| Literature DB >> 34917408 |
Anele Dube-Pule1, Brian C Zanoni2, Cathy Connolly3, Majahonkhe Shabangu4,5, Moherndran Archary6,7.
Abstract
BACKGROUND: Adherence to infant antiretroviral (ARV) postnatal prophylaxis and early infant diagnosis (EID) uptake is low in Africa. Promoting EID and adherence are necessary for this age group.Entities:
Keywords: HIV DNA PCR; PMTCT; SMS reminders; early infant diagnosis; high-risk mothers; infant prophylaxis; low-risk mothers; mHealth
Year: 2021 PMID: 34917408 PMCID: PMC8661286 DOI: 10.4102/sajhivmed.v22i1.1301
Source DB: PubMed Journal: South Afr J HIV Med ISSN: 1608-9693 Impact factor: 2.744
FIGURE 1Sample SMS message sent to mothers at 1, 4, 10 and 14 weeks post-delivery.
Description of maternal and infant characteristics.
| Characteristic | High risk ( | Low risk ( | Total ( |
| ||
|---|---|---|---|---|---|---|
|
| % |
| % | |||
|
| ||||||
| Age group | ||||||
| < 25 | 21 | 29.60 | 25 | 14.10 | 46 | 0.003 |
| 25–35 | 40 | 56.30 | 113 | 63.30 | 155 | |
| 36–44 | 10 | 14.10 | 40 | 22.60 | 50 | |
| Parity | ||||||
| Nulliparous | 19 | 26.76 | 48 | 27.00 | 67 | 0.9 |
| Multiparous | 52 | 73.24 | 130 | 73.03 | 182 | |
| Booking status | ||||||
| Early (< 20 weeks) | 28 | 38.36 | 85 | 47.70 | 113 | 0.06 |
| Late/unbooked | 31 | 42.47 | 77 | 43.30 | 108 | |
| Unrecorded | 14 | 21.90 | 16 | 9.00 | 32 | |
| CD4 count | ||||||
| < 100 | 1 | 1.37 | 2 | 1.10 | 3 | 0.12 |
| 100–250 | 4 | 5.48 | 13 | 7.30 | 17 | |
| 250–500 | 19 | 26.03 | 52 | 29.21 | 71 | |
| > 500 | 14 | 19.20 | 73 | 41.01 | 87 | |
| Unknown CD4 | 35 | 47.90 | 38 | 21.35 | 73 | |
| Infant | ||||||
| Birthweight | ||||||
| < 2500 g | 7 | 9.59 | 14 | 7.8 | 21 | 0.029 |
| 2500 g – 3999 g | 47 | 64.38 | 137 | 76.97 | 184 | |
| ≥ 4000 g | 2 | 2.74 | 10 | 5.62 | 12 | |
| Unrecorded | 17 | 23.29 | 17 | 9.55 | 34 | |
| Gestational age | ||||||
| Preterm (< 37/40 weeks) | 19 | 26.03 | 33 | 18.54 | 52 | 0.4 |
| Term | 48 | 66.00 | 128 | 71.91 | 176 | |
| Unrecorded | 6 | 8.22 | 17 | 9.55 | 34 | |
| Mode of delivery | ||||||
| Caesarean section | 36 | 51.43 | 114 | 64.04 | 150 | 0.04 |
| Natural vaginal delivery | 20 | 28.57 | 48 | 26.97 | 68 | |
| Unrecorded | 16 | 20.00 | 16 | 8.99 | 30 | |
Birth and 10-week polymerase chain reaction.
| HIV PCR | High risk ( | Low risk ( | Total ( |
| ||
|---|---|---|---|---|---|---|
|
| % |
| % | |||
|
| ||||||
| Negative | 64 | 87.67 | 174 | 97.50 | 238 | 0.002 |
| Indeterminate | 1 | 1.40 | 0 | 0.00 | 1 | 0.3 |
| Positive | 1 | 1.40 | 0 | 0.00 | 1 | 0.3 |
| Not obtained | 7 | 9.59 | 4 | 2.25 | 11 | 0.02 |
|
| ||||||
| Negative | 48 | 65.80 | 136 | 76.40 | 184 | 0.08 |
| Died | 1 | 1.40 | 0 | 0.00 | 1 | 0.29 |
| Not done | 24 | 32.88 | 42 | 24.00 | 66 | 0.16 |
PCR, polymerase chain reaction.
