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One-year continuation of postpartum intrauterine contraceptive device: findings from a retrospective cohort study in India.
Kumar, Somesh; Srivastava, Ashish; Sharma, Surendra; Yadav, Vivek; Mittal, Atul; Kim, Young-Mi; Nash-Mercado, Angela; Reijneveld, Sijmen A; Sood, Bulbul.
Afiliação
  • Kumar S; Jhpiego, an affiliate of Johns Hopkins University; University Medical Center Groningen, University of Groningen, Department of Health Sciences.
  • Srivastava A; Jhpiego, an affiliate of Johns Hopkins University. Electronic address: asheishsrivastava@gmail.com.
  • Sharma S; Jhpiego, an affiliate of Johns Hopkins University.
  • Yadav V; Jhpiego, an affiliate of Johns Hopkins University.
  • Mittal A; Jhpiego, an affiliate of Johns Hopkins University.
  • Kim YM; Jhpiego, an affiliate of Johns Hopkins University.
  • Nash-Mercado A; Jhpiego, an affiliate of Johns Hopkins University.
  • Reijneveld SA; University Medical Center Groningen, University of Groningen, Department of Health Sciences.
  • Sood B; Jhpiego, an affiliate of Johns Hopkins University.
Contraception ; 99(4): 212-216, 2019 04.
Article em En | MEDLINE | ID: mdl-30576637
ABSTRACT

OBJECTIVE:

To evaluate outcomes of a national postpartum (within 48 h of delivery) copper intrauterine device placement (PPCuIUD) program in six "high-focus states" with high unmet family planning need in India. STUDY

DESIGN:

We identified high-volume district hospitals that provided PPCuIUD in six (Bihar, Jharkhand, Uttar Pradesh, Uttarakhand, Madhya Pradesh and Chhattisgarh) Indian states (two per state). Each selected hospital maintained a list of PPCuIUD acceptors with contact phone numbers. We randomly selected 100 women at each site for inclusion in a telephone survey of IUD outcomes at 1 year. Questions regarded IUD expulsion, discontinuation because of symptoms (e.g., pain, bleeding, discharge), discontinuation for other reasons and use of alternative contraception if discontinuation reported.

RESULTS:

We could contact 844 of the 1200 randomly selected women, of whom 673 (79.7%) had postplacental insertion (within 10 min of delivery), while 171 (20.3%) had an early postpartum insertion (between 10 min to 48 h after delivery). Of those contacted, 530 women (62.8%) reported continuing with the method beyond 1 year, 63 (7.5%) reported having an expulsion, 163 (19.3%) reported having removals for associated side effects (bleeding, pain and discharge), and 88 (10.4%) reported having removals for other reasons. After removal or expulsion, almost half of the women (46.5%) did not switch to any other modern contraceptive method.

CONCLUSION:

PPCuIUD continuation rate at 1 year was 62.8%. Most removals within 1 year were due to associated side effects. Almost half of the women discontinuing PPCuIUD did not switch to an alternative modern contraceptive method. IMPLICATIONS The 1-year continuation rate of PPCuIUD achieved through a large-scale national program in India is satisfactory. The program though needs to address the low uptake of other modern contraceptive methods after discontinuation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dispositivos Intrauterinos de Cobre Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dispositivos Intrauterinos de Cobre Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2019 Tipo de documento: Article