Are anthropometric data a tool for determining the severity of OHSS? Yes, it could be!
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BACKGROUND: All management guidelines of ovarian hyperstimulation syndrome (OHSS) recommend daily monitoring of women's body weight, waist circumference and note that as indicators increase, the severity OHSS also increases. However, the dynamics of abdominal size and its relationship with markers of OHSS severity have not been highlighted. The purpose of this study is to assess the usefulness of various anthropometric indicators for determining the degree of OHSS severity as well as paracentesis indications. METHODS: Observational study including 76 women complaining with OHSS. Clinical history, physical examination, laboratory tests, and ultrasound measurement of the ovarian volume (OV) and ascites index (AsI) were done in all cases. Intra-abdominal pressure (IAP) was assessed using an intravesical manometer. The anteroposterior diameter of the abdomen (APD) and transverse diameter of the abdomen (TS) were measured with a pelvimeter. The APD/TS ratio was calculated. RESULTS: The APD/TS ratio increased progressively and tended to be the highest in the most symptomatic stage of OHSS (Kruskal-Wallis test, p < 0.001). The median APD/TS was significantly lower in patients with mild OHSS (0.55 [IQR, 0.44-0.64]) compared with severe OHSS (0.87 [IQR, 0.80-0.93]; p < 0.001) or critical OHSS (1.04 [IQR, 1.04-1.13]; p < 0.001). Similarly, the median APD/TS of the moderate OHSS group (0.65 [IQR, 0.61-0.70]) was significantly lower than that of the severe (p < 0.001) and critical OHSS group (p = 0.001). There was a strong positive correlation between APD/TS and IAP (Spearman's r = 0.886, p < 0.01). The APD/TS ratio showed a significant positive correlation with AsI (Spearman's r = 0.695, p < 0.01) and OV (Spearman's r = 0.622, p < 0.01). No significant differences were observed in age, height, weight, body mass index, hip circumference or waist circumference between moderate, severe and critical OHSS groups. CONCLUSIONS: The APD/TS ratio is related to the severity of OHSS. Monitoring APD/TS dynamics could be a method of indirectly controlling intra-abdominal volume, compliance of the abdominal wall and IAP. In conjunction with clinical and laboratory data, APD/TS might be an indicator for paracentesis.
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Abstract
Background: All management guidelines of ovarian hyperstimulation syndrome (OHSS) recommend daily moni‑
toring of women’s body weight, waist circumference and note that as indicators increase, the severity OHSS also
increases. However, the dynamics of abdominal size and its relationship with markers of OHSS severity have not been
highlighted. The purpose of this study is to assess the usefulness of various anthropometric indicators for determining
the degree of OHSS severity as well as paracentesis indications.
Methods
Observational study including 76 women complaining with OHSS. Clinical history, physical examination,
laboratory tests, and ultrasound measurement of the ovarian volume (OV) and ascites index (AsI) were done in all
cases. Intra‑abdominal pressure (IAP) was assessed using an intravesical manometer. The anteroposterior diameter of
the abdomen (APD) and transverse diameter of the abdomen (TS) were measured with a pelvimeter. The APD/TS ratio
was calculated.
Results
The APD/TS ratio increased progressively and tended to be the highest in the most symptomatic stage of
OHSS (Kruskal–Wallis test, p < 0.001). The median APD/TS was significantly lower in patients with mild OHSS (0.55
[IQR, 0.44–0.64]) compared with severe OHSS (0.87 [IQR, 0.80–0.93]; p < 0.001) or critical OHSS (1.04 [IQR, 1.04–1.13];
p < 0.001). Similarly, the median APD/TS of the moderate OHSS group (0.65 [IQR, 0.61–0.70]) was significantly lower
than that of the severe (p < 0.001) and critical OHSS group (p = 0.001). There was a strong positive correlation between
APD/TS and IAP (Spearman’s r = 0.886, p < 0.01). The APD/TS ratio showed a significant positive correlation with AsI
(Spearman’s r = 0.695, p < 0.01) and OV (Spearman’s r = 0.622, p < 0.01). No significant differences were observed in
age, height, weight, body mass index, hip circumference or waist circumference between moderate, severe and criti‑
cal OHSS groups.
