Diagnosis and Management of Placenta
Diagnosis and Management of Placenta
Diagnosis and Management of Placenta
10
The diagnosis of placenta accreta begins with clinical suspicion in patients at risk. Ultrasound and
Doppler are first-choice diagnostic methods because of their accessibility and high sensitivity.
Placental MRI is an accurate method of topographic stratification that makes it possible to define
anatomy, to plan the surgical approach and to consider other therapeutic possibilities. Manage-
ment of placenta percreta involves great technical dexterity and significant clinical support. The
main challenges include controlling the haemorrhage and dissection of the invaded tissues. Now-
adays, there are two treatment options: caesarean hysterectomy or a conservative approach.
With the latter, there is a choice between leaving the placenta in situ and waiting for its later
resolution, and a one-step surgery that addresses the problems of invasion, vascular control
and myometrial damage in a single surgical act.
Key words: conservative treatment; diagnosis; one-step surgery; placenta accreta; therapeutic
approach.
INTRODUCTION
* Av. Corrientes 5087 4 a C14141 AJD Ciudad Autónoma de Buenos Aires, Argentina. Tel./Fax: þ54 11
4857 1331.
E-mail address: jpalacios@fmed.uba.ar
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1134 J. M. Palacios-Jaraquemada
caesarean sections, and other myometrial injuries associated with dilatation and curet-
tage (D&C) and corrective surgeries, among others, are the main predisposing factors.
Ultrasound (US) and Doppler3,4 are two first-line methods for the diagnosis of pla-
centa accreta; both have a high degree of diagnostic sensitivity and both methods
have made it possible to establish diagnostic signs that allow the suspicion of an abnor-
mally implanted placenta in a high percentage of cases.
In addition, placental nuclear magnetic resonance imaging (pMRI) has proved to be
a noteworthy auxiliary when it comes to plan the surgery of placenta accreta.5 Placen-
tal MRI (pMRI) makes it possible to have total acquisition of images; its multiplane char-
acteristic allows a correct three-dimensional (3D) reconstruction, necessary for
surgical planning.
Placenta accreta causes morbidity and mortality due to haemorrhage, coagulopathy
and its inherent surgical difficulty; these facts make this disorder the first cause of
obstetric hysterectomy.6
Traditionally, the treatment of placenta accreta has consisted of puerperal hysterec-
tomy. This is a high-risk procedure, especially when haemorrhage and coagulation dis-
orders coexist. To minimize damage and conserve the reproductive potential in
women, a series of procedures that aim to preserve the uterus affected by placenta
accreta have been incorporated.7,8 These conservative tactics have proved to be effec-
tive and safe under controlled conditions.
Below, we provide a synthesis of the current knowledge about placenta accreta, in-
cluding practical data for obstetricians and surgeons. We emphasize early detection of
risk factors, diagnostic guidelines and treatment alternatives in accordance with the
human and technical resources available.
TERMINOLOGY
From a histopathological perspective, there are marked differences among placenta ac-
creta, increta and percreta. However, from a clinical–surgical point of view, sectors
that show a different degree of invasion can coexist in the same patient. This phenom-
enon leads to discrepancies between what is observed during surgery and the final
pathological diagnosis. This difference is not only semantic; it makes comparisons of
surgical techniques and clinical results from different authors virtually impossible.
Unlike other illnesses, the histopathological study of invasive placenta does not al-
ways constitute a diagnostic ‘‘gold standard’’. This phenomenon occurs when biopsy is
obtained in an area without invasion or with a degree of minor penetration. In these
cases, there is a mismatch between histology and the surgical finding. We prefer to
define placenta accreta according to its clinical–surgical characteristics.9,10
RISK FACTORS
DIAGNOSTIC METHODS
Ultrasound
Figure 1. Transvaginal ultrasound: anterior placenta percreta in patient with twin pregnancy. LMVL, loss of
myometrial-vesical layer; NFV, newly-formed vessels.
1136 J. M. Palacios-Jaraquemada
Ultrasound signs
Certain patterns have been associated with placenta accreta. One such sign is the
presence of placental lagoons, which, unlike those seen in the second trimester, are
large, irregular and multiple. The aetiology of these placental lagoons is unknown.
Their presence, characteristics and number are not directly related to the gravity of
placenta accreta. The sensitivity of this ultrasound sign is 79%, with a positive predic-
tive value of 92%, when identified between weeks 15 and 40.16
The loss of the retroplacental hypoecogenic zone, represented by the absence of
the retroplacental vascular bed, basal decidua and placental advancement over the my-
ometrium is another ultrasound sign associated with the presence of placenta accreta.
