Community Level Interventions for Pre-eclampsia

We have designed a two-phased community (including PHC-level) cRCT encompassing both rural and urban settings to be fully powered in each of: * Ogun State, Nigeria * Maputo and Gaza Province, Mozambique * Hyderabad and Matiari districts in Sindh Province, Pakistan. * Belgaum and Bagalkot districts in Karnataka State, India The trial will be phased from the Pilot CLIP trial to Definitive CLIP trial on the basis of a satisfactory rate of use (≥50%) of the CLIP 'package of care' in appropriate women in all countries but Mozambique. Mozambique will be unique in that they will rely on an extended period of feasibility to pilot test all Trial systems and tools before directly beginning a definitive trial. Foregoing the Pilot in Mozambique was felt to be appropriate based on their experience with community-based surveillance and will ensure timelines of the trial are met within a manageable budget. For all other countries, use of the package in the Pilot phase will be defined as appropriate referral (urgent or non-urgent) to a facility able to provide comprehensive emergency obstetric care (CEmOC) in appropriate women during the first six months of the Pilot CLIP trial. A primary component of the CLIP intervention is antenatal risk assessment guided by the PIERS on teh Move mHealth decision aid. The CLIP version of the PIERS on the Move tool (CLIP POM) integrates the miniPIERS predictive score and a clinical data collection system into a single application. Community health workers in each country will assess women according to the visit protocol, entering clinical data into the CLIP POM mobile application. The application will provide recommendations for care according to meeting one of the trigger events listed below, as per this protocol. Triggers identified that will indicate treatment and/or transport (urgently, defined as within 4hrs) to a CEmOC facility are as follows: 1. Unconsciousness (MgSO4 if sBP ≥160 mmHg \[to be reasonably sure that the unconsciousness is associated with severe pre-eclampsia and not due to obstetric sepsis\], urgent transport) 2. Signs of recent stroke or seizure (methyldopa if sBP ≥160 mmHg \[to ensure BP is not lowered too much\], MgSO4, urgent transport) 3. Significant vaginal bleeding (MgSO4 if sBP ≥140 mmHg \[presumed abruption associated with severe pre-eclampsia\], urgent transport). 4. No fetal movements felt in the previous 12 hrs (urgent transport \[a threshold for identifying at risk fetuses that are alive at the time of screening\] 39) 5. sBP ≥160 mmHg (or dBP ≥ 110 mmHg in Nigeria only) (methyldopa, MgSO4, urgent transport \[consistent with severe pre-eclampsia\]) 6. Heavy proteinuria (≥4+ by dipstick - predictive of stillbirth in miniPIERS cohort, urgent transport) 7. miniPIERS predicted probability ≥25% (MgSO4, urgent transport) 8. Shock index \>1.7 in Nigeria only (the Shock index is a ratio of pulse/sBP; high shock index is an indication of poor prognosis in women with postpartum haemorrhage) Non-urgent transport (by non-ambulance services), meaning assessment at a CEmOC facility within 24 hours, will be advised for all women with non-severe hypertension (sBP 140-159 mmHg) who do not meet criteria for one of the above 7/8 triggers. In Mozambique and Pakistan additional CLIP triggers based on use of the audio oximeter will also be included in the POM decision aid. As with the original miniPIERS model, the enhanced model including SpO2 uses a risk threshold of ≥25% predicted probability to identify high-risk cases. Recommendations based on the updated miniPIERS model will include treatment with MgSO4 and urgent referral. An additional independent trigger of SpO2\<93% will also be used in Mozambique and Pakistan to indicate urgent referral. In Nigeria where the updated Microlife CRADLE VSA blood pressure device is being used additional triggers will be included for severe diastolic blood pressure or severe shock index to coincide with the traffic light warning signs included in this device.