Announcement

Collapse
No announcement yet.

Rwanda - MoH announces "a few" Marburg cases - September 27, 2024 - MoH confirms 66 cases/15 deaths

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • #76
    Source: https://x.com/RwandaHealth/status/18...971470/photo/2

    Click image for larger version

Name:	image.png
Views:	160
Size:	881.8 KB
ID:	999532

    Comment


    • #77
      Marburg virus disease - Rwanda

      1 November 2024

      Situation at a glance

      It has been over a month since the declaration of the Marburg virus disease (MVD) outbreak in Rwanda on 27 September 2024. As of 31 October 2024, 66 confirmed cases, including 15 deaths (CFR: 23%), have been reported including two new confirmed cases since the previous Disease Outbreak News report. WHO continues to support the Government of Rwanda in responding to the outbreak. Enhanced surveillance, contact tracing and infection prevention and control measures must be maintained until the outbreak is declared over.

      Description of the situation


      Since the last Disease Outbreak News on this event was published on 25 October 2024, two additional laboratory-confirmed cases of Marburg virus disease (MVD) were reported in Rwanda on 26 and 30 October respectively. These cases are known contacts of a previously confirmed case and are currently in isolation and receiving treatment. As of 31 October 2024, 66 confirmed cases, including 15 deaths (CFR: 23%), have been reported. Among confirmed cases, 68% are males, and 45% are adults between 30 and 39 years of age. Health workers from two health facilities in Kigali account for almost 80% of all confirmed cases. Most cases are reported from the three districts in Kigali city.

      The highest number of new confirmed cases were reported in the first two epidemiological weeks of the outbreak with 26 cases reported in epidemiological week 39 (23 to 29 September 2024) and 23 cases in week 40 (30 September to 6 October). Following just one case reported in epidemiology week 42 (14 to 20 October), three cases were reported in epidemiology week 43 (21 to 27 October) and one case in week 44 (reported on 30 October).

      Since the declaration of the outbreak by the Government of Rwanda on 27 September and as of 31 October, 49 confirmed cases have recovered, and two cases are still receiving care at the designated Marburg treatment centre. As of 31 October 2024, 6099 tests for Marburg virus have been conducted, with approximately 100-350 samples being tested daily at the Rwanda Biomedical Center.

      Contact tracing is ongoing, with 559 contacts listed under follow-up as of 31 October 2024.

      WHO continues to support the Government of Rwanda to respond to the ongoing outbreak. Enhanced surveillance, contact tracing and infection prevention and control measures must be maintained until the outbreak is declared over.

      Figure 1. MVD cases by week of reporting in Rwanda, as of 31 October 2024, (n=66)

      Rwanda MVD epi curve

      * The epidemiological week 44 is not complete at the time of publication, it ends on 3 November 2024. Epidemiology


      MVD is a highly virulent disease that can cause haemorrhagic fever and is clinically similar to Ebola virus disease. Marburg and Ebola viruses are both members of the Filoviridae family (filovirus). People are infected with Marburg virus when they come into close contact with Rousettus bats, a type of fruit bat, that can carry the Marburg virus and are often found in mines or caves. Marburg virus then spreads between people via direct contact (through broken skin or mucous membranes) with the blood, secretions, organs or other bodily fluids of infected people, and with surfaces and materials (e.g. bedding, clothing) contaminated with these fluids. Health workers have previously been infected while treating patients with suspected or confirmed MVD. Burial ceremonies that involve direct contact with the body of the deceased can also contribute to the transmission of Marburg virus.

      The incubation period varies from two to 21 days. Illness caused by Marburg virus begins abruptly, with high fever, severe headache and severe malaise. Severe watery diarrhoea, abdominal pain and cramping, nausea and vomiting can begin on the third day. Although not all cases present with haemorrhagic signs, severe haemorrhagic manifestations may appear between five and seven days from symptoms onset, and fatal cases usually have some form of bleeding, often from multiple areas. In fatal cases, death occurs most often between eight and nine days after symptom onset, usually preceded by severe blood loss and shock. There is currently no approved treatment or vaccine for MVD. Some candidate vaccines and therapeutics are currently under investigation.


