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Timing of surgical intervention for compartment syndrome in different body region: systematic review of the literature

This article has been updated


Compartment syndrome can occur in many body regions and may range from homeostasis asymptomatic alterations to severe, life-threatening conditions. Surgical intervention to decompress affected organs or area of the body is often the only effective treatment, although evidences to assess the best timing of intervention are lacking. Present paper systematically reviewed the literature stratifying timings according to the compartmental syndromes which may beneficiate from immediate, early, delayed, or prophylactic surgical decompression. Timing of decompression have been stratified into four categories: (1) immediate decompression for those compartmental syndromes whose missed therapy would rapidly lead to patient death or extreme disability, (2) early decompression with the time burden of 3–12 h and in any case before clinical signs of irreversible deterioration, (3) delayed decompression identified with decompression performed after 12 h or after signs of clinical deterioration has occurred, and (4) prophylactic decompression in those situations where high incidence of compartment syndrome is expected after a specific causative event.


The ability to tolerate rise in pressure of a closed area of the body, depends on three main factors: the compliance—the extent to which that region can expand to adjust the increasing pressure—the degree of vascular and nervous damage that occurs in the area, and the physiological effects that the increasing pressure generate on the body homeostasis. It is explicit that some compartments can only briefly tolerate an acute rise in pressure due to its detrimental effect like hemodynamic instability seen in tension pneumothorax or cardiac tamponade even if those pathological entities seldom are included among “compartmental syndromes”. In fact, compartment syndrome properly defined is the pressure increase inside a defined body compartment. When tissue interstitial pressure becomes higher than the capillary one, cells get insufficient blood supply. To revert those scenarios, generally urgent intervention may be required. Uncertainty exists in regard to the timing of intervention of more complex, urgent compartmental syndromes. The resistance of the different tissues to hypoxia and hypoperfusion is unknown. Different tissues, in fact, have different capability to resist to blood flow reduction due to pressure increase. Several compartments exist in the human body. Most of them may potentially develop compartment syndrome but only a few of them may impact on the body homeostasis or may be surgically decompressed. Moreover, only a small part of these areas has been investigated in terms of compartment syndrome effects and management. Present paper included among compartment syndromes even those clinical conditions characterized by a pressure increase impairing the function even if not directly reducing the blood supply to tissues. In fact, tension pneumothorax and cardiac tamponade, with a sudden increase of pressure inside un-expandable districts, may determine life-threatening conditions that must be solved as soon as possible through surgical decompression. The aim of this paper is to evaluate the current evidence in order to assess the optimal timing for surgical intervention in these main compartments. The deep understanding of pathophysiology underlining at the development of each compartment syndrome is beyond the proposal of this paper and will not be addressed.

Material and methods

A systematic computerized search was done in different databanks (MEDLINE, Scopus, EMBASE) citations were included for the period between January 1981 and April 2020 for articles regarding the timing of decompression in compartment syndrome in all body regions. Primary search strategy utilized the following words: abdominal, limb*, ocular, orbital, thora*, hand, compartment, compartmental, compartment* syndr*, lower-limb, upper-limb*, decompressive, decompression, laparotomy, thoracotomy, fasciotomy, acute, vascular, cardiac, non-operative, medical, management, timing, surgery, craniotomy, craniectomy, brain, and cerebral combined with AND/OR. No search restrictions were imposed. The dates were selected to allow comprehensive published abstracts of clinical trials, consensus conference, comparative studies, congresses, guidelines, government publication, multicenter studies, systematic reviews, meta-analysis, large case series, original articles, and randomized controlled trials. Narrative review articles were also analyzed to determine other possible studies. Included articles were enlisted in the tables and selection process is explained in the PRISMA flow chart (Fig. 1).

Fig. 1

PRISMA flow chart


A total of 499 articles were retrieved. Among them 58 articles were considered in results analysis (Fig. 1). Included articles are reported in Tables 1, 2, and 3 divided by anatomical regions. Extensive discussion of the results is reported below. Decompression timing was stratified according to priority (Table 4).

Table 1 Summary of studies about decompressive procedures in orbital compartment syndrome (residual visual acuity has been uniformed whenever requested from Snellen Imperial to Snellen metric according to Elliott and Flanagan [1])
Table 2 Summary of studies about decompressive craniotomy timing
Table 3 Summary of studies about decompressive laparotomy timing in abdominal compartment syndrome
Table 4 Decompression timing

Orbital compartment syndrome

Orbital compartment syndrome (OCS) is identified as one of the most feared ophthalmic emergencies [51]. It is a sight-threatening condition due to optic nerve and retinal compromise secondary to ischemic process deriving from a rapid and uncompensated increase of infraorbital pressure. Trauma and retrobulbar hemorrhage are the most common causes of OCS along with massive resuscitation after burn injuries. OCS is generally associated to trauma (45%) and surgery (32%) [51]. Only small increases in orbital volume can compensate thanks to the anterior globe movement and fat prolapse. Normal intraocular pressure is 3–6 mmHg (0.4–0.8 kPa). Orbital content volume is around 30 mL, including the eyeball, nerves, vessels, lacrimal glands, fat, and muscles. Orbital space and content are not fully confined and follow the pressure-volume dynamics with a pathophysiology comparable to the other compartment syndromes of the body [51, 52]. Visual loss can occur after only 60–100 min of increased pressure within the orbit [53]. Clinical judgment is of foremost importance and it should lead to the decision to decompress ocular compartment by lateral canthotomy and inferior cantholysis as soon as suggestive clinical signs (proptosis, ocular pain, loss of sight, lateral gaze limitation, evident hematoma formation) appears in the setting of a suspect for OCS [3, 4, 30].

No dedicated laboratory exams are necessary in these patients. Imaging (i.e., CT-scan of magnetic resonance-RMN) may help in defining the cause of the OCS and in differential diagnosis but they are limited to the stable patients and in case of RMN it is usually not viable in emergency setting. It is to be pointed out that imaging is to be considered complimentary and not mandatory in case of patients not amenable to be transferred especially in those with high suspicion of OCS being treated for other severe and life-threatening lesions. However, it has been demonstrated the association between a posterior globe angle of fewer than 120° and acute proptosis on CT-scan with a poorer prognosis and a higher risk of permanent vision loss [54].

