| Literature DB >> 30178780 |
Ruiqing Di1, Guowen Li1.
Abstract
BACKGROUND We explored the intervention effect of a smartphone medical app on complications and quality of life of patients with nasopharyngeal carcinoma who underwent radiotherapy and chemotherapy. MATERIAL AND METHODS We divided 132 patients with nasopharyngeal carcinoma who received radiotherapy and chemotherapy for the first time, in accordance with the random number table method, into a control group (67 patients) and an intervention group (65 patients). Patients in control group were discharged with standard care and patients in the intervention group used a smartphone medical app after discharge. Data on adverse effects of radiotherapy and chemotherapy, complications, and quality of life were collected and analyzed. RESULTS There was no difference between the complications of radiotherapy and chemotherapy and quality of life between the 2 groups at discharge (P>0.05). The incidence of oral mucositis, xerostomia, mouth-opening difficulties, and nasal congestion in the intervention group was significantly lower than in the control group at 6 months after discharge and quality of life was significantly higher than in the control group (P<0.05). CONCLUSIONS Reasonable use of this smartphone app can improve the exercise compliance of discharged patients with nasopharyngeal carcinoma who underwent radiotherapy and chemotherapy, reduce the adverse reactions and complications of radiotherapy and chemotherapy, and improve quality of life and satisfaction of patients after discharge.Entities:
Mesh:
Year: 2018 PMID: 30178780 PMCID: PMC6134889 DOI: 10.12659/MSM.908146
Source DB: PubMed Journal: Med Sci Monit ISSN: 1234-1010
Demographic and health characteristics of the participants.
| Items | Classification | Intervention group (N1=65) | Control group (N2=67) | t/χ2 | P |
|---|---|---|---|---|---|
| Gender | Male | 39 (60.0) | 44 (65.7) | 0.009 | 0.924 |
| Female | 26 (40.0) | 23 (34.3) | |||
| Age (Yr) | 44.32±11.03 | 42.28±10.37 | 0.883 | 0.463 | |
| Course of disease | IV stage | 11 (16.9) | 13 (19.4) | 1.067 | 0.587 |
| III stage | 28 (43.1) | 29 (43.3) | |||
| II stage and below | 26 (40.0) | 25 (37.3) | |||
| Chemotherapy regimen | Single chemotherapy | 45 (69.2) | 49 (73.1) | 0.135 | 0.714 |
| Combination chemotherapy | 20 (30.8) | 18 (26.9) | |||
| Radiotherapy regimen | Conventional radiotheraphy | 18 (27.7) | 16 (23.9) | 0.025 | 0.875 |
| Intensity modulated radiation therapy | 47 (72.3) | 51 (76.1) |
Comparison of side effects and complications of radiotherapy and chemotherapy in two groups [N (%)].
| Items | Grade | At discharge | 6 months after discharge | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Group C | Group I | Z/χ2 | P | Group C | Group I | Z/χ2 | P | ||
| Oral mucositis | 0 | 8 (12) | 13 (19) | −0.757 | 0.449 | 34 (52) | 52 (78) | −2.138 | 0.033 |
| I~II | 40 (61) | 40 (59) | 29 (45) | 12 (19) | |||||
| III~IV | 17 (27) | 14 (22) | 2 (3) | 3 (3) | |||||
| Mouth opening difficulties | 0 | 16 (24) | 15 (22) | 0.000 | 1.000 | 23 (36) | 45 (68) | −2.397 | 0.017 |
| I~II | 38 (58) | 42 (63) | 31 (48) | 14 (22) | |||||
| III~IV | 11 (18) | 10 (15) | 11 (16) | 8 (10) | |||||
| Xerostomia | 0~I | 39 (60) | 43 (64) | −0.503 | 0.615 | 42 (65) | 51 (76) | −2.335 | 0.020 |
| II~III | 26 (40) | 24 (36) | 23 (35) | 16 (24) | |||||
| Hearing loss | Without | 20 (31) | 19 (29) | 0.010 | 0.919 | 22 (34) | 24 (36) | 0.545 | 0.460 |
| Exist | 45 (69) | 46 (71) | 43 (66) | 43 (64) | |||||
| Nasal congestion | 0 | 12 (18) | 17 (25) | 1.220 | 0.223 | 25 (39) | 37 (56) | −2.084 | 0.037 |
| I~II | 29 (45) | 35 (53) | 25 (39) | 25 (38) | |||||
| II~III | 24 (37) | 15 (22) | 15 (22) | 5 (6) | |||||
Group C is control group, and Group I is intervention group.
