Refugee Attitudes Towards Patient Autonomy-Based Ethics of Informed Consent

Refugee Attitudes Towards Patient Autonomy-Based Ethics of Informed Consent
Book Chapter
Sukran Sevimli
Practices, Challenges, and Prospects of Digital Ethnography as a Multidisciplinary Method, 2022 [IGIG Global]
Abstract
The objective of this study was to identify refugees’ attitudes concerning the autonomy-based ethics of informed consent and to determine whether these attitudes varied by gender. A quantitative methodology was adopted for this study. Questions were scored using a Likert-type scale and face-to-face interviews were conducted with 610 refugees who had migrated to Turkey from MENA and Caucasia countries. Refugees from eleven countries participated in the survey, of whom the majority were men (62.5% male versus 37.5% female). Autonomy is a fundamental principle of human rights and medical ethics. Refugees from MENA countries, where the concept of autonomy is contrary to the deeply-held traditional religious views of much of the population, in general, have a poor grasp of informed consent as a patient right. Traditional values steeped in patriarchy constitute an obstacle to women making decisions regarding their own lives in MENA and Caucasia countries. Therefore, the practice of informed consent is of critical importance in helping to reduce gender differentials in healthcare.

Informed consent for surgical case reports

Informed consent for surgical case reports
Mohamed Onyango, Brian Kariuki
The Annals of African Surgery, 30 June 2022
Open Access
Excerpt
Informed consent is one of the most essential pillars of medical research ethics (1). It encompasses the medical ethical principle of autonomy which enables the participants to decide on whether or not to partake in a study without any coercion (2). It also enables patients to make informed decisions after critically analyzing the implications of the facts presented by the surgeon (3). It is of great importance that surgeons apply specific informed consent rules for specific study designs they undertake. The majority of studies submitted to surgical journals are case reports, but the process for obtaining quality informed consent is still insufficient. In addition, some journals do not have well-defined informed consent protocols for case report studies. This editorial thus aims to highlight case report specific rules for informed consent for surgeons to employ prior to commencement of their research…

Are Consent Forms Used in Cardiology Clinics Easy to Read?

Are Consent Forms Used in Cardiology Clinics Easy to Read?
İbrahim Etem Dural
Archives of the Turkish Society of Cardiology, 30 June 2022
Open Access
Abstract
Objective
Informed consent forms are a contract between the patient and the doctor before the medical diagnosis and treatment. It is extremely important that the patient can read and understand such forms. The purpose of the present study was to investigate the readability levels of consent forms recommended by the Turkish Society of Cardiology used in cardiology clinics.
Methods
The number of words, syllables, letters, and characters of 20 consent forms that are used in cardiology clinics were calculated. The readability scores were calculated by using the formulas of Ateşman and Bezirci–Yılmaz.
Results
It was found that the cardiology consent forms were readable at the 11th or 12th grade according to the Ateşman Index and at the high school level according to the Bezirci–Yılmaz Index.
Conclusion
We suggest that the informed consent forms recommended by the Turkish Society of Cardiology must be simplified from the level that requires high school education to the level that requires 6 years of education, which is the average schooling year in Turkey.

Patients’ Choice, Consent, and Ethics in Patient Blood Management

Patients’ Choice, Consent, and Ethics in Patient Blood Management
James P. Isbister, Bronwyn L. Pearse, Alana S. Delaforce, Shannon L. Farmer
Anesthesia & Analgesia, September 2022; 135(3) pp 489-500
Infographic
Picture 1
Abstract
…Patients must be informed of their diagnosis, the nature, severity and prognosis of the disease, and treatment options along with risks and benefits. They should be involved in decision-making regarding their management. However, as part of this process, there are multifaceted medical, legal, ethical, and economic issues, encompassing shared decision-making, patient choice, and informed consent. Furthermore, variability in patient circumstances and preferences, the complexity of medical science, and the workings of health care systems in which consent takes place can be bewildering, not only for the patient but also for clinicians obtaining consent…

How Informed Is Your Informed Consent: Evaluating Differences Between Resident and Attending Obtained Consents for Cholecystectomy

