Injection: History
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An injection (often and usually referred to as a "shot" in US English, a "jab" in UK English, or a "jag" in Scottish English and Scots) is the act of administering a liquid, especially a drug, into a person's body using a needle (usually a hypodermic needle) and a syringe. An injection is considered a form of parenteral drug administration; it does not involve absorption in the digestive tract. This allows the medication to be absorbed more rapidly and avoid the first pass effect. There are many types of injection, which are generally named after the body tissue the injection is administered into. This includes common injections such as subcutaneous, intramuscular, and intravenous injections, as well as less common injections such as intraperitoneal, intraosseous, intracardiac, intraarticular, and intracavernous injections. Injections are among the most common health care procedures, with at least 16 billion administered in developing and transitional countries each year. Of these, 95% are used in curative care or as treatment for a condition, 3% are to provide immunizations/vaccinations, and the rest are used for other purposes, including blood transfusions. The term injection is sometimes used synonymously with inoculation, but injection does not only refer to the act of inoculation. Injections generally administer a medication as a bolus (or one-time) dose, but can also be used for continuous drug administration. After injection, a medication may be designed to be released slowly, called a depot injection, which can produce long-lasting effects. An injection necessarily causes a small puncture wound to the body, and thus may cause localized pain or infection. The occurrence of these side effects varies based on injection location, the substance injected, needle gauge, procedure, and individual sensitivity. Rarely, more serious side effects including gangrene, sepsis, and nerve damage may occur. Fear of needles, also called needle phobia, is also common and may result in anxiety and fainting before, during, or after an injection. To prevent the localized pain that occurs with injections the injection site may be numbed or cooled before injection and the person receiving the injection may be distracted by a conversation or similar means. To reduce the risk of infection from injections, proper aseptic technique should be followed to clean the injection site before administration. If needles or syringes are reused between people, or if an accidental needlestick occurs, there is a risk of transmission of bloodborne diseases such as HIV and hepatitis. Unsafe injection practices contribute to the spread of bloodborne diseases, especially in less-developed countries. To combat this, safety syringes exist which contain features to prevent accidental needlestick injury and reuse of the syringe after it is used once. Furthermore, recreational drug users who use injections to administer the drugs commonly share or reuse needles after an injection. This has led to the development of needle exchange programs and safe injection sites as a public health measure, which may provide new, sterile syringes and needles to discourage the reuse of syringes and needles. Used needles should ideally be placed in a purpose-made sharps container which is safe and resistant to puncture. Some locations provide free disposal programs for such containers for their citizens.

  • inoculation
  • public health
  • intraperitoneal

1. Types

Needle insertion angles for 4 types of injection: intramuscular, subcutaneous, intravenous, and intradermal. https://handwiki.org/wiki/index.php?curid=1437016

Injections are classified in multiple ways, including the type of tissue being injected into, the location in the body the injection is designed to produce effects, and the duration of the effects. Regardless of classification, injections require a puncture to be made, thus requiring sterile environments and procedures to minimize the risk of introducing pathogens into the body. All injections are considered forms of parenteral administration, which avoids the first pass metabolism which would potentially affect a medication absorbed through the gastrointestinal tract.

1.1. Systemic

Many injections are designed to administer a medication which has an effect throughout the body. Systemic injections may be used when a person cannot take medicine by mouth, or when the medication itself would not be absorbed into circulation from the gastrointestinal tract. Medications administered via a systemic injection will enter into blood circulation, either directly or indirectly, and thus will have an effect on the entire body.

Intravenous

Intravenous injections, abbreviated as IV, involve inserting a needle into a vein, allowing a substance to be delivered directly into the bloodstream.[1] An intravenous injection provides the quickest onset of the desired effects because the substance immediately enters the blood, and is quickly circulated to the rest of the body.[2] Because the substance is administered directly into the bloodstream, there is no delay in the onset of effects due to the absorption of the substance into the bloodstream. This type of injection is the most common and is used frequently for administration of medications in an inpatient setting.