Whenever OCS is suspected and clinically highly probable, the specialist should be convoked, and immediate treatment should be provided by an experienced physician. Proptosis, intraocular pressure > 40 mmHg (> 5 kPa) (whenever measured), bradycardia, and patients with lowering of the level of consciousness are indications to proceed with orbital decompression. In literature, only case reports and few case series about OCS exist. However delayed surgical intervention appears to be the most important factor affecting the rate of visual loss due to OCS [52] with a high rate of fully recovered vision in patients who are early decompressed. In general, patients treated before the 2 h from the symptoms start achieve a final Snellen visual acuity of 6/12 or better, almost 15% reach a final outcome of less than 6/12 [2, 5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27]. Outcomes in patients treated after more than 2 h are worst and almost 25% of them reach final visual acuity of 6/12 or better [5, 15, 20, 23, 24, 28, 29, 31,32,33,34,35,36, 55]. In those cases, who reached a visual acuity of 6/12 or better even if treated after 2 h, it should be clarified that more than 50% of them presented a visual acuity of 6/12 or better at the admission. Lastly, recovery of vision may be not immediate and require up to 4 weeks to reach the best outcome possible.

Intracranial pressure and compartment syndrome of the brain

Within all compartments, the brain is reasonably the one that less tolerates a rise in pressure. Since the skull is non-expansible, a rise in brain tissue volume (e.g., edema) or blood content (e.g., hematoma) can rapidly increase the intracranial pressure (ICP) leading to a compartment syndrome that, if untreated, could bring to brain herniation and death [56, 57].

Generally, in traumatic brain injury (TBI) setting, a stepwise approach to intracranial hypertension is suggested [58]. This strategy consists of a step by step increase in the level of therapy in patients with elevated ICP reserving more aggressive interventions, generally associated with greater risks/adverse effects, when no response is observed [58]. Decompressive craniectomy (DC) is a neurosurgical procedure consisting in the removal of a part of the skull and opening the dura mater (generally by duraplasty) [59]. In this way, the increase in cranial volume allows to accommodate brain swelling because the skull is converted from a closed box (with finite volume) to an open box [59]. DC can be performed after evacuation of an intracranial lesion in the acute phase (primary, not ICP driven) or delayed (secondary) to control ICP that is refractory to maximal medical therapy [59]. DC is very effective in the ICP reduction but is considered and “extreme” therapy (being associated with several complications such as central nervous system and wound infections, cerebral hematomas, hydrocephalus) to be reserved for selected patients with refractory intracranial hypertension (IH) [58, 60]. Recent trials in TBI patients have shown differences in neurological outcome. In the DECRA trial [61], bifrontal secondary DC decreased ICP and ICU stay but was associated with more unfavorable outcomes in patients with diffuse brain injury. In the RESCUE-ICP trial [62], secondary DC (mainly unilateral) resulted in lower mortality but higher rates of vegetative state, lower severe disability, and upper severe disability. A better profile was observed in patients aged ≤ 40 years. Secondary DC was associated with a reduction in mortality in TBI but the effects on long-term neurological outcome remain controversial [63]. In this regard, future studies should focus in identifying the patients who can benefit most from this procedure considering also the most appropriate surgical techniques as well as the best timing [63]. In this regard, some studies (Table 2) suggest a benefit of early DC in terms of mortality and functional outcome [37, 38]. Literature focusing on timing of decompression however is scarce and of low quality. Even if early decompression seems to improve results, no definitive indication can be obtained from the existing trials.

DC seemed to be of benefit (decreased mortality and increased Glasgow Outcome Scale) when performed within 5 h after injury in younger patients (≤ 50 years) with a Glasgow coma scale score > 5 [38]. A retrospective analysis of 213 severe combat-related TBI undergoing DC showed a lower postoperative mortality when DC was initiated within 5.33 h from injury [37]. DC is also utilized in the management of patients with ischemic and hemorrhagic stroke [39, 46, 64]; even in this setting, the timing of DC is a matter of debate (Table 2).

The effects of DC on malignant middle cerebral artery (MCA) infarction in relation to the timing and the age of the patient has not been completely defined. Several studies and meta-analysis showed as DC undertaken within 48 h from stroke, reduced mortality, and increased the number of patients with a favorable functional outcome [39, 64]. Even analyzing narrower timeframes as before or after 6 h data confirmed the necessity to proceed with early DC before the neurological compromise arises [65]. A single-center retrospective study (66 patient) investigating the association between the timing of DC and the neurological outcome in patients with space-occupying MCA infarction showed as the 48 h cut-off in performing DC did not influence the outcome [46]. Regarding subarachnoid hemorrhage (SAH), as ingle retrospective analysis of 245 patients (171 primary DC and 74 secondary DC) focused on the value of DC timing [40]. It showed that early DC (within 24 h after ictus) significantly improves the functional outcome of SAH patients. In TBI and stroke patients, early decompression (respectively, within 6 and 24 h from injury or at least before herniation in stroke) seems to be associated with better neurological outcome. However, more data deriving from well powered clinical trial are necessary to define the appropriate timing of DC in these settings.

Thoracic and mediastinal compartment syndrome

Different compartmental syndromes can occur within the thorax and most of them are immediately life-threatening if left untreated. Most of them are related to elective cardiac surgery. The “tight mediastinum” was described for the first time in 1975 [42].

Thoracic and mediastinal compartment syndrome has been described and open chest management has been recognized as a viable option in unstable patients who may not tolerate the chest wall closure due to an increase of intra-thoracic pressure that precipitate hemodynamic collapse at the attempt [45, 66]. During thoracic wall closure, the rise in peak inspiratory pressure may be considered an early warning for thoracic compartment syndrome [67]. Thoracic decompression must be immediate followed by open chest management with delayed sternal closure. Sternum and subcutaneous layer should be left open after surgery and mediastinal cavity should be covered with protective devices interposed between the two skin edges or the skin may eventually be temporarily sutured [67, 68]. Open chest management should be protracted until the hemodynamic conditions require it. Generally, the reported average time ranges from 2 to 7 days [69]. Decision to close may follow increasing in cardiac output, decreasing in filling pressure and improving in lung function [45]. Forcing diuresis is generally suggested; however, it should be pointed out that it may generate difficult management in patients suffering from traumatic shock.

In trauma setting, although not being officially recognized as compartmental syndromes, tension pneumothorax and cardiac tamponade both share similar pathophysiology as other component syndromes such as abdominal, in term of the rise of pressure within a space that in normal situation bears different forces. Tension PNX and cardiac tamponade must be treated by immediate decompression. Generally, there is not enough time to obtain a radiological definitive diagnosis and operative decisions must be taken on clinical conditions and suspicion [70]. E-FAST (extended focus assessment with sonography for trauma) [71] eventually is generally fundamental in corroborating the clinical suspicion. Emergency treatments range from needle decompression, to intercostal drainage, to sub-xiphoidal window, to lateral thoracotomy up to clam-shell thoracotomy.

