Morbidity, Mortality And Risk Factors of Mpox in HIV Negative High Risk Sexual Health Clinic Attenders and People Living With HIV
- Conditions
- MonkeypoxHIV Coinfection
- Interventions
- Other: No intervention
- Registration Number
- NCT05965427
- Lead Sponsor
- NEAT ID Foundation
- Brief Summary
This data collection study aims to describe and compare the outcomes of Mpox on people living with HIV (PLHIV) and HIV-negative individuals who are on pre-exposure prophylaxis (PrEP). The study also aims to identify risk factors for specific Mpox outcomes.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 2000
- Diagnosis of MPX was more than 90 days prior to data collection
- Confirmed MPX infection by documented PCR testing of lesions between 1st May 2022 to 1st December 2023
- At least 18 years of age
- Cases (PLWHIV + MPX) i) Documented HIV-1 infection
- Cases (PrEP users + MPX) i) Attended a clinic to receive PrEP
- MPX diagnosed based on clinical criteria only
- MPX diagnosis was within the last 90 days
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description PLHIV and Mpox coinfection No intervention - HIV negative PrEP users with Mpox infection No intervention -
- Primary Outcome Measures
Name Time Method Death From date of disease onset (first symptom) until date of death related to Mpox (up to 3 months) Clinical complications associated with Mpox From date of disease onset (first symptom) until date of clinical resolution e.g. lesion resolution, hospital discharge or death(up to 3 months) Complications which will be collected are as follows:
* Severe rectal and/or perianal pain (i.e. due to perianal/anal abscess, proctitis)
* Tonsillitis and/or dysphagia
* Secondary bacterial infection on affected skin
* Urological complications (genital oedema, urinary retention)
* Ocular involvement (conjunctivitis, corneal involvement, periorbital cellulitis)
* Central nervous system involvement (encephalitis, meningitis, focal neurology signs)
* Pneumonia/pulmonary abscess or necrotizing involvement
* Myocarditis
* Diarrhoea
The definition of a mental health condition will be that reported by the patient and recognized in the ICD-10 classification.Percentage of hospitalisations 1st May 2022 to 1st December 2023 percentage of hospitalisations for clinical reasons only (i.e. not for precautionary measures or quarantine).
Severity of Mpox lesions From date of disease onset (first symptom) until date of peak number of lesions and sites recorded (up to 3 months) Severity of lesions will be assessed by the peak number of lesions and peak number of sites.
Skin lesion at peak severity score:
* Not presenting with skin lesions (0 skin lesions)
* Mild (\<25 lesions)
* Moderate (25-99 skin lesions)
* Severe (100-250 skin lesions)
* Very severe (\>250 skin lesions)
Site of lesion will also be collected as part of the severity assessment:
* Genital lesions (defined as involvement of either vulva or vaginal mucosa or penis, pubic area)
* Ano-rectal/perianal lesions
* Oral mucosa (lips/gums/oral/pharynx) lesions
* Face
* Trunk (chest/torso/abdomen/back)
* Limbs (arms/forearms/legs/hands/feet) on the body.Differences in the clinical manifestation of MPX in PLWHIV and PrEP users From date of disease onset (first symptom) until date of clinical resolution e.g. lesion resolution, hospital discharge or death(up to 3 months) Clinical manifestations will include: Severity and time to resolution of lesions, severity of disease, clinical complications, drug treatments, length of hospitalisations, and number of deaths.
severe disease is defined as:
* Adults with severe clinical illness (e.g. National Early Warning Score \[NEWS\] 2 score of ≥5), which may include significant lower respiratory symptoms, confusion/encephalitis, and other complications (e.g. secondary bacterial infection, sepsis)
* Widely disseminated lesions and very many in number (≥100)
* Suspected infection of the cornea
* Severe, refractory pain from lesions requiring hospitalisation to achieve symptomatic control
* Lesions associated with complications due to pain or swelling (e.g., constipation, urinary retention, inability to swallow)
* Confirmed infection, regardless of severity, in immunocompromised people, pregnant women, or children aged ≤16 years.Differences in the clinical manifestation of MPX in PLWHIV by CD4 and VL. From date of disease onset (first symptom) until date of clinical resolution e.g. lesion resolution, hospital discharge or death(up to 3 months) Clinical manifestations will include: Severity and time to resolution of lesions, severity of disease, clinical complications, drug treatments, length of hospitalisations, and number of deaths.
severe disease is defined as:
* Adults with severe clinical illness (e.g. National Early Warning Score \[NEWS\] 2 score of ≥5), which may include significant lower respiratory symptoms, confusion/encephalitis, and other complications (e.g. secondary bacterial infection, sepsis)
* Widely disseminated lesions and very many in number (≥100)
* Suspected infection of the cornea
* Severe, refractory pain from lesions requiring hospitalisation to achieve symptomatic control
* Lesions associated with complications due to pain or swelling (e.g., constipation, urinary retention, inability to swallow)
* Confirmed infection, regardless of severity, in immunocompromised people, pregnant women, or children aged ≤16 years.
- Secondary Outcome Measures
Name Time Method Number of MPX patients attending as a percentage of total number of patients the sites have seen over a set period of time (from first Mpox patient to last Mpox patient) 1st May 2022 to 1st December 2023 Length of stay in hospital for inpatients treated for Mpox From date of hospital admission for Mpox until date of hospital discharge (up to 3 months) Differences in the clinical manifestation of MPX in PLWHIV and PrEP users by co-morbidities. From date of disease onset (first symptom) until date of clinical resolution e.g. lesion resolution, hospital discharge or death(up to 3 months) Clinical manifestations will include: Severity and time to resolution of lesions, severity of disease, clinical complications, drug treatments, length of hospitalisations, and number of deaths.
severe disease is defined as:
* Adults with severe clinical illness (e.g. National Early Warning Score \[NEWS\] 2 score of ≥5), which may include significant lower respiratory symptoms, confusion/encephalitis, and other complications (e.g. secondary bacterial infection, sepsis)
* Widely disseminated lesions and very many in number (≥100)
* Suspected infection of the cornea
* Severe, refractory pain from lesions requiring hospitalisation to achieve symptomatic control
* Lesions associated with complications due to pain or swelling (e.g., constipation, urinary retention, inability to swallow)
* Confirmed infection, regardless of severity, in immunocompromised people, pregnant women, or children aged ≤16 years.Time to lesion resolution (if known) From date of disease onset (first symptom) until date of lesion resolution (up to 3 months)
Trial Locations
- Locations (5)
Hôpital Bichat Claude Bernard
🇫🇷Paris, France
Hôpital Pitié-Salpêtrière
🇫🇷Paris, France
Chelsea and Westminster Hospital
🇬🇧London, United Kingdom
Hospital Universitari Vall d'Hebron
🇪🇸Barcelona, Spain
Euroguidelines
🇵🇱Warsaw, Poland