Conclusions
The APD/TS ratio is related to the severity of OHSS. Monitoring APD/TS dynamics could be a method of
indirectly controlling intra‑abdominal volume, compliance of the abdominal wall and IAP . In conjunction with clinical
and laboratory data, APD/TS might be an indicator for paracentesis.
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Open Access
*Correspondence: [email protected]
1 Clinic Institute of Gynecology, Obstetrics and Neonatology, Faculty
of Medicine, University of Barcelona, Hospital Clinic‑Institut d´Investigacions
Biomèdiques August Pi i Sunyer (IDIBAPS), Villarroel 170, 08036 Barcelona,
Spain
Full list of author information is available at the end of the article
Page 2 of 7Petrenko et al. BMC Women’s Health (2022) 22:155
Background
Ovarian hyperstimulation syndrome (OHSS) is a largely
iatrogenic condition, associated with significant mor -
bidity and even mortality of healthy women undergoing
fertility treatment [1, 2]. Generally, OHSS is triggered
by human chorionic gonadotropin (hCG) and it’s mainly
due to excessive ovarian secretion of vascular endothe -
lial growth factor and other angiogenic factors, increas -
ing vascular permeability and causing fluid leakage into
the third space [3, 4]. Thus, OHSS is characterized by
enlarged ovaries with hypovolemia and haemoconcen -
tration, in more severe cases including ascites, hyperco -
agulation, renal failure and even multiple organ failure in
the critical ones [2]. The main principles in moderate and
severe OHSS treatment are correction of hypovolemia,
electrolyte imbalance, hypoalbuminemia and paracente -
sis, if necessary [5].
Ascites progression and ovarian enlargement with
OHSS leads to an increase in intra-abdominal pressure
(IAP), and in severe and critical formsto the abdominal
compartment syndrome (ACS) and associated severe
organ dysfunction, which is the main factor of poor
outcome among women with this syndrome [6, 7]. Our
previous study revealed OHSS as a classic model of intra-
abdominal hypertension (IAH) syndrome, where IAP is
an important diagnostic marker, allied with the OHSS
severity [8]. It has been proposed, there was provided to
use the IAH level and ascites index (AsI), for paracente -
sis’s indications in combination with clinical and labora -
tory data. The IAP measuring through a Foley catheter
by using a pressure transducer is the gold standard [9],
but, unfortunately, it has not yet become widespread in
gynecological and obstetric practice. Finding a simpler
and more convenient method for indirect controlling
intra-abdominal volume (IAV), abdominal wall compli -
ance (Cab) and IAP without the use independently of
complex and expensive techniques would be useful for
OHSS management.
All OHSS management guidelines recommend daily
monitoring of women’s body weight, waist circumference
(WC) and note that as indicators increase, the severity of
OHSS also increases [5, 10–12]. However, according to
the literature data, the dynamics of abdominal size and
its relationship with markers of OHSS severity have not
been highlighted.
The purpose of this study is to assess the usefulness of
various anthropometric indicators in determining degree
of OHSS severity as well as indications for paracentesis.
Methods
Sample
A total of 76 infertile women who were in an in vitro fer -
tilization program and presented OHSS were included
in this study. Sample size was established based on the
fact that according to the Ministry of Health of the Sara -
tov Region, during the period from 2015 to 2019, 4800
cycles of ART were performed in all medical institutions
of the region. Complications presented by various forms
of OHSS requiring outpatient monitoring and hospitali -
zation, were recorded in 95 cases (1.9%). Thus, using the
statistical software to calculate the sample size with a
5% maximum acceptable error, 95% confidence level, we
obtained a sample size of 76 women with OHSS. All of
them were admitted into the gynaecological department
of the city clinical hospital No.1 named after Yu.Ya. Gor -
deev (Saratov, Russian Federation). Anthropometrical,
laboratory and clinical data were recorded in all included
subjects (Additional file 1: Table S1, Additional file 2:
Table S2 and Additional file 3: Table S3). The age range
of the study participants was from 20 to 40 years old and
the body mass index (BMI) was from 16.9 to 24.1 kg/m2.