Abdominal compartment syndrome

Abdominal compartment syndrome (ACS) is defined as increased intra-abdominal pressure (IAP) > 20 mmHg in association with new onset organ failure; it may result in multiorgan dysfunction (i.e., cardiovascular, respiratory, renal, splanchnic, musculoskeletal, and central nervous systems) [72,73,74,75]. Due to ACS high morbidity and mortality rates, the identification of patients at risk, early recognition, appropriate staging, and timely intervention are fundamental [72].

Intra-abdominal hypertension (IAH) and ACS management must always be step-up. All medical intensive treatment must be posed into practice before proceeding to surgical decompression [76].

Clinical environment plays a pivotal role in early diagnosis and subsequent early treatment. In fact, surgical wards and surgical intensive care units (SICU) are more familiar and better trained in recognizing and timely treating IAH and ACS. Early ACS recognition and treatment increase survival rate up to 33.6% [77]. A recent study compared patients with traumatic ACS managed medical ICU (MICU) and in SICU. Median time from admission to suspicion of ACS was 60 h in the MICU vs. 13 h in SICU. After the diagnosis was done, mean time to surgery was similar in the two groups (60 vs. 53 min, respectively). Mortality was 83% in MICU and 12.5% in SICU [78]. Once diagnosed as ACS, if medical and eventual percutaneous treatments fail, it must be treated as soon as possible with decompressive laparotomy [9, 72].

De Waele et al. conducted a prospective study on 33 patients undergoing decompressive laparotomy for ACS [49, 79]. With an average time from diagnosis to decompressive laparotomy of 3 h, the overall observed 28-day mortality was of 36%, and 1-year mortality of 55%. Literature reported mortality in similar cohorts of patients was up to 50% in the first month [79]. The lowering in mortality observed in this cohort may be due to the earlier decision to proceed to decompressive laparotomy.

Specific consideration should be dedicated to IAH and ACS due to severe acute pancreatitis. In fact, indications to surgical decompression are still not clearly defined. Severe acute pancreatitis is a disease that should be treated as much as possible with intensive medical care. A step-up approach should always be adopted during the first hours from the diagnosis [80]. If no reversal was achieved with intensive medical treatment and minimally invasive attempts, proceeding to decompressive laparotomy without further waiting is mandatory [47, 75, 81]. Generally, in not improving patients with ACS, the cut-off time frame to proceed to early decompression with improved results is ≤ 6 h within the diagnosis [81]. Mentula et al. showed that early decompression (first 4 days) was associated with significantly less deaths, compared with late decompression (after 4 days) [47].

Decompressive laparotomy in severe acute pancreatitis, whenever indicated may be achieved with laparotomy (midline or transverse subcostal) or through a less invasive subcutaneous linea alba fasciotomy [82]. Some patients for sure may benefit from it (Table 3). However, despite its effectiveness in decreasing IAP and the improvement in physiological variables, no definitive data exist about the effects of surgical decompression on organ function and outcomes. Laparotomy and subsequent open abdomen management in fact are associated to significant morbidity. Davis et al. reported a comparable hospital mortality among patients with severe acute pancreatitis treated with and without decompressive laparotomy [48].

No definitive data exist on humans and some trials on animal may help in defining the effects of decompressive laparotomy (DL). Some animal models showed clearly the positive effect of early DL on metabolic derangements. A porcine model evaluating the timing of DL for ACS in severe acute pancreatitis compared four groups and found an increased survival rate in the 6 h group who underwent DL earlier (after 6 h). It was associated with a return of the normal value of urine output, blood oxygenation, and lactate clearance [83]. In another porcine model, early DL resulted in improved intestinal blood flow and could normalize the lactate/pyruvate ratio, a marker of intestinal hypoperfusion [84].

In secondary ACS, due to a reason which is not primarily abdomino-pelvic (i.e., over resuscitation), the timing of the decompressive laparotomy should be different since the pathophysiology is different as well. In patients suffering for severe burns, decompressive laparotomy may be beneficial in order to revert the effects of compartment syndrome [50, 85] (Table 3).

Ramirez et al. retrospectively analyzed a group of 46 patients with burn injury and ACS to evaluate survival comparing the timing of decompressive laparotomy [50]. Three groups were created dividing patients according to the cause of ACS development: (1) initial injury resuscitation, (2) perioperative resuscitation, and (3) sepsis. 45 patients over 46 underwent immediate laparotomy (within 1 h from ACS diagnosis) with overall survival of 56%; the age and total body surface area (TBSA) of the burn was similar in survivors and non-survivor groups. In patients with ACS associated to inhalation injury, higher mortality was observed (61% vs. 39%). The group with the highest survival rate (up to 80%) was the one of immediate DL after ACS due to initial injury resuscitation and the difference in survival was not explained by TBSA since the population with better outcome tended to have more frequently a bigger burn size and therefore more aggressively resuscitated. The authors noted increased survival rate in their population in respect of other series on ACS for a burn injury in which DL was used as the last resource, therefore concluded with the suggestion of immediate DL in ACS patients with burn injuries. It has to be stressed however that although after DL hemodynamic parameters rapidly improve, acute lung injury, and multiorgan dysfunction syndrome may be more severe after DL and more severe than in similar severely burned patients without IAH [86]. Moreover, DL is associated with higher mortality in patients aged 80 years or older. Whenever possible, DL should be avoided in frail patients [87].

Extremities compartment syndrome

Acute extremity compartment syndrome (ECS) is due to the raise of pressure within a closed fascial compartment, causing local tissue hypoxia, and at the last stage, ischemia. ECS most often develops in the context of severe trauma, especially—nearly 75% of all cases—in long bone fractures, such as tibial and forearm fractures and crush injuries. However, it may also develop from both minor traumas, when treated with tight bandage or constrictive cast, or in non-traumatic cases. Non-traumatic ECS can develop after prolonged immobilization in unconscious patients, because of positional imbalance of the limb due to incorrect patient positioning during anesthesia in postoperative sedation [88,89,90], after intramuscular drug abuse or as a consequence of thermal injuries. In particular full-thickness burns may trigger ECS, causing edema and large fluid shifts in extravascular space; furthermore, the eschar may enhance the constrictive effect. Even in open fractures and open injuries, such as extremities penetrating trauma, ECS should always be ruled out. Lastly, young and fit patients seem to be more prone to develop post-traumatic ECS [91]. The diagnosis is generally clinical, and no definitive sensible and specific tools exist to undoubtedly recognize or rule out ECS. Historically, the cornerstones of clinical diagnosis were the 6 p’s: pain, pallor, poikilothermia, paresthesia, paralysis, and pulselessness. But in ECS, generally, pulses are present; if absent, other causative events should be ruled out (i.e., systemic hypotension, arterial occlusion, or vascular injury). Furthermore, the other signs are typical of delayed, missed ECS; so, for an early diagnosis, particular attention has to be paid to the pain, that is generally out of proportion and exacerbated by passive stretching of the muscles involved.

