Peritoneal Lavage
Peritoneal Lavage
Peritoneal Lavage
To cite this article: Osman Temizkan, Osman Asıcıoglu, Kemal Güngördük, Berhan Asıcıoglu,
Pınar Yalcin & Isil Ayhan (2015): The effect of peritoneal cavity saline irrigation at cesarean
delivery on maternal morbidity and gastrointestinal system outcomes, The Journal of
Maternal-Fetal & Neonatal Medicine
Article views: 30
ORIGINAL ARTICLE
Abstract Keywords
Objective: The objective of this study is to investigate the effect of peritoneal cavity saline Cesarean, emesis, irrigation, nausea
irrigation during cesarean section (CS) on gastrointestinal disturbance and postoperative
infectious morbidity (PIM). History
Methods: This prospective randomized clinic trial included 430 women who underwent elective
or primary CS. The participants were randomized to either an irrigation of the abdominal cavity Received 14 January 2015
or the control group. The primary outcome measured was the rate of antiemetic drugs required Accepted 2 February 2015
in the postoperative period following CS. Secondary outcome measures included the rate of Published online 24 February 2015
PIM.
Results: Participants in both groups had similar demographic and clinical characteristics.
The rate of antiemetic drugs required by patients was significantly higher in the irrigation
group when compared with the control group (15.8% versus 8.4%, p ¼ 0.018). The rate
of intraoperative nausea and emesis (p 0.001) and the rate of postoperative nausea and
emesis (p 0.001 and p ¼ 0.018, respectively) were significantly higher in the irrigation group
compared with the control group.
Conclusions: Irrigation with saline at the time of CS increases both intraoperative and
postoperative nausea and emesis without any beneficial effects on PIM. Routine use of saline
irrigation in the abdominal cavity does not seem to be reasonable.
gastrointestinal disease were excluded. Elective CS was and temperature). Uterine tonus was monitored every 15 min
defined as CS performed before the presence of labor with for 2 h, and then every 4 h. The Foley catheter was removed
or without previous CS history. Primary CS was defined as on the first postoperative day. The physician staff responsible
women with no previous CS history. for collection of patient reported nausea symptoms were
Following informed consent, all participants completed a blinded to group randomization. Examination of the surgi-
form providing information on age, parity, body mass index, cal incision, notation of return of GI function, and a
existing comorbidities, and use of tobacco or alcohol. After complete blood count were standard orders for the first
this, the participants were randomized to either an irrigation postoperative day.
group or a control group. Assignment to one of the two The primary outcome measured was the rate of antiemetic
treatment groups was determined using a random number drugs required in the postoperative period following cesarean
table. The assigned treatments were written on cards and delivery. Secondary outcome measures included the rate of
sealed in secure opaque envelopes numbered in sequence. The PIM. Other outcomes evaluated were nausea and emesis
surgeons were not blinded to the procedure allocation. The occurring during the postoperative hospitalization. These
allocated envelope was opened by the surgeon just before were determined via routine physician assessment of nausea,
surgery, and the procedure allocation was recorded on each emesis, and requirement of antiemetic drugs during the
woman’s chart. postoperative period. Return of bowel function was defined as
Before CS, a Foley catheter was inserted, and the hair on passage of flatus. Postoperative physicians were blinded to
the abdomen was shaved. The skin was cleaned with povidone group assignment to avoid any potential bias; however, the
iodine solution. All operations were performed under regional surgeon who performed the operative procedure cared for
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anesthesia and the anesthetist used 5 mL of 0.5% bupivacaine the patient in the postoperative period, thus, was not blinded
(Marcaine Spinal Heavy, AstraZeneca, Istanbul, Turkey). All to the study group. Postpartum endometritis was defined as a
operations were performed by the first and second authors body temperature greater than 38.5 C with concomitant foul
(obstetrics and gynecology surgeons: O. A. and O. T.). smelling discharge or abnormally tender uterus on bimanual
Pfannenstiel incisions were used on all patients. The fascial examination. Febrile morbidity was defined as an elevated
aponeurosis was freed from the underlying rectus abdominis temperature of 38 C or higher for a minimum of 24 h
muscles in both cranial and caudal directions. After the following surgery, not associated with lower abdominal or
caudal-cut aponeurosis was elevated under tension, the rectus pelvic tenderness, or other signs of infection. Wound infection
muscles were separated on midline. The peritoneum was was characterized by partial or total separation of the incision,
opened in an identical manner using a vertical midline as well as the presence of purulent or serous wound discharge
incision. A bladder flap was not created routinely. The uterine with induration, warmth, and tenderness.