OHSS was classified according to the Royal College of
Obstetricians & Gynaecologists guidelines [5]. Therefore,
patients were allocated into four groups depending on
the severity of OHSS: mild OHSS (group I, n = 25), mod-
erate OHSS (group II, n = 25), severe OHSS (group III,
n = 21), and critical OHSS (group IV, n = 5). Early-onset
OHSS was defined when the syndrome was initiated dur -
ing the first 9 days after trigger administration of hCG,
and late OHSS was defined when the syndrome was
initiated from 10 days after. The current study included
19 (25%) women with early OHSS and 57 (75%) women
with late OHSS. The IAP was measured 4 [IQR, 3–5]
days after hCG administration in case of early OHSS
and 17 [IQR, 13–19] days after hCG triggering in case of
late OHSS. The average length of stay for subjects with
early OHSS was 10 [IQR, 7–12] days; the average length
of a hospital stay for women with late OHSS was 9 [IQR,
7–11] days. All women admitted with the diagnosis of
OHSS were considered for inclusion in the study. Those
who voluntarily refused to participate were excluded.
Procedures
Anthropometrical and clinical data were recorded in all
included subjects (Additional file 2: Table S2 and Addi-
tional file 3: Table S3). The anteroposterior diameter
of the abdomen (APD) and transverse diameter of the
Keywords
Ovarian hyperstimulation syndrome, Anthropometic indicators, Intra‑abdominal pressure, Intra‑
abdominal hypertension, Ascites index, Compliance of the abdominal wall
Page 3 of 7
Petrenko et al. BMC Women’s Health (2022) 22:155
abdomen (TS) were measured with a pelvimeter. The
APD was defined as the distance between the spine at
the L3–4 level and the abdomen apex, then the pelvimeter
branches were rotated in the same plane, set along the
midaxillary lines, and after that, TS measurement was
made. The APD/TS ratio was calculated.
BMI was evaluated by the Quetelet’s equation, and in
all cases blood and urine samples were obtained. Ovar -
ian size and pelvic and abdominal free fluid were assessed
by ultrasound (Accuvix XG [Samsung MEDISON Co.
Ltd. Korea]) using 3.5 MHz sectoral sensors. The ovarian
volume (OV) using the prolate ellipsoid formula [13] and
the AsI [14] was measured as previously described [8].
Finally, the IAP was determined using a Foley catheter
with a pressure transducer [9].
Statistical analysis
The data were analysed using a personal computer-based
software package (SPSS 26.0, SPSS Inc. Headquarters,
233 South Wacker Drive, 11th Floor, Chicago, IL 60606,
USA). The Shapiro–Wilk test was used to determine the
normal distribution of the sample. Data for non-normally
distributed variables are given as the median [interquar -
tile range]. Homogeneity of within-group variances was
evaluated by Levene’s test. The Kruskal–Wallis test was
used to analyse differences between groups. Statistically
significant results were followed by Mann–Whitney
U-tests with Bonferroni adjustment to detect subgroup
differences. Spearman’s correlation coefficients were
used to check the association between continuous vari -
ables. All probability tests were two-sided and a p-value
of < 0.05 was considered significant.
Results
Anthropometrical data are given in Additional file 3:
Table S3. The age range of the study participants was
from 20 to 40 years old and the BMI was from 16.9 to
24.1 kg/m2.
Significant differences between groups were observed
regarding APD measurements (p < 0.001). The median
APD of the mild OHSS group (16 [IQR, 15–19]) was
found to be significantly lower than that of the severe
(24 [IQR, 23–27], p < 0.001) and critical OHSS group (26
[IQR, 24–28], p = 0.001). Besides that, the median APD
of the moderate OHSS group (19 [IQR, 17–24]) was sig -
nificantly lower than that of the severe (p < 0.005) and
critical OHSS group (p 0.05).
As expected, APD/TS increased progressively and
tended to be the highest in the most symptomatic stage
of OHSS (p < 0.001). Figure 1 represents the intergroup
comparison of APD/TS. The median APD/TS was sig -
nificantly lower in patients with mild OHSS (0.55 [IQR,
0.44–0.64]) compared with severe OHSS (0.87 [IQR,
0.80–0.93]; p < 0.001) or critical OHSS (1.04 [IQR, 1.04–
1.13]; p < 0.001). Similarly, the median APD/TS of the
moderate OHSS group (0.65 [IQR, 0.61–0.70]) was sig -
nificantly lower than that of the severe (p 0.05).