Maternal and infant risk factors for not obtaining a 10-week polymerase chain reaction.
| Risk factors | 10-week PCR not obtained ( | 10-week PCR obtained ( | Total ( |
| ||
|---|---|---|---|---|---|---|
|
| % |
| % | |||
|
| ||||||
| Low | 42 | 62.69 | 136 | 73.91 | 178 | 0.08 |
| High | 25 | 37.31 | 48 | 26.09 | 73 | |
|
| ||||||
| Age group | ||||||
| < 25 | 13 | 20.00 | 33 | 18.03 | 46 | 0.9 |
| 25–35 | 40 | 61.54 | 112 | 61.20 | 152 | |
| 36–44 | 12 | 18.46 | 38 | 20.77 | 50 | |
| Parity | ||||||
| Nulliparous | 15 | 23.08 | 52 | 28.26 | 67 | 0.42 |
| Multiparous | 50 | 76.92 | 132 | 71.74 | 182 | |
| Prenatal care | ||||||
| Early (< 20 weeks) | 29 | 47.54 | 84 | 52.50 | 113 | 0.51 |
| Late/none | 32 | 52.46 | 76 | 47.50 | 108 | |
| CD4 count | ||||||
| < 500 | 17 | 42.50 | 74 | 53.62 | 91 | 0.22 |
| > 500 | 23 | 57.50 | 64 | 46.38 | 87 | |
| Infant | ||||||
| Birthweight | ||||||
| < 2500 g | 6 | 10.34 | 15 | 9.43 | 21 | 0.88 |
| 2500 g – 3999 g | 48 | 82.76 | 136 | 85.52 | 184 | |
| ≥ 4000 g | 4 | 6.90 | 8 | 5.03 | 12 | |
| Gestational age | ||||||
| Preterm (< 37 weeks) | 7 | 11.86 | 45 | 26.63 | 52 | 0.02 |
| Term | 52 | 88.14 | 124 | 73.73 | 176 | |
PCR, polymerase chain reaction.
Interviewed versus non-interviewed women.
| Maternal parameters | Interviewed ( | Not interviewed ( |
| ||||||
|---|---|---|---|---|---|---|---|---|---|
| High risk ( | Low Risk ( | High risk ( | Low risk ( | ||||||
|
| % |
| % |
| % |
| % | ||
|
| |||||||||
| < 25 | 7 | 36.8 | 7 | 14.9 | 14 | 26.9 | 18 | 13.8 | 0.74 |
| 26–35 | 10 | 52.6 | 34 | 72.3 | 30 | 57.7 | 78 | 60.0 | |
| > 36 | 2 | 10.5 | 6 | 12.8 | 8 | 15.4 | 34 | 26.2 | 0.16 |
|
| |||||||||
| Nulliparous | 7 | 36.8 | 15 | 31.9 | 12 | 23.1 | 33 | 25.2 | 0.24 |
| Multiparous | 12 | 63.2 | 32 | 68.1 | 40 | 76.9 | 98 | 74.8 | 0.37 |
HR, high risk; LR, low risk.
, HR interviewed versus HR not interviewed;
, LR interviewed versus LR not interviewed;
, HR interviewed versus HR not interviewed;
, LR interviewed versus LR not interviewed.
During the enrolment phase, when you signed up for the programme, did you experience any of the following?
| Reaction | Response | Comments | |
|---|---|---|---|
| Yes (1) | No (2) | ||
| 1. Trouble understanding purpose of research project and your role in it | |||
| 2. Discomfort giving name to research staff member | |||
| 3. Discomfort giving personal phone number to research staff member | |||
| 4. Unease with phone number confirmation procedure (i.e. replying with ‘yes’ or ‘ yebo’ to initial SMS) | |||
| 5. Worry that collected personal information could be lost | |||
| 6. Worry that collected personal information could be shared with third parties, for example telemarketers | |||
| 7. Other concerns | |||
In the course of the study, when you were receiving SMS reminders for your appointments, did you experience any of the following?
| Reaction | Response | Comments | |
|---|---|---|---|
| Yes (1) | No (2) | ||
| 1. Problems (not) receiving SMS reminders at the right (wrong) time | |||
| 2. Problems with inaccurate/inappropriate SMS content (e.g. names mix up) | |||
| 3. Problems understanding the SMS content | |||
| 4. Fear/worry that others might see the SMS reminder on your phone | |||
| 5. Feel bothered by the SMS (e.g. felt like it was spam) | |||
| 6. Other people asking you about the SMS | |||
| 7. Trouble opting out of the programme (for those who have opted out) | |||
| 8. Any other adverse experiences | |||
What effect did the reminders have on your remembering of your appointments? How?
| Effect | Comment |
|---|---|
| Positive | |
| Neutral/no effect | |
| Negative |
What effect did the reminders have on your attendance of your appointments? How?
| Effect | Comment |
|---|---|
| Positive | |
| Neutral/no effect | |
| Negative |
Would you recommend that other mothers enrol for the programme? Why?
| Response | Comment |
|---|---|
| Yes | |
| No |
Overall how much did you like using/being a part of the Sawubona SMS reminder programme?
| Effect | Comment |
|---|---|
| Liked it | |
| Neutral | |
| Did not like it |