incision was initially created with a scalpel to incise the lower Estimated blood loss was calculated using the difference
uterine segment transversely for 1–2 cm in the midline. The in hematocrit values taken before and 48 h after cesarean
uterine incision was then expanded using blunt methods. delivery, according to the following formula:
The placenta was delivered by controlled cord traction. The
anesthetist administered a 5 IU intravenous bolus of oxytocin Estimated blood loss
0 1
(Syntocinon, Novartis, Basel, Switzerland) over 5–10 s to Preoperative hematocrit
each woman when the umbilical cord was clamped. Then, B C
Estimated blood volume @ Postoperative A
30 IU of oxytocin in 500 mL lactated Ringer solution was
administered at a rate of 125 mL/h, and this was continued for hematocrit
¼
4 h. A total of 1 -g cefazolin diluted in 20 mL normal saline Preoperative hematocrit
was administered over a 5-min period. Patients were not given
any additional drugs intraoperatively. The uterine incision was where the estimated blood volume in milliliters ¼ woman’s
sutured without exteriorization of the uterus. After hemostasis weight in kilograms 85 [15].
was secured, the irrigation group underwent irrigation of the All data were recorded and analyzed by another researcher,
abdominal cavity using 500 mL of warm normal saline after who was blinded to the group assignments.
closure of the uterine incision but before closure of the Viney et al. [14] reported that the rate of use of antiemetic
abdominal wall. All blood clots, vernix, and other debris were drugs was 18%. Based on this previously reported rate of
evacuated from the paracolic gutters, anterior and posterior antiemetic drug use, a sample size of 215 per group was
cul-de sacs, and under the bladder flap when employed. In required to detect to a 50% difference in the rate of antiemetic
patients assigned to the control group without irrigation, all drug use between groups, with a power of 80% and level of
clots, vernix, and other debris were left in place. The significance of 5%. Chi-squared tests were used to analyze
abdominal wall was closed in layers without closure of the categorical variables. Student’s t-test and Mann–Whitney’s
peritoneum. Occasional cauterization of subcutaneous tissue U-test were used for continuous variables. The relative risk
was performed to secure hemostasis. The skin was closed (RR), with 95% confidence interval (CI), was calculated.
using 3-0 Vicryl sutures. If patients had nausea or emesis Statistical significance was set at p50.05.
during the cesarean delivery, the observation was recorded
Results
systematically by the anesthetist who was blinded to the
treatment group. Between October 2012 and August 2014, 430 patients who
The postpartum care for both groups was identical and underwent elective cesarean delivery were randomized, with
included monitoring of vital signs (blood pressure, pulse rate, 215 randomized into the control group and 215 randomized
DOI: 10.3109/14767058.2015.1015415 Saline irrigation at CS 3
Figure 1. Participant flow chart (control Assessed for
group: without irrigation of the abdominal eligibility (n:1835)
cavity; irrigation group: irrigation of the
abdominal cavity using 500 mL of warm
normal saline after closure of the uterine
incision but before closure of the abdominal Excluded (n:1405)
wall). ENROLLMENT
*Refused the parcipitate
(n:55)
430 Randomized *Other reason (n:106)
*Not meeng inclusion
criteria (n:1244)
Analyzed ( n:215)
Analyzed (n:215) ANALYSIS
Table 4. Findings related to neonatal outcome. to peritoneal irritation from the peritoneal saline irrigation.
