Ambrosia Health-Tech Care Ltd

Predicting recovery. Connecting care.

Decision support and care coordination for the weeks after hospital discharge.

Patient R.M. · Day 6 after discharge

62

Medium risk
  • Mobility reduced against baseline
  • Two missed medication check-ins
  • Reported low confidence at home

Queued for coordinator review · 14:20

Discharge is not the same as recovery

A patient can be medically fit to leave hospital and still be at risk. Responsibility spreads across family, GPs, community nurses, pharmacies and support providers — with no single view of how recovery is actually going.

An older man and a young child sitting together on a sofa at home in daylight

47.5%

received enough support after leaving hospital

32%

felt unprepared when they were discharged

18%

were contacted afterwards to assess their support needs

A review of 23 studies found that inadequate social support after discharge was associated with increased readmission risk. When patient information, family concerns and referrals sit in separate systems, deterioration can be missed and no shared record of action exists.

One pathway, from information to action

Ambrosia turns structured recovery updates into prioritised, human-reviewed action, and records what happened — so every risk event has a traceable outcome.

Onboard

Consent is secured and the patient's recovery profile is created: reason for discharge, recovery goals, expected pathway, known vulnerabilities, existing support and nominated contacts.

The PRSO Engine

Predictive Risk Stratification and Optimisation

PRSO combines five domains of recovery information, compares them against each patient's own baseline, and produces a visible score, an explainable set of reasons, and a defined review priority.

Baseline and recovery context

Reason for discharge, recovery goals, expected pathway, known vulnerabilities, existing support and nominated contacts.

Symptoms and change

Pain, fatigue, wounds, new concerns, and whether symptoms are improving, stable or deteriorating.

Medication and daily function

Medication concerns, adherence, mobility, daily activities, nutrition and hydration.

Behavioural and social context

Mood, confidence, isolation, family observations, home safety and access to practical support.

Optional health observations

Manually entered or connected-device readings, supported by range, trend, missing-data and quality checks.

The assessment is strengthened by how these signals interact. A single symptom in isolation says little; a symptom alongside a drop in mobility, a missed medication and a fall in confidence says a great deal.

Recovery signals

55
62
58
44
30

Red-flag indicators

PRSO readout

52
Medium risk

Reason codes

  • Symptom pattern changed against personal baseline
  • Two missed medication check-ins in the last 72 hours
  • Mobility 22 points below baseline
  • Reported low confidence managing at home
  • Incomplete observation data for one scheduled check-in

Resulting action

Case enters the coordinator review queue. Context checked with the patient or nominated carer.

The PRSO demonstration is illustrative. Thresholds, reason-code logic and red-flag indicators shown are proposed initial design values, and require clinical review, testing and approval before any live use.

Explainable reason codes

Every score displays the contributing signals, the changes from baseline, any red-flag triggers, the source information and timestamps.

Meaningful human review

Medium and high-risk cases enter a prioritised queue. An appropriately trained reviewer examines the context before any significant intervention or escalation.

Challenge and correction

Patients can correct information they have submitted. Reviewers can override a recommendation, but must record their reason for doing so.

Versioned audit trail

Every event retains the input data, rule version, score, reason codes, named reviewer, action taken and recorded outcome.

Unlike black-box risk scoring, every PRSO output can be understood, challenged, and traced back to the information that produced it.

Three bands, three defined responses

Every assessment produces a band, and every band has a defined response.

Low risk · 0–39

  • Stable or expected recovery pattern
  • No red-flag indicator identified
  • Routine monitoring and check-ins continue
  • Education and reminders remain active
  • Reasons stay visible to both patient and reviewer
  • Reassessed when new information is submitted

Medium risk · 40–69

  • Deteriorating trend or combined concerns
  • Monitoring frequency increases
  • Case enters the coordinator review queue
  • Context checked with the patient or nominated carer
  • Appropriate education, referral or intervention arranged
  • Decision and follow-up recorded

High risk · 70–100

  • Serious concern, rapid deterioration or red-flag trigger
  • Immediate priority within the review queue
  • Qualified human review required
  • Escalation follows the approved clinical pathway
  • No automated diagnosis or clinical decision
  • Complete action and outcome audit trail

Red-flag triggers override the numerical score and escalate a case immediately.