Another use for intravenous injections includes for the administration of nutrition to people who cannot get nutrition through the digestive tract. This is termed parenteral nutrition and may provide all or only part of a person's nutritional requirements. Parenteral nutrition may be pre-mixed or customized for a person's specific needs.[3] Intravenous injections may also be used for recreational drugs when a rapid onset of effects is desired.[4][5]

Intramuscular

Intramuscular injections, abbreviated as IM, deliver a substance deep into a muscle, where they are quickly absorbed by the blood vessels into systemic circulation. Common injection sites include the deltoid, vastus lateralis, and ventrogluteal muscles.[6] Medical professionals are trained to give IM injections, but people who are not medical professionals can also be trained to administer medications like epinephrine using an autoinjector in an emergency.[7] Some depot injections are also administered intramuscularly, including medroxyprogesterone acetate among others.[8] In addition to medications, most inactivated vaccines, including the influenza vaccine, are given as an IM injection.[9]

Subcutaneous

Subcutaneous injections, abbreviated as SC or sub-Q, consist of injecting a substance into the fat tissue between the skin and the muscle.[10] Absorption of the medicine from this tissue is slower than in an intramuscular injection. Since the needle does not need to penetrate to the level of the muscle, a thinner and shorter needle can be used. Subcutaneous injections may be administered in the fatty tissue behind the upper arm, in the abdomen, or in the thigh. Certain medications, including epinephrine, may be used either intramuscularly or subcutaneously.[11] Others, such as insulin, are almost exclusively injected subcutaneously. Live or attenuated vaccines, including the MMR vaccine (measles, mumps, rubella), varicella vaccine (chickenpox), and zoster vaccine (shingles) are also injected subcutaneously.[12]

Intradermal

A tuberculin sensitivity test being administered intradermally. https://handwiki.org/wiki/index.php?curid=1986487

Intradermal injections, abbreviated as ID, consist of a substance delivered into the dermis, the layer of skin above the subcutaneous fat layer, but below the epidermis or top layer. An intradermal injection is administered with the needle placed almost flat against the skin, at a 5 to 15 degree angle.[13] Absorption from an intradermal injection takes longer than when the injection is given intravenously, intramuscularly, or subcutaneously. For this reason, few medications are administered intradermally. Intradermal injections are most commonly used for sensitivity tests, including tuberculin skin tests and allergy tests, as well as sensitivity tests to medications a person has never had before. The reactions caused by tests which use intradermal injection are more easily seen due to the location of the injection, and when positive will present as a red or swollen area. Common sites of intradermal injections include the forearm and lower back.[13]

Intraosseous

An intraosseous injection or infusion is the act of administering medication through a needle inserted into the bone marrow of a large bone. This method of administration is only used when it is not possible to maintain access through a less invasive method such as an intravenous line, either due to frequent loss of access due to a collapsed vessel, or due to the difficulty of finding a suitable vein to use in the first place.[14] Intraosseous access is commonly obtained by inserting a needle into the bone marrow of the humerus or tibia, and is generally only considered once multiple attempts at intravenous access have failed, as it is a more invasive method of administration than an IV.[14] With the exception of occasional differences in the accuracy of blood tests when drawn from an intraosseous line, it is considered to be equivalent in efficacy to IV access. It is most commonly used in emergency situations where there is not ample time to repeatedly attempt to obtain IV access, or in younger people for whom obtaining IV access is more difficult.[14][15]

1.2. Localized

Injections may be performed into specific parts of the body when the medication's effects are desired to be limited to a specific location, or where systemic administration would produce undesirable side effects which may be avoided by a more directed injection.

Injections to the corpus cavernosum of the penis, termed intracavernous injections, may be used to treat conditions which are localized to the penis. They can be self-administered for erectile dysfunction prior to intercourse or used in a healthcare setting for emergency treatment for a prolonged erection with an injection to either remove blood from the penis or to administer a sympathomimetic medication to reduce the erection.[16] Intracavernosal injections of alprostadil may be used by people for whom other treatments such as PDE5 inhibitors are ineffective or contraindicated. Other medications may also be administered in this way, including papaverine, phentolamine, and aviptadil.[17] The most common adverse effects of intercavernosal injections include fibrosis and pain, as well as hematomas or bruising around the injection site.[17]

Medications may also be administered by injecting them directly into the vitreous humor of the eye. This is termed an intravitreal injection, and may be used to treat endophthalmitis (an infection of the inner eye), macular degeneration, and macular edema.[18] An intravitreal injection is performed by injecting a medication through the pupil into the vitreous humor core of the eye after applying a local anesthetic drop to numb the eye and a mydriatic drop to dilate the pupil. They are commonly used in lieu of systemic administration to both increase the concentrations present in the eye, as well as avoid systemic side effects of medications.[18]