      Seventeen outbreaks of MVD have previously been reported globally. The most recent outbreaks were reported in Equatorial Guinea and the United Republic of Tanzania between February and June 2023. Additional countries that previously reported outbreaks of MVD in the African Region include Angola, the Democratic Republic of the Congo, Ghana, Guinea, Kenya, South Africa, and Uganda.

      Public health response
      • The Government of Rwanda is coordinating the response with support from WHO and partners.
      • A surge team from WHO has been deployed to support the in-country response across the functions of incident management, epidemiology, health operations, case management, infection prevention and control, laboratory, health logistics, therapeutics and vaccines research, and partner coordination.
      • WHO is continuously engaged with its viral hemorrhagic fever collaborating centers and other reference laboratories and partners to support Rwanda in assessing laboratory test performance and providing technical support.
      • WHO is supporting the Government in the establishment of a programme for recovered patients, by sharing technical guidance and protocols for the establishment of a national programme and by supporting the Rwanda Ministry of Health (MOH) implementation effort.
      • WHO is supporting the implementation of the nationally approved and recently launched Marburg therapeutics clinical trial. The trial is enrolling patients as they are admitted to the established MVD treatment center. WHO supported MOH in assessing the national Infection Prevention and Control (IPC) and Water, Sanitation and Hygiene (WASH) readiness for response capabilities to MVD outbreak
      • WHO and partners supported MOH in developing and finalising the national IPC operational guidance for MVD adapted from WHO IPC guidelines. This operational guidance, together with IPC standard operating procedures, is being rapidly disseminated to all health facilities.
      • WHO supported MOH in developing and finalizing the training materials for the upcoming national IPC training of trainers targeting the national IPC focal persons.
      • WHO is collaborating with MOH to enhance IPC capacities by continuing onsite training activities for healthcare workers and providing mentorship and supervision in different priority health facilities.
      • WHO supported MOH in the enhancing of IPC measures in the isolation sites.
      • WHO has provided technical advice to public health authorities in Rwanda and at-risk countries on the implementation of evidence-informed and risk-based health measures; the strengthening of detection, reporting and management capacities at points of entry and across borders; and travel advice.
      • WHO has published interim guidance on the Considerations for border health and points of entry for filovirus disease outbreaks, which applies to but is not limited to the current MVD outbreak in Rwanda.
      • WHO has also published a statement advising against any travel restrictions and against any trade restrictions with Rwanda in the context of the ongoing MVD outbreak.
      • WHO is providing support in surrounding countries to assess the readiness of healthcare facilities, points of entry and border communities within surrounding countries and specifically risk mapping for areas bordering Rwanda.
      • WHO is supporting the MVD treatment center with direct support from clinical experts in infectious disease, ICU and nursing as well as health logistics and WASH expertise.
      • WHO is conducting training of clinical staff at MVD treatment on general aspects of MVD health operations, case management and optimized supportive care. MoH providing to trainees.
      • WHO is supporting the national case management pillar to collect standardized patient level data based on WHO electronic case report form from the WHO Global Clinical Platform and making descriptive reports of case management responses to outbreak.
      WHO risk assessment


      Marburg virus disease (MVD) is caused by the same family of viruses (Filoviridae) that causes Ebola virus disease. MVD is an epidemic-prone disease associated with high CFR (24-88%). In the early course of the disease, MVD is challenging to distinguish from other infectious diseases such as malaria, typhoid fever, shigellosis, meningitis and other viral haemorrhagic fevers. Epidemiologic features can help differentiate between viral hemorrhagic fevers (including history of exposure to bats, caves, or mining) and laboratory testing is important to confirm the diagnosis.

      With 66 confirmed cases reported, this is the third largest MVD outbreak reported to date, with almost 80% of confirmed cases reported among health workers. Healthcare-associated infections (also known as nosocomial infections) of this disease can lead to further spread if not controlled early. The importance of screening all persons entering health facilities as well as inpatient surveillance for prompt identification, isolation, provision of care and notification cannot be overemphasized. This is in addition to the importance of contact identification and listing and daily follow-up of all contacts.

