Much of our initial knowledge about IAH and ACS originates from patients with specific conditions such as ruptured aortic aneurysms, abdominal trauma, severe burns and severe acute pancreatitis [8
]. These diagnostic groups, however, account for a minority of admissions in most ICUs. Although we have learned much about the pathophysiology and treatment of IAH from these studies, the true prevalence, impact on outcome, and risk factors of IAH remain to be clarified. To avoid bias from the preselection of patients, one should seek studies where all consecutive ICU admissions, independent of diagnosis, length of stay, mode of ventilation, etc. were included and the epidemiology of IAH addressed. We are not aware of any study meeting these criteria. The data on epidemiology presented below are, therefore, based on extrapolations from those studies that most resembled these ideal criteria and measured IAP in the general ICU populations.
The results of relevant studies are summarised in Table [6
]. The studies on IAH are directly comparable only since 2006, when consensus definitions were published [7
]. Two papers from 2004 and 2005, however, are so far the only multicentre studies; they used almost the same definitions as later in WSACS consensus statement and are, therefore, included in the analysis. The original definition of IAH, sustained or repeated IAP ≥ 12 mmHg, is not always easy to apply because intermittent measurements without fixed intervals are mostly used in practice. Therefore, a definition of IAH of the mean IAP ≥ 12 mmHg on one day was used in parallel.
Prevalence, incidence and risk factors of IAH in mixed ICU populations
In 2004, the first study of IAH epidemiology in a mixed ICU population was performed. In it, 97 patients treated in 13 ICUs in six countries for at least 24 h were enrolled for 1-day point-prevalence assessments. IAH, defined as a maximum IAP ≥ 12 mmHg, was observed in 58.8% of cases [3
], whereas defining IAH according to the mean IAP resulted in a prevalence of 23.7%. A second multicentre study included 265 consecutive patients (mean Acute Physiology and Chronic Health Evaluation II score (APACHE) II score 17.4; 46.8% of the medical profile) who stayed in the ICU for at least 24 h [4
]. IAH, defined as the mean IAP > 12 mmHg, was observed in 32.1% and ACS in 4.2% of these patients on admission, whereas the development of IAH during the ICU stay was an independent predictor of mortality. Independent predictors of IAH were liver dysfunction (defined as decompensated or compensated cirrhosis or other liver failure with ascites), abdominal surgery (with or without laparoscopy, reduction of a hernia, tight closure, or abdominal banding with a postoperative Velcro belt to prevent incisional hernia), massive fluid resuscitation (defined as 3.5 L of colloids or crystalloids in the 24 h before the study) and ileus. At the same time, there was no difference in the prevalence of IAH between medical and surgical patients.
Vidal et al. collected prospective data on 83 critically ill patients staying in an ICU for at least 24 h (mean APACHE II 19; 47% of the medical profile) [12
]. Considering mean IAP, 23% of patients had IAH on admission, but another 31% developed it afterwards. Twelve per cent of patients suffered from ACS. Patients with IAH were sicker and had a higher mortality rate, whereas the maximum IAP was identified as an independent predictor of mortality.
Dalfino et al. followed 123 consecutive patients staying in an ICU for at least 24 h, and they observed a 30.1% incidence of IAH [13
]. The raw hospital mortality rate was significantly higher in patients with IAH; however, risk-adjusted rates were not different. IAH was significantly associated with age, cumulative fluid balance, shock, sepsis and abdominal surgery, whereas only the first three were independent risk factors.
In a study of 264 mechanically ventilated patients who presented at least one additional predisposing factor associated with IAH (admission due to severe trauma, abdominal surgery, pancreatitis or post-cardiopulmonary resuscitation status; fluid resuscitation above 5 L/24 h; vasoactive or inotropic support; or renal replacement therapy), the development of IAH was identified as an independent risk factor of death [14
]. The incidence of IAH was 37.0%. The patients with IAH had higher age, BMI, fluid gain and disease severity scores during the admission day in the univariate analysis, whereas independent risk factors for IAH were not defined.
In the largest study so far, Reintam Blaser et al. investigated 563 out of 635 consecutive patients who were mechanically ventilated and stayed over 24 h in the ICU. During the entire ICU period, IAH occurred in 32.3% of patients [15
]. ACS developed in six patients (1.1%). A checklist was developed to facilitate the decisions for IAP monitoring at bedside. However, the single-centre design of the study and the fact that not all consecutive patients were studied limit its practical value.
The preliminary results of a multicentre study analysing 358 patients from 39 ICUs, which included consecutive patients requiring mechanical ventilation for at least 6 h [16
], assessed the validity of predisposing conditions of IAH proposed by the consensus statement [7
]. This study found that considerable proportion of patients (22.0%) without any aetiological factor other than mechanical ventilation still developed IAH. Furthermore, among the patients presenting five or more predisposing factors, more than one-third did not develop IAH.