When an effect is only required in one joint, a joint injection (or intra-articular injection) may be administered into the articular space surrounding the joint. These injections can range from a one-time dose of a steroid to help with pain and inflammation to complete replacement of the synovial fluid with a compound such as hyaluronic acid.[19] The injection of a steroid into a joint is used to reduce inflammation associated with conditions such as osteoarthritis, and the effects may last for up to 6 months following a single injection.[19] Hyaluronic acid injection is used to supplement the body's natural synovial fluid and decrease the friction and stiffness of the joint.[19] Administering a joint injection[20] generally involves the use of an ultrasound or other live imaging technique to ensure the injection is administered in the desired location, as well as to reduce the risk of damaging surrounding tissues.[21]

1.3. Long-Acting

Long-acting injectable (LAI) formulations of medications are not intended to have a rapid effect, but instead release a medication at a predictable rate continuously over a period of time. Both depot injections and solid injectable implants are used to increase adherence to therapy by reducing the frequency at which a person must take a medication.[22]:3

Depot

A depot injection is an injection, usually subcutaneous, intradermal, or intramuscular, that deposits a drug in a localized mass, called a depot, from which it is gradually absorbed by surrounding tissue. Such injection allows the active compound to be released in a consistent way over a long period.[23] Depot injections are usually either oil-based or an aqueous suspension. Depot injections may be available as certain salt forms of a drug, such as decanoate salts or esters. Examples of depot injections include haloperidol decanoate, medroxyprogesterone acetate,[23] and naltrexone.[24]

Implant

Injections may also be used to insert a solid or semi-solid into the body which releases a medication slowly over time. These implants are generally designed to be temporary, replaceable, and ultimately removed at the end of their use or when replaced. There are multiple contraceptive implants marketed for different active ingredients, as well as differing duration of action - most of these are injected under the skin.[25] A form of buprenorphine for the treatment of opioid dependence is also available as an injectable implant.[26] Various materials can be used to manufacture implants including biodegradable polymers, osmotic release systems, and small spheres which dissolve in the body.[22]:4, 185, 335

2. Adverse Effects

2.1. Pain

The act of piercing the skin with a needle, while necessary for an injection, also may cause localized pain. The most common technique to reduce the pain of an injection is simply to distract the person receiving the injection. Pain may be dampened by prior application of ice or topical anesthetic, or pinching of the skin while giving the injection. Some studies also suggest that forced coughing during an injection stimulates a transient rise in blood pressure which inhibits the perception of pain.[27] For some injections, especially deeper injections, a local anesthetic is given.[27] When giving an injection to young children or infants, they may be distracted by giving them a small amount of sweet liquid, such as sugar solution,[28] or be comforted by breastfeeding [29] during the injection, which reduces crying.

2.2. Infection

A needle tract infection, also called a needlestick infection, is an infection that occurs when pathogens are inadvertently introduced into the tissues of the body during an injection. Contamination of the needle used for injection, or reuse of needles for injections in multiple people, can lead to transmission of hepatitis B and C, HIV, and other bloodstream infections.[30][31][32] Injection drug users have high rates of unsafe needle use including sharing needles between people.[33] The spread of HIV, Hepatitis B, and Hepatitis C from injection drug use is a common health problem,[34] in particular contributing to over half of new HIV cases in North America in 1994.[4]

Other infections may occur when pathogens enter the body through the injection site, most commonly due to improper cleaning of the site before injection. Infections occurring in this way are mainly localized infections, including skin infections, skin structure infections, abscesses, or gangrene.[35] An intravenous injection may also result in a bloodstream infection (termed sepsis) if the injection site is not cleaned properly prior to insertion. Sepsis is a life-threatening condition which requires immediate treatment.[13]:358;373

2.3. Others

Injections into the skin and soft tissue generally do not cause any permanent damage, and the puncture heals within a few days. However, in some cases, injections can cause long-term adverse effects. Intravenous and intramuscular injections may cause damage to a nerve, leading to palsy or paralysis. Intramuscular injections may cause fibrosis or contracture.[36] Injections also cause localized bleeding, which may lead to a hematoma. Intravenous injections may also cause phlebitis, especially when multiple injections are given in a vein over a short period of time.[37] Infiltration and extravasation may also occur when a medication intended to be injected into a vein is inadvertently injected into surrounding tissues.[38] Those who are afraid of needles may also experience fainting at the sight of a needle, or before or after an injection.[39]

