Estimating serious fungal disease burden in the Philippines

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Presentation transcript:

Estimating serious fungal disease burden in the Philippines Maria Christina R. Batac1, David W. Denning1,2,3 1University of Manchester, Manchester, United Kingdom, 2Global Action Fund for Fungal Infections, 3Leading International Fungal Education Background Aim The Philippines is a low middle-income, tropical country in Southeast Asia. Infectious diseases including tuberculosis, remain the main causes of morbidity. Fungal disease surveillance has not been done, and its burden has never been estimated. Populations at risk of acquiring serious fungal diseases continue to increase, which include immunocompromised patients, drawn from patients with AIDS, TB, malignancies, and disease states requiring chronic steroid use. To estimate the incidence and prevalence of serious fungal diseases based on results from previous epidemiological studies, populations at risk and epidemiological databases. Methods Using the methodology of the LIFE program (www.LIFE-worldwide.org), estimates were derived from data gathered from WHO, UNAIDS, Philippine Health Statistics 2011, Philippine Dermatological Society Health Information System database, HIV/AIDS and ART registry of the Philippines, epidemiological studies like The TREAT Asia HIV Observational Database 2005, and personal communication. Results The population of the Philippines is 98,394,000, with 34% under the age of 15 and 6% are above 60. The median age is 23. The population is composed of 50.5% males and 49.5% females, 25.6% are 40 years old and above, and 25.9% are women between 15-50 years old. We estimate that in 2016, a total of 1,852,137 (1.9%) were affected by severe fungal infections in the Philippines. The table below shows the incidence and prevalence for selected serious fungal infections. Table. Prevalence and incidence of selected serious fungal infections in the Philippines, 2016 Serious Fungal Infection Estimation method Totals   Rate/100,000 Cryptococcal meningitis 7% of new AIDS diagnosis 84 Annual incidence 0.09 Pneumocystis pneumonia 31% of new AIDS diagnosis 391 0.40 Invasive aspergillosis 10% of AML, 0.5% of renal transplant patients, 4% of liver transplant patients, and 1.3% of patients hospitalized for chronic obstructive pulmonary disease (COPD) 3,085 3 Chronic pulmonary aspergillosis (CPA) 22% of cavitary pulmonary TB, 2% of non-cavitary pulmonary TB 77,172 Prevalence 78 Allergic bronchopulmonary aspergillosis (ABPA) 2.5% of adult asthmatics 121,113 123 Severe asthma with fungal sensitisation (SAFS) 33% of the most severe 10% of adult asthmatics 159,869 162 Candidaemia 2/100,000 general population, 1.5 in non-ICU and 0.5 in ICU 1,968 2 Candida peritonitis 50% of incidence of candidemia in ICU 246 0.25 Oral candidiasis 90% of HIV patients not on antiretrovirals and CD4 <200 x 106/L 3467 3.5 Oesophageal candidiasis 20% of HIV patients not on antiretrovirals and CD4 <200 x 106/L + 5% of HIV patients on antiretrovirals 1522 1.5 Recurrent Candida vaginitis (>4x/year) 5% of women 15-50 years of age 1,481,899 3,012 Mucormycosis 0.2 cases per 1,000,000 population 20 0.02 Fungal keratitis Based on cases seen at a tertiary government hospital in the NCR in 2015 358 0.36 Tinea capitis Based on cases seen at Philippine Dermatological Society training institutions in 2015 846 0.86 Mycetoma 97 0.10 Total serious fungal infection burden 1,852,137 Future directions Epidemiological studies are needed to validate these estimates, facilitating appropriate medical care of patients and proper prioritization of limited resources. HIV/AIDS cases are increasing over the past 5 years. They are at risk of acquiring cryptococcal meningitis, pneumocystis pneumonia and oral candidiasis. Hand in hand with an effective AIDS prevention program and prompt and adequate treatment of cases with antiretroviral drugs, should be the proper management of opportunistic fungal infections. TB and COPD are both associated with CPA. It is probable that there are many undiagnosed CPA cases, with some of them managed as resistant TB cases. It is important to determine baseline prevalence using available serological tests.