ECS early diagnosis and treatment are fundamental to avoid subsequent severe disability.

In general, longer period of ECS-related ischemia correlates with worst outcomes. Data regarding the possibility of muscles to tolerate ischemia derive from tourniquet model. These showed as muscles can tolerate up to 6–8 h of ischemia before necrosis occurs. Compartment syndrome pathophysiology in crush injury or long bone fractures setting; however, may elicit different cellular response compared to tourniquet-induced ischemia. This may result in a shorter tolerance period of ischemia by muscle bellies [92]. In fact, it was noted that victims of trauma could develop ECS even more quickly and muscle necrosis may occur even faster than the theoretical limit of 6 h [93]. There is not an exactly defined time period after which irreversible muscle damage occurs [94]. A retrospective cohort analysis showed that 37 among 76 patients who timely underwent surgery for ECS had some degree of muscle necrosis; it was estimated that nearly 37% of patients may have muscle necrosis after 3 h from injury [95]. Current surgical recommendation is based on a disease model that probably underrates the real amount of muscle damage consequent to hypoxia and ischemia. Fasciotomies for compartment syndrome performed in trauma centers of the UK were reviewed and it was found an average time of 2 h from diagnosis to fasciotomy [93]. This demonstrated that very early decompression, even in a hospital dedicated to trauma care, is uneasy to obtain, generally due to logistical issues. Authors observed a major complication rate of 34%, including limb loss, but failed to demonstrate a time-effect relationship with treatment delay [93].

ECS represents a surgical emergency: time limit for fasciotomy is within 8 h from the diagnosis of acute ECS [82, 94, 96]. In presence of obvious clinical symptoms associated with a measurement of compartment pressure higher than 40 mmHg, surgical decompression should occur within an hour.

In case of late presentation or missed diagnosis of ECS, some authors suggest non-operative management, since surgical decompression can be harmful and non-counter-balanced by reasonable benefit. It has been demonstrated that fasciotomies performed later than 8 h after diagnosis of ECS were associated with a significantly higher risk of infection [97]. In these situations, case by case evaluation is mandatory.

Lower leg fasciotomies should be performed with two incisions to decompress all the four compartment of the leg. Debridement and dressing of the surgical incisions should be performed every 48 h or more frequently if indicated [98].

Revascularization after limb vascular trauma or limb acute ischemia is the two most common causes of delayed ECS. In fact, in such cases, ECS may develop up to several hours after the end of the operation. That is why, after vascular repair procedures, it is debated if ECS should be prevented (prophylactic decompression fasciotomies) or treated once it appears.

A retrospective analysis of 612 patients who faced early or delayed (< 8 h or > 8 h) prophylactic fasciotomy (after vascular repair for lower extremity arterial injury) showed as patients with early fasciotomy had a lower rate of limb amputation (8.5 vs. 24.6% p > 0.001). The authors concluded that there is high suggestion to perform fasciotomy at the time of vascular repair.

Kara at al. investigated the relationship between the timing of fasciotomy and outcomes after revascularization procedures for acute limb ischemia [99]. Fasciotomies were classified as prophylactic (at the time of operation of revascularization) or delayed. One hundred and thirty-eight patients with acute limb ischemia where analyzed; 42 underwent 4-compartment fasciotomy; those who underwent delayed fasciotomy resulted in higher amputations rate within 30 days (50% vs. 5.9%, p = 0.002). Patients who underwent prophylactic fasciotomy had a higher Rutherford classification score.

No definitive indication can be given in regard to the prophylactic fasciotomy in acute limb ischemia. It may be performed at the time of revascularization if there is suspect of ischemia lasting for more than 6 h or of inadequate collateral flow or in the setting of trauma with a combined arterial and venous injury [100,101,102,103]. However, fasciotomy is not a riskless procedure so, in a well pondered risk-benefit balance, it may be possible to perform it only whenever ECS arises. However, it should be taken into consideration that the amputation rate with the latter approach may be higher.

Timing of intervention

With the currently available evidence, a stratification of timing for surgical decompression has been proposed for the different body areas (Table 4). Four timing categories have been defined:

  1. 1.

    Immediate decompression for those compartmental syndromes whose missed therapy would rapidly lead to patient death or extreme disability

  2. 2.

    Early decompression with the time burden of 3–12 h and in any case before clinical signs of irreversible deterioration

  3. 3.

    Delayed decompression identified with decompression performed after 12 h or after signs of clinical deterioration has occurred

  4. 4.

    Prophylactic decompression in those situations where high incidence of compartment syndrome is expected after a specific causative event


Different compartments respond with a variable degree of cellular damage and physiological decline to increased pressure; consequently, not all compartment syndromes would find benefit in timely treatment at the same extent. Although early decompression could be beneficial in some conditions, physicians must be aware of the potential harm of decompression and relative procedural hazards, thus aiming to maximize the medical effort to reduce the rate of intervention when feasible, without hesitating surgical intervention lengthy till there is no longer room for bettering outcomes. Better evidence is needed to further assess the impact of timely surgical intervention in ameliorating outcomes of patients suffering from compartmental syndromes; RTCs tailored on different body regions and timing of intervention are lacking. Given the impact of the compartment syndrome on morbi-mortality, more studies are necessary.

Availability of data and materials

Not applicable

Change history

  • 18 November 2020

    The original article has been updated to present author, Luigi Branca Vergano's name correctly.



Abdominal compartment syndrome


Orbital compartment syndrome


Extremities compartmental syndrome


Decompressive laparotomy


Total body surface area


Modified Rankin Score


Intracranial pressure


Decompressive craniectomy


Traumatic brain injury


Compartment syndrome


Extended focus assessment with sonography for trauma


  1. 1.

    Schwab S, Steiner T, Aschoff A, Schwarz S, Steiner HH, Jansen O, et al. Early hemicraniectomy in patients with complete middle cerebral artery infarction. Stroke. 1998;29:1888–93.

    CAS  PubMed  Google Scholar 

  2. 2.

