemorrhage, midline cranial shift, or
basal cistern effacement, and an ICP of more
than 15 mmflg is a poor candidate for early
fracture reduction. Consideration should be
given to delayed surgical treatment. However,
even those patients with a low likelihood for
neurologic recovery (unless they are clinically
brain dead) still should be considered for delayed
surgical reduction of facial fractures, when ICP
reduction permits, to avoid the later develop-
ment of grotesque facial deformity. Restoration
of correct facial anatomy may be of benefit not
only to the patient with the unexpected and
surprisingly good recovery, but as well to the
family of the patient with persistent severe brain
injury, since it may reduce their tendency toward
“familial” social isolation as a result of the pa-
tient’s facial deformity.
John A. Persing, M.D.
Division of Craniofacial Surgery
Box 376
University of Virginia Health Sciences Center
Charlottesville, Va. 22908
ACKNOWLEDGMENTS
‘Theauthors wish to thank Jeff Adams and Nancy Tisdale,
R. N,, for assistance in data organization and retrieval and
Debra Shaffer for excellent editorial assistance.
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