      Based on the outbreak investigation which included record review in health facilities, review of epidemiological data, serology and genomic sequencing, as well as environmental and animal testing, the source of the outbreak is reported to be of zoonotic origin, linked to exposure in a cave inhabited by fruit bats. However, the dates of symptom onset of cases are still unknown to WHO.

      On 30 September, WHO assessed the risk of this outbreak as very high at the national level, high at the regional level, and low at the global level. However, based on the evolution of the outbreak and ongoing investigations, this risk assessment may be revised. MVD is not easily transmissible (i.e. in most instances it requires contact with the body fluids of a sick patient presenting with symptoms or with surfaces contaminated with these fluids). In addition, there are ongoing public health measures in place, including active surveillance in facilities and communities, testing suspected cases, isolation and treatment of cases and contact tracing.

      WHO advice


      MVD outbreak control relies on using a range of interventions, including prompt isolation and case management; surveillance including active case search, case investigation and contact tracing; a laboratory service; infection prevention and control, including prompt safe and dignified burial; and social mobilization – community engagement is key to successfully controlling MVD outbreaks. Raising awareness of risk factors for Marburg virus infection and protective measures that individuals can take is an effective way to reduce human transmission. WHO advises the following risk reduction measures as an effective way to reduce MVD transmission in healthcare facilities and in communities:
      • To reduce human infections and deaths, it is essential to raise community awareness about the risk factors for Marburg virus infection particularly of human-to-human transmission, and the protective measures individuals can take to minimize exposure to the virus. This includes encouraging anyone with symptoms to seek immediate care at a health facility or designated treatment center to lower the risk of community transmission and improve their chances for recovery.
      • Reducing the risk of bat-to-human transmission arising from prolonged exposure to mines or caves inhabited by fruit bat colonies. People visiting or working in mines or caves inhabited by fruit bat colonies should wear gloves and other appropriate protective clothing (including masks).
      • Surveillance activities, including the wide dissemination of the MVD case definition, should be strengthened in all affected districts, including contact tracing and active case finding.
      • Patient-care activities should be undertaken in a clean and hygienic environment that facilitates practices related to the prevention and control of health-care-associated infections (HAIs) as outlined in Essential environmental health standards in health care. Safe water, adequate sanitation and hygiene infrastructure and services should be provided in healthcare facilities. For details on recommendations and improvement, follow the WASH FIT implementation Package
      • A comprehensive strategy to manage deceased individuals in communities should be implemented. Safe and dignified burials should be carried out, with strong engagement of communities.
      • Rapid qualitative assessments should be implemented to collect socio-behavioural data, which can then be utilized to guide the response.
      • Results of the phone Knowledge, Attitude and Practices (KAP) survey and other surveys should be integrated into the response strategy and interventions.
      • Timely laboratory testing of all suspected cases needs to be maintained and supported with a reliable sample transportation system.
      • WHO encourages the sharing of genomic sequencing data to inform the public health response.
      • Border health readiness and response capacities should be strengthened at points of entry and in communities bordering areas reporting MVD cases and onboard conveyances, and public health advice should be provided to travellers in line with WHO’s interim guidance on considerations for border health and points of entry for filovirus disease outbreaks.
      • WHO encourages all countries to send the first samples that tested positive for Marburg virus and a subset of negative samples to a WHO Collaborating Centre or a regional reference laboratory for inter-laboratory comparison.
      • WHO recommends that clinical data from suspected and confirmed Marburg virus disease cases be systematically collected to improve the limited understanding of the clinical course and direct causes and risk factors for poor outcomes. This can be done by contributing anonymized data to the WHO Global Clinical Platform for viral haemorrhagic fevers.
      • WHO advises that all patients with MVD receive holistic care including optimized supportive care including critical care and mental health services in a treatment center designed for optimal patient care and patient centered experience with biosecurity measures such as unidirectional patient and staff flow and WASH services in place.

