| Literature DB >> 31429414 |
Charlotte E J Sandberg1, Stephen R Knight2, Ahmad Uzair Qureshi3, Samir Pathak4,5,6.
Abstract
BACKGROUND: A high burden of preventable morbidity and mortality due to surgical site infections (SSIs) occurs in low- and middle-income countries (LMICs), and most of these SSIs occur following discharge. There is a high loss to follow-up due to a wide geographical spread of patients, and cost of travel can result in delayed and missed diagnoses.Entities:
Keywords: developing country; follow-up; low- and middle-income countries; postoperative; surgical site infection; telemedicine; wound infection
Mesh:
Year: 2019 PMID: 31429414 PMCID: PMC6718082 DOI: 10.2196/13309
Source DB: PubMed Journal: JMIR Mhealth Uhealth ISSN: 2291-5222 Impact factor: 4.773
Figure 1Preferred reporting items for systematic reviews and meta-analysis flow diagram.
Included study characteristics.
| Characteristics | Aiken et al | Nguhuni et al | Pathak et al |
| Publication year | 2013 | 2017 | 2015 |
| Geographic location | Kenya | Tanzania | India |
| Number of included patients | 1172 | 374 | 536 |
| Study population | All patients undergoing surgical procedure | Obstetric patients | All patients undergoing surgical procedure |
| Included surgical procedures | Caesarean section, laparotomy, hernia repair, orthopedic lower limb surgery, salpingectomy, cystectomy | Caesarean section only | Hernia repair, colonic and urogenital surgery |
| Method of telemedicine intervention | Telephone calls with predetermined questionnaire | Telephone calls with predetermined questionnaire | Telephone calls with predetermined questionnaire |
| Follow-up frequency | 2 | 3 | 1 |
| Follow up performed | Days 14 & 28 | Days 6, 12 & 28 | Day 30 |
| Length of follow up | 30 days | 30 days | 30 days |
| SSIa diagnosis criteria | CDCb criteria for diagnosis of SSI | CDC criteria for diagnosis of SSI | Local SSI criteria |
| SSI rate | 7.90% | 12.0% | 6.34% |
aSSI: surgical site infection
bCDC: centers for disease control and prevention
Summary of findings.
| Findings | Aiken et al | Nguhuni et al | Pathak et al |
| Patients providing a telephone number, % | >90 | 84 | 100 |
| Patients with ≥1 successful telephone follow up who had provided a telephone number, % | Not stated | 87 | 71 |
| Patients contacted by phone and seen in clinic, % | Not stated | 73 | 69 |
| Patients undergoing surgical procedure | 89 | 484 | 10 |
| Patients with SSIsa that participated in telephone screening, % | Not stated | 72 | Not stated |
| SSIs detected over phone or clinic review at day 7 | Not stated | 11/14 | Not stated |
| SSIs detected over phone or by clinical review at day 14 | Not stated | 7/11 | Not stated |
| SSIs detected over phone or by clinical review at day 30 | Not stated | 0/0 | Not stated |
| Total SSIs detected over phone or by clinical review | 16 / 23 | 18 / 25 | 10 / 10 |
aSSI: surgical site infection
Methodological index for nonrandomized studies criteria for each paper.
| Criteria | Studies | |||||
| Aiken et al [ | Nguhuni et al [ | Pathak et al [ | ||||
| Score | Description | Score | Description | Score | Description | |
| 1a | 2 | —b | 2 | — | 2 | — |
| 2c | 2 | — | 1 | Did not state reason some patients were excluded | 1 | No inclusion criteria stated |
| 3d | 1 | References a pilot study | 0 | Doesn't report a pilot or protocol | 0 | No pilot or protocol mentioned |
| 4e | 2 | SSIsf diagnosed in reference to the standardized CDC-NHNSg risk criteria | 2 | SSIs diagnosed in reference to the standardized CDC-NHNS risk criteria | 0 | No criteria for SSI diagnosis explained |
| 5h | 1 | Not stated whether those in clinic were blinded to the telephone outcomes | 1 | Not stated whether those in clinic were blinded to the telephone outcomes | 1 | Not stated whether those in clinic were blinded to the telephone outcomes |
| 6i | 2 | 30 days | 2 | 30 days | 2 | 30 days |
| 7j | 0 | The loss to follow up was not commented on | 1 | Loss to follow up was 13%, but 26% of those who had been contacted by phone did not return to clinic | 2 | No loss to follow up |
| 8k | 2 | Specificity, sensitivity | 2 | Specificity, sensitivity, positive predictive values, negative predictive values | 1 | Not recorded |
| 9l | 2 | Compared against clinical diagnosis | 2 | Compared against clinical diagnosis | 2 | Compared against clinical diagnosis |
| 10m | 2 | Patients were their own control | 2 | Patients were their own control | 2 | Patients were their own control |
| 11n | 0 | No Table 1 referenced | 2 | — | 0 | No data on group equivalence mentioned |
| 12o | 2 | — | 2 | — | 1 | No statistics mentioned for SSI detection via mobile phone |
| Total scorep | 18 | — | 19 | — | 14 | — |
aHas a clearly stated aim.
bNot applicable/no description given.
cIncludes all eligible patients.
dCollected data according to a preestablished protocol.
eThere was an appropriate endpoint to the aim of the study.
fSSI: surgical site infection.
gCDC-NHNS: Centers for Disease Control and Prevention-National Healthcare Safety Network.
hThere was an unbiased assessment of the study endpoint.
iHad an appropriate follow-up period.
jHad a loss to follow up less than 5%.
kProspectively calculated the study size.
lUtilized an adequate control group.
mStudy group was managed during the same time period as the control.
nBaseline equivalence of the study group and control group.
oAdequate statistical analysis.
pOut of 24.
Mobile health evidence and reporting assessment checklist.
| Criteria | Aiken et al [ | Nguhuni et al [ | Pathak et al [ |
| Infrastructure (population level) | No | No | No |
| Technology platform | Yes | Yes | Yes |
| Interoperability or HISa context | Yes | Yes | Yes |
| Intervention delivery | Yes | Yes | Yes |
| Intervention content | Yes | Yes | Yes |
| Usability/content testing | No | No | No |
| User feedback | No | No | No |
| Access of individual participants | No | No | Yes |
| Cost assessment | No | Yes | No |
| Adoption inputs/ program entry | Yes | Yes | Yes |
| Limitations for delivery at scale | No | No | Yes |
| Contextual adaptability | No | No | No |
| Replicability | Yes | Yes | Yes |
| Data security | No | No | No |
| Compliance with national guidelines or regulatory statutes | No | No | No |
| Fidelity of the intervention | Yes | Yes | Yes |
| Total (out of 16) | 7 | 8 | 9 |
aHIS: health information systems.
Figure 2World Health Organization Mobile health evidence and reporting assessment schematic depiction of the six stages of the intervention maturity life-cycle, from preprototype to national level deployment.