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Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study

PURPOSE: Etonogestrel subdermal implants are a commonly used contraceptive device placed in the medial upper arm. Plastic and orthopedic surgeons may be consulted for difficult implant removals. We performed a case–control study comparing patients undergoing surgical and uncomplicated in-office remo...

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Autores principales: Katabi, Leila, Stevens, Erica, Ascha, Mona, Arora, Kavita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373992/
https://www.ncbi.nlm.nih.gov/pubmed/35968271
http://dx.doi.org/10.2147/OAJC.S368250
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author Katabi, Leila
Stevens, Erica
Ascha, Mona
Arora, Kavita
author_facet Katabi, Leila
Stevens, Erica
Ascha, Mona
Arora, Kavita
author_sort Katabi, Leila
collection PubMed
description PURPOSE: Etonogestrel subdermal implants are a commonly used contraceptive device placed in the medial upper arm. Plastic and orthopedic surgeons may be consulted for difficult implant removals. We performed a case–control study comparing patients undergoing surgical and uncomplicated in-office removal at our institution. PATIENTS AND METHODS: We identified patients who underwent operative removal of implantable contraceptive devices by plastic or orthopedic surgeons at our institution from January 2014 to October 2019. Patients who underwent uncomplicated office removal during the same time were compared. Demographic and surgical variables were collected, and descriptive statistics were calculated. Univariate and multivariate logistic regression was performed with surgical versus outpatient removal as the outcome of interest. RESULTS: A total of 669 patients undergoing etonogestrel subdermal implant removals were identified during the five-year study period, of which thirteen patients required surgical removal (1.9%) and 326 were selected as uncomplicated removal comparisons. There were no significant differences in median (IQR) body mass index (BMI) (31.1 [28.2, 35.2] versus 29.3 [24.0, 35.1], p = 0.19), median (IQR) weight gain since device placement (5 [−0.6, 14.7] kilograms versus 1.6 [−1.2, 5.8] kilograms, p = 0.15), or length of time since device insertion (2.3 [0.8, 2.8] years versus 1.0 [0.4, 2.2] years, p = 0.17). Of those who needed surgical removal, the most common indication for implant removal was device expiration (n = 5, 38.5%). Devices placed by OBGYN attendings were less likely to require surgical removal (p = 0.02). Family medicine attendings were more likely to refer patients for surgical removal (p = 0.02). No significant findings were detected on univariate or multivariate regression. Among surgical removals, radiography was the most frequently used imaging modality. Implants were most frequently subdermal (n = 11, 84.6%) though intramuscular placement was also identified (n = 2, 15.4%). Only one patient had residual paresthesia along the length of the incision. No other complications were identified. CONCLUSION: We did not identify risk factors associated with the difficult removal of etonogestrel subdermal implants. Practitioners should consult upper extremity surgeons if they encounter difficult removals.
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spelling pubmed-93739922022-08-13 Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study Katabi, Leila Stevens, Erica Ascha, Mona Arora, Kavita Open Access J Contracept Original Research PURPOSE: Etonogestrel subdermal implants are a commonly used contraceptive device placed in the medial upper arm. Plastic and orthopedic surgeons may be consulted for difficult implant removals. We performed a case–control study comparing patients undergoing surgical and uncomplicated in-office removal at our institution. PATIENTS AND METHODS: We identified patients who underwent operative removal of implantable contraceptive devices by plastic or orthopedic surgeons at our institution from January 2014 to October 2019. Patients who underwent uncomplicated office removal during the same time were compared. Demographic and surgical variables were collected, and descriptive statistics were calculated. Univariate and multivariate logistic regression was performed with surgical versus outpatient removal as the outcome of interest. RESULTS: A total of 669 patients undergoing etonogestrel subdermal implant removals were identified during the five-year study period, of which thirteen patients required surgical removal (1.9%) and 326 were selected as uncomplicated removal comparisons. There were no significant differences in median (IQR) body mass index (BMI) (31.1 [28.2, 35.2] versus 29.3 [24.0, 35.1], p = 0.19), median (IQR) weight gain since device placement (5 [−0.6, 14.7] kilograms versus 1.6 [−1.2, 5.8] kilograms, p = 0.15), or length of time since device insertion (2.3 [0.8, 2.8] years versus 1.0 [0.4, 2.2] years, p = 0.17). Of those who needed surgical removal, the most common indication for implant removal was device expiration (n = 5, 38.5%). Devices placed by OBGYN attendings were less likely to require surgical removal (p = 0.02). Family medicine attendings were more likely to refer patients for surgical removal (p = 0.02). No significant findings were detected on univariate or multivariate regression. Among surgical removals, radiography was the most frequently used imaging modality. Implants were most frequently subdermal (n = 11, 84.6%) though intramuscular placement was also identified (n = 2, 15.4%). Only one patient had residual paresthesia along the length of the incision. No other complications were identified. CONCLUSION: We did not identify risk factors associated with the difficult removal of etonogestrel subdermal implants. Practitioners should consult upper extremity surgeons if they encounter difficult removals. Dove 2022-08-08 /pmc/articles/PMC9373992/ /pubmed/35968271 http://dx.doi.org/10.2147/OAJC.S368250 Text en © 2022 Katabi et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Katabi, Leila
Stevens, Erica
Ascha, Mona
Arora, Kavita
Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title_full Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title_fullStr Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title_full_unstemmed Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title_short Characteristics of Patients Requiring Surgical Removal of Subdermal Contraceptive Implants: A Case–Control Study
title_sort characteristics of patients requiring surgical removal of subdermal contraceptive implants: a case–control study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373992/
https://www.ncbi.nlm.nih.gov/pubmed/35968271
http://dx.doi.org/10.2147/OAJC.S368250
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