Also Viney et al. [14] reported that postoperative nausea,
Control Irrigation
group group
emesis, and requirement rate of antiemetic drugs required
Neonatal outcome (n ¼ 215) (n ¼ 215) p value RR (CI 95%) were similar between groups. These findings differed from
the present study. In the present study, postoperative GI
Birth weight (g) 3314 ± 457 3372 ± 374 0.150 _
5-min Apgar 3 2 (0.9) 2 (0.9) _ _ outcomes, such as emesis, nausea, and requirement rate of
NICU admission 1 (0.5) 2 (0.9) 0.562 0.5 (0.04–5.4) antiemetic drug were significantly higher in the irrigation
group than those in the control group, resulting in impaired
Data are expressed as the mean ± standard deviation or n (%). NICU,
neonatal intensive care unit.
postoperative patient comfort. This finding was attributed to
the insufficient drainage of saline from abdominal cavity
intraoperatively, with residual saline resulting in peritoneal
irrigation on intraoperative nausea and vomiting. Viney et al. irritation. Furthermore, no significant differences were
[14] evaluated the effect of intraoperative irrigation on detected in neonatal outcomes between groups. Only
intraoperative nausea and vomiting and postoperative return Harrigill et al. [13] has evaluated neonatal outcomes with
of bowel function after cesarean delivery. However, the study saline irrigation, and they found similar findings to the
did not include an adequate sample size to detect differences. present study.
Furthermore, in that study, the type of anesthesia during CS On one hand, the present study had several strengths. It
was not specified. Intraoperative nausea and emesis can be was a large prospective randomized investigation that
impacted by the anesthetic technique, as well as visceral included an adequate sample size. This investigation was
irritation. Therefore, the present study was designed as a conducted in a tertiary referral center in western Turkey.
prospective clinic trial with sufficient patient numbers, with Furthermore, there were similar demographic and pregnancy
all patients undergoing regional anesthesia. The primary profiles between groups. Experienced obstetricians performed
outcome was the rate of antiemetic drug use required in the all cesarean deliveries, and the average blood loss was
postoperative period, because postoperative patient comfort evaluated using an objective method. In addition, all cesarean
especially during early breastfeeding time was considered deliveries were performed under regional anesthesia. On the
important. other hand, the present study had several limitations. The
Viney et al. [14] reported that irrigation at the time of primary limitation was that only elective CS was included,
cesarean delivery increases intraoperative nausea, without and high-risk patients, such as those with corioamnionitis,
beneficial effects on maternal infectious morbidity. The HELLP syndrome, pre-eclampsia, and abnormal placentation,
present study results were similar to the intraoperative were excluded. Furthermore, there was potential for bias in
findings reported in that previous study. This was attributed determining intra and postoperative outcomes. However, the
DOI: 10.3109/14767058.2015.1015415 Saline irrigation at CS 5
clinical study was designed such that the study participants, 5. Bashore RA, Phillips WH, Brankman III CR. A comparison of the
morbidity of midforceps and cesarean delivery. Am J Obstet
anesthetist, postpartum physician staff, and data analyzer Gynecol 1990;162:1428–35.
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In conclusion, the present study demonstrates that irriga- 1987;157:557–62.
7. Magann EF, Dodson MK, Ray MA, et al. Preoperative skin
tion at the time of CS increases both intraoperative and preparation and intraoperative pelvic irrigation: impact on post-
postoperative nausea and vomiting, without any beneficial cesarean endometritis and wound infection. Obstet Gynecol 1993;
effects on maternal PIM. In the light of these findings, routine 81:922–5.
use of saline irrigation in the abdominal cavity does not seem 8. Cernadas M, Smulian JC, Giannina G, Ananth CV. Effects of
placental delivery method and intraoperative glove changing on
to be reasonable. Larger studies, involving subjects undergo-
postcesarean febrile morbidity. J Matern Fetal Med 1998;7:100–4.
ing emergency CS or in high-risk patients, are necessary to 9. Merchavy S, Levy A, Holcberg G, et al. Method of placental
confirm these findings. removal during cesarean delivery and postpartum complications.
Int J Gynaecol Obstet 2007;98:232–6.
10. Morales M, Boulvain M, Ceysens G, et al. Spontaneous versus
Acknowledgements manual placental delivery during cesarean section: a randomized
controlled trial. Am J Obstet Gynecol 2002;187:58–62.
We gratefully acknowledge the investigators, coinvestigators, 11. Magann EF, Washburne JF, Harris RL, et al. Infectious morbidity,
study coordinators, and the patients who participated in operative blood loss, and length of the operative procedure after
this trial. cesarean delivery by method of placental removal and site of
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12. Keblawi A, Dawley BL. Does saline irrigation in the peritoneal
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