TY - JOUR
T1 - A prospective study comparing conventional methods against a structured method of gaining patients' informed consent for tonsillectomy
AU - Nixon, Iain
AU - Balaji, N.
AU - Hilmy, O.
AU - Fu, B.
AU - Brown, C.
PY - 2005/10/1
Y1 - 2005/10/1
N2 - Objective: By providing junior members of medical staff with appropriate guidelines one can achieve an improved standard of informed consent for tonsillectomy, than is provided at present. Design: A prospective study of 138 consecutive patients. Setting: District General Hospital. Participants: A total of 138 patients undergoing routine tonsillectomy split into two groups. Group A (n = 87), the conventional group, gave consent in our unit's standard manner to various grades of doctors by using a hospital general surgical consent form. Most gave their consent as outpatients, while some consented on admission. Group B (n = 51), the structured consent group, gave their consent in pre-admission clinic, to an SHO using a standardized tonsillectomy consent form and a structured interview technique. Main outcome measures: A preoperative questionnaire regarding the knowledge of tonsillectomy. Results: Improvement of the awareness of the risks involved with tonsillectomy was achieved by the structured consent Group B; 82% of Group A were aware of postoperative pain compared with 94% of group B (P = 0.04); 63% of group A were aware of infection compared with 82% of group B (P = 0.02); 100% of group B had read the consent form before signing compared with 80% of group A (P < 0.01). There was no statistical difference in the awareness of postoperative haemorrhage (91 versus 98%, P = 0.15). Conclusion: By providing junior medical staff with guidelines, senior staff retain responsibility for consent while improving the standard of informed consent for tonsillectomy.
AB - Objective: By providing junior members of medical staff with appropriate guidelines one can achieve an improved standard of informed consent for tonsillectomy, than is provided at present. Design: A prospective study of 138 consecutive patients. Setting: District General Hospital. Participants: A total of 138 patients undergoing routine tonsillectomy split into two groups. Group A (n = 87), the conventional group, gave consent in our unit's standard manner to various grades of doctors by using a hospital general surgical consent form. Most gave their consent as outpatients, while some consented on admission. Group B (n = 51), the structured consent group, gave their consent in pre-admission clinic, to an SHO using a standardized tonsillectomy consent form and a structured interview technique. Main outcome measures: A preoperative questionnaire regarding the knowledge of tonsillectomy. Results: Improvement of the awareness of the risks involved with tonsillectomy was achieved by the structured consent Group B; 82% of Group A were aware of postoperative pain compared with 94% of group B (P = 0.04); 63% of group A were aware of infection compared with 82% of group B (P = 0.02); 100% of group B had read the consent form before signing compared with 80% of group A (P < 0.01). There was no statistical difference in the awareness of postoperative haemorrhage (91 versus 98%, P = 0.15). Conclusion: By providing junior medical staff with guidelines, senior staff retain responsibility for consent while improving the standard of informed consent for tonsillectomy.
UR - http://www.scopus.com/inward/record.url?scp=26244442107&partnerID=8YFLogxK
U2 - 10.1111/j.1365-2273.2005.01021.x
DO - 10.1111/j.1365-2273.2005.01021.x
M3 - Article
C2 - 16232244
AN - SCOPUS:26244442107
SN - 1749-4478
VL - 30
SP - 414
EP - 417
JO - Clinical Otolaryngology
JF - Clinical Otolaryngology
IS - 5
ER -