3. Technique

Proper needle use is important to perform injections safely,[40] which includes the use of a new, sterile needle for each injection. This is partly because needles get duller with each use and partly because reusing needles increases risk of infection. Needles should not be shared between people, as this increases risk of transmitting blood-borne pathogens. The practice of using the same needle for multiple people increases the risk of disease transmission between people sharing the same medication.[40] In addition, it is not recommended to reuse a used needle to pierce a medication bag, bottle, or ampule designed to provide multiple doses of a medication, instead a new needle should be used each time the container must be pierced. Aseptic technique should always be practiced when administering injections. This includes the use of barriers including gloves, gowns, and masks for health care providers. It also requires the use of a new, sterile needle, syringe and other equipment for each injection, as well as proper training to avoid touching non-sterile surfaces with sterile items.[41]

To help prevent accidental needlestick injury to the person administering the injection, and prevent reuse of the syringe for another injection, a safety syringe and needle may be used.[42] The most basic reuse prevention device is an "auto-disable" plunger, which once pressed past a certain point will no longer retract. Another common safety feature is an auto-retractable needle, where the needle is spring-loaded and either retracts into the syringe after injection, or into a plastic sheath on the side of the syringe. Other safety syringes have an attached sheath which may be moved to cover the end of the needle after the injection is given.[42] The World Health Organization recommends the use of single-use syringes with both reuse prevention devices and a needlestick injury prevention mechanism for all injections to prevent accidental injury and disease transmission.[42]

Novel injection techniques include drug diffusion within the skin using needle-free micro-jet injection (NFI) technology.[43][44]

3.1. Disposal of Used Needles

Used needles should be disposed of in specifically designed sharps containers to reduce the risk of accidental needle sticks and exposure to other people.[45] In addition, a new sharps container should be begun once it is ​3⁄4 full. A sharps container which is ​3⁄4 filled should be sealed properly to prevent re-opening or accidental opening during transportation.[46] Some locations offer publicly accessible "sharps take-back" programs where a sharps container may be dropped off to a public location for safe disposal at no fee to the person. In addition, some pharmaceutical and independent companies provide mail-back sharps programs, sometimes for an additional fee.[46] In the United States, there are 39 states that offer programs to provide needle or syringe exchange.[47]

Over half of non-industrialized countries report open burning of disposed or used syringes. This practice is considered unsafe by the World Health Organization.[48]

3.2. Aspiration

The aspiration is the technique of pulling back on the plunger of a syringe prior to the actual injection. If blood flows into the syringe it signals that a blood vessel has been hit.[49]

4. Society and Culture

Due to the prevalence of unsafe injection practices, especially among injection drug users, many locations have begun offering supervised injection sites and needle exchange programs, which may be offered separately or colocated. These programs may provide new sterile needles upon request to mitigate infection risk, and some also provide access to on-site clinicians and emergency medical care if it becomes required. In the event of an overdose, a site may also provide medications such as naloxone, used as an antidote in opioid overdose situations, or other antidotes or emergency care. Safe injection site have been associated with lower rates of death from overdose, less ambulance calls, and lower rates of new HIV infections from unsafe needle practices.[50]

As of 2019, at least ten countries currently offer safe injection sites, including Australia, Canada, Denmark, France, Germany, Luxembourg, The Netherlands, Norway, Spain and Switzerland. In total, there are at least 120 sites operating.[51] Although the United States does not currently have any safe injection sites, some cities such San Francisco, Philadelphia, and Denver are considering opening them, and some localities offer needle exchange programs.[47] In 2018, the California State Assembly passed Assembly Bill 186 to launch a three-year pilot program in San Francisco for California's first safe injection sites, but this bill was not signed by the governor.[52] Colorado and Pennsylvania have also expressed interest in offering safe injection sites. Court rulings in Pennsylvania have determined that safe injection sites are not illegal under federal law.[53]

5. Plants and Animals

Many species of animals use injections for self-defence or catching prey. This includes venomous snakes which inject venom when they bite into the skin with their fangs. Common substances present in snake venom include neurotoxins, toxic proteins, and cytotoxic enzymes. Different species of snakes inject different formulations of venom, which may cause severe pain and necrosis before progressing into neurotoxicity and potentially death.[54] The weever is a type of fish which has venomous spines covering its fins and gills and injects a venom consisting of proteins which cause a severe local reaction which is not life-threatening.[55] Sting rays use their spinal blade to inject a protein-based venom which causes localized cell death but is not generally life-threatening.[56]