How Informed Is Your Informed Consent: Evaluating Differences Between Resident and Attending Obtained Consents for Cholecystectomy
Kathleen E. Singer, Jennifer E. Baker, Nora C. Elson, Taylor E. Wallen, Ann Salvator, Ralph C. Quillin, Jeffrey J. Sussman, Amy T. Makley, Michael D. Goodman
Journal of Surgical Education, 24 August 2022
Abstract
Objective
There is considerable variability in surgeons’ approach to write and obtain informed consent for surgery, particularly among resident trainees. We analyzed differences in procedures and complications described in documented surgical consents for cholecystectomy between residents and attendings. We hypothesized that attending consents would describe more comprehensive procedures and complications than those done by residents.
Design
This is a retrospective analysis of 334 patients who underwent cholecystectomy. Charts were queried for demographics, surgical approach, whether the consent was completed electronically, and which provider completed the consent. Specifically, consents were evaluated for inclusion of possible conversion to open procedure, intraoperative cholangiogram, bile duct injury, injury to nearby structures, reoperation, bile leak, as well as if the consent matched the actual procedure performed.
Setting
This study was conducted at an accredited general surgery training program at an academic tertiary care center in the Midwest.
Participants
This was a review of 334 patients who underwent cholecystectomy over a 1 year period.
Results
Of all documented consents analyzed, 153 (47%) specifically included possible intraoperative cholangiogram, 156 (47%) included bile duct injury, 76 (23%) included injury to nearby structures, 22 (7%) included reoperation, and 62 (19%) included bile leak. In comparing residents and attendings, residents were more likely to consent for bile duct injury (p = 0.002), possible intraoperative cholangiogram (p = 0.0007), injury to nearby structures (p < 0.0001), reoperation (p < 0.0001), and bile leak (p < 0.0001).
Conclusions
Significant variation exists between documentation between resident and attending cholecystectomy consents, with residents including more complications than attendings on their consent forms. These data suggest that experience alone does not predict content of written consents, particularly for common ambulatory procedures. Education regarding the purpose of informed consent and what should be included in one may lead to a reduction in variability between providers.

Shared Consent: Acknowledging the Subjectivity of Surgical Decision-making

Shared Consent: Acknowledging the Subjectivity of Surgical Decision-making
Surgical Perspectives
Paul J.Kepper, Sean C. Wightman, Baddr A. Shakhsheer
Annals of Surgery, 22 August 2022
Excerpt
Surgeons aspire to make data-driven decisions to provide the highest level of patient care. Evidence-based medicine mandates utilization of the best available data to guide decision making. The decision to offer an operation, however, is more than an evaluation of clinical evidence. Clinical expertise applies evidence-based medicine to a specific patient and tailors the practice of medicine to individual patient situations and preferences. Clinicians fill the gaps in the evidence with expertise developed over years of experience and training. Bridging these gaps is often described as the “art of surgery”; it is inherently subjective. Shared consent is the process that acknowledges subjectivity in decision-making. Shared consent is the foundation for a cooperative cognitive model between patient and surgeon, interpreting the available data through the lens of patient preference while relying on surgeon expertise…

Regional Audit: Valid and Informed Consent for Lower Limb Arthroplasty in Orthopaedic Surgery: Are We Doing Enough?

Regional Audit: Valid and Informed Consent for Lower Limb Arthroplasty in Orthopaedic Surgery: Are We Doing Enough?
Z Sohail, R Mills, O Adebayo, G Mamarelis, F Acquaah, S Subhash, I Liew
British Journal of Surgery, 19 August 2022; 109(Supplement 6)
Abstract
Aim
To investigate regionally the validity of the patient consent process for lower limb arthroplasty, compared to set data standards, with a view to investigating whether the consent process could be improved, and if so, how?
Method
Regional data from 8 hospital trusts (50 data sets collected from each hospital) across England was collected retrospectively from May 1st, 2021, (25 THR, 25 TKR), collated and collectively analysed against agreed, pre-determined set criterion. Data standards included ascertaining whether alternatives to surgery were offered and exploring the likely benefits and risks. Capacity to consent for procedure-specific surgery was measured as patients’ ability to understand, weigh up, retain, and communicate their decisions regarding surgery. Hospitals regional data was collectively analysed.
Results
Capacity was only successfully fulfilled and documented regionally in 11.6% of hip and 13.9% of knee replacement surgeries, despite Consent Form 1 having been filled out in 94.8% and 88.5% of cases respectively, which were procedure specific in only 74.0% and 72.1% of cases.
Conclusions
Significant improvement can clearly be made to an area of already such high clinical negligence claims. We propose a novel solution involving the digitalisation of the consent process, including multimedia surgical videos to better inform patients and reliably assist in establishing the validity of a patient’s consent. The implications of this are limited not only to Orthopaedic surgery but could have far-reaching consequences across all surgical (and indeed medical) specialties, where obtaining valid and informed consent for procedures remains integral to quality patient care.