This sign does not have great significance when found in isolation. Certain authors
question its importance due to its low diagnostic and predictive sensitivity and
a false-positive rate of nearly 50%.
Progressive thinning of the retroplacental myometrium indicates the extreme prox-
imity of the placental tissue to the peritoneal serosa or to the neighbouring organs,
another sign of placenta accreta. Segmental myometrial thinning of less than 1 mm
is suggestive of abnormal placental adherence, with sensitivity of 93%, specificity of
79% and predictive value of 73%.17
Thinning or disruption of the uterine–vesical serosa occurs due to the lack of my-
ometrial tissue, leaving the visceral serosa exposed. It is not easy to make a differential
diagnosis between placenta accreta and the irregularities of the vesical wall. Disruption
of the serosa indicates a higher degree of compromise; the presence of extrauterine
placental parenchyma confirms placenta percreta.
US grey-scale general capacity is enough to diagnose placenta accreta with sensitiv-
ity 87%, specificity 98%, a positive predictive value 93% and a negative predictive value
98%.18
The presence of vessels perpendicular to the uterine axis indicates the presence of pla-
cental vessels from and towards the myometrium or other neighbouring tissues17–19; this
pattern is associated with the presence of different degrees of placenta accreta.
Initially, the aim was to determine whether placental magnetic resonance imaging (pMRI)
can improve the diagnostic sensitivity of ultrasound in the detection of placenta ac-
creta.20–22 The first prospective study was performed in 1997. The report included 18
patients and did not find any diagnostic differences between the techniques, although it
did identify a higher diagnostic sensitivity in pMRI in the case of posterior placenta accreta.
In 2005, a prospective series comprising 300 cases showed that pMRI adequately
outlined the topographic anatomy of the invasion, relating it to the regional anasto-
motic vascular distribution. The characteristics of the invasion confirmed the possibil-
ity of bleeding, the occurrence of complications, and the inherent technical difficulty in
certain cases. It is the only published study to date that has been able to confirm the
presence of parametrial invasion (axial slices)5; an important factor associated with the
possibility of urethral damage during surgery.
Technical aspects
Like other diagnostic methods, pMRI has certain technical details that can enhance or
emphasize its diagnostic accuracy. The main aim of the imaging study is to obtain the
best definition of the uterine–placental interphase and its relation to the bladder
(Figure 2).
Figure 2. pMRI (sagital slice): isodense placental tissue is present inside the bladder, a characteristic sign of
placenta percreta.
1138 J. M. Palacios-Jaraquemada
Newly formed vessels (NFV) secondary to the development of placenta accreta are
underdeveloped in the middle layer. This particularity requires the pMRI study to be
performed with a semi-full bladder, to avoid false negatives as a result of overdisten-
sion and/or collapse of the NFV, as well as false negatives due to an empty bladder. It is
important that the bladder is only partially full; an empty bladder next to the pubic
bone would prevent an adequate sign of the uterine–vesical interphase, resulting in
diagnostic error.
The use of ultrafast techniques that minimize artefacts produced by fetal movement
is recommended.23 T2-weighted imaging highlights urine as a naturally white contrast,
thus allowing better delineation of the vesical muscle in relation to the placenta and
the underlying myometrium.24
In the presence of risk factors (multiple D&C, myomectomies or corrective sur-
gery), if there are clinical antecedents for the T2 mode allowing a naturally white con-
trast and a suspicion of posterior placenta accreta, the use of gadolinium is
recommended to improve diagnostic accuracy. Without this, a combination of pla-
centa, myometrium, abdominal viscera and the vertebrae form a complex image, which
makes an adequate diagnosis of posterior myometrial placental invasion virtually
impossible.
So far, gadolinium has not shown any side effects during pregnancy, and there are no
toxicity reports. However, and as a precaution, its use is generally recommended for
cases in which diagnosis by other techniques is not possible.25,26
It is prudent to use pMRI in all cases with a resulting non-conclusive ultrasound or
Doppler examination, when it is important to rule out or confirm the presence of par-
ametrial invasion. Therapeutic options depend on the size of the invasions and exact
anatomy of the lesion.5,27,28
Preoperative evaluation
Surgical strategy
The primary objective is to perform the caesarean section in the safest conditions pos-
sible, according to the resources available. Placental removal is s not an essential step
and can be postponed. However, initiation of the removal manoeuvre is usually the
point of no return. If placental detachment, dissection or proximal vascular control
is ineffective, serious complications are generally immediate.