Some types of insects also utilize injection for various purposes. Bees use a stinger located in their hind region to inject a venom consisting of proteins such as melittin, which causes a localized painful and itching reaction.[57] Leeches can inject an anticoagulant peptide called hirudin after attaching to prevent blood from clotting during feeding. This property of leeches has been used historically as a natural form of anticoagulation therapy, as well as for the use of bloodletting as a treatment for various ailments.[58] Some species of ants inject forms of venom which include compounds which produce minor pain such as the formic acid, which is injected by members of the Formicinae subfamily.[59] Other species of ants, including Dinoponera species, inject protein-based venom which causes severe pain but is still not life-threatening.[60] The bullet ant (Paraponera clavata) injects a venom which contains a neurotoxin named poneratoxin which causes extreme pain, fever, and cold sweats, and may cause arrhythmias.[61]

Plants may use a form of injection which is passive, where the injectee pushes themselves against the stationary needle. The stinging nettle plant has many trichomes, or stinging hairs, over its leaves and stems which are used to inject a mix of irritating chemicals which includes histamine, serotonin, and acetylcholine. This sting produces a form of dermatitis which is characterized by a stinging, burning, and itching sensation in the area.[62] Dendrocnide species, also called stinging trees, use their trichomes to inject a mix of neurotoxic peptides which causes a reaction similar to the stinging nettle, but also may result in recurring flares for a much longer period after the injection.[63] While some plants have thorns, spines, and prickles, these generally are not used for injection of any substance, but instead it is the act of piercing the skin which causes them to be a deterrent.[64]