No significant differences were observed in age, height,
weight, body mass index, hip circumference or waist cir -
cumference between moderate, severe and critical OHSS
groups (Additional file 2: Table S2). There was also no
significant difference between the early and late OHSS
groups (p > 0.05).
Correlation analysis was used to identify whether
the APD/TS was independently associated with other
anthropometric indicators and IAP , AsI or OV. As antici-
pated, there was a strong positive correlation between
APD/TS and IAP (Spearman’s r = 0.886, p < 0.01; Fig. 2a).
Besides that, APD/TS showed a significant positive cor -
relation with AsI (Spearman’s r = 0.695, p < 0.01; Fig. 2b)
and OV (Spearman’s r = 0.622, p < 0.01; Fig. 2c). No sig -
nificant correlation was present between APD/TS and
any of the other anthropometric indicators, except for a
weak inverse correlation with WC (Spearman’s r = −0.24,
p < 0.05). A significant but weak inverse correlation was
observed between APD/TS and the age (Spearman’s
r = −0.285, p < 0.05).
Discussion
In a previous study, we made an analogy between OHSS
and IAH syndrome documenting the importance of
dynamic monitoring of IAP , AsI and OV. All these
II II II IV
0.0
0.5
1.0
1.5
OHSS
APD/TS
Fig. 1 APD/TS according to severity of ovarian hyperstimulation
syndrome. Data are plotted as median with range
Page 4 of 7Petrenko et al. BMC Women’s Health (2022) 22:155
parameters were significantly associated with the OHSS
severity [8]. In the present research, we studied the
women’s anthropometric data and their relationship with
OHSS severity.
All OHSS management guidelines emphasize the
importance of daily monitoring of weight and WC in
women and simply state the fact that the severity of
OHSS increases with increasing these parameters [5,
10–12]. In our work, we did not observe significant dif -
ferences in weight, BMI, HC or WC between moderate,
severe and critical OHSS groups. Our data are consistent
with those by Ma et al., who noted that increasing BMI is
not a risk factor for OHSS severity [15]. Malbrain et al.,
when examining patients in intensive care, also stated
that there was no significant correlation between abdom-
inal circumference and IAP level [16].
It is a well-known that IAP is determined by two ele -
ments—the IAV and Cab [17]. The WC in women
reflects approximate IAV, but not Cab and associated
IAP . Women can have the same ascetic fluid amount, but
different Cab, different possibilities for abdominal cavity
accommodation and, as a result, different IAP . According
to the World Society of Abdominal Compartment Syn -
drome (WSACS) experts, Cab plays a key role in under -
standing the negative effects of unadapted IAV on IAP
and organ perfusion, although it is currently one of the
most neglected parameters in critically ill patients [18].
Cab extension indicates a loss of abdominal wall elastic -
ity, while a decrease in Cab means that the same change
in IAV will result in a larger change in IAP .
Malbrain et al., in their fundamental work, studied the
stages of changing in the abdominal shape in critically ill
patients with IAH/ACS and revealed a change from an
ellipse to a sphere with a maximum increase in IAP val -
ues. The authors described three phases of the ongoing
processes: the reshaping, stretching, and pressurisation
phases [19].
In the presented study, we obtained similar results. In
the absence of significant intergroup differences in WC,
the median APD in the moderate OHSS group was sig -
nificantly lower than in the severe and critical OHSS
group. Obviously, with the progression of ascites, APD
increases most of all. The APD/TS ratio progressively
increased and was highest at the most symptomatic stage
of OHSS (Fig. 1). When the ratio APD/TS is approach -
ing to 1, i.e. when the transverse and anteroposterior
dimensions became equal, the abdomen took the sphere
form with the transition from severe to critical OHSS.
No significant difference in the APD/TS between mild
and moderate OHSS can be explained by the fact that
in moderate form there is a small amount of ascitic fluid
with a sufficient elasticity reserve of the anterior abdom -
inal wall and APD, as well as TS change insignificantly.