      Based on the current risk assessment, WHO advises against any travel restrictions or any trade restrictions with Rwanda at this time. For further information, please see WHO advice for international traffic in relation to the Marburg virus disease outbreak in Rwanda.​

      ...
      It has been over a month since the declaration of the Marburg virus disease (MVD) outbreak in Rwanda on 27 September 2024. As of 31 October 2024, 66 confirmed cases, including 15 deaths (CFR: 23%), have been reported including two new confirmed cases since the previous Disease Outbreak News report. WHO continues to support the Government of Rwanda in responding to the outbreak. Enhanced surveillance, contact tracing and infection prevention and control measures must be maintained until the outbreak is declared over.

      Comment


      • #78
        medRxiv

        Genomic characterization uncovers transmission dynamics of Marburg Virus in Rwanda following a single zoonotic spillover event


        Posted November 05, 2024.​

        View ORCID ProfileYvan Butera, View ORCID ProfileLeon Mutesa, View ORCID ProfileEdyth Parker, View ORCID ProfileRaissa Muvunyi, View ORCID ProfileEsperance Umumararungu, View ORCID ProfileAlisen Ayitewala, View ORCID ProfileJean Pierre Musabyimana, View ORCID ProfileAlhaji Olono, View ORCID ProfilePlacide Sesonga, View ORCID ProfileOlusola Ogunsanya, Emmanuel Kabalisa, View ORCID ProfileOluwatobi Adedokun, Nelson Gahima, Laetitia Irankunda, Chantal Mutezemariya, Richard Niyonkuru, Arlene Uwituze, Ithiel Uwizera, James Kagame, Arlette Umugwaneza, John Rwabuhihi, Fidele Umwanankabandi, Valens Mbonitegeka, View ORCID ProfileEdouard Ntagwabira, View ORCID ProfileEtienne Kayigi, Gerard Izuwayo, Herve Murenzi, Therese Mukankwiro, Nasson Tuyiringire, Jean Marie Vianney Uwimana, Agnes Gasengayire, Reuben Sindayiheba, Glory-Ugochi Onyeugo, Merawi Aragaw, Lenny Gitundu, Radjabu Bigirimana, Mosoka Fallah, Adaora Ejikeme, Senga Sembuche, Alice Kabanda, Jean Claude Mugisha, Emmanuel Edwar Siddig Francis, Pierre Gashema, Jerome Ndayisenga, View ORCID ProfileAlexis Rugamba, View ORCID ProfileFaustin Kanyabwisha, View ORCID ProfileGad Murenzi, View ORCID ProfileAnise Happi, Jean Claude Semuto Ngabonziza, View ORCID ProfileMisbah Gashegu, View ORCID ProfileAyman Ahmed, View ORCID ProfileNoella Bigirimana, Edson Rwagasore, Muhammed Semakula, View ORCID ProfileJean Paul Rwabihama, View ORCID ProfileClarisse Musanabaganwa, View ORCID ProfileEric Seruyange, View ORCID ProfileMenelas Nkeshimana, View ORCID ProfileTheogene Twagirumugabe, David Turatsinze, Eric Remera, View ORCID ProfileNoel Gahamanyi, View ORCID ProfileSofonias Kifle Tessema, View ORCID ProfileIsabelle Mukagatare, Sabin Nsanzimana, View ORCID ProfileChristian Happi, View ORCID ProfileClaude Mambo Muvunyi
        doi: https://doi.org/10.1101/2024.11.01.24316374


        This article is a preprint and has not been certified by peer review [what does this mean?]. It reports new medical research that has yet to be evaluated and so should not be used to guide clinical practice.
        00000052Abstract


        The ongoing outbreak of Marburg virus disease (MVD) in Rwanda marks the third largest historically, though it has exhibited the lowest fatality rate. Genomic analysis has identified a lineage with limited internal diversity most closely related to a genome sequence from a sporadic case sampled in 2014 in Uganda, though the lineages have diverged from a common ancestor that was circulating for decades in the animal reservoir. Notably, the data also provide evidence that the outbreak resulted from a single zoonotic transmission event with limited human-to-human transmission, rather than multiple independent zoonotic transmission events. The Rwandan MVD outbreak prompted a thorough investigation that included contact tracing, clinical assessment, travel history, sequencing, and serology testing, to trace the virus's origin. Results of investigations linked the index case to a mining cave inhabited by Rousettus aegyptiacus (the Egyptian fruit bat), where three individuals tested seropositive for IgG and IgM, further supporting the zoonotic origin of the outbreak through human-animal interactions.