    Goodall KL, Brahma A, Bates A, Leatherbarrow B. Lateral canthotomy and inferior cantholysis: an effective method of urgent orbital decompression for sight threatening acute retrobulbar haemorrhage. Injury. 1999;30(7):485–90.

    CAS  PubMed  Google Scholar 

  3. 3.

    Vassallo S, Hartstein M, Howard D, Stetz J. Traumatic retrobulbar hemorrhage: emergent decompression by lateral canthotomy and cantholysis. J Emerg Med. 2002;22(3):251–6.

    PubMed  Google Scholar 

  4. 4.

    Katz B, Herschler J, Brick DC. Orbital hemorrhage and prolonged blindness: a treatable posterior optic neuropathy. Br J Ophthalmol. 1983;67:549–53.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Sun MT, Chan WO, Selva D. Traumatic orbital compartment syndrome: importance of the lateral canthomy and cantholysis. Emerg Med Australas. 2014;26(3):274–8.

    PubMed  Google Scholar 

  6. 6.

    Castro E, Seeley M, Kosmorsky G, Foster JA. Orbital compartment syndrome caused by intraorbital bacitracin ointment after endoscopic sinus surgery. Am J Ophthalmol. 2000;130(3):376–8.

    CAS  PubMed  Google Scholar 

  7. 7.

    Wladis EJ, Peebles TR, Weinberg DA. Management of acute orbital hemorrhage with obstruction of the ophthalmic artery during attempted coil embolization of a dural arteriovenous fistula of the cavernous sinus. Ophthal Plast Reconstr Surg. 2007;23(1):57–9.

    PubMed  Google Scholar 

  8. 8.

    Jenkins TL, Zheng CX, Murchison AP, Bilyk JR. Orbital compartment syndrome following post-traumatic subgaleal hematoma. Ophthal Plast Reconstr Surg. 2017;33(2):e33–6.

    PubMed  Google Scholar 

  9. 9.

    Key SJ, Ryba F, Holmes S, Manisali M. Orbital emphysema – the need for surgical intervention. J Cranio Maxillofacial Surg. 2008;36(8):473–6.

    Google Scholar 

  10. 10.

    See A, Gan EC. Orbital compartment syndrome during endoscopic drainage of subperiosteal orbital abscess. Am J Otolaryngol. 2015;36(6):828–31.

    PubMed  Google Scholar 

  11. 11.

    Colletti G, Deganello A, Bardazzi A, et al. Complications after treatment of head and neck venous malformations with sodium tetradecyl sulfate foam. J Craniofac Surg. 2017;28(4):e388–92.

    PubMed  Google Scholar 

  12. 12.

    Huang S, Sun MT, Davis G, Fitzgerald J, Selva D, Henderson T. Bilateral orbital compartment syndrome in a patient with disseminated intravascular coagulation. Orbit. 2018;37(5):361–3.

    PubMed  Google Scholar 

  13. 13.

    Saussez S, Choufani G, Brutus JP, Cordonnier M, Hassid S. Lateral canthotomy: a simple and safe procedure for orbital haemorrhage secondary to endoscopic sinus surgery. Rhinology. 1998;36(1):37–9.

    CAS  PubMed  Google Scholar 

  14. 14.

    Gillum WN, Anderson RL. Reversible visual loss in subperiostealhematoma of the orbit. Ophthalmic Surg. 1981;12(3):203–9.

    CAS  PubMed  Google Scholar 

  15. 15.

    Korinth MC, Ince A. BanghardW, Huffmann BC, Gilsbach JM. Pterional orbital decompression in orbital hemorrhage and trauma. J Trauma. 2002;53(1):73–8.

    PubMed  Google Scholar 

  16. 16.

    Larsen M, Wieslander S. Acute orbital compartment syndrome after lateral blow-out fracture effectively relieved by lateral cantholysis. Acta Ophthalmol Scand. 1999;77(2):232–3.

    CAS  PubMed  Google Scholar 

  17. 17.

    Susarla SM, Nam AJ, Dorafshar AH. Orbital compartment syndrome leading to visual loss following orbital floor reconstruction. Craniomaxillofac Trauma Reconstr. 2016;9(2):152–7.

    PubMed  Google Scholar 

  18. 18.

    Schwitkis AE, Pollack TL, Torbati SS. Orbital compartment syndrome following mechanical fall. Clin Pract Cases Emerg Med. 2018;2(3):268–9.

    PubMed  PubMed Central  Google Scholar 

  19. 19.

    Tran KD, Scawn RL, Whipple KM, Korn BS, Kikkawa DO. Mastication induced retrobulbar hemorrhage. Orbit. 2013;32(6):387–8.

    PubMed  Google Scholar 

  20. 20.

    Sampath R, Shah S, Leatherbarrow B. The management of an optic nerve compromising acute retrobulbar haemorrhage: report of a case. Eye (Lond). 1995;9(Pt 4):533–5.

    Google Scholar 

  21. 21.

    McInnes G, Howes DW. Lateral canthotomy and cantholysis: a simple, vision-saving procedure. CJEM. 2002;4(1):49–52.

    PubMed  Google Scholar 

  22. 22.

    Carrim ZI, Anderson IWR, Kyle PM. Traumatic orbital compartment syndrome: importance of prompt recognition and management. Eur J Emerg Med. 2007;14(3):174–6.

    PubMed  Google Scholar 

  23. 23.

    Jamal BT, Diecidue RJ, Taub D, Champion A, Bilyk JR. Orbital hemorrhage and compressive optic neuropathy in patients with midfacial fractures receiving low-molecular weight heparin therapy. J Oral Maxillofac Surg. 2009;67(7):1416–9.

    PubMed  Google Scholar 

  24. 24.

    Maurer P, Conrad-Hengerer I, Hollstein S, Mizziani T, Hoffmann E, Hengerer F. Orbital haemorrhage associated with orbital fractures in geriatric patients on antiplatelet or anticoagulant therapy. Int J Oral Maxillofac Surg. 2013;42(12):1510–4.

    CAS  PubMed  Google Scholar 

  25. 25.

    Pamukcu C, Odabaşı M. Acute retrobulbar haemorrhage: an ophthalmologic emergency for the emergency physician. Ulus Travma Acil Cerrahi Derg. 2015;21(4):309–14.

    PubMed  Google Scholar 

  26. 26.

    Li KK, Meara JG, Rubin PA. Orbital compartment syndrome following orthognathic surgery. J Oral Maxillofac Surg. 1995;53(8):964–8.

    CAS  PubMed  Google Scholar 

  27. 27.