In summary, IAH, depending on the sample population, may occur in 20% to 40% of intensive care patients. The incidence of ACS in general cohorts is 5% to 10% in earlier reports but considerably less in recent studies. This fact leads us to speculate that awareness of IAH, and its proper medical treatment may have reduced the incidence of progression from IAH to ACS. Importantly, no study has assessed the incidence of IAH in all consecutive admissions to the ICU. The studies that included patients who were expected to stay for at least 24 h in the ICU must certainly have missed some patients who actually stayed for more than 24 h. Therefore, the exact incidence of IAH/ACS in mixed ICU patient populations remains unclear.
IAH/ACS in specific patient groups
IAH/ACS has frequently been described in severe trauma patients
. The incidence of ACS in trauma patients undergoing emergency laparotomy/damage-control surgery ranges from 5% to 14% depending on the severity of the insult and the extent of abdominal packing applied [9
]. The liberal use of open-abdomen techniques has decreased the incidence of ACS in these patients [18
]; however, monitoring IAP is still mandatory, as ACS can develop in cases of open abdomen [19
]. IAH/ACS may also be observed in patients without abdominal injuries and is then associated with severe shock that requires aggressive fluid resuscitation; the incidence of IAH/ACS is 0.07% of all trauma admissions and 9% of shock trauma patients [21
]. Among all trauma victims admitted to ICUs, IAP above 20 mmHg can be observed in 2% of cases [22
]. Thus, severe trauma, especially when abdominal injuries are involved, carries a considerable risk of IAH and ACS.
IAH/ACS is also reported in a number of small series of severely burned patients
] and is currently considered a life-threatening complication of thermal injury [25
]. Extensive swelling and ascites due to profound systemic inflammation combined with massive volume resuscitation cause increased IAP in these patients. IAP above 20 mmHg is common in patients with burns > 40% of their total body surface area, particularly if the patient is exposed to inhalational injury, poorly guided fluid resuscitation therapy or abdominal wall burns [25
Severe acute pancreatitis
is associated with IAH/ACS [6
], with IAH occurring in 59% to 78% and ACS in 27% to 56% of these patients [27
]. The combination of both primary (due to abdominal collections and inflammation) and secondary (due to fluid resuscitation) IAH is often observed, and this explains the high incidence of IAH/ACS in severe acute pancreatitis.
The term ACS was introduced by Kron et al. in 1984, who reported ACS after aortoiliac surgery [8
]. Since then, the syndrome has been repeatedly described after ruptured abdominal aortic aneurysm
(rAAA) repair [30
]. Although only few population-based studies have specifically addressed rAAA, it is reasonable to count IAH/ACS as an important complication in these patients. Therefore, IAP monitoring after surgical or endovascular repair of rAAA is strongly recommended [33
While IAH/ACS frequently occurs after major abdominal surgery
, its true incidence is difficult to establish, as earlier studies use different definitions for IAH and do not always differentiate between IAH and ACS. Defining IAH as IAP ≥ 25 mmHg, Biancofiore et al. found a 32% incidence in liver transplant patients [35
]. Sugrue et al. reported that 46% of emergency gastrointestinal surgery patients requiring intensive care had IAP ≥ 18 mmHg [36
There are no clear data on the incidence and risk factors of IAH in spontaneously breathing patients
. To our knowledge, the only study that included exclusively spontaneously breathing patients is by Serpytis and Ivaskevicius, who enrolled 77 non-infectious patients after major abdominal surgery [37
]. They observed a high incidence of IAH (45.5% on the first postoperative day) and a positive correlation between positive fluid balance and IAP. The bladder pressure was measured with a 50 ml instillation volume, while the patients were asked to relax. This instillation volume may result in overestimation of IAP in mechanically ventilated and sedated patients [38
], but it is not known how it may influence the results in spontaneously breathing patients. In studies on consecutive patients, especially when enrolling only the patients hospitalised for at least 24 h in the ICU, the majority of patients would expectedly be mechanically ventilated. In the prevalence study by Malbrain et al., 63% of patients with IAH and 70% of patients without IAH were on mechanical ventilation. IAH patients had a lower pO2
ratio, but ventilation groups were not separately analysed [4
]. The only study of consecutive ICU patients where mechanical ventilation was identified as a risk factor of IAH is the report by Vidal et al. [12
]. In that study, 75% of IAH patients compared to 37% of non-IAH patients were mechanically ventilated. Other studies either do not report the proportion of MV [13
] or enrolled only MV patients based on pathophysiological arguments of thoraco-abdominal interaction [14
]. Thus, studies on the importance of IAH as well as IAP monitoring methods in spontaneously breathing intensive/intermediate care patients are warranted. Considering the major changes in physiological and pathophysiological conditions associated with mechanical ventilation, we caution against the free transmission of evidence between these two patient groups.
