Supine Hypotensive Syndrome
Conditions
Brief summary
The aim of this study is to examine the effect of pelvic floor muscle exercises on the hemodynamic responses of the vena cava inferior in pregnant and non-pregnant women.
Detailed description
The IVC is responsible for approximately two-thirds of the total venous return to the heart. The blood flow in the IVC is affected by the respiratory and cardiac cycle. One of the factors affecting blood flow is pregnancy. Studies have shown that the hemodynamic responses of the IVC may vary depending on the position, and that the supine position puts pressure on the IVC during pregnancy. Compression of the growing fetus against the IVC can cause supine hypotensive syndrome and fetal danger. However, there is no definite finding about the effects of exercise performed in the supine position. Jefferys et al. reported that the reduction in blood flow at rest is twice that that occurs during exercise and that the level of blood flow should not be a cause for concern in healthy asymptomatic women who choose to exercise in the supine position in late pregnancy. Based on this information, we predict that pelvic floor muscle exercises can change the hemodynamic responses of the IVC and reduce the compression on it. In order to evaluate the effect of pelvic floor muscle exercises on hemodynamic responses of IVC and compression on it, pregnant and non-pregnant women will be measured by ultrasonography. Women eligible for the study will be seated and rested for 30 minutes before taking the measurement. Then, he will be taken to the supine position, rested for 2 minutes, and the first measurements will be taken at the 3rd minute. pelvic floor muscle exercises will be applied for 5 minutes as stated in the literature. Ultrasonographic measurements will be repeated in the supine position immediately after the pelvic floor exercises and 5 minutes after the exercise. Measurements will be applied to all participants in the same order. During the exercises blood pressure, heart rate and peripheral oxygen saturation will be monitored. Before and after the exercises, the heart rate and blood pressure parameters of the women will be recorded.
Interventions
Before the pelvic floor exercises are taught to all women participating in the study, a brief informational training about the function and structure of the pelvic floor and pelvis will be given using visuals. The application protocol will be given by experienced specialist physiotherapists who have received special training on pelvic floor muscle training. In this study, the training protocol described by Mørkved et al and Bø et al will be used. An exercise series will consist of slow and fast muscle contractions of the pelvic floor muscles. The exercise series will include 10 reps of maximum pelvic floor muscle contraction held for 6 seconds followed by three rapid muscle contractions. A 10-second rest period will be given between each exercise series. A total of 5 minutes, 4 repetitions of pelvic floor muscle contraction series will be applied, including the rest period.
Sponsors
Izmir University of Economics
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)
Masking description
Double (Participant, Outcomes Assessor)
Intervention model description
This research is a prospective and controlled study. The data of the study will be collected from pregnant women (Experimental group) and non-pregnant women (Control group).
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
Experimental group * Being pregnant between the ages of 18-40, * At least primary school graduate and able to read and write, * The gestational age is 20-40 weeks, * Not having any mental problems that prevent cooperation and understanding. Control group * Being a non-pregnant woman who is in the same age range as the experimental group, * At least primary school graduate and able to read and write, * Not having any mental problems that prevent cooperation and understanding.
Exclusion criteria
* Pregnant women with acute or chronic diseases with poor placental adaptation and vascular damage such as diabetes, chronic arterial hypertension and preeclampsia, as the fetus is closer to the threshold of hypoxia and acidemia and adaptive phenomena may fail, * Pregnant women with intra-uterine growth restriction and fetal anomaly, * Pregnant women with cardiovascular disease, * Pregnant women considered as high risk by the obstetrician, * Pregnant women with premature, premature birth or miscarriage risk, * Pregnant women diagnosed with neurological disease, * Obese women (body mass index \> 30), * Women whose IVC measurements cannot be made with ultrasonography, * Women with severe low back pain (not able to do housework regularly), * Women who have been diagnosed with a psychiatric illness, * Women with a history of gynecological surgery, * Women with pelvic floor dysfunction, * Women who cannot lie in the supine position.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of the collapsibility index (%) of IVC | immediately after the intervention | The collapsibility index (%) of IVC will be calculated using the formula: \[(Maximum IVC diameter - Minimum IVC diameter)/Maximum IVC diameter\] × 100. |
| Change of Pulsatility index of IVC | immediately after the intervention | Doppler (Toshiba Medical Systems, Aplio 400, Berlin) flow velocimetry will be evaluated. |
| Changes of IVC diameters | immediately after the intervention | M mode ultrasonography will be used for expiratory (IVC d min) and end-inspiratory (IVC d min) diameter measurement. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of the collapsibility index (%) of IVC | 5 minutes after the intervention | The collapsibility index (%) of IVC will be calculated using the formula: \[(Maximum IVC diameter - Minimum IVC diameter)/Maximum IVC diameter\] × 100. |
| Change of Pulsatility index of IVC | 5 minutes after the intervention | Doppler (Toshiba Medical Systems, Aplio 400, Berlin) flow velocimetry will be evaluated. |
| Changes of IVC diameters | 5 minutes after the intervention | M mode ultrasonography will be used for expiratory (IVC d min) and end-inspiratory (IVC d min) diameter measurement. |
Countries
Turkey (Türkiye)
Outcome results
None listed