The content is sourced from: https://handwiki.org/wiki/Medicine:Injection

References

  1. "Chapter 6. Absorption/Transport Mechanisms". Handbook of Basic Pharmacokinetics … Including Clinical Applications, Seventh Edition. The American Pharmacists Association. 2009-01-01. doi:10.21019/9781582121260.ch6. ISBN 978-1-58212-126-0.  https://dx.doi.org/10.21019%2F9781582121260.ch6
  2. "Pharmacokinetics". Biochemical Pharmacology. Special Issue: Pharmacology in 21st Century Biomedical Research 87 (1): 93–120. January 2014. doi:10.1016/j.bcp.2013.09.007. PMID 24055064.  https://dx.doi.org/10.1016%2Fj.bcp.2013.09.007
  3. "Standardized versusindividually customized parenteral nutrition solutions: a comparison ofserum electrolyte values". P&T 25 (2): 78–80, 83, 87. 2000. http://www.ptcommunity.com/ptjournal/fulltext/25/2/2502078.pdf. Retrieved 2010-09-17. 
  4. "Injection drug use in North America". Infectious Disease Clinics of North America 16 (3): 535–51, vii. September 2002. doi:10.1016/S0891-5520(02)00010-7. PMID 12371114.  https://dx.doi.org/10.1016%2FS0891-5520%2802%2900010-7
  5. "Injection drug use: an understudied cause of venous disease". Archives of Dermatology 143 (10): 1305–9. October 2007. doi:10.1001/archderm.143.10.1305. PMID 17938345.  https://dx.doi.org/10.1001%2Farchderm.143.10.1305
  6. Injection (Intramuscular): Clinician Information. The Joanna Briggs Institute. 2016. 
  7. "Anaphylaxis". April 23, 2015. https://www.niaid.nih.gov/topics/anaphylaxis/Pages/default.aspx. 
  8. "Drugs@FDA: FDA Approved Drug Products". United States Food and Drug Administration. http://www.accessdata.fda.gov/scripts/cder/daf/. 
  9. "Pinkbook: Vaccine Administration: Epidemiology of VPDs". Centers for Disease Control and Prevention (CDC). 2017-10-04. https://www.cdc.gov/vaccines/pubs/pinkbook/vac-admin.html. 
  10. "What Is a Subcutaneous Injection?". Healthline. https://www.healthline.com/health/subcutaneous-injection#overview1. 
  11. EpiPen/EpiPen Jr (epinephrine) [prescribing information]. Morgantown, WV: Mylan Specialty LP; August 2018.
  12. "Administer the Vaccine(s)". Centers for Disease Control and Prevention (CDC). 2017-09-01. https://www.cdc.gov/vaccines/hcp/admin/administer-vaccines.html. 
  13. Fundamentals of nursing : the art and science of nursing care (7th ed.). Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. 2011. pp. 749, 788. ISBN 978-0-7817-9383-4. https://books.google.com/books?id=Dg1uQgAACAAJ. 
  14. Petitpas, F.; Guenezan, J.; Vendeuvre, T.; Scepi, M.; Oriot, D.; Mimoz, O. (December 2016). "Use of intra-osseous access in adults: a systematic review". Critical Care 20 (1): 102. doi:10.1186/s13054-016-1277-6. PMID 27075364.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4831096
  15. Joanne, Garside; Stephen, Prescott; Susan, Shaw (May 2016). "Intraosseous vascular access in critically ill adults-a review of the literature: IO vascular access in critically ill adults". Nursing in Critical Care 21 (3): 167–177. doi:10.1111/nicc.12163. PMID 25688586. http://eprints.hud.ac.uk/id/eprint/23501/1/Intraosseous_vascular_access_in_adults__BACCN_11_08.pdf. 
  16. Salonia, Andrea; Eardley, Ian; Giuliano, François; Hatzichristou, Dimitrios; Moncada, Ignacio; Vardi, Yoram et al. (February 2014). "European Association of Urology Guidelines on Priapism". European Urology 65 (2): 480–489. doi:10.1016/j.eururo.2013.11.008. PMID 24314827.  https://dx.doi.org/10.1016%2Fj.eururo.2013.11.008
  17. Duncan, Catriona; Omran, Ghadir J.; Teh, Jiasian; Davis, Niall F.; Bolton, Damien M.; Lawrentschuk, Nathan (June 2019). "Erectile dysfunction: a global review of intracavernosal injectables". World Journal of Urology 37 (6): 1007–1014. doi:10.1007/s00345-019-02727-5. PMID 30895359.  https://dx.doi.org/10.1007%2Fs00345-019-02727-5
  18. Doshi, Rishi R.; Bakri, Sophie J.; Fung, Anne E. (May 2011). "Intravitreal Injection Technique". Seminars in Ophthalmology 26 (3): 104–113. doi:10.3109/08820538.2010.541318. PMID 21609222.  https://dx.doi.org/10.3109%2F08820538.2010.541318
  19. Yaftali, Nina A.; Weber, Kathleen (1 January 2019). "Corticosteroids and Hyaluronic Acid Injections". Clinics in Sports Medicine 38 (1): 1–15. doi:10.1016/j.csm.2018.08.006. PMID 30466716.  https://dx.doi.org/10.1016%2Fj.csm.2018.08.006
  20. "MSK Ultrasound Guided Injection" (in en-US). https://r3medicaltraining.com/events/msk-ultrasound-guided-injection-course/. 
  21. Courtney, Philip; Doherty, Michael (April 2013). "Joint aspiration and injection and synovial fluid analysis". Best Practice & Research Clinical Rheumatology 27 (2): 137–169. doi:10.1016/j.berh.2013.02.005. PMID 23731929.  https://dx.doi.org/10.1016%2Fj.berh.2013.02.005
  22. Wright, Jeremy C.; Burgess, Diane J. (2012). Long acting injections and implants. New York, NY: Springer. ISBN 978-1-4614-0554-2. 
