OBJECTIVES: To estimate the proportion of TB patients who have access to mobile phones and to describe mobile phone utilization practices of TB patients.
METHODS: Six public and six private TB clinics representing the four districts of Metro Manila and one institution in Cavite were purposively selected for this cross-sectional survey conducted in 2006. Using an interviewer-administered questionnaire, patients suspected to have TB, those newly diagnosed and those currently on treatment under either DOTS or non-DOTS were interviewed.
RESULTS: Of the 337 patients interviewed, 65% (95% CI 60.2 to 70.6) have access to mobile phones (45% currently own a mobile phone and 20% share a mobile phone with a household member). The mean duration of ownership was 1.8 years (SD1.7). Almost all had prepaid subscriptions (99%) and 72% had some credit/load in their mobile phones at the time of interview. Of the three existing networks, subscription to SMART was highest, followed by the Globe network. Most of them use their phones for social purposes and emergency-related communications. Most of the respondents were male (60%) in the age group of 20-39 (54%) and 40-59 years old (33%). Half of the respondents were from public TB clinics (52%). On multivariable analysis, patients consulting in private clinics [OR 2.25, 95% CI 1.36 to 3.74], belonging to the younger age of < 20 [OR 4.54, 95% CI 1.48 to 13.89] and 20 - 39 years old [OR 2.56, 95% CI 1.48 to 4.39], who had college education [OR 4.97, 95% CI 1.84 to 13.43] and currently employed [OR 3.23, 95% CI 1.92 to 5.47] were more likely to have access to mobile phones.
CONCLUSION: Considering the fair access (65%) to mobile phones of the patients interviewed, it is feasible to conduct a pilot intervention using SMS as a strategy to improve adherence to treatment. The intervention should consider that majority use prepaid subscriptions and that sharing of phones among household members is a common practice.

Human ; Male ; Ownership ; Syndactyly, Type I ; Pilot Projects ; Cell Phone ; Health Facilities ; Communication

Goltz syndrome(focal dermal hypoplasia) is a rare disorder characterized by ectodermal and mesodermal dysplasia described in 1962 by Goltz. In Korea, one case of Goltz syndrome was reported in 1994. The inheritance mode is mostly X-linked dominant. Skin abnormality is the most common manifestation including hypoplasia of the dermis. Skeletal involvement such as syndactyly, polydactyly, scoliosis, kyphosis and spina bifida occulta may be present, also ocular and dental abnormalities are reported. Radiologic findings are the osteopathy and striation of the long bone. We experienced a case of Goltz syndrome in a 9-year old female who was presented with right side hypotrophy, focal dermal hypoplasia, ocular(anidria, microcornea), dental(oligodontia, amelogenesis) and skeletal(syndactyly) abnormalities. Skin biopsy was performed and showed decreased expression of type I collagen gene with Northern blotting.
Biopsy ; Blotting, Northern ; Child ; Collagen Type I ; Dermis ; Ectoderm ; Female ; Focal Dermal Hypoplasia* ; Humans ; Korea ; Kyphosis ; Mesoderm ; Polydactyly ; Scoliosis ; Skin ; Skin Abnormalities ; Spina Bifida Occulta ; Syndactyly ; Wills