Diagnosis and management of placenta accreta 1139
Figure 3. Characteristic deformity of anterior placenta percreta. The invaded surface is cribbed by newly
formed vessels among the placenta, uterus and bladder. This patient underwent a one-step surgery.
Regional irrigation
The pelvic vascular system widely interconnects the internal iliac, external iliac and
femoral systems.17–29 External and internal compression of the abdominal aorta
1140 J. M. Palacios-Jaraquemada
Obstetric hysterectomy
The primary objective of surgery for placenta accreta consists of applying the sim-
plest and most efficient procedure that minimizes the risk of haemorrhage.
The presence of pericervical or lower-segment varicose veins proper of placenta
praevia can be confused with the neovascularization of placenta accreta. In these
cases, surgical exploration will make a differential diagnosis, thus avoiding unneces-
sary hysterectomies.
Surgical difficulties and possibility of complications in placenta accreta are directly
related to the invaded anatomical area, its specific circulation and to the dissection
of the organs involved.
When total hysterectomy must be performed in the presence of non-dissectable
lower-segment invasion, it is useful to apply some kind of aortic vascular control
(internal compression, endoluminal balloon or loop) before performing dissection
of the invaded tissues.
Indications for hysterectomy in placenta accreta include: (1) anticipated technical
problems with the technical impossibility of repair; (2) the technical impossibility
of performing a safe haemostasis; and (3) when, after performing conservative tech-
niques, complications such as infection or untreatable haemorrhage arise.
Neoformation vessels should not be electrocoagulated because of poor develop-
ment of the middle layer. This procedure can be the cause of bleeding difficult to
control, or of a postsurgical haemorrhage.
CONSERVATIVE TREATMENT
Figure 4. Control MRI (sagittal slice) from the patient seen in Figure 2. Note the homogeneous thickness of
the reconstructed anterior wall.
Diagnosis and management of placenta accreta 1143
Figure 5. Post-reconstruction segment caesarean performed 2 years after the surgery for anterior placenta
percreta (patient in Figure 2). The uterine segment can be observed, in perfect condition, opening up to the
fetal head.
1144 J. M. Palacios-Jaraquemada
pregnancies have been reported in patients who underwent a one-step surgery; 43 had
posterior of fundal placenta, and in 2 cases, anterior placenta. Only one recurrence
was reported, in a patient who became pregnant a few months after the repair
(Palacios-Jaraquemada, unpublished data).
As mentioned above, there is no unique approach to the management of placenta
accreta. Surgical team expertise, availability of resources and local conditions are de-
termining factors when choosing the safest procedure. Table 2 shows the choice of
procedures according to the technical and material resources available; these actions
have proved to be the safest procedures that make it possible to solve the problem
delivery with an acceptable maternal risk.
POSTSURGICAL CARE
Figure 6. The placenta is gradually reduced in size, and no corrective measure in the invaded uterine or
vesical area is taken (sagittal slice).
SUMMARY
procedure. This measure, together with adequate dissection of the interfascial planes,
is the key to safe surgery. The two options for conservative treatments differ in their
complexity, complication rates and follow up. As caesarean rates are growing globally,
and with these the cases of placenta accreta, the best strategy for the future consists
of identifying the aetiological factors and avoiding them as much as possible.
Research agenda
REFERENCES
1. Center for Disease Control and Prevention. Births: final data for 2002. Natl Vital Stat Rep 2003; 52:
1–114.
2. Kozak LJ & Weeks JD. U.S. trends in obstetric procedures, 1990–2000. Birth 2002; 29: 157–161.
*3. Finberg HJ & Williams JW. Placenta accreta: prospective sonographic diagnosis in patients with placenta
previa and prior cesarean section. J Ultrasound Med 1992; 11: 333–343.
*4. Chou MM, Ho ES, Lu F et al. Prenatal diagnosis of placenta previa/accreta with color Doppler ultra-
sound. Ultrasound Obstet Gynecol 1992; 2: 293–296.
5. Palacios Jaraquemada JM & Bruno CH. Magnetic resonance imaging in 300 cases of placenta accreta:
surgical correlation of new findings. Acta Obstet Gynecol Scand 2005; 84: 716–724.
6. Catanzarite VA, Stanco LM, Schrimmer DR et al. Managing placenta previa/accreta. Contemp Ob Gyn
1996; 41: 66–95.