Four interfaces, one recovery record

Patients record recovery. Care teams review and prioritise. Operations coordinates services. Management sees performance. All four work from the same record.

Ambrosia patient app: daily recovery check-ins and care plan

09:14Wi-Fi · 82%

Good morning, John

Thursday 12 November · Day 6 after discharge

6/14

Recovery progress

Day 6 of your 14-day recovery plan

Today's check-in

4 questions, about 2 minutes

Today's readings

  • Heart rate72 bpm
  • Blood pressure130/80
  • Steps2,450
  • MoodGood

Amoxicillin, 2pm

Course day 6 of 7

Person resting at home with a warm drink

Managing fatigue in your first two weeks

4 minute read

Sarah, Care Coordinator

Checking in on how your mobility has been this week.

08:40

Margaret Wilson has access to your recovery updates.

Open the full patient app

These are design mock-ups of the intended interface. The working platform is in development, with the MVP scheduled for delivery in January 2027.

Founder-led, clinically challenged

Ambrose originated the PRSO methodology. Independent clinical and governance advisers review and challenge it.

Ambrose Osaze Jegede, Founder and Chief Executive Officer of Ambrosia Health-Tech Care

Ambrose Osaze Jegede

Founder and Chief Executive Officer

Ambrose originated the PRSO methodology and owns Ambrosia's product vision, leading the recovery-data framework, decision rules, workflows and functional requirements. He oversees MVP development, independent clinical and governance review, technology and service partnerships, and the boundary between digital coordination and regulated care. His healthcare experience spans acute NHS hospitals, community care, rehabilitation, residential services and specialist complex-care settings, including clinical observations using NEWS2, deterioration recognition and escalation, discharge planning, safeguarding and multidisciplinary working. In a previous Healthcare Supervisor role he led staff and volunteers across daily care coordination, referrals, care plans, rotas and handovers, giving him direct insight into the fragmented support patients face after discharge.

He holds an MSc in Philosophy of Science from the University of Liverpool, a BSc in Psychology and Philosophy from Imo State University, a BSc in Psychology and Sociology from the Pontifical Urban University, Rome, and an Advanced Certificate in Formator and Leadership from SIST, Rome. He is currently undertaking an Advanced Professional Certificate in Leadership and Management, with ongoing research engagement in clinical psychology and behavioural science.

Dr Joseph Patrick Akitoye Puplampu-Dove

Dr Joseph Patrick Akitoye Puplampu-Dove

Independent Clinical Adviser. MBChB, MSc. GMC-registered doctor and Specialty Registrar in Internal Medicine Training. Provides independent medical review and challenge of the PRSO Engine, clinical governance, patient safety, risk stratification and escalation pathways.

Onyinyechi Okpalaenwe, BSc

Onyinyechi Okpalaenwe, BSc

Independent Clinical Lead. Registered Adult Nurse and A&E Specialist Nurse. Reviews the recovery data framework, risk rules, red-flag indicators, escalation pathways and patient-safety controls.

Victoria Louise Morgan

Victoria Louise Morgan

Governance and Quality Adviser. CQC Registered Manager and independent care consultant. Supports service-boundary decisions, regulatory readiness, governance policies, safeguarding and quality assurance.

Regulation is built into each stage, not added at the end

Progression from launch to provider contracts to NHS adoption is gated by the safety and data-protection requirements relevant to each stage.

01

Gate 1 · Before live MVP use

  • Confirm final intended use and obtain advice on applicable CQC and MHRA requirements
  • Maintain a clear boundary between coordination and regulated clinical or personal care
  • Complete the DPIA, lawful-basis assessment, consent process and data-retention controls
  • Appoint a Clinical Safety Officer and prepare the hazard log and safety case
  • Apply DCB0129 requirements where relevant
  • Complete security testing, incident-response planning and controlled release approval
02

