9 research outputs found
Using Range Condition Assessment to Optimize Wildlife Stocking in Tindress Wildlife Sanctuary, Nakuru District, Kenya
Over 70% of Kenya’s wildlife resources occur outside protected areas, in areas where land use practices do not necessarily conform to wildlife conservation standards. Ensuring that land use practices in these areas accommodate wildlife conservation is vital in effectively conserving wildlife in this country. Tindress Farm in Rift Valley offers a good example of a place where economic activities and wildlife conservation can work harmoniously. The farm has set up a 320-ha wildlife sanctuary in the hilly parts of the property to provide a haven for wildlife displaced by human settlements in the surrounding environs. The Tindress Farm management needed to know the diversity and optimum number of wildlife species that the sanctuary could accommodate. This study set out to 1) outline a set of models for objectively calculating wildlife stocking levels and 2) demonstrate the practical use of these models in estimating optimum stocking levels for a specific wildlife sanctuary. After comparing models using forage inventory methods models and utilization-based methods (UM), we opted to use UM models because of their focus on ecological energetics. This study established that the range condition in Tindress Wildlife Sanctuary varied from poor to good (29-69%) and recommended a total stocking density of 158.9 grazer units and 201.4 browser units shared out by the various herbivore species. These estimates remain a best-case scenario. The effects of rainfall, range condition, and condition of the animals should be monitored continuously to allow for adjustments through active adaptive management.The Rangeland Ecology & Management archives are made available by the Society for Range Management and the University of Arizona Libraries. Contact [email protected] for further information.Migrated from OJS platform August 202
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Plasma nevirapine concentrations predict virological and adherence failure in Kenyan HIV-1 infected patients with extensive antiretroviral treatment exposure
Treatment failure is a key challenge in the management of HIV-1 infection. We conducted a mixed-model survey of plasma nevirapine (NVP) concentrations (cNVP) and viral load in order to examine associations with treatment and adherence outcomes among Kenyan patients on prolonged antiretroviral therapy (ART). Blood plasma was collected at 1, 4 and 24 hours post-ART dosing from 58 subjects receiving NVP-containing ART and used to determine cNVP and viral load (VL). Median duration of treatment was 42 (range, 12–156) months, and 25 (43.1%) of the patients had virologic failure (VF). cNVP was significantly lower for VF than non- VF at 1hr (mean, 2,111ng/ml vs. 3,432ng/ml, p = 0.003) and at 4hr (mean 1,625ng/ml vs. 3,999ng/ml, p = 0.001) but not at 24hr post-ART dosing. Up to 53.4%, 24.1% and 22.4% of the subjects had good, fair and poor adherence respectively. cNVP levels peaked and were > = 3μg.ml at 4 hours in a majority of patients with good adherence and those without VF. Using a threshold of 3μg/ml for optimal therapeutic nevirapine level, 74% (43/58), 65.5% (38/58) and 86% (50/58) of all patients had sub-therapeutic cNVP at 1, 4 and 24 hours respectively. cNVP at 4 hours was associated with adherence (p = 0.05) and virologic VF (p = 0.002) in a chi-square test. These mean cNVP levels differed significantly in non-parametric tests between adherence categories at 1hr (p = 0.005) and 4hrs (p = 0.01) and between ART regimen categories at 1hr (p = 0.004) and 4hrs (p<0.0001). Moreover, cNVP levels correlated inversely with VL (p< = 0.006) and positively with adherence behavior. In multivariate tests, increased early peak NVP (cNVP4) was independently predictive of lower VL (p = 0.002), while delayed high NVP peak (cNVP24) was consistent with increased VL (p = 0.033). These data strongly assert the need to integrate plasma concentrations of NVP and that of other ART drugs into routine ART management of HIV-1 patients
Trajectory plasma nevirapine concentrations and association with viral load.
<p>Plasma nevirapine concentration (cNVP) is compared for various groups over 24 hour period according to adherence (A:- open circle, good adherence; closed diamonds, fair adherence; open triangle, poor adherence; solid line, mean), and according to virologic response or gender (B:- open diamond, virologic failure; closed circle, virologic success or non-virologic failure; closed triangle, male; crosses, female). Patients with good and fair adherence and those with virologic success (non-virologic failure) had peak cNVP at 4 hours while cNVP for virologic failure patients started low at 1hr and peaked later at 24hrs. Significant inverse correlations are observed between same day viral load with cNVP at 1 hour (C) and at 4 hours (D). Circles, virologic success; triangles, virologic failure.</p
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