Oligohydramnios Imaging 

  • Author: Jason K Baxter, MD; Chief Editor: Eugene C Lin, MD   more...
 
Updated: Apr 11, 2011
 

Overview

Multiple definitions of oligohydramnios are used because no ideal cutoff level for intervention exists.[1, 2, 3, 4, 5, 6, 7]

Oligohydramnios is characterized by the following features:

  • Diminished amniotic fluid volume (AFV)
  • Amniotic fluid volume of less than 500 mL at 32-36 weeks' gestation - Amniotic fluid volume depends on the gestational age; therefore, the best definition may be AFI less than the fifth percentile.
  • Single deepest pocket (SDP) of less than 2 cm
  • Amniotic fluid index (AFI) of less than 5 cm or less than the fifth percentile

See the images below.

Sonogram obtained before second-trimester amnioinfSonogram obtained before second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands. Sonogram obtained after second-trimester amnioinfuSonogram obtained after second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands.

The earlier in pregnancy that oligohydramnios occurs, the poorer the prognosis. Fetal mortality rates as high as 80-90% have been reported with oligohydramnios diagnosed in the second trimester. Most of this mortality is a result of major congenital malformations and pulmonary hypoplasia secondary to PROM before 22 weeks' gestation. Midtrimester PROM (premature rupture of membranes) often leads to pulmonary hypoplasia, fetal compression syndrome, and amniotic band syndrome. The inspiration of amniotic fluid at regular intervals is probably needed for terminal alveolar development.

The assessment of amniotic fluid volume is important in pregnancies complicated by abnormal fetal growth or IUGR. AFV has been shown to be predictive in discriminating normal from decreased growth. Oligohydramnios is a frequent finding in pregnancies involving IUGR and is most likely secondary to decreased fetal blood volume, renal blood flow, and, subsequently, fetal urine output. Pregnancies complicated by severe oligohydramnios have been shown to be at increased risk for fetal morbidity.[8, 9]

AFV is an important predictor of fetal well-being in pregnancies beyond 40 weeks' gestation. AFV must be closely monitored, with measurements obtained at least once per week. The diagnosis of oligohydramnios may help in identifying postterm fetuses in jeopardy.

AFV is a predictor of the fetal tolerance of labor, and it is associated with an increased risk of abnormal heart rate, meconium-stained amniotic fluid, and cesarean delivery. An increased incidence of cord compression is associated with oligohydramnios; this can lead to variable decelerations, with cord occlusion as the proximate cause of fetal distress.

For more information, see Polyhydramnios and Oligohydramnios.

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Workup

Ultrasonography

The diagnosis is confirmed by means of ultrasonography (see the images below). Oligohydramnios may be discovered incidentally during routine ultrasonography and noted during antepartum surveillance for other conditions. The diagnosis may be prompted by a lag in sequential fundal height measurements (size less than that expected for the dates) or by fetal parts that are easily palpated through the maternal abdomen.[10, 11, 12, 13, 14, 15]

During ultrasonography of the fetal anatomy, normal-appearing fetal kidneys and fluid-filled bladder may be observed to rule out renal agenesis (see the following 2 images), cystic dysplasia, and ureteral obstruction. Check fetal growth to rule out intrauterine growth restriction (IUGR) leading to oliguria.

Sonogram obtained before second-trimester amnioinfSonogram obtained before second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands. Sonogram obtained after second-trimester amnioinfuSonogram obtained after second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands.

Sterile speculum examination

Sterile speculum examination may be performed to check for range of motion (ROM). Amniotic fluid may pool in the vagina, and an arborization or ferning pattern may be observed when dried posterior vault fluid is examined microscopically. Cervical mucous may cause false-positive results, as can semen and blood. Nitrazine paper turns blue. The amniotic fluid is more basic (pH 6.5-7.0) than normal vaginal discharge (pH 4.5).

Measurement of amniotic fluid volume

Initial studies to objectively measure amniotic fluid volume (AFV) involved dye dilution techniques. The techniques were accurate, although they required amniocentesis, an invasive procedure that increased the risk of perinatal morbidity.

The routine use of ultrasonography has created a safe, reliable, and repeatable method of measuring AFV. Early methods of assessing AFV with ultrasonography involved nonquantitative assessments, including sonographers' subjective impression of AFV.