        ...

        The ongoing outbreak of Marburg virus disease (MVD) in Rwanda marks the third largest historically, though it has exhibited the lowest fatality rate. Genomic analysis has identified a lineage with limited internal diversity most closely related to a genome sequence from a sporadic case sampled in 2014 in Uganda, though the lineages have diverged from a common ancestor that was circulating for decades in the animal reservoir. Notably, the data also provide evidence that the outbreak resulted from a single zoonotic transmission event with limited human-to-human transmission, rather than multiple independent zoonotic transmission events. The Rwandan MVD outbreak prompted a thorough investigation that included contact tracing, clinical assessment, travel history, sequencing, and serology testing, to trace the virus's origin. Results of investigations linked the index case to a mining cave inhabited by Rousettus aegyptiacus (the Egyptian fruit bat), where three individuals tested seropositive for IgG and IgM, further supporting the zoonotic origin of the outbreak through human-animal interactions. ### Competing Interest Statement The authors have declared no competing interest. ### Funding Statement Government of Rwanda and Development Partners. ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The study was approved by the Rwanda National Ethics Committee (FWA Assurance No. 00001973 IRB 00001497 of IORG0001100-Protocol approval notice: N° 121/RNEC/2024). I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes All the sequence data are available upon request on https://github.com/rbx-bfx/illumina_vsp

        Comment


        • #79
          Translation Google

          Recovered Marburg patients are urged not to breastfeed and not to have unprotected sex

          By André Gakwaya — November 3, 2024

          Do not breastfeed and do not have unprotected sex, this is the final recommendation made by the Ministry of Health (MINISANTE) to people who have been cured of the Marburg virus. This message is justified by the fact that the Marburg virus remains intact in some parts for more than a year and that the cured person can still contaminate his fellow men.

          The virus is still intact in the tear secretions of the eye, sperm and breast milk. This is why a person who has recovered from Marburg should avoid unprotected sex, throw away used condoms or breastfeed their child.

          The MINISANTE recommends that these precautions should remain in effect until the treating physician confirms that the patient does not have Marburg in any part of the body.

          Dr. Menelaus Nkeshimana, Director of Personnel Reinforcement at MINISANTE, says that the Marburg virus remains in certain parts of the human body of the cured person for more than a year.

          "The cured person looks like other normal humans. But the virus continues to remain intact in some parts such as the eye and sperm. People cured of Marburg can contaminate other people if care is not taken. The health care staff must be more vigilant and attentive when the person cured of Marburg goes to be treated for another disease. These cured people will be more hygienic in their lives. They will be followed by the health care staff, because they are likely to show other after-effects, certainly less serious, following Marburg," he indicated.

          The person cured of Marburg may suffer from retinal damage and may not have good vision. He may sometimes display extreme fatigue. He may suffer from pain in the joints and veins. He may display severe anxiety problems. This is why such cases are closely monitored by medical personnel. (End)

          Ne pas allaiter et ne pas avoir des rapports sexuels non protégés, tel est l’ultime recommandation faite par le Ministère de la Sante (MINISANTE) en direction des personnes qui ont été guéries du v…


          ------------------------------​

          Ministry of Health | Rwanda
          @RwandaHealth

          "Those who have recovered from the Marburg virus may still retain parts of the virus in specific areas of their body, particularly in semen and the inner parts of their eyes. For this reason, they undergo follow-up monitoring for several weeks"~ Minister @NsanzimanaSabin

          Click image for larger version  Name:	image.png Views:	1 Size:	408.2 KB ID:	999944
          12:05 PM · Nov 4, 2024​​

          Comment

          Working...
          X