Standardizing Consent Forms for Outpatient Urology Procedures

Standardizing Consent Forms for Outpatient Urology Procedures
S Shrestha, E Jiang, A Sandhu, P Pinnamaraju, T Swallow, A Pai
British Journal of Surgery, 19 August 2022; 109(Supplement 6)
Abstract
Introduction
British Association of Urological Surgeons (BAUS) guidelines have provided comprehensive and standardized guidelines for urological procedures, including indications, benefits, risks involved, and alternatives. At our institution, currently, consent forms are handwritten resulting in generalized or incomplete information given to patients.
Aim
To improve patient understanding of the procedures they are undergoing by providing standardized consent form stickers for procedures as per BAUS guidelines.
Method
Single institution data were collected retrospectively for flexible cystoscopy, stent removal, transrectal ultrasonography (TRUS), and transurethral laser ablation (TULA). Consent forms compared to BAUS guidelines. A standardized consent form sticker for each procedure was developed in accordance with BAUS guidelines and reviewed via the trust’s clinical governance process. Clinicians were educated in their use for future consenting.
Results
Consent forms of consecutive patients over a two-month period were analyzed. The initial audit showed that the proportion of patients who had all risks included was 0% for flexible cystoscopy, 0% for TRUS, and 100% for stent removal. Common and rare, but serious risks were not mentioned in all cases. 100% of patients had all risks mentioned for TULA. After education on the consent process and the introduction of consent form stickers, all risks (100%) were mentioned for all procedures.
Conclusions
It is imperative that patients are fully informed about the risks, indications, and alternatives of their treatment. Failure to provide this information in full may lead to unnecessary angst, morbidity, and litigation. Simple quality improvement projects can lead to measurable improvement in patient information.

Improving Consent Forms for Laparoscopic Cholecystectomy; a Visual Consent Form Toolkit

Improving Consent Forms for Laparoscopic Cholecystectomy; a Visual Consent Form Toolkit
M Jeilani, J Super, M Riad, B Jayasankar
British Journal of Surgery, 19 August 2022; 109(Supplement 6)
Abstract
Aim
Laparoscopic cholecystectomy is a common elective operation with significant complication risks. GMC guidance on consent emphasises informed consent, and failure to warn patients of significant complications can lead to medico-legal implications. We aimed to assess the quality of risk documentation for laparoscopic cholecystectomies performed at our trust. In particular, we aimed to assess improvement since previous cycles after circulation of our boutique ‘Visual Consent Form Toolkit’, an easily accessible resource for risks associated with common procedures.
Method
Consent forms for 49 elective laparoscopic cholecystectomies performed at a busy district general hospital between September and November 2021 were retrospectively analysed. Risk documentation was audited against a standard of 15 common complications associated with laparoscopic cholecystectomy.
Results
There was significant improvement across the board. Risks previously documented at 100% remained at this level (infection & bleeding). Those previously well-documented showed further improvement (CBD injury, bile leak, damage to local structures, open conversion & VTE). Of those not previously well-documented (the rest), all except two (diarrhoea & pancreatitis) showed improvement. In particular anaesthetic risks, which was emphasised in our toolkit, saw the largest improvement.
Conclusions
Risk documentation on consent forms has overall considerably improved with the circulation of our ‘Visual Consent Form Toolkit’. More risks now fully or partially meet the expected standard. From those risks not meeting the expected standard despite numerous audit cycles, we understand that surgeons do not feel these risks should be documented in all situations for all patients, and therefore that an expected standard does not necessarily apply for these risks.

Improving the Quality of Consent Forms in Emergency Laparotomy

Improving the Quality of Consent Forms in Emergency Laparotomy
S Probert, N Ballanamada Appaiah, L Khan
British Journal of Surgery, 19 August 2022; 109(Supplement 6)
Abstract
Aim
To improve the quality and completion of consent forms for patients undergoing emergency laparotomy.
Methods
A standard for emergency laparotomy consent forms, guided by recommendations from the National Emergency Laparotomy Audit (NELA) was established. This standard was used to score consent forms. Our initial audit of 20 consent forms scored an average of 41.9%. A template sticker, specific to emergency laparotomy, was created. This contains all of the information deemed important by our standard. The sticker allows the surgeon completing the consent process to simply tick off the individual components once discussed with the patient and apply it to the regular consent form. The stickers were introduced to all of those involved in consenting patients, and their use was strongly encouraged.
Results
Consent forms were collected and scored over the following 2-months. Of the 18 consent forms, 33% made use of the consent form sticker, with an average score of 65.2% (improvement of 23.3%). In analysing scores for both the pre- and post-intervention consent forms, we found a P value of < 0.0001.
Conclusions
The use of consent templates specific to surgical procedures improves the quality of consent forms and ensures that all possible complications are discussed with patients. The use of stickers for emergency laparotomy has improved the quality of our consent forms. With ongoing use, we aim to ensure that all patients undergoing this procedure are adequately consented. There remains room for continued improvement, and we believe ongoing exposure to these stickers will lead to an up-take in use.