    Yang P, Toomey C, Lin J, Kikkawa DO, Korn BS, Harrison A. Beware of the sneeze. Surv Ophthalmol. 2020;65(5):592–6.

  28. 28.

    Amorim Correa JL, Acioly MA. The enigma of orbital compartment syndrome after lumbar spine surgery in the prone position: case report and literature review. World Neurosurg. 2018;110:309–14.

    PubMed  Google Scholar 

  29. 29.

    Voss JO, Hartwig S, Doll C, Hoffmeister B, Raguse J-D, Adolphs N. The “tight orbit”: incidence and management of the orbital compartment syndrome. J Craniomaxillofac Surg. 2016;44(8):1008–14.

    PubMed  Google Scholar 

  30. 30.

    Lee KYC, Tow S, Fong KS. Visual recovery following emergent orbital decompression in traumatic hemorrhage. Ann Acad Med Singapore. 2006;35:831–2.

    PubMed  Google Scholar 

  31. 31.

    Popat H, Doyle PT, Davies SJ. Blindness following retrobulbar haemorrhage—it can be prevented. Br J Oral Maxillofac Surg. 2007;45(2):163–4.

    CAS  PubMed  Google Scholar 

  32. 32.

    Amagasaki K, Tsuji R, Nagaseki Y. Visual recovery following immediate decompression of traumatic retrobulbar hemorrhage via transcranial approach. Neurol Med Chir (Tokyo). 1998;38(4):221–4.

    CAS  Google Scholar 

  33. 33.

    Gauden AJ, Hardy T, Mack HG, Danesh-Meyer HV, Kaye AH. Orbital compartment syndrome following aneurysm surgery. J Clin Neurosci. 2012;19(7):1032–6.

    PubMed  Google Scholar 

  34. 34.

    Pahl FH, de Oliveira MF, Dal Col Lúcio JE, Souza E, Castro EF. Orbital compartment syndrome after frontotemporal craniotomy: case report and review of literature. World Neurosurg. 2018;109:218–21.

    PubMed  Google Scholar 

  35. 35.

    Yu Y-H, Chen W-J, Chen L-H, Chen W-C. Ischemic orbital compartment syndrome after posterior spinal surgery. Spine (Phila Pa 1976). 2008;33(16):E569–72.

    Google Scholar 

  36. 36.

    Colletti G, Valassina D, Rabbiosi D, et al. Traumatic and iatrogenic retrobulbar hemorrhage: an 8-patient series. J Oral Maxillofac Surg. 2012;70(8):e464–8.

    PubMed  Google Scholar 

  37. 37.

    Shackelford SA, Del Junco DJ, Reade MC, et al. Association of time to craniectomy with survival in patients with severe combat-related brain injury. Neurosurg Focus. 2018;45(6):E2.

    PubMed  Google Scholar 

  38. 38.

    Barthélemy EJ, Melis M, Gordon E, Ullman JS, Germano IM. Decompressive craniectomy for severe traumatic brain injury: a systematic review. World Neurosurg. 2016;88:411–20.

    PubMed  Google Scholar 

  39. 39.

    Dasenbrock HH, Robertson FC, Vaitkevicius H, et al. Timing of decompressive hemicraniectomy for stroke: a nationwide inpatient sample analysis. Stroke. 2017;48(3):704–11.

    PubMed  Google Scholar 

  40. 40.

    Jabbarli R, Oppong MD, Dammann P, et al. Time is brain! Analysis of 245 cases with decompressive craniectomy due to subarachnoid hemorrhage. World Neurosurg. 2017;98:689–94.

    PubMed  Google Scholar 

  41. 41.

    Elsawaf A, Galhom A. Decompressive craniotomy for malignant middle cerebral artery infarction: optimal timing and literature review. World Neurosurg. 2018;116:e71–8.

    PubMed  Google Scholar 

  42. 42.

    Riahi M, Tomatis LA, Schlosser RJ, et al. Cardiac compression due to closure of the median sternotomy in open heart surgery. Chest. 1975;67:113–4.

    CAS  PubMed  Google Scholar 

  43. 43.

    Mori K, Nakao Y, Yamamoto T, Maeda M. Early external decompressive craniectomy with duroplasty improves functional recovery in patients with massive hemispheric embolic infarction: timing and indication of decompressive surgery for malignant cerebral infarction. Surg Neurol. 2004;62:420–9 discussion 429–30.

    PubMed  Google Scholar 

  44. 44.

    Wang KW, Chang WN, Ho JT, Chang HW, Lui CC, Cheng MH, et al. Factors predictive of fatality in massive middle cerebral artery territory infarction and clinical experience of decompressive hemicraniectomy. Eur J Neurol. 2006;13:765–71.

    PubMed  Google Scholar 

  45. 45.

    Balogh ZJ, Butcher NE. Compartment syndromes from head to toe. Crit Care Med. 2010;38(9 Suppl):S445–51.

    PubMed  Google Scholar 

  46. 46.

    Goedemans T, Verbaan D, Coert BA, et al. Outcome after decompressive craniectomy for middle cerebral artery infarction: timing of the intervention. Neurosurgery. 2020;86(3):E318–25.

    PubMed  PubMed Central  Google Scholar 

  47. 47.

    Mentula P, Hienonen P, Kemppainen E, Puolakkainen P, Leppäniemi A. Surgical decompression for abdominal compartment syndrome in severe acute pancreatitis. Arch Surg. 2010;145(8):764–9.

    PubMed  Google Scholar 

  48. 48.

    Davis PJ, Eltawil KM, Abu-Wasel B, Walsh MJ, Topp T, Molinari M. Effect of obesity and decompressive laparotomy on mortality in acute pancreatitis requiring intensive care unit admission. World J Surg. 2013;37:318–32.

    PubMed  Google Scholar 

  49. 49.

    De Waele JJ, Kimball E, Malbrain M, Nesbitt I, Cohen J, Kaloiani V. Decompressive laparotomy for abdominal compartment syndrome. British J Surg. 2016;103:709–15.

    Google Scholar 

  50. 50.

    Ramirez JI, Sen S, Palmieri TL, Greenhalgh DG. Timing of laparotomy and closure in burn patients with abdominal compartment syndrome: effects on survival. J Am Coll Surg. 2018;226(6):1175–80.

    PubMed  Google Scholar 

  51. 51.

    Lima MD. Orbital compartment syndrome: the ophthalmic surgical emergency. Surv Ophthalmol. 2009;54:441–9.

    PubMed  Google Scholar 

  52. 52.