Subjective oligohydramnios criteria have included the following:

  • The absence of fluid pockets throughout the uterine cavity
  • Crowding of the fetal limbs
  • The absence of pockets surrounding the fetal legs
  • Overlapping of the fetal ribs (in severe cases)

The 2 most commonly used objective methods of determining AFV include measurement of the single deepest pocket (SDP) and the summation of the SDPs in each quadrant, or the amniotic fluid index (AFI).[16] These tests are routinely performed with the patient in the supine or semi-Fowler position, although studies have demonstrated accuracy in the lateral decubitus position as well.[17, 18, 9, 19]

The ultrasound transducer is held along the maternal longitudinal axis and maintained perpendicular to the floor while the SDP of the amniotic fluid is measured. Pockets should be free of fetal limbs and the umbilical cord, although some authors allow for a single loop of cord to be within the fluid pocket. AFV may be artificially increased if the transducer is not maintained perpendicular to the floor. Excessive pressure on the maternal abdomen with the transducer may lead to an artificially reduced measurement (see the image below).

Amniotic fluid index (AFI) measurement technique. Amniotic fluid index (AFI) measurement technique.

Phelan et al described the AFI as a quantitative measurement to predict a poor pregnancy outcome and the success of external cephalic versions.[1] The pregnant abdomen is divided into 4 quadrants by using the umbilicus as a reference point to divide the uterus into upper and lower halves and by using the linea nigra to divide the uterus into left and right halves. The 4 measurements are summed to obtain the AFI in centimeters.[18, 19]

In gestations earlier than 20 weeks, measurements from the 2 halves are divided by the linea nigra to obtain the AFI. Tables of the normal limits for AFI, based on the gestational age, have been published for singleton and multiple pregnancies (see an example below). The mean AFI for normal pregnancies is 11-16 cm.

Amniotic fluid index (AFI) during a normal human sAmniotic fluid index (AFI) during a normal human singleton pregnancy. The solid line is the mean AFI, the lower dotted line is the 5th percentile value, and the upper dotted line is the 95th percentile value (data adapted from Moore, 1990). Image courtesy of Christopher L. Sistrom, MD.

The test is reproducible, with interobserver and intraobserver variations of about 10-15% or 1-2 cm in pregnancies with normal AFVs. The margin of error is less in patients with decreased amounts of amniotic fluid.

Oligohydramnios has been defined as an AFI less than 5 cm, although 8 cm has occasionally been used as a cut-off threshold. Because the AFV depends on the gestational age, oligohydramnios has been defined as an AFI less than the fifth percentile (corresponding to an AFI of < 6.8 cm at term).

Oligohydramnios has been defined as an SDP less than 2 cm. Perinatal morbidity rates have been shown to increase sharply with SDPs below this value. Some have suggested that an SDP of 2.5-3.0 cm is a better lower limit for separating normal SDPs from those consistent with oligohydramnios.

Many studies have shown that the SDP and the AFI methods have equal diagnostic accuracies. The SDP technique may be a better means of assessing the AFV in twin gestations and in pregnancies at an early gestational age. Some study results have shown that the AFI has greater sensitivity and a higher predictive value than the SDP in diagnosing abnormally high and low AFVs. Most obstetricians prefer to assess a broader area of the uterine cavity by using the AFI because the single measurement of the SDP does not allow for an asymmetric fetal position in the uterus.

Other examinations

MRI and 3-dimensional (3D) ultrasonography are newer (and more expensive) modalities for accurately assessing the AFV.[20]

Amniotic wrinkle

Finberg reported a possible pitfall in the sonographic analysis of amniotic fluid in twin pregnancies, the "amniotic wrinkle," which may give the misleading impression of adequate amniotic fluid for both twins when one twin actually has little to none.

The author reevaluated sonograms of twin pregnancies in which an initial sonographer's assessment was adequate fluid for each twin but which the author's own imaging assessment on the same day showed oligohydramnios in one twin.

