The Psychosocial Experience of Patients with End-Stage Renal Disease and Its Impact on Quality of Life: Findings from a Needs Assessment to Shape a Service

<table class="table-group" id="tab1"><tr><td><table class="table"><tr><td class="thead-hr" colspan="3"><hr/></td></tr><tr class="thead"><td align="left"> </td><td align="center">Number of Patients who participated</td><td align="center">Number of carers who participated</td></tr><tr><td class="thead-hr" colspan="3"><hr/></td></tr><tr><td align="left">Males</td><td align="center">74</td><td align="center">3</td></tr><tr><td align="left">Females</td><td align="center">44</td><td align="center">9</td></tr><tr class="table-tr"><td colspan="3"><hr class="tbody-hr"/></td></tr></table></td></tr></table>

details of sample characteristics; patients and carers. 

International Scholarly Research Notices

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Table 1

Table 1: The Psychosocial Experience of Patients with End-Stage Renal Disease and Its Impact on Quality of Life: Findings from a Needs Assessment to Shape a Service 

Table 1 | The Psychosocial Experience of Patients with End-Stage Renal Disease and Its Impact on Quality of Life: Findings from a Needs Assessment to Shape a Service 