Also, between severe and critical OHSS, there was no
significant difference in the APD/TS. It can be due to
the fact, that in severe form with exhaustion of abdomi -
nal stretching allowance, even a small addition of ascitic
a
01 02 03 0
0.0
0.5
1.0
1.5
Spearman’s r = 0.886, p<0.01
IAP, mmHg
APD/TS
b
01 00 2003 00 400
0.0
0.5
1.0
1.5
Spearman’s r = 0.695, p<0.01
Ascites index, mm
APD/TS
c
02 00 4006 00 800 1000
0.0
0.5
1.0
1.5
Spearman’s r = 0.622, p<0.01
Ovarian volume, ml
APD/TS
Fig. 2 Scatter plots of APD/TS related to intra‑abdominal pressure
(a), ascites index (b) and ovarian volumes (c)
Page 5 of 7
Petrenko et al. BMC Women’s Health (2022) 22:155
fluid slightly changes both, APD and TS, but causes an
exponential increase in IAP with the transition to critical
OHSS. Correlation analysis also confirmed a significant
positive correlation between APD/TS and OHSS sever -
ity markers, where the strongest positive correlation was
between APD/TS and IAP .
It can be assumed that women with severe OHSS had
an initially lower Cab compared with mild OHSS, and
an increase in additional IAV with limited Cab led to a
progressive IAP increase. Unfortunately, Cab measure -
ment and estimation are difficult at the patient’s bed -
side and can only be done in a case of change (removal
or addition) in IAV [20]. This limitation also applies to
IAV, which can be assessed by three-dimensional ultra -
sound, water-suppressed magnetic resonance imaging
and computed tomography [19]. These are complex and
expensive techniques which have not yet gained access
to widespread clinical practice. Weak inverse correla -
tion of APD/TS with WC seems illogical, although it
can be explained by the fact that with increasing sever -
ity of OHSS, the median WC and BMI in the groups
decreased, and the median Height increased (Additional
file 2: Table S2). Thus, it can be stated that, asthenic type
of constitution prevailed in the groups with severe and
critical OHSS. The obtained results are consistent with
the literature data, where asthenic habitus is indicated as
one of the leading risk factors for the OHSS development
[2, 10].
In a study assessing the IAV physiology during preg -
nancy, the authors confirm that the IAV capacity and the
tensile properties of pregnant women’s abdominal wall
can be predicted by the dynamics of the anteroposte -
rior and transverse abdominal diameters [21]. It should
be pointed out that the current clinical guidelines rep -
resent pregnancy as a chronic compensated state of
IAP , where the abdominal wall slowly stretches, its Cab
gradually increases, and the pregnant woman has time
to adapt to slowly increasing IAP levels [22]. Whereas
OHSS is a dynamic condition, a rapid increase in volume
and/or pressure exceeds Cab, because there is no time
for tissue adaptation and moderate OHSS can progress
to severe OHSS within a few hours [6]. Many authors
confirm that in such cases, paracentesis is the single
most important treatment modality for life-threatening
OHSS which isn’t controlled by medical therapy [23–26].
Having the absence of the ability to measure IAP and
Cab, the dynamics of the APD/TS ratio can be a surro -
gate indicator of the IAH degree, IAV increase, reserve
capabilities of the abdominal wall’s extensibility and can
help in establishing indications for timely performed
paracentesis.
Conclusions
The APD/TS ratio and its dynamics are important
markers of OHSS severity. The APD/TS ratio increases
progressively, reaching the highest values in the most
symptomatic stage of OHSS.
IAP showed the strongest positive correlation with the
APD/TS ratio; however, significant correlations were also
found between APD/TS and AsI and OV.
When the ratio APD/TS is approaching to 1, and the
anteroposterior and transverse abdominal dimensions
become equal, the abdomen changes from an ellipse
to a sphere, the reserve of abdominal wall stretching is
depleted, and IAP exponential growth is observed with
the transition from severe to critical OHSS. The APD/
TS monitoring can be a method of indirectly control -
ling IAP , Cab and IAV reserve, without using com -
plex and expensive techniques. The inclusion of APD/
TS monitoring in the standard for the management of
OHSS might be useful in specifying the severity and
timely initiation of treatment, including methods to
reduce IAP , prevent further organ dysfunction, and
avoid the transition to a more severe stage of IAH and
ACS. Finally, in the absence of IAP monitoring capabil -
ities, the APD/TS ratio in conjunction with clinical and
laboratory data might be an additional tool for indica -
tion for paracentesis.