  23. "Long-acting injectable antipsychotics: What to do about missed doses" (in en). Current Psychiatry 17 (7): 10–12, 14–19, 56. 2018. https://www.mdedge.com/psychiatry/article/168776/schizophrenia-other-psychotic-disorders/long-acting-injectable. 
  24. H. Thomas Milhorn (17 October 2017). Substance Use Disorders: A Guide for the Primary Care Provider. Springer International Publishing. pp. 88–. ISBN 978-3-319-63040-3. https://books.google.com/books?id=wH86DwAAQBAJ&pg=PA88. 
  25. Ramdhan, Rebecca C.; Simonds, Emily A.; Wilson, Charlotte; Loukas, Marios; Oskouian, Rod J.; Tubbs, R. Shane (31 January 2018). "Complications of Subcutaneous Contraception: A Review". Cureus 10 (1): e2132. doi:10.7759/cureus.2132. PMID 29610715.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5878093
  26. Rosenthal, Richard N.; Goradia, Viral V. (28 August 2017). "Advances in the delivery of buprenorphine for opioid dependence". Drug Design, Development and Therapy 11: 2493–2505. doi:10.2147/DDDT.S72543. PMID 28894357.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5584886
  27. "Reducing venipuncture pain by a cough trick: a randomized crossover volunteer study". Anesthesia and Analgesia 98 (2): 343–5, table of contents. February 2004. doi:10.1213/01.ANE.0000094983.16741.AF. PMID 14742367.  https://dx.doi.org/10.1213%2F01.ANE.0000094983.16741.AF
  28. "Efficacy of sweet solutions for analgesia in infants between 1 and 12 months of age: a systematic review". Archives of Disease in Childhood 95 (6): 406–13. June 2010. doi:10.1136/adc.2009.174227. PMID 20463370.  https://dx.doi.org/10.1136%2Fadc.2009.174227
  29. "Breastfeeding for procedural pain in infants beyond the neonatal period". The Cochrane Database of Systematic Reviews 2020 (10): CD011248. October 2016. doi:10.1002/14651858.cd011248.pub2. PMID 27792244.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=6461192
  30. "CDC Grand Rounds: Preventing Unsafe Injection Practices in the U.S. Health-Care System". https://www.cdc.gov/mmwr/preview/mmwrhtml/mm6221a3.htm. 
  31. "A patient Safety Threat – Syringe Reuse: Injection Safety". Centers for Disease Control and Prevention (CDC). 2019-04-26. https://www.cdc.gov/injectionsafety/patients/syringereuse_faqs.html. 
  32. "Illicit drug use and harms, and related interventions and policy in Canada: A narrative review of select key indicators and developments since 2000". The International Journal on Drug Policy 27: 23–35. January 2016. doi:10.1016/j.drugpo.2015.08.007. PMID 26359046.  https://dx.doi.org/10.1016%2Fj.drugpo.2015.08.007
  33. "HIV infection and intravenous drug use: critical issues in transmission dynamics, infection outcomes, and prevention". Reviews of Infectious Diseases 10 (1): 151–8. January 1988. doi:10.1093/clinids/10.1.151. PMID 3281219.  https://dx.doi.org/10.1093%2Fclinids%2F10.1.151
  34. "Global burden of disease attributable to illicit drug use and dependence: findings from the Global Burden of Disease Study 2010" (in en). Lancet 382 (9904): 1564–74. November 2013. doi:10.1016/S0140-6736(13)61530-5. PMID 23993281. https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(13)61530-5/abstract. 
  35. "Intramuscular Injection". StatPearls. January 2020. PMID 32310581.  http://www.ncbi.nlm.nih.gov/pubmed/32310581
  36. "Sciatic nerve injection injury". Journal of International Medical Research 42 (4): 887–897. August 2014. doi:10.1177/0300060514531924. PMID 24920643.  https://dx.doi.org/10.1177%2F0300060514531924
  37. "Clinically-indicated replacement versus routine replacement of peripheral venous catheters". The Cochrane Database of Systematic Reviews 1: CD007798. 23 January 2019. doi:10.1002/14651858.CD007798.pub5. ISSN 1469-493X. PMID 30671926.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=6353131
  38. "The rate of adverse events during IV conscious sedation". General Dentistry 60 (5): e341-4. 2012. PMID 23032244.  http://www.ncbi.nlm.nih.gov/pubmed/23032244
  39. Hamilton, JG (August 1995). "Needle phobia: a neglected diagnosis.". The Journal of Family Practice 41 (2): 169–75. PMID 7636457.  http://www.ncbi.nlm.nih.gov/pubmed/7636457
  40. "Background | Injection Safety | CDC". 2019-06-20. https://www.cdc.gov/injectionsafety/providers/provider_faqs.html. 
  41. "Aseptic Technique: Uses, Benefits, and Complications". October 2015. https://www.healthline.com/health/aseptic-technique. 
  42. WHO (2016). WHO guideline on the use of safety-engineered syringes for intramuscular, intradermal and subcutaneous injections in health care settings.. Geneva: World Health Organization. ISBN 9789241549820. https://apps.who.int/iris/bitstream/handle/10665/250144/9789241549820-eng.pdf;jsessionid=7867B228706D99961582E656727DC5D6?sequence=1. Retrieved 18 September 2020. 
  43. Cu, K., Bansal, R., Mitragotri, S. et al. Delivery Strategies for Skin: Comparison of Nanoliter Jets, Needles and Topical Solutions. Ann Biomed Eng 48, 2028–2039 (2020). https://doi.org/10.1007/s10439-019-02383-1
