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1.
Clin Infect Dis ; 54 Suppl 4: S313-6, 2012 May.
Article in English | MEDLINE | ID: mdl-22544194

ABSTRACT

Monitoring human immunodeficiency virus drug resistance (HIVDR) early warning indicators (EWIs) can help national antiretroviral treatment (ART) programs to identify clinic factors associated with HIVDR emergence and provide evidence to support national program and clinic-level adjustments, if necessary. World Health Organization-recommended HIVDR EWIs were monitored in Zimbabwe using routinely available data at selected ART clinics between 2007 and 2009. As Zimbabwe's national ART coverage increases, improved ART information systems are required to strengthen routine national ART monitoring and evaluation and facilitate scale-up of HIVDR EWI monitoring. Attention should be paid to minimizing loss to follow-up, supporting adherence, and ensuring clinic-level drug supply continuity.


Subject(s)
Anti-Retroviral Agents/pharmacology , HIV Infections/drug therapy , HIV Infections/epidemiology , Adult , Anti-Retroviral Agents/supply & distribution , Anti-Retroviral Agents/therapeutic use , Drug Resistance, Viral , Humans , Lost to Follow-Up , National Health Programs , Patient Compliance/statistics & numerical data , Population Surveillance , World Health Organization , Zimbabwe/epidemiology
2.
Br J Ophthalmol ; 93(11): 1474-8, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19692371

ABSTRACT

BACKGROUND: To compare the efficacy of intravitreal pegaptanib (IVP) with panretinal laser photocoagulation (PRP) in the treatment of active proliferative diabetic retinopathy (PDR). METHODS: A prospective, randomised, controlled, open-label, exploratory study. Twenty subjects with active PDR were randomly assigned at a 1:1 ratio to receive treatment in one eye either with IVP (0.3 mg) every 6 weeks for 30 weeks or with PRP laser. Efficacy endpoints included regression of retinal neovascularisation (NV), changes from baseline in best-corrected visual acuity (BCVA) and foveal thickness. Safety outcomes included observed and reported adverse events. RESULTS: In 90% of randomised eyes to IVP, retinal NV showed regression by week 3. By week 12, all IVP eyes were completely regressed and maintained through week 36. In the PRP-treated group, at week 36, two eyes demonstrated complete regression, two showed partial regression, and four showed persistent active PDR. The mean change in BCVA at 36 weeks was +5.8 letters in pegaptanib-treated eyes and -6.0 letters in PRP-treated eyes. Only mild to moderate transient ocular adverse events were reported with pegaptanib. CONCLUSIONS: IVP produces short-term marked and rapid regression of diabetic retinal NV. Regression of NV was maintained throughout the study and at the final visit.


Subject(s)
Angiogenesis Inhibitors/administration & dosage , Aptamers, Nucleotide/administration & dosage , Diabetic Retinopathy/drug therapy , Retinal Neovascularization/drug therapy , Adult , Aged , Angiogenesis Inhibitors/adverse effects , Aptamers, Nucleotide/adverse effects , Diabetic Retinopathy/surgery , Female , Humans , Injections, Intralesional , Laser Coagulation/methods , Male , Middle Aged , Pilot Projects , Prospective Studies , Retinal Neovascularization/surgery
3.
Malawi Med J ; 13(3): 27-9, 2001 Sep.
Article in English | MEDLINE | ID: mdl-27528899

ABSTRACT

A cross sectional study was done between October 1999 and February 2000 to determine antimicrobial susceptibility patterns of consecutive bacterial isolates of 102 clinical samples among surgical in-patients at Lilongwe Central Hospital (LCH), Malawi. Antimicrobial susceptibility was determined using comparative disc diffusion techniques. 83 (81.4%) samples were culture positive for bacterial growth while 19 (18.6%) grew nothing. Of the 93 culture positive specimens, Staphylococcus aureus was the predominant organism 43(51.8%) followed by Proteus species 8(9.6%) and E. coli 7(8.4%). Overall, 98.6% of all isolates tested against ciprofloxacin were susceptible, and against gentamicin and flucloxacin were 84.8% and 66.7% respectively. 59.3% of isolates tested against chloramphenicol were resistant. We recommend a review on the use of chloramphenicol as first-line antimicrobial therapy among surgical in-patients at Lilongwe Central Hospital. We also recommend restricted use of antimicrobials so as to minimise development of drug resistance. Periodic susceptibility studies are necessary to guide judicious use of antibiotics.

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