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1 IUD malposition was an exploratory outcome.
2 IUD use at 6 months was similar between the groups: 141
3 IUDs are now considered by many experts as a first-line
4 s (subdermal implant, 45% to 78% [P < .001]; IUD, 61% to 83% [P < .001]; injection, 28% to 44% [P = .
6 (odds ratio [OR], 1.23; 95% CI, 1.07-1.42), IUD or implant (OR, 1.79; 95% CI, 1.28-2.48), and D&C (O
9 eeking medical care in the first month after IUD placement occurred in 5.2% of participants in the le
10 was the rate of IUD expulsion 6 months after IUD insertion; an expulsion rate 8 percentage points hig
11 -genital-tract infection is negligible after IUD insertion, with or without the administration of pro
14 who were aged 50 years or younger and had an IUD insertion between Jan 1, 2001, and April 30, 2018.
17 gonorrhoea or chlamydial infection having an IUD inserted have a higher risk of salpingitis than do u
19 lpingitis than do uninfected women having an IUD inserted; however, the risk appears similar to that
24 ng 575 women who underwent randomization, an IUD was inserted in 100% (258 of 258) of the women in th
25 g the 294 participants (73%) who received an IUD and completed 6-month follow-up, complete expulsion
29 ted odds ratio, 1.24; 95% CI, 1.06-1.44) and IUD (adjusted odds ratio, 1.19; 95% CI, 1.06-1.32) use a
32 ]; heterogeneity chi23 = 7.3; p = 0.06), and IUDs = 1.21 (95% CI [1.14 to 1.28]; heterogeneity chi24
33 rates among users of subdermal implants and IUDs, as well as varying pregnancy and continuation rate
36 he primary outcome for this analysis was any IUD-related uterine perforation diagnosis for the first
37 and Expulsion of Intrauterine Devices (APEX-IUD) cohort study included women aged 50 years or younge
39 ed risk of perforation with breastfeeding at IUD insertion, the benefits of breastfeeding and effecti
40 non-post-partum and post-partum intervals at IUD insertion in the full cohort, and by breastfeeding s
41 non-post-partum and post-partum intervals at IUD insertion, and among post-partum individuals, to ass
43 We enrolled 71 non-ART (36 LNG-IUS, 31 C-IUD; 2 declined and 2 were ineligible) and 134 ART-using
44 ligible) and 134 ART-using (65 LNG-IUS, 67 C-IUD; 1 declined and 1 could not complete IUC insertion)
49 gnificantly different comparing LNG-IUS to C-IUD across 6 (adjusted odds ratio [AOR]: 0.78, 95% confi
52 used transvaginal ultrasonography to confirm IUD presence and position at the 6-month postpartum foll
56 t study of HIV-positive women using a copper IUD suggests that there is no significant increase in th
57 associated with the previous use of a copper IUD was 1.0 (95 percent confidence interval, 0.6 to 1.7)
62 in 321 (0%; 95% CI, 0 to 1.1) in the copper IUD group; the between-group absolute difference in both
65 ], .65-.97) for DMPA-IM compared with copper IUD, 0.86 (95% CI, .71-1.05) for DMPA-IM compared with L
67 past use of contraceptives, including copper IUDs, previous sexual relationships, and history of geni
69 trel IUDs and 356 assigned to receive copper IUDs, 317 and 321, respectively, received the interventi
72 edroxyprogesterone acetate (DMPA-IM), copper-IUD, and the levonorgestrel (LNG) implant on cervical T
77 s were used to (1) evaluate BV risk among Cu-IUD users relative to women using no/another nonhormonal
78 n, evaluations of the association between Cu-IUD and BV have not included more than 6 months of follo
79 cts on the vaginal environment induced by Cu-IUD initiation, which may adversely impact sexual and re
80 contraceptive copper intrauterine device (Cu-IUD) may increase bacterial vaginosis (BV) risk, possibl
81 (LNG), and a copper intrauterine device (Cu-IUD) on the vaginal environment after one and six consec
83 IUS, n = 11), copper intrauterine device (cu-IUD, n = 13) or levonorgestrel-containing combined oral
88 16, 2.00) higher in the first 6 months of Cu-IUD use and remained elevated over 18 months of use (P <
91 tivation compared to controls whereas the cu-IUD transcriptome was indistinguishable from luteal phas
93 ter contraceptive initiation, women using Cu-IUD had increased concentrations of 25/27 cytokines comp
96 ver, the effects of immediate versus delayed IUD insertion after uterine aspiration on rates of compl
98 l, patch, and/or ring), intrauterine device (IUD) and/or contraceptive implant, and dilation and cure
100 the United States with intrauterine device (IUD) insertions during 2011-2018, there was no increased
101 e a convenient time for intrauterine device (IUD) placement; the placement could then coincide with e
104 the United States, more intrauterine device (IUD) users select levonorgestrel IUDs than copper IUDs f
