Management of Nausea and Vomiting of Pregnancy
Słowa kluczowe
Abstrakcyjny
Opis
Upto 80% of all pregnant women experience some form of nausea and vomiting during their pregnancy (NVP). The International Statistical Classification of Disease and Related Health Problems ICD-10 defines hyperemesis gravidarum (HG) as persistent and excessive vomiting starting before the end of the 22nd week of gestation, and further subdivides the condition into mild and severe, severe being associated with metabolic disturbances such as carbohydrate depletion, dehydration or electrolyte imbalance. HG is a diagnosis of exclusion, characterized by prolonged and severe nausea and vomiting, dehydration, large ketonuria and > 5% bodyweight loss.
HG affects approximately 0.3- 2.0% of pregnancies and is the commonest indication for admission to hospital in the first half of pregnancy and second only to preterm labor as a cause of hospitalisation overall. According to the Hyperemesis Education and Research Foundation, conservative estimates indicate that HG can cost a minimum of $200 million annually in house hospitalizations in the United states. Taking into account other factors such as emergency room treatments, potential complications of severe HG and the fact that up to 35% of women with paid employment will lose time from work through nausea the actual cost of NVP to the economy is significantly higher.
NVP can be extremely debilitating for the patient and if inadequately managed can cause significant morbidities including malnutrition and electrolyte imbalances, thrombosis, Wernicke's encephalopathy, depressive illness and poor pregnancy outcomes such as prematurity and small for gestational age fetuses.
Day care has proven to be beneficial and safe mode of care for patients in other clinical settings. Studies have demonstrated that day care management of patients with NVP appears acceptable and feasible but no systematic reviews or randomized controlled trials have been performed which examine the effects of introducing day care on rates of hospital admission, duration of inpatient stay and patient satisfaction.
We aim to conduct a prospective open label randomized controlled trial to test the hypothesis that the availability of day care services for the initial treatment of NVP reduces the mean duration of stay in hospital by 1 day (28.6%) and results in significantly greater patient satisfaction compared with standard inpatient management.
The null hypothesis states there is no difference in the amount of inpatient hospital days when women with NVP are treated initially in day care or by standard inpatient admission.
All pregnant women under 22 weeks gestation, who have not already been treated for NVP in their current pregnancy, presenting with the diagnosis of NVP are eligible for inclusion in the trial. The treatment group will be day care treatment of NVP. The comparison group will be the inpatient treatment of NVP.
Daktyle
| Ostatnia weryfikacja: | 12/31/2013 |
| Pierwsze przesłane: | 11/19/2008 |
| Szacowana liczba przesłanych rejestracji: | 11/19/2008 |
| Wysłany pierwszy: | 11/20/2008 |
| Ostatnia aktualizacja przesłana: | 01/12/2014 |
| Ostatnia opublikowana aktualizacja: | 01/14/2014 |
| Rzeczywista data rozpoczęcia badania: | 03/31/2009 |
| Szacowana data zakończenia podstawowej działalności: | 08/31/2012 |
| Szacowana data zakończenia badania: | 08/31/2012 |
Stan lub choroba
Interwencja / leczenie
Procedure: Day care
Procedure: Inpatient
Faza
Grupy ramion
| Ramię | Interwencja / leczenie |
|---|---|
| Experimental: Day care Patients randomised to day care treatment of NVP will be instructed to present to the day services unit where they will receive a pre-agreed fluid and anti emetic regimen. | Procedure: Day care Patients randomised to day care treatment of NVP will be instructed to present to the day services unit where they will receive a pre-agreed fluid and anti emetic regimen. |
| Active Comparator: Inpatient Patients randomised to inpatient management of NVP will be admitted to hospital where they will receive a pre-agreed fluid and anti emetic regimen. | Procedure: Inpatient Patients randomised to inpatient management of NVP will be admitted to hospital where they will receive a pre-agreed fluid and anti emetic regimen. |
Kryteria kwalifikacji
| Płeć kwalifikująca się do nauki | Female |
| Przyjmuje zdrowych wolontariuszy | tak |
| Kryteria | Inclusion Criteria: Women (no age limits) will be admitted to the study if they have two or more of the following criteria - Ongoing viable intrauterine pregnancy/ pregnancies < 22 weeks gestation - Persistent vomiting (>x3 episodes/ 24 hours) not attributable to other causes - Severe nausea not attributable to other causes. - Dehydration diagnosed by the presence of ketonuria. - Electrolyte imbalance not attributable to other causes. Exclusion Criteria: Women will not be admitted to the study if any of the following criteria are present. - Women with a confirmed urinary tract infection (mid stream urine isolation of a single strain of uropathogen >105 bacteria/ml) - Women with molar pregnancies - Women with non viable pregnancies. - Women who have already received treatment for NVP outside of this trial. - Pregnant women who present who will not be booking at CUMH for their pregnancy or are not resident in the South West of Ireland i.e. day care treatment is not an option. - Women who do not have a good understanding of English. |
Wynik
Podstawowe miary wyników
1. The primary outcome will be the number of inpatient nights spent in hospital secondary to NVP from initial presentation until 22 weeks gestation. An inpatient night will be defined as requiring an inpatient bed between the hours of 20.00 and 08.00. [Following discharge]
Miary wyników wtórnych
1. Total number of hours spent in hospital secondary to NVP from initial presentation until 22 weeks gestation. [22 weeks gestation]
2. Total amount of intravenous fluids administered secondary to NVP from initial presentation until 22 weeks gestation [22 weeks gestation]
3. Total amount of anti-emetics administered secondary to NVP from initial presentation until 22 weeks gestation. [22 weeks gestation]
4. Total Multivitamin complexes administered secondary to NVP from initial presentation until 22 weeks gestation [22 weeks gestation]
5. Patient satisfaction will be measured by the Client Satisfaction Questionnaire. [Following first presentation]
6. Incidence of miscarriage [22 weeks gestation]
7. Infant birth weight at delivery [Following delivery]
8. Gestational age at delivery. [following delivery]
9. Total days lost at work secondary to NVP from initial presentation until 22 weeks gestation. (Asked at 16 weeks gestation) [16 weeks gestation]