Because IAH has mainly been studied in mixed or surgical ICU populations, the data on medical patients
are scarce. Malbrain et al. reported no difference in the prevalence of IAH between the patients of medical (54.4%) and surgical (45.6%) profile [3
], no difference in the incidence of IAH was observed in the second study by the same authors [4
]. In a study by Reintam et al., almost all patients with primary IAH and approximately 50% of patients with secondary IAH were of surgical profile [5
]. Worse outcomes of secondary compared with primary IAH were observed. Daugherty et al. studied 40 medical patients with a minimum net positive fluid balance of 5 L/24 h [41
]. In this small group, equal to 8.5% of all medical ICU admissions screened, the incidence of IAH was 85% and of ACS 33%. Positive fluid balance was also identified as an independent risk factor for IAH in several studies [4
], whereas some other studies with mixed ICU patients failed to observe positive fluid balance as an independent risk factor for IAH [3
]. Although the evidence is not entirely consistent and the cut-off value for positive fluid balance is not clear, routine IAP monitoring should be considered in medical patients with large-volume resuscitation.
Limited information is available about the prevalence of IAH in septic patients
. Regueira et al. reported that 76.5% of their septic shock patients exhibited IAH during the first 72 h after admission [2
]. Surprisingly many (27/67 (40%)) septic shock patients with IAH developed ACS. Other studies have demonstrated that the proportion of septic patients among IAH patients is higher than in the total ICU population [4
]. The simultaneous presence of other factors, such as intra-abdominal infections, massive fluid resuscitation and ileus, may explain the high prevalence of IAH in this subgroup of patients.
In which patients should IAP be measured?
Many literature reviews list all clinical conditions that have been associated with increased IAP and mistakenly call them possible risk factors of IAH [7
]. Such an overwhelming list of all possible clinical conditions, including sepsis, oliguria, acidosis and others, would be of little help to an attending clinician to identify patients who would benefit from IAP assessment. Measuring IAP requires labour and money; therefore, its blind application in all patients should be avoided. From a critical analysis of the prevalence and risk factors above, the following summary can be made. More than one study has identified high BMI, abdominal surgery, liver dysfunction/ascites, hypotension/vasoactive therapy, respiratory failure and excessive fluid balance as risk factors of IAH in general ICU populations (Table ). Importantly, recent studies that have incorporated IAH prevention may have identified different risk factors compared to earlier studies. To create a uniform and explicit list of independent risk factors applying to all ICU patients will probably be impossible. Different approaches seem unavoidable for different patient groups. Epidemiologic studies, analysing different groups only after including all consecutive patients, should be encouraged. We need to be careful when drawing conclusions about the incidence or risk factors of IAH based on studies including only selected patients.
At present, we suggest IAP be measured routinely in certain patient groups. Given the high risk of ACS, monitoring IAP is mandatory in ICU patients with severe burns, severe trauma, severe acute pancreatitis, liver failure or ruptured aortic aneurysms. Increased IAP in these patients is related to (1) decreased abdominal wall compliance (laparotomy, high BMI, respiratory mechanics and abdominal eschar); (2) increased intra-abdominal volume (ascites and intra-abdominal bleeding); (3) increased intraluminal volume (ileus, gastrointestinal bleeding and bowel oedema); or (4) capillary leaking and fluid overload (pancreatitis and shock/sepsis). IAP measurements are strongly indicated if the patient has any of these conditions.
Some evidence suggests [15
] that the risk for IAH is minimal in mechanically ventilated ICU patients without pancreatitis, acute hepatic failure/cirrhosis with ascites, gastrointestinal bleeding or laparotomy and in the absence of BMI > 30, positive end-expiratory pressure > 10 cmH2
< 300 and the use of vasopressors/inotropes on admission day. This list might be advocated to identify those ICU patients in whom IAP measurement can be forgone. It needs to be underlined that this evidence originates from one single-centre study in ventilated patients only, and most likely, this list would be different in different ICUs. However, similar local checklist might be the first step in decision-making process for IAP monitoring. The complexity of abdomino-thoracic interactions and the pathophysiology of polycompartment syndrome should always be kept in mind, as should the probable necessity of measuring IAP in each individual patient [43
]. In addition to the standardised IAP measurements in at-risk patients, a routine clinical assessment of the signs of IAH should be a part of every patient's bedside evaluation, leading to prompt IAP monitoring in case of the slightest suspicion of (the development of) IAH. The detection of IAH should lead to the complex management of the syndrome, for which the management guidelines from WSACS provide good support [47