Abbreviations
ACS: Abdominal compartment syndrome; APD: Anteroposterior diameter
of the abdomen; AsI: Ascites index; Cab: Compliance of the abdominal wall;
IAH: Intra‑abdominal hypertension; IAP: Intra‑abdominal pressure; IAV: Intra‑
abdominal volume; OHSS: Ovarian hyperstimulation syndrome; OV: Ovarian
volume; TS: Transverse diameter of the abdomen.
Supplementary Information
The online version contains supplementary material available at https:// doi.
org/ 10. 1186/ s12905‑ 022‑ 01701‑5.
Additional file 1: Table S1. Baseline patients’ characteristics.
Additional file 2: Table S2. Clinical and laboratory data according to the
severity of ovarian hyperstimulation syndrome.
Additional file 3: Table S3. Anthropometric markers according to the
degree of severity of the ovarian hyperstimulation syndrome.
Acknowledgements
The authors would like to thank all the women who kindly accepted to partici‑
pate in this study.
Author contributions
AP , DM and MB took part in patient recruitment for the study and conducted
clinical trials. AP , CCB, DM, and EN designed the study. AP , CCB, DM, and EN
took part in the analysis and interpretation of data and revision of the draft. AP ,
CCB, DM, and EN wrote the manuscript. CCB, AK, and ES revised critically for
important intellectual content. All authors approved the final version of the
manuscript. All authors had full access to all of the data in the study (including
statistical reports and tables) and can take responsibility for the integrity of the
Page 6 of 7Petrenko et al. BMC Women’s Health (2022) 22:155
data and accuracy of the data analysis. All authors read and approved the final
manuscript.
Funding
This research received no specific grant from any funding agency in the pub‑
lic, commercial, or not‑for‑profit sectors.
Availability of data and materials
The study was registered at the ISRCTN registry; identifier: ISRCTN66235250,
http:// www. isrctn. com/ ISRCT N6623 5250 and https:// doi. org/ 10. 1186/ ISRCT
N6623 5250; Data are available at: Castelo‑Branco, Camil (2021), “Severity Mark‑
ers in Women with Ovarian Hyperstimulation Syndrome” , Mendeley Data, V1,
https:// doi. org/ 10. 17632/ ryhtp s673s.1.
Declarations
Ethics approval and consent to participate
Written informed consent was obtained from all the patients. The study was
approved by the Ethics Committee of the Saratov State Medical University
named after V. I. Razumovsky, Saratov, Russian Federation (IORG0004384, P .№7;
6 March 2018) and was performed in accordance with the Declaration of
Helsinki II and the ICH Guidelines for Good Clinical Practice.
Consent for publication
Not applicable.
Competing interests
On behalf of all authors, the corresponding author states that there is no
conflict of interest.
Author details
1 Clinic Institute of Gynecology, Obstetrics and Neonatology, Faculty
of Medicine, University of Barcelona, Hospital Clinic‑Institut d´Investigacions
Biomèdiques August Pi i Sunyer (IDIBAPS), Villarroel 170, 08036 Barcelona,
Spain. 2 Department of Emergency Anesthesiology‑Resuscitation Care
and Simulation Technologies in Medicine, Saratov State Medical University
named after V. I. Razumovsky, Saratov, Russian Federation. 3 Department
of Anesthesiology and Critical Care, State Budgetary Healthcare Institution
of Moscow Region M.F. Vladimirsky Moscow’s Regional Research Clinical Insti‑
tute, Moscow, Russian Federation. 4 City Clinical Hospital №1 named after Yu.
Ya. Gordeev, Saratov, Russian Federation. 5 Department of Hospital Surgery,
Saratov State Medical University named after V. I. Razumovsky, Saratov, Russian
Federation.
Received: 3 November 2021 Accepted: 5 April 2022
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