  44. Rivas, David Fernandez; Galvez, Loreto Alejandra Oyarte (2020). Jet injection system. https://research.utwente.nl/en/publications/jet-injection-system. 
  45. "Sharps injury reduction: a six-year, three-phase study comparing use of a small patient-room sharps disposal container with a larger engineered container". Journal of Infection Prevention 15 (5): 170–174. September 2014. doi:10.1177/1757177414543088. PMID 28989381.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5074232
  46. "Sharps Containers at Home". https://www.nationwidechildrens.org/family-resources-education/health-wellness-and-safety-resources/helping-hands/sharps-containers-at-home. 
  47. "Supervised injection sites are coming to the United States. Here's what you should know.". 2019-05-02. https://nursing.usc.edu/blog/supervised-injection-sites/. 
  48. "Injection safety". Health Topics A to Z. World Health Organization. http://allcountries.org/health/injection_safety.html. 
  49. "Aspiration in injections: should we continue or abandon the practice?". 1 March 2017. doi:10.12688/f1000research.1113.3. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333604/. 
  50. "Does evidence support supervised injection sites?". Canadian Family Physician 63 (11): 866. November 2017. PMID 29138158.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5685449
  51. "Supervised Consumption Services". http://www.drugpolicy.org/issues/supervised-consumption-services. 
  52. "Supervised injection sites are coming to the United States. Here's what you should know.". 2019-05-02. https://nursing.usc.edu/blog/supervised-injection-sites/. 
  53. Allyn, Bobby. "Judge McHugh's Federal Ruling on Safehouse". https://www.documentcloud.org/documents/6444521-2019-10-02-Memorandum-on-Safehouse.html. 
  54. "Bites of venomous snakes.". The New England Journal of Medicine 347 (5): 347–56. 1 August 2002. doi:10.1056/NEJMra013477. PMID 12151473.  https://dx.doi.org/10.1056%2FNEJMra013477
  55. "Venomous Bites, Stings, and Poisoning". Infectious Disease Clinics of North America 33 (1): 17–38. March 2019. doi:10.1016/j.idc.2018.10.001. PMID 30712761.  https://dx.doi.org/10.1016%2Fj.idc.2018.10.001
  56. "A Severe Accident Caused by an Ocellate River Stingray (Potamotrygon motoro) in Central Brazil: How Well Do We Really Understand Stingray Venom Chemistry, Envenomation, and Therapeutics?". Toxins 7 (6): 2272–88. 18 June 2015. doi:10.3390/toxins7062272. PMID 26094699.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4488702
  57. "Melittin, the Major Pain-Producing Substance of Bee Venom". Neuroscience Bulletin 32 (3): 265–272. June 2016. doi:10.1007/s12264-016-0024-y. PMID 26983715.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5563768
  58. "The Leech and the Physician: Biology, Etymology, and Medical Practice with Hirudinea medicinalis". World Journal of Surgery 24 (7): 878–883. July 2000. doi:10.1007/s002680010141. PMID 10833259.  https://dx.doi.org/10.1007%2Fs002680010141
  59. "The Biochemical Toxin Arsenal from Ant Venoms". Toxins 8 (1): 30. 20 January 2016. doi:10.3390/toxins8010030. PMID 26805882.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4728552
  60. Haddad Junior, Vidal; Cardoso, João Luiz Costa; Moraes, Roberto Henrique Pinto (August 2005). "Description of an injury in a human caused by a false tocandira (Dinoponera gigantea, Perty, 1833) with a revision on folkloric, pharmacological and clinical aspects of the giant ants of the genera Paraponera and Dinoponera (sub-family Ponerinae)". Revista do Instituto de Medicina Tropical de São Paulo 47 (4): 235–238. doi:10.1590/S0036-46652005000400012. PMID 16138209.  https://dx.doi.org/10.1590%2FS0036-46652005000400012
  61. Szolajska, E; Poznanski, J; Ferber, ML; Michalik, J; Gout, E; Fender, P et al. (June 2004). "Poneratoxin, a neurotoxin from ant venom. Structure and expression in insect cells and construction of a bio-insecticide.". European Journal of Biochemistry 271 (11): 2127–36. doi:10.1111/j.1432-1033.2004.04128.x. PMID 15153103.  https://dx.doi.org/10.1111%2Fj.1432-1033.2004.04128.x
  62. "Mechanism of action of stinging nettles.". Wilderness & Environmental Medicine 22 (2): 136–9. June 2011. doi:10.1016/j.wem.2011.01.001. PMID 21396858.  https://dx.doi.org/10.1016%2Fj.wem.2011.01.001
  63. Gilding, Edward K.; Jami, Sina; Deuis, Jennifer R.; Israel, Mathilde R.; Harvey, Peta J.; Poth, Aaron G. et al. (1 September 2020). "Neurotoxic peptides from the venom of the giant Australian stinging tree". Science Advances 6 (38): eabb8828. doi:10.1126/sciadv.abb8828. PMID 32938666.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=7494335
  64. Bagella, S.; Filigheddu, R.; Benesperi, R.; Giordani, P.; Minuto, L.; Viciani, D. et al. (2 January 2019). "Thorn, spine and prickle patterns in the Italian flora". Plant Biosystems 153 (1): 118–133. doi:10.1080/11263504.2018.1474961.  https://dx.doi.org/10.1080%2F11263504.2018.1474961
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