*7. Bretelle F, Courbiere B, Mazouni C et al. Management of placenta accreta: morbidity and outcome. Eur J
Obstet Gynecol Reprod Biol 2007; 133(1): 34–39.
*8. Palacios Jaraquemada JM, Pesaresi M, Nassif JC et al. Anterior placenta percreta: surgical approach, he-
mostasis and uterine repair. Acta Obstet Gynecol Scand 2004; 83: 738–744.
9. Gielchinsky Y, Rojansky N, Fasouliotis SJ et al. Placenta accreta-summary of 10 years: a survey of 310
cases. Placenta 2002; 23(2-3): 210–214.
*10. Irving FC & Hertig AT. A study of placenta accreta. Surg Gynecol Obstet 1937; 64: 178–200.
11. Miller DA, Chollet JA & Goodwin TM. Clinical risk factors for placenta previa-placenta accreta. Am J
Obstet Gynecol 1997; 177: 210–214.
12. Hung TH, Shau WY, Hsieh CC et al. Risk factors for placenta accreta. Obstet Gynecol 1999; 93: 545–550.
13. Ota Y, Watanabe H, Fukasawa I et al. Placenta accreta/increta. Review of 10 cases and a case report.
Arch Gynecol Obstet 1999; 263: 69–72.
Diagnosis and management of placenta accreta 1147
14. Cravello L, Agostini A, Roger V et al. Intrauterine pregnancy after thermal balloon ablation. Acta Obstet
Gynecol Scand 2001; 80(7): 671.
15. Timor Tritsch IE & Yunis RA. Confirming the safety of transvaginal sonography in patientes suspected
placenta previa. Obstet Gynecol 1993; 81: 742–744.
16. Oyelese Y & Smulian JC. Placenta previa, placenta accreta, and vasa previa. Obstet Gynecol 2006; 107(4):
927–941.
*17. Hudon L, Belfort MA & Broome DR. Diagnosis and management of placenta percreta: a review. Obstet
Gynecol Surv 1998; 53(8): 509–517.
18. Haratz-Rubinstein N, Malone FD & Shevell T. Prenatal diagnosis of placenta accreta. Contemp Ob Gyn
2002; 4: 116–142.
19. Megier P, Gorin V & Desroches A. Ultrasonography of placenta previa at the third trimester of preg-
nancy: research for signs of placenta accreta/percreta and vasa previa. Prospective color and pulsed
Doppler ultrasonography study of 45 cases. J Gynecol Obstet Biol Reprod 1999; 28(3): 239–244.
*20. Comstock CH. Antenatal diagnosis of placenta accreta: a review. Ultrasound Obstet Gynecol 2005; 26(1):
89–96.
21. Maldjian C, Adam R, Pelosi M et al. MRI appearance of placenta percreta and placenta accreta. Magn
Reson Imaging 1999; 17(7): 965–971.
22. Levine D, Hulka CA, Ludmir J et al. Placenta accreta: evaluation with color Doppler US, power Doppler
US, and MR imaging. Radiology 1997; 205: 773–776.
23. Kim JA & Narra VR. Magnetic resonance imaging with true fast imaging with steady-state precession
and half-Fourier acquisition single-shot turbo spin-echo sequences in cases of suspected placenta ac-
creta. Acta Radiol 2004; 45: 692–698.
24. Lax A, Prince MR, Mennitt KW et al. The value of specific MRI features in the evaluation of suspected
placental invasion. Magn Reson Imaging 2007; 25: 87–93.
25. Junkermann H. Indications and contraindications for contrast-enhanced MRI and CT during pregnancy.
Radiologe 2007; 47(9): 774–777.
26. Webb JA, Thomsen HS, Morcos SK & Members of Contrast Media Safety Committee of European
Society of Urogenital Radiology (ESUR). The use of iodinated and gadolinium contrast media during
pregnancy and lactation. Eur Radiol 2005; 15: 1234–1240.
*27. Mazouni C, Gorincour G, Juhan V et al. Placenta accreta: a review of current advances in prenatal
diagnosis. Placenta 2007; 28: 599–603.
28. Masselli G, Manfredi R, Vecchioli A et al. MR imaging and MR cholangiopancreatography in the preop-
erative evaluation of hilar cholangiocarcinoma: correlation with surgical and pathologic findings. Eur Ra-
diol 2008 May 8 [Epub ahead of print].
