Sir,
The questions raised by Garg & Tyagi1 illustrate a fundamental challenge related to the limitations and heterogeneity of published original research on intra-abdominal pressure (IAP) in pregnancy. We sought to coalesce data into clinically meaningful recommendations for the diagnosis and management of intra-abdominal hypertension (IAH) and abdominal compartment syndrome (ACS) in pregnancy.2 We defined IAH as pre-delivery IAP ≥14 mm Hg or postpartum IAP ≥12 mm Hg. These cutoffs are supported by Tyagi et al3, who performed the only known study of IAP in critically ill obstetric patients. Each patient with IAH was pregnant when diagnosed and had an IAP ≥14 mm Hg. Postpartum, IAP decreased to <12 mm Hg in four patients, but persisted ≥12 mm Hg despite delivery in two women who died. Our definitions would have captured all IAH patients in the Tyagi study, while excluding patients with phys iologic IAP elevations.
Tyagi et al found IAP had no impact on organ function or mortality.3 The median sequential organ failure assessment (SOFA) cardiovascular, renal and hepatic sub-scores were zero. Higher neurologic sub-scores contributed most to organ dysfunction, but these may be susceptible to false calculation (such as when seda tives were used). Therefore, this case mix may not be comparable to previous data obtained in critically ill patients.4 Furthermore, it is unclear how many patients required mechanical ventilation for >24 hours, vasopressor/inotrope support or renal replacement therapy, nor were Acute Physiology and Chronic Health (APACHE)-II or APACHE-III scores or Simplified Acute Physiology Score (SAPS)-II or SAPS-III provided. Nevertheless, the authors deserve congratulations for this study in obstetric patients. The data are reassuring in that positive fluid balance was associated with poor outcome. While generalizations are impossible, notable findings include: (1) IAP on intensive care unit (ICU) admission was higher among pregnant than non-pregnant patients (13.3 ± 2.2 vs 8.1 ± 1.5, P < 0.001), and (2) total SOFA score was higher among non-survivors than survivors (11.3 ± 3.7 vs 5.7 ± 3.4, P < 0.001). These findings suggest that pregnant patients with high IAP may indeed have organ dysfunction.
We suggest clinicians consider left uterine displacement effect on IAP while recommending measurements be performed in the supine position. This is consistent both with guidelines from the World Society of the Abdominal Compartment Syndrome (WSACS)5 and with the Tyagi study methods.3
Most data on IAP in pregnancy come from patients undergoing elective cesarean delivery under spinal anesthesia. The anesthetic effects cause increased abdominal wall compliance and lower IAP. Despite this, mean IAP values in most studies (Table 1) are similar to those in unanesthetized, critically ill obstetric patients.3 As ICU patients are unlikely to have neuraxial anesthesia, our proposed definitions are appropriately calibrated.
TABLE 1.
Intra-abdominal pressure measurements of obstetric patients
| Author | n | Gestation (wk) | Patient position | IAP (mm Hg) mean ± SD | Transducer position | Delivery characteristics | Comments |
|---|---|---|---|---|---|---|---|
| Pre-delivery measurements | |||||||
| Paramore, 1913 | 23 | 6 mo-term | Supine; left side; knee chest; standing | 15–44 | Rectal manometer | ||
| Al-Khan, 2011 | 100 | 36–41 | Leftward tilt | 22 ± 2.9 | Not specified | Elective CD | 50-mL saline injection |
| Chun, 2012 | 20 | 38–40 | Supinel0° leftward tilt | 10.8 ± 4.7 8.9 ± 4.9 |
MAL at iliac crest | Elective CD; spinal | 25-mL saline injection |
| Fuchs, 2013 | 70 | 38.1 | Supine, end-expiration | 14.2a | Pubic symphysis | Elective CD; spinal | 25-mL saline injection |
| Staelens, 2014 | 23 | 39.0 | Supine, flat, end-expiration | 14.0 ± 2.6 | MAL at iliac crest | Elective primary or repeat CD | 25-mL saline injection |
| Tyagi, 20173 | 8 | 10–39 | Supine, end-expiration | 13.2 ± 2.2 | MAL | Critical, ICU admission-Vaginal delivery in ICU | 20-mL saline injection |
| Marshalov, 2017 | 117b | 38–39 | Supine | 17.8 ± 3.6 | Pubic symphysis | 38 SVD, 79 elective CD | 20-mL saline injection |
| Author | n | Hours Postpartum | Patient position | IAP (mmHg) mean ± SD | Transducer position | Delivery Characteristics | Comments |
| Post-delivery measurements | |||||||
| Abdel-Razeq, 2010 | 21 | 1 | Supine | 6.4 ± 5.2 | Pubic symphysis | Elective CD | 25-mL saline injection |
| Fuchsc, 2013 | 70 | 2 | Supine, end-expiration | 10.7a | Pubic symphysis | Elective CD | 25-mL saline injection |
| Staelensc, 2014 | 23 | 1 | Supine, flat, end-expiration | 9.8 ± 3.0 | MAL at iliac crest | Elective primary or repeat CD | 25-mL saline injection |
| Tyagi, 20173 | 93 | Variable | Supine, end-expiration | 8.1 ± 1.5 | MAL | Critical, ICU admission | IAP measured daily |
| Marshalovc, 2017 | 117 | 1 | Supine | 9.6 ± 0.89 | Pubic symphysis | 38 SVD, 79 elective CD | 20-mL saline injection |
Adapted and reproduced with permission from Lozada et al (Management of peripartum intra-abdominal hypertension and abdominal compartment syndrome. Acta Obstet Gynecol Scand 2019 under Open Access CC BY License 4.0).
Complete list of references available in the original publication.
CD, cesarean delivery; IAP, intra-abdominal pressure; MAL, mid-axillary line; SVD, spontaneous vaginal delivery.
Standard deviation not reported.
Control group data only presented.
Same patient cohort as pre-delivery (above).
The request by Garg & Tyagi for more evidence1 comes more than 100 years after Paramore first measured IAP in pregnant patients. Even with ongoing research, nothing suggests that practice changing data are imminent. Our proposed recommendations are a framework upon which future updates can build. We welcome in sight from others and encourage collaboration to produce consensus guidelines. This would strengthen our recommendations and benefit patients around the world.
REFERENCES
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