    Hislop WS, Dutton GN. Retrobulbar hemorrhage: can blindness be prevented? Injury. 1994;25:663.

    CAS  PubMed  Google Scholar 

  53. 53.

    Hayreh SS, Kolder WE, Weingeist TA. Central retinal artery occlusion and retinal tolerance time. Ophthalmology. 1980;87:75–8.

    CAS  PubMed  Google Scholar 

  54. 54.

    Cheung CA, Rogers-Martel M, Golas L, Chepurny A, Martel JB, Martel JR. Hospital-based ocular emergencies: epidemiology, treatment, and visual outcomes. Am J Emerg Med. 2014;32:221–4.

    PubMed  Google Scholar 

  55. 55.

    Mootha VV, Cowden TP, Sires BS, Dortzbach RK. Subperiosteal orbital hemorrhage from retrobulbar injection resulting in blindness. Arch Ophthalmol. 1997;115(1):123–4.

    CAS  PubMed  Google Scholar 

  56. 56.

    Czosnyka M, Pickard JD, Steiner LA. Principles of intracranial pressure monitoring and treatment. Handb Clin Neurol. 2017;140:67–89.

    CAS  PubMed  Google Scholar 

  57. 57.

    Carney N, Totten AM, O’Reilly C, Ullman JS, Hawryluk GWJ, Bell MJ, et al. Guidelines for the management of severe traumatic brain injury, fourth edition. Neurosurgery. 2016;0:1–10.

    Google Scholar 

  58. 58.

    Stocchetti N, Maas AI. Traumatic intracranial hypertension. N Engl J Med. 2014;370(22):2121–30.

    PubMed  PubMed Central  Google Scholar 

  59. 59.

    Kolias AG, Kirkpatrick PJ, Hutchinson PJ. Decompressive craniectomy: past, present and future. Nat Rev Neurol. 2013;9(7):405–15.

    CAS  PubMed  Google Scholar 

  60. 60.

    Stiver SI. Complications of decompressive craniectomy for traumatic brain injury. Neurosurg Focus. 2009;26(6):E7.

    PubMed  Google Scholar 

  61. 61.

    Cooper DJ, Rosenfeld JV, Murray L, et al. Decompressive craniectomy in diffuse traumatic brain injury. N Engl J Med. 2011;364(16):1493–502.

    CAS  PubMed  Google Scholar 

  62. 62.

    Hutchinson PJ, Kolias AG, Timofeev IS, et al. Trial of decompressive craniectomy for traumatic intracranial hypertension. N Engl J Med. 2016;375(12):1119–30.

    PubMed  Google Scholar 

  63. 63.

    Sahuquillo J, Dennis JA. Decompressive craniectomy for the treatment of high intracranial pressure in closed traumatic brain injury. Cochrane Database Syst Rev. 2019;12(12):CD003983.

    PubMed  PubMed Central  Google Scholar 

  64. 64.

    Lu X, Huang B, Zheng J, et al. Decompressive craniectomy for the treatment of malignant infarction of the middle cerebral artery. Sci Rep. 2014;4:7070.

    PubMed  PubMed Central  Google Scholar 

  65. 65.

    Cho DY, Chen TC, Lee HC. Ultra-early decompressive craniectomy for malignant middle cerebral artery infarction. Surg Neurol. 2003;60:227–32 discussion 232–223.

    PubMed  Google Scholar 

  66. 66.

    Christenson JT, Maurice J, Simonet F, et al. Open chest and delayed sternal closure after cardiac surgery. Eur J Cardiothorac Surg. 1996;10:305–11.

    CAS  PubMed  Google Scholar 

  67. 67.

    Kaplan LJ, Trooskin SZ, Santora TA. Thoracic compartment syndrome. J Trauma. 1996;40:291–3.

    CAS  PubMed  Google Scholar 

  68. 68.

    Rizzo AG, Sample GA. Thoracic compartment syndrome secondary to a thoracic procedure. Chest. 2003;124:1161–8.

    Google Scholar 

  69. 69.

    Kouchoukos NT, Blackstone EH, Doty DB, et al. Kirklin/Barratt-Boyes cardiac surgery, vol. 1. 3rd ed. New York: Churchill Livingstone; 2003. p. 112.

    Google Scholar 

  70. 70.

    ATLS 10th edition ISBN 78-0-9968262-3-5. Accessed 20 Sep 2020.

  71. 71.

    Kirkpatrick AW, Sirois M, Laupland KB, Liu D, Rowan K, Ball CG, et al. Hand-held thoracic sonography for detecting post-traumatic pneumothoraces: the extended focused assessment with Sonography for trauma (EFAST). J Trauma. 2004;57(2):288–95.

    CAS  PubMed  Google Scholar 

  72. 72.

    Kirkpatric, et al. WSACS guidance intensive. Care Med. 2013;39:1190–206.

    Article  Google Scholar 

  73. 73.

    Walker J, Criddle LM. Pathophysiology and management of abdominal compartment syndrome. Am J Crit Care. 2003;12:367–71.

    PubMed  Google Scholar 

  74. 74.

    Bailey J, Shapiro MJ. Abdominal compartment syndrome. Crit Care. 2000;4:23–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  75. 75.

    Hunter JD, Damani Z. Intra-abdominal hypertension and the abdominal compartment syndrome. Anaesthesia. 2004;59:899–907.

    CAS  PubMed  Google Scholar 

  76. 76.

    Coccolini F, Roberts D, Ansaloni L, Ivatury R, Gamberini E, Kluger Y, et al. The open abdomen in trauma and non-trauma patients: WSES guidelines. World J Emerg Surg. 2018;13:7.

    PubMed  PubMed Central  Google Scholar 

  77. 77.

    Parsak CK, Seydaoglu G, Sakman G, et al. Abdominal compartment syndrome: current problems and new strategies. World J Surg. 2008;32:13–9.

    PubMed  Google Scholar 

  78. 78.

    Nguyen J, Noory M, Capano-Wehrle L, Gaughan J, Hazelton JP. Expeditious diagnosis and laparotomy for patients with acute abdominal compartment syndrome may improve survival. Am Surg. 2018;84(11):1836–40.

    PubMed  Google Scholar 

  79. 79.

    De Waele JJ, Kimball E, Malbrain M, Nesbitt I, Cohen J, Kaloiani V, et al. Decompressive laparotomy for abdominal compartment syndrome – a critical analysis. Crit Care. 2006;10:R51.

    PubMed  PubMed Central  Google Scholar 

  80. 80.