He found either of the following may occur when oligohydramnios of one twin is present:

  • The intertwin membrane may fold in on itself, creating an amniotic wrinkle (a short linear structure that extends perpendicularly away from the twin with decreased amniotic fluid in toward the amniotic space of the other twin)
  • An intrauterine sling or "cocoon" may be present, in which a fetus appears to be suspended within the amniotic space of the other twin may be present

Finberg recommended showing the intertwin membrane in all images used to document each twin's amniotic fluid, with additional right-angle images to identify amniotic wrinkles.[21]

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Contributor Information and Disclosures
Author

Jason K Baxter, MD  Fellow in Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Thomas Jefferson University Hospital

Jason K Baxter, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, American Medical Association, Association of Professors of Gynecology and Obstetrics, Sigma Xi, and Society for Maternal-Fetal Medicine

Disclosure: Nothing to disclose.

Coauthor(s)

Harish M Sehdev, MD  Associate Professor of Clinical Obstetrics and Gynecology, Department of Obstetrics and Gynecology, University of Pennsylvania; Consulting Staff, Pennsylvania Hospital, University of Pennsylvania Health System

Harish M Sehdev, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Obstetricians and Gynecologists, American Institute of Ultrasound in Medicine, Phi Beta Kappa, and Society for Maternal-Fetal Medicine

Disclosure: Nothing to disclose.

John W Breckenridge, MD, FACR  Clinical Assistant Professor, Department of Radiology, Division of Ultrasound, Thomas Jefferson University Hospital; Chair, Department of Radiology, Abington Memorial Hospital

John W Breckenridge, MD, FACR is a member of the following medical societies: Alpha Omega Alpha, American College of Radiology, American Institute of Ultrasound in Medicine, American Medical Association, and Pennsylvania Medical Society

Disclosure: Nothing to disclose.

Specialty Editor Board

Christopher L Sistrom, MD  Associate Chair for Research, Assistant Professor, Department of Radiology, University of Florida School of Medicine

Christopher L Sistrom, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Radiology, American Institute of Ultrasound in Medicine, American Roentgen Ray Society, Association of University Radiologists, Phi Beta Kappa, and Radiological Society of North America

Disclosure: Nothing to disclose.

Bernard D Coombs, MB, ChB, PhD  Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand

Disclosure: Nothing to disclose.

Karen L Reuter, MD, FACR  Professor, Department of Radiology, Lahey Clinic Medical Center

Karen L Reuter, MD, FACR is a member of the following medical societies: American Association for Women Radiologists, American College of Radiology, American Institute of Ultrasound in Medicine, American Roentgen Ray Society, and Radiological Society of North America

Disclosure: Nothing to disclose.

Robert M Krasny, MD  Resolution Imaging Medical Corporation

Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America

Disclosure: Nothing to disclose.

Chief Editor

Eugene C Lin, MD  Consulting Radiologist, Virginia Mason Medical Center; Clinical Assistant Professor of Radiology, University of Washington School of Medicine

Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, and Society of Nuclear Medicine

Disclosure: Nothing to disclose.

References
  1. Phelan JP, Smith CV, Broussard P, Small M. Amniotic fluid volume assessment with the four-quadrant technique at 36-42 weeks' gestation. J Reprod Med. Jul 1987;32(7):540-2. [Medline].

  2. Dasari P, Niveditta G, Raghavan S. The maximal vertical pocket and amniotic fluid index in predicting fetal distress in prolonged pregnancy. Int J Gynaecol Obstet. Feb 2007;96(2):89-93. [Medline].

  3. Fok WY, Chan LY, Lau TK. The influence of fetal position on amniotic fluid index and single deepest pocket. Ultrasound Obstet Gynecol. Aug 2006;28(2):162-5. [Medline].

  4. Johnson JM, Chauhan SP, Ennen CS, Niederhauser A, Magann EF. A comparison of 3 criteria of oligohydramnios in identifying peripartum complications: a secondary analysis. Am J Obstet Gynecol. Aug 2007;197(2):207.e1-7; discussion 207.e7-8. [Medline].

  5. Moore TR, Cayle JE. The amniotic fluid index in normal human pregnancy.. Am J Obstet Gynecol. May 1990;162(5):1168-73. [Medline].

  6. Peipert JF, Donnenfeld AE. Oligohydramnios: a review. Obstet Gynecol Surv. Jun 1991;46(6):325-39. [Medline].

  7. Sherer DM. A review of amniotic fluid dynamics and the enigma of isolated oligohydramnios. Am J Perinatol. Jul 2002;19(5):253-66. [Medline].