Comparison of rehabilitation exercise compliance between two groups of patients after discharge [N (%)].
| Items | 3 months after discharge | 6 months after discharge | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Group C | Group I | Z/χ2 | P | Group C | Group I | Z/χ2 | P | ||
| Compliance of mouth opening exercise | Full compliance | 8 (12) | 20 (19) | 6.610 | 0.037 | 5 (12) | 8 (19) | 7.369 | 0.013 |
| Partial compliance | 40 (61) | 36 (59) | 23 (6) | 33 (59) | |||||
| Non-compliance | 17 (27) | 11 (22) | 37 (2) | 26 (22) | |||||
| Compliance of nasal irrigation | Full compliance | 12 (12) | 24 (19) | 3.685 | 0.048 | 8 (12) | 16 (19) | 8.356 | 0.015 |
| Partial compliance | 20 (61) | 16 (59) | 34 (61) | 19 (59) | |||||
| Non-compliance | 33 (27) | 27 (22) | 23 (27) | 32 (22) | |||||
Group C is control group, and Group I is intervention group.
QLQ-C30 questionnaire of two groups at discharge and 6 months after discharge.
| Field | At discharge | 6 months after discharge | |||||||
|---|---|---|---|---|---|---|---|---|---|
| Group C | Group I | P | Group C | Group I | P | ||||
| Functional field | PF | 59.62±12.18 | 58.79±10.58 | 0.293 | 0.771 | 80.22±11.35 | 91.36±8.63 | 4.444 | <0.001 |
| RF | 55.86±16.53 | 56.33±14.69 | 0.121 | 0.904 | 63.54±14.23 | 72.18±10.13 | 2.812 | 0.007 | |
| EF | 53.29±12.36 | 54.18±12.68 | 0.287 | 0.775 | 62.53±11.34 | 73.62±10.21 | 4.139 | <0.001 | |
| CF | 73.22±13.25 | 74.37±14.76 | 0.331 | 0.742 | 77.63±12.31 | 83.14±10.64 | 1.928 | 0.049 | |
| SF | 57.89±17.46 | 56.37±16.35 | 0.362 | 0.719 | 70.54±15.14 | 76.91±12.19 | 1.572 | 0.121 | |
| Symptom field | FA | 52.09±16.49 | 53.82±18.32 | 0.400 | 0.690 | 38.64±13.32 | 22.14±12.54 | 5.139 | <0.001 |
| NV | 20.98±12.69 | 21.56±11.02 | 0.196 | 0.845 | 2.54±5.61 | 2.13±4.96 | 0.311 | 0.756 | |
| PA | 55.46±20.41 | 57.21±21.35 | 0.338 | 0.737 | 8.24±11.75 | 3.12±8.36 | 2.018 | 0.048 | |
| DY | 10.21±14.56 | 12.84±13.24 | 0.761 | 0.449 | 2.34±9.63 | 2.11±8.54 | 0.102 | 0.919 | |
| SL | 61.02±22.12 | 59.74±21.36 | 0.237 | 0.813 | 13.14±20.11 | 6.13±16.58 | 1.531 | 0.131 | |
| AP | 73.82±23.12 | 71.21±21.58 | 0.481 | 0.632 | 9.62±10.54 | 3.28±8.56 | 2.657 | 0.009 | |
| CO | 15.34±16.57 | 16.40±15.80 | 0.264 | 0.792 | 8.11±12.33 | 3.82±9.22 | 1.585 | 0.118 | |
| DI | 5.39±10.50 | 6.10±9.44 | 0.286 | 0.776 | 5.10±8.51 | 5.86±8.47 | 0.361 | 0.719 | |
| FI | 43.85±34.17 | 41.28±35.11 | 1.867 | 0.067 | 39.66±30.12 | 38.22±31.01 | 0.190 | 0.850 | |
| Overall quality of life field | QL | 34.15±10.31 | 32.14±9.65 | 0.811 | 0.420 | 62.15±11.17 | 72.03±9.07 | 3.908 | <0.001 |
Group C is control group, and Group I is intervention group. PF – physical functionong; RF – role functioning; EF – emotional functioning; CF – cognitive functioning; SF – social functioning; FA – fatigue; NV – nausea and vomiting; PA – pain; DY – dyspnoea; SL – sleep loss; AP – appetite loss; CO – constipation; DI – diarrhoea; FI – financial difficulties; QL –: quality of life.