    Leppäniemi A, Tolonen M, Tarasconi A, Segovia-Lohse H, Gamberini E, Kirkpatrick AW, et al. 2019 WSES guidelines for the management of severe acute pancreatitis. World J Emerg Surg. 2019;14:27.

    PubMed  PubMed Central  Google Scholar 

  81. 81.

    De Waele JJ. Abdominal compartment syndrome in severe acute pancreatitis - when to decompress? Eur J Trauma Emerg Surg. 2008;34(1):11–6.

    PubMed  Google Scholar 

  82. 82.

    Leppäniemi AK, Hienonen PA, Siren JE, Kuitunen AH, Lindström OK, Kemppainen EA. Treatment of abdominal compartment syndrome with subcutaneous anterior abdominal fasciotomy in severe acute pancreatitis. World J Surg. 2006;30(10):1922–4.

    PubMed  Google Scholar 

  83. 83.

    Ni HB, Tong ZH, Li WQ, Li N, Li JS. The importance of timing of decompression in severe acute pancreatitis combined with abdominal compartment syndrome. J Trauma Acute Care Surg. 2013;74:1060–6.

    PubMed  Google Scholar 

  84. 84.

    Skoog P, Hörer TM, Nilsson KF, Norgren L, Larzon T, Jansson K. Abdominal hypertension and decompression: the effect on peritoneal metabolism in an experimental porcine study. Eur J Vasc Endovasc Surg. 2014;47:402–10.

    CAS  PubMed  Google Scholar 

  85. 85.

    Struck MF, Reske AW, Schmidt T, Hilbert P, Steen M, Wrigge H. Respiratory functions of burn patients undergoing decompressive laparotomy due to secondary abdominal compartment syndrome. Burns. 2014;40:120–6.

    PubMed  Google Scholar 

  86. 86.

    Strang SG, Van Lieshout EMM, Breederveld RS, Van Waes OJF. A systematic review on intra-abdominal pressure in severely burned patients. Burns. 2014;40:9–16.

    PubMed  Google Scholar 

  87. 87.

    Oda J, Yamashita K, Inoue T, Hosotsubo H, Aoki Y, Ode Y, et al. Acute lung injury and multiple organ dysfunction syndrome secondary to intra-abdominal hypertension and abdominal decompression in extensively burned patients. J Trauma. 2007;62:1365–9.

    PubMed  Google Scholar 

  88. 88.

    McLaren AC, Ferguson JH, Miniaci A. Crush syndrome associated with the use of the fracture- table: a case report. J Bone Joint Surg Am. 1987;69:1447–9.

    CAS  PubMed  Google Scholar 

  89. 89.

    Morin RJ, Swan KG, Tan V. Acute forearm compartment syndrome secondary to local arterial injury after penetrating trauma. J Trauma. 2009;66:989–93.

    PubMed  Google Scholar 

  90. 90.

    Newton EJ, Love J. Acute complications of extremity trauma. Emerg Med Clin North Am. 2007;25:751–61.

    PubMed  Google Scholar 

  91. 91.

    Badhe S, Baiju D, Elliot R, Rowles J, Calthorpe D. The ‘silent’ compartment syndrome. Injury. Int J Care Injured. 2009;40:220–2.

    CAS  Google Scholar 

  92. 92.

    Heppenstall RB, Scott R, Sapega A, Park YS, Chance BA. Comparative study of the tolerance of skeletal muscle to ischemia. Tourniquet application compared with acute compartment syndrome. J Bone Joint Surg Am. 1986;68(6):820–8.

    CAS  PubMed  Google Scholar 

  93. 93.

    Bodansky D, Doorgakant A, Alsousou J, Iqbal HJ, Fischer B, Scicluna G. At al. Acute compartment syndrome: do guidelines for diagnosis and management make a difference? Injury. 2018;49(9):1699–702.

    CAS  PubMed  Google Scholar 

  94. 94.

    McQueen MM, Duckworth AD. The diagnosis of acute compartment syndrome: a review. Eur J Trauma Emerg Surg. 2014;40(5):521–8.

    CAS  PubMed  Google Scholar 

  95. 95.

    Vaillancourt C, Shrier I, Falk M, Rossignol M, Vernec A, Somo- gyi D. Quantifying delays in the recognition and management of acute compartment syndrome. Can J Emerg Med. 2001;3(1):26–30.

    CAS  Google Scholar 

  96. 96.

    McQueen MM, Christie J, Court-Brown CM. Acute compartment syndrome in tibial diaphyseal fractures. J Bone Joint Surg Br. 1996;78(1):95–8.

    CAS  PubMed  Google Scholar 

  97. 97.

    Velmahos GC, Theodorou D, Demetriades D, Chan L, Berne TV, Asensio J, et al. Complications and non closure rates of fasciotomy for trauma and related risk factors. World J Surg. 1997;21:247–53.

    CAS  PubMed  Google Scholar 

  98. 98.

    British Orthopaedic Association and British Association of Plastic, Reconstructive and Aesthetic Surgeons. The standard for trauma – 2014 Boast 10: diagnosis and management of compartment syndrome of the limbs. Accessed 20 Sep 2020.

  99. 99.

    Rothenberg KA, et al. Delayed fasciotomy is associated with higher risk of major amputation in patients with acute limb ischemia. Ann Vasc Surg. 2019;59:195–201.

    PubMed  Google Scholar 

  100. 100.

    Modrall CJ. Compartment syndrome. In: Rutherford’s vascular surgery. 8th ed. Amsterdam: Elsevier; 2014. p. 2544–54.

  101. 101.

    Haljamae H, Enger E. Human skeletal muscle energy metabolism during and after complete tourniquet ischemia. Ann Surg. 1975;182(1):9–14.

    CAS  PubMed  PubMed Central  Google Scholar 

  102. 102.

    Cone J, Inaba K. Trauma Surg Acute Care Open. 2017;2:1–6.

    Google Scholar 

  103. 103. Last access May 2020.

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FCo and MI: manuscript conception, literature revision, and analysis. AB, DT, MC, NDA, LBV, EP, FCa, PF, and MS: helped with the analysis. FCo and MI: drafted the paper that was critically reviewed by FCo, MI, EP, NDA, LBV, FCa, MC, PF, MS, and AWK. The authors read and approved the final version of the manuscript.

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Coccolini, F., Improta, M., Picetti, E. et al. Timing of surgical intervention for compartment syndrome in different body region: systematic review of the literature. World J Emerg Surg 15, 60 (2020).

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  • Hypertension
  • Decompressive craniectomy
  • Compartment syndrome
  • Extremities
  • Ocular
  • Plycompartment