Gate 2 · Before provider delivery

  • Verify partner qualifications, registration, insurance and safeguarding arrangements
  • Define service boundaries, escalation responsibilities and response standards
  • Agree data-controller and processor responsibilities
  • Put service-level, information-sharing and business-continuity agreements in place
  • Monitor referral completion, incidents, complaints and service performance
03

Gate 3 · Before an NHS or ICB pilot

  • Prepare the required NHS assurance and procurement documentation
  • Provide system architecture, privacy, cybersecurity and penetration-testing evidence
  • Submit clinical-safety documentation and supplier due-diligence information
  • Demonstrate business continuity, incident management and interoperability readiness
  • Agree a controlled pilot protocol, evaluation measures and governance structure

Data protection by design

The platform is built on an encrypted database with role-based access control, UK GDPR-compliant security controls and full audit logging. Development and testing use synthetic data only. Ambrosia is the data controller for all personal data processed through the platform.

A closer look at the app

Four screens from the patient app mock-up.

Ambrosia patient app Home screen

Home

Daily check-in and readings

Ambrosia patient app Your recovery screen

Your recovery

Progress since discharge

Ambrosia patient app Alerts screen

Alerts

Messages and reminders

Ambrosia patient app Profile screen

Profile

Care plan and consent

Rules first, evidence second, models only when both support them.

Ambrosia will not present an untrained algorithm as predictive intelligence.

A person recovering at home, sitting on a sofa with a warm drink in afternoon light

Built in stages, gated by evidence

A twelve-week MVP delivery, then evidence, then models.

  1. Weeks 1–2

    Discovery and technical planning

    2–15 Nov 2026

  2. Weeks 3–4

    Interface design across four portals

    16–29 Nov 2026

  3. Weeks 5–8

    Core development

    30 Nov – 27 Dec 2026

  4. Week 9

    PRSO Engine integration

    28 Dec 2026 – 3 Jan 2027

  5. Week 10

    Testing and quality assurance

    4–10 Jan 2027

  6. Week 11

    User acceptance testing

    11–17 Jan 2027

  7. Week 12

    Deployment and handover

    18–24 Jan 2027

Phase 1 · Explainable MVP

  • Founder-authored PRSO rulebook and decision tables
  • Clinically reviewed thresholds and red-flag triggers
  • Transparent 0–100 score, risk band and reason codes
  • Human review built into every significant action
  • Live launch only after safety approval

Phase 2 · Evidence and model development

  • Capture consented longitudinal recovery information
  • Define outcome labels and prediction horizons
  • Link patient signals, interventions and outcomes
  • Measure missing data, label quality and potential bias
  • Test interpretable candidate models in shadow mode against the rules engine

Phase 3 · Validated predictive intelligence

  • Deploy only after performance and safety validation
  • Test calibration, accuracy and subgroup performance
  • Provide reviewer-visible explanations
  • Monitor drift and version changes
  • Retain human authority and the rules engine as safeguards

One configurable core, many pathways

The same platform serves individual patients, provider cohorts and NHS pathways without being rebuilt.

Reusable technology core

  • PRSO scoring architecture, reason codes and human-review workflow
  • Patient, coordinator and partner interfaces
  • Outcome-linked audit trail and model-governance framework
  • Central security, reporting and performance monitoring

Configurable per market

  • Condition-specific questions, thresholds and escalation pathways
  • Local languages, consent processes and data-retention requirements
  • Approved clinical, community and practical-support providers
  • Jurisdiction-specific regulatory requirements

Routes to market

  • Direct access for patients and families
  • Managed cohorts for care providers and private healthcare organisations
  • Controlled pilots with NHS Trusts and Integrated Care Boards
  • The same platform serves all three without being rebuilt

18.5 million

finished admission episodes recorded in England, 2024–25

4.3 million

UK residents aged 65 and over living alone

5

documented adviser and partner relationships

Talk to us

If you are a care provider, healthcare organisation, investor, patient or family member, we would like to hear from you.

ambrosia.healthtechcare@gmail.com

Lime Studio, Dock Road
Birkenhead, Wirral
Merseyside, CH41 1BS
United Kingdom
A clinician in a white coat greeting a smiling woman with a handshake in a bright room

Care. Innovation. Better health.

Predicting recovery. Connecting care.