105 A), implant, pills, and intrauterine device (IUD)) were promoted and provided to women not using a re
106 thods-DMPA-IM, a copper intrauterine device (IUD), and a levonorgestrel (LNG) implant-on human immuno
107 nthly dispensations of intrauterine devices (IUDs) and oral contraceptive pills (OCPs) per 1000 femal
108 methods, which include intrauterine devices (IUDs) and subdermal hormonal implants, are used by only
109 eptive methods include intrauterine devices (IUDs) and subdermal implants and show great promise for
110 raceptive implants and intrauterine devices (IUDs) are long-acting reversible contraceptives (LARCs)
111 ptive effectiveness of intrauterine devices (IUDs) has been attributed in part to a foreign body reac
112 w discusses the use of intrauterine devices (IUDs) in United States teens as a potential strategy to
113 ration risk related to intrauterine devices (IUDs) inserted immediately post partum and among non-pos
115 lling and insertion of intrauterine devices (IUDs) or progestin implants and 20 to provide standard c
117 contraception (LARC), intrauterine devices (IUDs), implants, short-acting hormonal injection, and ba
119 Previous studies of intrauterine devices (IUDs), many of which are no longer in use, suggested tha
122 progestagen-releasing intrauterine devices (IUDs): ORs = 1.23 (95% CI [1.14 to 1.32]; p < 0.001), 1.
124 ersible contraception (intrauterine devices [IUDs] and implants) with other commonly prescribed contr
126 ants were randomly assigned to undergo early IUD placement and 201 to undergo interval IUD placement
127 condary outcomes were partial IUD expulsion, IUD removal, pelvic infection, patient satisfaction, ute
129 ing should be based on individual desire for IUD contraception and patient convenience to assure an I
130 was a significant increase in the level for IUDs of 0.64 (95% CI, 0.02-1.26) and for OCPs of 13.2 (9
131 and a significant decrease in the level for IUDs of 0.82 (95% CI, -1.55 to -0.09) after OHIP- in Ont
132 the likelihood that a woman would retain her IUD at 90 days or the frequency of postinsertion medical
133 No statistically significant changes in IUD or OCP dispensations were observed in areas with hig
134 rison group, overdiagnosis of salpingitis in IUD users, and inability to control for the confounding
135 P+, there was an immediate level increase in IUDs dispensed to Ontario females aged 15 to 24 years (i
136 3.6 to 4.4) with every 5 years since initial IUD use (P-trend = .03), while CRP increased an average
137 ly IUD placement and 201 to undergo interval IUD placement (mean [SD] age, 29.9 [5.4] years; 46 [11.4
139 n 5.2% of participants in the levonorgestrel IUD group and 4.9% of those in the copper IUD group.
142 randomly assigned to receive levonorgestrel IUDs and 356 assigned to receive copper IUDs, 317 and 32
146 orgestrel-releasing intrauterine device (LNG-IUD; n = 27), oral contraceptive pills (n = 32), or no h
148 orgestrel-releasing intrauterine system (LNG-IUD), gonadotropin-releasing hormone analogues (GnRHa; n
150 cts an understanding of the safety of modern IUDs, the potential for this highly effective method to
152 orical concerns regarding the association of IUD and infection; however, modern studies have shown th
153 lity was not associated with the duration of IUD use, the reason for the removal of the IUD, or the p
159 ediate insertion resulted in higher rates of IUD use at 6 months, without an increased risk of compli
161 es was to compare the incidence and risks of IUD-related uterine perforations by non-post-partum and
165 y, eliminate user error, and, in the case of IUDs, have extremely low or no systemic drug absorption.
166 f 1344 participants, increases in the use of IUDs in South Carolina were noted after the implementati
168 trol sites reported receiving counselling on IUDs or implants (565 [71%] of 797 vs 271 [39%] of 693,
171 djusted HRs using women with non-post partum IUD insertion as the referent were 5.34 (95% CI, 4.47-6.
174 intended pregnancy; how timing of postpartum IUD insertion and breastfeeding are associated with risk
175 s [61.1%]), with lower proportions providing IUD or implant (4059 physicians [18.5%]) and D&C (152 ph
178 hern California enrolled women who requested IUD insertion and were at low risk of sexually transmitt
183 f IUD use, the reason for the removal of the IUD, or the presence or absence of gynecologic problems
186 s were randomly assigned (in a 5:6 ratio) to IUD insertion immediately after the procedure or 2 to 6
187 ease, we examined the association of OC use, IUD use, and tubal ligation with plasma levels of C-reac
189 though the risk for uterine perforation with IUD insertion 4 days to 6 weeks or less post partum is n