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The purpose of this study is to determine if women subjected to laparoscopic supracervical hysterectomy in a day-case setting would be less satisfied with the length of hospital stay when compared with women who had an overnight stay following their surgical procedure. The null hypothesis was that there was no difference in satisfaction with length of hospital stay.
Objective: To determine whether women having day-case laparoscopic supracervical hysterectomy (LSH) are as satisfied with the length of stay in hospital as women who stay overnight following the procedure.
Design: randomised controlled trial (RCT).
Setting: Ulleval university hospital, Oslo, Norway.
Population: 49 women scheduled for LSH were enrolled and 45 patients completed the study (22 in the inpatient group and 23 in the day-case group).
Methods: Women were randomised to either day-case care or overnight hospital stay following a routine supracervical hysterectomy. The primary outcome measure was satisfaction with the length of stay in the hospital (measured on a 10-point visual analogue scale) and secondary measures were health-related quality of life (measured using the EuroQol EQ5D), anxiety (measured using the State-Trait Anxiety Inventory for Adults (STAI) and general questions about their experiences of having the operation. Readmissions, prolonged hospitalisations, complications and any contact with a health professional after discharge were also recorded. Measures were taken on the day of surgery (postoperatively), and on days 1, 2, 4 and 7 following surgery. The data were analysed based on an intention to treat.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| inpatient LSH | Active Comparator | LSH means laparoscopic supracervical hysterectomy |
|
| Day-case LSH | Experimental | LSH means laparoscopic supracervical hysterectomy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| day-case laparoscopic supracervical hysterectomy | Procedure | patients discharged home the same day of the operation |
|
| Measure | Description | Time Frame |
|---|---|---|
| satisfaction with the length of stay in the hospital | satisfaction was measured on a 10-point visual analogue scale | on the 7th postoperative day |
| Measure | Description | Time Frame |
|---|---|---|
| health-related quality of life | health-related quality of life (measured using the EuroQol EQ5D), anxiety (measured using the State-Trait Anxiety Inventory for Adults (STAI) and general questions about their experiences of having the operation. Readmissions, prolonged hospitalisations, complications and any contact with a health professional after discharge were also recorded | measured on days 1, 2, 4 and 7 following surgery |
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Inclusion Criteria:.
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jelena Kisic-Trope, MD, Msc | Oslo University Hospital, Ullevål | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Oslo University Hospital, Ullevål | Oslo | Oslo | 0407 | Norway |
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| ID | Term |
|---|---|
| D000556 | Ambulatory Surgical Procedures |
| D007291 | Inosine Monophosphate |
| ID | Term |
|---|---|
| D013514 | Surgical Procedures, Operative |
| D007292 | Inosine Nucleotides |
| D011685 | Purine Nucleotides |
| D011687 | Purines |
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| inpatient LSH | Procedure | patients discharged home the day after the operation |
|
|
| D006574 |
| Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
| D006571 | Heterocyclic Compounds |
| D009711 | Nucleotides |
| D009706 | Nucleic Acids, Nucleotides, and Nucleosides |
| D012265 | Ribonucleotides |