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A rare cause of early post-partum haematuria
secondary to uterovesical fistula
Tahrir Basheer, Dominic Lee, Warren Davis, Rahul
Rindani
Uterovesical fistulae are uncommon, constituting 1–4%
of all urogenital fistulae.6,8 Although the
least common type of urogenital fistulae, they cannot be considered a rarity as
there are about 800 published cases.11 Most
Units report 1–5 cases over 5–15 year
periods.3 Presentation is variable, ranging
between 3–7 years post-delivery. There are few case reports about this
condition following vaginal birth after caesarean
(VBAC).8
In this article we outline the immediate diagnosis and the
management of a case involving this complication.
Case reportA 26-year-old woman, Gravida 2 Para 1, underwent labour. She
had a previous delivery by emergency lower-segment caesarean section at 40 weeks
gestation after a failed attempt at vacuum delivery. There was no other
significant past medical or surgical history.
The current pregnancy was complicated by intrauterine growth
restriction (IUGR) and multiple presentations for management of possible
antepartum haemorrhage in the last trimester. She was induced at 39 weeks by
artificial rupture of membranes (ARM) and syntocin infusion. She had an epidural
and in her third stage of labour she developed decelerations in her
cardiotocograph (CTG), which became deeper and wider. She progressed to a
vacuum-assisted and Wrigley’s forceps delivery. She had persistent frank
haematuria post-delivery with haemodynamic instability but mild pain and
generalised abdominal tenderness. A 50 ml saline bladder wash was performed;
unexpectedly the saline discharged from the vagina.
Dehiscence of the previous caesarean scar with formation of
a uterovesical fistula was the initial diagnosis. This was confirmed by
cystogram, ultrasound scan, and cystoscopy after involvement of the Urology Team
(see Figure 1). Conservative management with transurethral catheter was
instituted which failed after 4 months with persistent intermittent urine leak
per vaginum, and menouria.
Further discussion of surgical treatment by laparotomy was
conducted; a total abdominal hysterectomy and bladder repair with omental patch
was decided after considerable counselling.
Intraoperatively, dense
fibrous adhesions were noted between the lower segment of the uterus and the
bladder. A 2–3 cm fistula was located in the lower segment scar area
towards the left side of the uterus. The trigone and ureters were not involved.
The hysterectomy was completed and the bladder was repaired with an omental
patch. A transurethral catheter was left in situ on free drainage for 2
weeks. At 6 weeks post-surgery, she was continent.
Figure 1.
Uterovesical fistula (arrows) on ultrasound scan
![]() DiscussionWhile injury to the lower urinary tract is uncommon,
occurring in only 0.1–0.3% of births,3
however it is expected to increase worldwide because of an increase in caesarean
section rates. This complication is important from clinical, social, and
medicolegal aspects.
The causes of peripartum bladder and uterine injury
resulting in fistulae formation are nearly always iatrogenic. Risk factors
include severe dystocia, instrumental deliveries, manual removal of the
placenta, placenta accreta, uterine rupture, and previous caesarean
section.3 Labour induction with prostaglandins,
in particular ARM and IV syntocin, may be associated with an increased risk of
scar dehiscence in comparison to a spontaneous onset of labour this should be
emphasized in the consent process with women who have previously delivering via
caesarean section.
The development of a fistula
is believed to relate to higher attachment of the bladder relative to the lower
segment, usually secondary to scarring from previous surgery. With an
unrecognised bladder injury or suture transfixion of the bladder, a tract may
develop between the bladder and uterine wall. Other risk factors associated with
uterovesical fistula are malignancy, irradiation, and intrauterine
devices.
Józwik and
Józwik have proposed a classification for uterovesical fistula which is
based on the route of menstrual flow.7 Type 1
(Youssef syndrome) is menouria, amenorrhoea, and complete continence of urine.
Type 2 is dual direction menstrual flow via bladder and vagina. Type 3 is normal
vaginal menses but lack of menouria. The management of vesicouterine fistula can
be either conservative or surgical.
Conservative management is
indicated when the fistula is diagnosed early and is
small.1,2,10 Spontaneous healing is reported in
5% of women.1 Surgical treatment is indicated
when conservative treatment has failed or in cases involving a large fistula.
This is either through laparoscopy or laparotomy immediately after the diagnosis
(in 48 hours) or 3–4 months after diagnosis.
The operation can be
transperitoneal or retroperitoneal. Either repair of the uterus and the bladder
with excision of the fistulous track; or total abdominal hysterectomy and repair
of the bladder if the patient has completed her family; can be performed. A
transvesical approach involving fulguration of vesical
opening6 has also been described but with a
high recurrence rate. The pregnancy rate after repair has been reported to be
31.25–37.5% with a rate of term deliveries of
25%.1,14
Fistulae are prevented by
meticulous practice of surgical principles at caesarean section with
investigations for intraoperative haematuria, caudal retraction of the bladder,
and identification of the anatomical landmarks with suturing.
As authors, we recommend that
the management should be tailored by the size of the fistula. With small
fistulae, conservative management is recommended with expectation of spontaneous
closure in 4 months, while big fistulae need surgical treatment.
Author information: Tahrir Basheer,
Obstetrics Fellow; Dominic Lee, Urology Registrar; Warren Davis, Obstetrics and
Gynaecology Specialist; Rahul Rindani, Urologist; Department of Obstetrics and
Gynaecology, Department of Urology, The Wollongong Hospital, Wollongong, NSW,
Australia
Correspondence: Dr Dominic Lee, Department
of Obstetrics and Gynaecology, Department of Urology, The Wollongong Hospital,
Crown Street, Wollongong, NSW, Australia. Email: domi_2020@yahoo.com.au
References:
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