Treatment FAQ

what is the difference between a standard and a protocol in medical treatment

by Zetta Bins Published 2 years ago Updated 2 years ago
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What is the difference between a protocol, standard of care delivery, and policy at the practice, state, and federal levels? Briefly outline each. A protocol is the set of clinical practice guidelines and standards that the health practitioners, mostly clinicians, use in clinical decision-making, and define the care that is involved.

Full Answer

What is the difference between a protocol and a standard?

Standards are guidelines, these are more abstract. You can have products that meet the standard, exceed the standard or below a certain standard. Protocols are rules. They define exactly how data is exchanged and the expected behavior. These are rules you must follow exactly or your device will not be able...

What are protocols?

Protocols are rules. They define exactly how data is exchanged and the expected behavior. These are rules you must follow exactly or your device will not be able to communicate at all with other devices. You can not exceed the protocol but its possible that you do not implement all the features...

What is the difference between procedure and standard?

Procedure tells us step by step what to do while standard is the lowest level control that can not be changed. Policy is a high level statement uniform across organization. Let’s explore these terms individually and develop a better understanding:

What is the purpose of clinical guidelines and care protocols?

DOI: 10.1016/j.iccn.2003.08.002 Abstract Clinical guidelines and care protocols are intended to provide information, based on an appraisal of the current best evidence of clinical and cost-effectiveness, regarding therapeutic interventions for given conditions.

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What is a protocol in medical treatment?

Listen to pronunciation. (PROH-tuh-KOL) A detailed plan of a scientific or medical experiment, treatment, or procedure. In clinical trials, it states what the study will do, how it will be done, and why it is being done.

What does Standard mean in medical terms?

Listen to pronunciation. (STAN-durd MEH-dih-kul kayr) Treatment that is accepted by medical experts as a proper treatment for a certain type of disease and that is widely used by healthcare professionals. Also called best practice, standard of care, and standard therapy.

What is the difference between a protocol standard of care delivery?

This protocol has a set of guidelines that can be followed and carried out without a physicians order. Standard of care delivery describes the care patients should be offered by health professionals and health services for a specific clinical condition or defined clinical pathway in line with current best evidence.

What is a protocol in a hospital?

Definition. A medical protocol is considered to be a set of predetermined criteria that define appropriate nursing interventions that articulate or describe situations in which the nurse makes judgments relative to a course of action for effective management of common patient care problems.

What is standard of patient care?

Standard of care can be defined as "…not a guideline or list of options; instead, it is a duty determined by a given set of circumstances that present in a particular patient, with a specific condition, at a definite time and place" [2]. In other words, standard of care is sensitive to time, place, and person.

What is an example of standard of care?

The term “standard of care” refers to the reasonable degree of care a person should provide to another person, typically in a professional or medical setting. For example, standard of care in the case of a cancer patient could include a recommendation of chemotherapy or surgery.

What is the difference between a protocol and procedure?

A Protocol defines a set of Procedures or steps to be followed for the accomplishment of a given task. Procedures are task oriented. Procedures provide step-by-step instructions on how to do a task.

Do doctors follow protocols?

Physician protocols do not place legal limitations on the physicians; they are characterized by their allowance for independent medical judgment. They are a voluntary agreement by the physicians to follow certain patterns when practicing within the group.

What is called a protocol?

protocol, in computer science, a set of rules or procedures for transmitting data between electronic devices, such as computers. In order for computers to exchange information, there must be a preexisting agreement as to how the information will be structured and how each side will send and receive it.

Why do hospitals have protocols?

The use of clinical protocols allows health care providers to offer appropriate diagnostic treatment and care services to patients, variance reports to purchasers and quality training to clinical staff.

Why do we have protocols in healthcare?

Protocols provide a clear logical structure and therefore added confidence for clinical management. In order to create the most pertinent protocols and guidelines for your practice consider engaging the whole team to create your own set – you will then know that these are appropriate and easy to follow.

Why is the term "protocol" confusing?

The term protocols is confusing sometimes because it is used differently from location to location, state to state. In general, protocols have to be very carefully written, or midwives damage themselves legally.

What is a clinical guidelines midwife?

The terms guidelines and standards should NOT be interchanged. Standards provide the midwife with process. Clinical guidelines provide research-based information. Standards are rigid.

Do midwives use written protocols?

The same is true for any midwife whose practice uses written protocols. Most of the time protocols are a group decision by a group of practitioners and serve to insulate the group from legal action should one of the members deviate from them.

What is clinical guidelines?

Clinical guidelines and care protocols are intended to provide information, based on an appraisal of the current best evidence of clinical and cost-effectiveness, regarding therapeutic interventions for given conditions.

What is the Department of Health?

The Department of Health also aims to introduce nationally agreed multidisciplinary care protocols which will dictate how certain conditions are to be managed. These developments have the potential to enhance healthcare provision and nursing practice.

Who put strict rules on clinical studies?

Strict rules for clinical studies have been put in place by National Institutes of Health and the FDA. Some studies involve promising new treatments that may directly benefit participants. Others do not directly benefit participants, but may help scientists learn better ways to help people.

What are the criteria for clinical trials?

All clinical trials have guidelines, called eligibility criteria, about who can participate. The criteria are based on such factors as age, sex, type and stage of disease, previous treatment history, and other medical conditions.

What to do before joining a clinical trial?

Before joining a clinical trial, it is important to learn as much as possible. Discuss your questions and concerns with members of the health care team conducting the trial. Also, discuss the trial with your health care provider to determine whether or not the trial is a good option based on your current treatment.

Why is confidentiality important in clinical research?

Confidentiality is an important part of clinical research and ensures that personal information is seen only by those authorized to have access. It also means that the personal identity and all medical information of clinical trial participants is known only to the individual patient and researchers.

Why do people participate in clinical trials?

Some people participate in clinical trials because none of the standard (approved) treatment options have worked, or they are unable to tolerate certain side effects. Clinical trials provide another option when standard therapy has failed.

Why is it important to test drugs and medical products in the people they are meant to help?

It is also important to conduct research in a variety of people, because different people may respond differently to treatments. FDA seeks to ensure that people of different ages, races, ethnic groups, and genders are included in clinical trials.

What is clinical research?

Clinical research is much different from the medical treatment you receive in a Healthcare Provider's office. Answers specific questions through research involving numerous research volunteers. Address the needs of individual patients.

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