  8. Lee SE, Romero R, Lee SM, Yoon BH. Amniotic fluid volume in intra-amniotic inflammation with and without culture-proven amniotic fluid infection in preterm premature rupture of membranes. J Perinat Med. 2010;38(1):39-44. [Medline].

  9. Ross MG, Beall MH, Christenson PD. Amniotic fluid volume and perinatal outcome. Am J Obstet Gynecol. Mar 2007;196(3):e17. [Medline].

  10. Chamberlain PF, Manning FA, Morrison I, et al. Ultrasound evaluation of amniotic fluid volume. I. The relationship of marginal and decreased amniotic fluid volumes to perinatal outcome. Am J Obstet Gynecol. Oct 1 1984;150(3):245-9. [Medline].

  11. Jaba B, Mohiuddin AS, Dey SN, Khan NA, Talukder SI. Ultrasonographic determination of amniotic fluid volume in normal pregnancy. Mymensingh Med J. Jul 2005;14(2):121-4. [Medline].

  12. Magann EF, Chauhan SP, Barrilleaux PS, Whitworth NS, McCurley S, Martin JN. Ultrasound estimate of amniotic fluid volume: color Doppler overdiagnosis of oligohydramnios. Obstet Gynecol. Jul 2001;98(1):71-4. [Medline].

  13. Moore TR. Sonographic screening for oligohydramnios: does it decrease or increase morbidity?. Obstet Gynecol. Jul 2004;104(1):3-4. [Medline].

  14. Zlatnik MG, Olson G, Bukowski R, Saade GR. Amniotic fluid index measured with the aid of color flow Doppler. J Matern Fetal Neonatal Med. Apr 2003;13(4):242-5. [Medline].

  15. Vink J, Hickey K, Ghidini A, Deering S, Mora A, Poggi S. Earlier gestational age at ultrasound evaluation predicts adverse neonatal outcomes in the preterm appropriate-for-gestational-age fetus with idiopathic oligohydramnios. Am J Perinatol. Jan 2009;26(1):21-5. [Medline].

  16. Nabhan AF, Abdelmoula YA. Amniotic fluid index versus single deepest vertical pocket: a meta-analysis of randomized controlled trials. Int J Gynaecol Obstet. Mar 2009;104(3):184-8. [Medline].

  17. Magann EF, Doherty DA, Chauhan SP, Busch FW, Mecacci F, Morrison JC. How well do the amniotic fluid index and single deepest pocket indices (below the 3rd and 5th and above the 95th and 97th percentiles) predict oligohydramnios and hydramnios?. Am J Obstet Gynecol. Jan 2004;190(1):164-9. [Medline].

  18. Moore TR. Superiority of the four-quadrant sum over the single-deepest-pocket technique in ultrasonographic identification of abnormal amniotic fluid volumes. Am J Obstet Gynecol. Sep 1990;163(3):762-7. [Medline].

  19. Rutherford SE, Phelan JP, Smith CV, Jacobs N. The four-quadrant assessment of amniotic fluid volume: an adjunct to antepartum fetal heart rate testing. Obstet Gynecol. Sep 1987;70(3 Pt 1):353-6. [Medline].

  20. Pistorius LR, Hellmann PM, Visser GH, Malinger G, Prayer D. Fetal neuroimaging: ultrasound, MRI, or both?. Obstet Gynecol Surv. Nov 2008;63(11):733-45. [Medline].

  21. Finberg HJ. The amniotic wrinkle: a pitfall in evaluating amniotic fluid for twins. J Ultrasound Med. Feb 2010;29(2):249-54. [Medline].

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Sonogram obtained before second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands.
Sonogram obtained after second-trimester amnioinfusion. This fetus has bilaterally absent kidneys consistent with a diagnosis of Potter syndrome. The cystic structures in the renal fossae are most likely the adrenal glands.
Amniotic fluid index (AFI) during a normal human singleton pregnancy. The solid line is the mean AFI, the lower dotted line is the 5th percentile value, and the upper dotted line is the 95th percentile value (data adapted from Moore, 1990). Image courtesy of Christopher L. Sistrom, MD.
Amniotic fluid index (AFI) measurement technique.
 
 
 
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