29. Palacios Jaraquemada JM. Estudio de la circulación arterial de la pelvis: consideraciones quirúrgicas.
[Anatomy study of arterial circulation of the pelvis. Surgical considerations] Doctorate thesis (in Span-
ish). School of Medicine, University of Buenos Aires, 1997.
30. Palacios Jaraquemada JM, Pesaresi M, Nassif JC et al. Aortic cross-clamping in obstetrics. Available from:
www.obgyn.net/displayarticle.asp?page¼/english/pubs/features/POV-aortic_cross [On line September
2001].
31. Keogh J & Tsokos N. Aortic compression in massive postpartum hemorrhage-An old but lifesaving
technique. Aust NZ Obstet Gynaecol 1997; 37: 237–238.
32. Greenberg JI, Suliman A, Iranpour P et al. Prophylactic balloon occlusion of the internal iliac arteries to
treat abnormal placentation: a cautionary case. Am J Obstet Gynecol 2007; 197(5): 470.e1–470.e4.
33. Bodner LJ, Nosher JL, Gribbin C et al. Balloon-assisted occlusion of the internal iliac arteries in patients
with placenta accreta/percreta. Cardiovasc Intervent Radiol 2006; 29: 354–361.
*34. Burchell RC. Arterial physiology of the human female pelvis. Obstet Gynecol 1968; 31: 855–860.
*35. Palacios Jaraquemada JM, Garcı́a Mónaco R, Barbosa NE et al. Lower uterine blood supply: extrauterine
anastomotic system and its application in the surgical devascularization techniques. Acta Obstet Gynecol
Scand 2007; 86: 228–234.
36. El-Shalakany AH, Nasr El-Din MH, Wafa GA et al. Massive vault necrosis with bladder fistula after uter-
ine artery embolisation. BJOG 2003; 110: 215–216.
37. Chou YJ, Cheng YF, Shen CC et al. Failure of uterine arterial embolization: placenta accreta with pro-
fuse postpartum hemorrhage. Acta Obstet Gynecol Scand 2004; 83: 688–690.
1148 J. M. Palacios-Jaraquemada
38. Torreblanca Neve E, Merchan Escalante G, Walter Tordecillas MA et al. Ligation of the hypogastric
arteries. Analysis of 400 cases. Ginecol Obstet Mex 1993; 61: 242–246.
39. Guillot E, Raynal P, Fuchs F et al. Failure of a conservative treatment of a placenta accreta. Gynecol Obstet
Fertil 2006; 34: 1055–1057.
40. Capechi E. Placenta accreta abbondonata in utero cesarizzato. Ritorno progressivo di questo allo stato
normale sensa alcuna complicanza (reàsorbimiento autodigestione uterina della placenta?). Policlin 1933;
40: 347.
41. Legro RS, Price FV & Caritis SN. Successful conservative treatment of placenta percreta. Am J Obstet
Gynecol 1995; 172: 1648–1649.
42. Courbiere B, Bretelle F, Porcu G et al. Conservative treatment of placenta accreta. J Gynecol Obstet Biol
Reprod 2003; 32(6): 549–554.
43. Palacios Jaraquemada JM, Monge F & Paesani F. One step conservative surgery in anterior placenta per-
creta by Pfannenstiel incision. Available from: http://www.obgyn.net/hysterectomy-alternatives/hyster-
ectomy-alternatives.asp?page¼articles/jaraquemada_placenta-percreta [On line February 2008].
44. Crespo R, Lapresta M & Madani B. Conservative treatment of placenta increta with methotrexate. Int J
Gynaecol Obstet 2005; 91: 162–163.
45. Chiang YC, Shih JC & Lee CN. Septic shock after conservative management for placenta accreta. Taiwan
J Obstet Gynecol 2006; 45: 64–66.
46. Samama CM, Albaladejo P, Benhamou D et al. Venous thromboembolism prevention in surgery and ob-
stetrics: clinical practice guidelines. Eur J Anaesthesiol 2006; 23: 95–116.
47. Chou MM. Prenatal diagnosis and management of placenta previa accreta: past, present and future.
Taiwan J Obstet Gynecol 2004; 43: 64–71.
48. Uszyński W & Uszyński M. Placenta accreta: epidemiology, molecular mechanism (hypothesis) and
some clinical remarks. Ginekol Pol 2004; 75: 971–978.
49. Tseng JJ & Chou MM. Differential expression of growth-, angiogenesis and invasion-related factors in
the development of placenta accreta. Taiwan J Obstet Gynecol 2006; 45: 100–106.