More Details on Number Needed to Treat
Definition
The NNT is the number of patients who need to be treated in order to prevent one additional bad outcome. It is the inverse of the Absolute Risk Reduction (ARR).How to Calculate NNTs
NNT = 1/ARR
ARR = |CER - EER|
where
CER = control group event rate
EER = experimental group event rate
Sample Calculation
The results of the Diabetes Control and Complications Trial (Ann Intern Med 1995; 122:561-8) into the effect of intensive diabetes therapy on the development and progression of neuropathy indicated that neuropathy occurred in 9.6% of patients randomised to usual care and 2.8% of patients randomised to intensive therapy. The number of patients we need to treat with the intensive diabetes therapy to prevent one additional occurrence of neuropathy can be determined by calculating the absolute risk reduction as follows:
ARR = |CER - EER| = |9.6% - 2.8%| = 6.8%
NNT = 1/ARR = 1/6.8% = 14.7 or 15
We therefore need to treat 15 diabetic patients with intensive therapy to prevent one from developing neuropathy.
Practice Calculation
In a randomised controlled trial (Stroke 1997; 28:1861-6) looking into the long-term outcome for stroke patients treated in stroke units (SU) compared with patients treated in general wards (GW), the mortality rate 5 years after the onset of stroke was 59.1% in the patients treated in SU and 70.9% in those treated in the GW. How many patients need to be treated in stroke units to prevent one additional death?
NNT = _______
See our answer and compare
ARR = |CER - EER| = |0.709 - 0.591| = 0.118
NNT = 1/ARR = 1/0.118 = 9
Nine patients would need to be treated in stroke units to prevent one additional death.
Examples
Criteria for Inclusion of Examples
(Modified from criteria used by ACP Journal Club)- Random allocation of participants to comparison groups.
- ≥ 80% follow-up of people enrolled.
- Outcome of clinical significance.
Disciplines
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Acute myocardial infarction1 | Angiotensin-converting enzyme (ACE) inhibitors vs. placebo | Mortality | 30 days | 7.6 | 7.1 | 210 (125 to 662) |
Acute myocardial infarction2 | Angiotensin-converting enzyme (ACE) inhibitors vs. placebo | Nonfatal heart failure | 30 days | 15.2 | 14.6 | 165 (111 to 488) |
Cardiology Chronic heart failure (CHF)3 | b-blockers vs. placebo | Hospitalisation for CHF | 7 months | 17 | 13 | 24 (16 to 51) |
Cardiology Chronic heart failure (CHF)4 | b-blockers vs. placebo | All-cause mortality | 7 months | 12 | 9 | 40 (24 to 149) |
Congestive heart failure5 | Spironolactone vs. placebo | Mortality | 24 months | 46 | 35 | 9 (7 to 16) |
Non-Q-wave coronary events (unstable angina or non-Q-wave MI)6 | Enoxaparin vs. unfractionated heparin | Composite end point of death, MI or recurrent angina | 14 days | 19.7 | 16.6 | 31 (17 to 191) |
Coronary events in healthy persons with low HDL cholesterol levels7 | Lovastatin vs. placebo | First acute major coronary events and adverse events | 5.2 years | 6 | 4 | 50 (33 to 97) |
Cardiovascular events in treated hypertension8 | Aspirin vs. placebo | Major cardiovascular events | 3.8 years | 3.9 | 3.4 | 176 (90 to 3115) |
Myocardial infarction (MI) | 1.4 | 0.9 | 208 (127 to 551) | |||
Myocardial infarction and average cholesterol levels in older patients9 | Pravastatin vs. placebo | Major coronary events | 5 years | 28.1 | 19.7 | 11 (8 to 24) |
Stroke | 7.3 | 4.5 | 34 (22 to 333) | |||
Death from coronary artery disease | 10.3 | 5.8 | 22 (15 to 53) | |||
Coronary artery bypass grafting | 11.0 | 6.6 | 21 (15 to 56) | |||
Chronic heart failure (CHF)10 | Exercise vs. no exercise | Death | 3.4 years | 40.8 | 18 | 5 (3 to 21) |
All cardiac events | 75.5 | 34 | 3 (2 to 5) | |||
Hospitalization for CHF | 28.6 | 10 | 6 (3 to 32) | |||
Severe vasovagal syncope; patients with ≥6 syncopal episodes and a positive tilt-table test result with syncope or presyncope and relative bradycardia11 | Pacemaker vs. usual care | First recurrence of syncope | 2 years | 70.4 | 22.2 | 3 (1 to 5) |
Congestive heart failure12 | Home-based intervention vs. usual care | Proportion of patients with the combined end point of unplanned readmission or out-of-hospital death | 18 months | 81.3 | 67.3 | Not significant |
Out-of-hospital death | 18.8 | 4.1 | 7 (3 to 44) | |||
Coronary Heart Disease13 | Patients invited to attend nurse led secondary prevention clinics vs. Patients who received regular care | Presence, frequency and course of chest pain | 12 months | 11 | 7 | 24 (16 to 170) |
Hospital admissions | 28 | 20 | 13 (9 to 35) | |||
Adults at high risk for cardiovascular events14 | Ramipril vs. placebo | Myocardial Infarction, stroke and cardiovascular mortality | 4 years | 18 | 14 | 26 (19 to 43) |
Patients surviving Myocardial Infarction who had contraindications to b-blockers15 | Amiodarone vs. placebo | Cardiac mortality | 1 year | 11 | 6 | 23 (12 to 1323) |
Arrhythmias | 19 | 8 | 9 (6 to 16) | |||
Recent-onset atrial fibrillation in patients with or without heart disease16 | Oral propafenone vs. placebo | Rates of conversion to sinus rhythm at 3 and 8 hours | 8 hours | 3 hrs: 18 | 3 hrs: 24 | 3 hrs: 4 (3 to 6) |
8 hrs: 37 | 8 hrs: 76 | 8 hrs: 3 (2 to 4) | ||||
Patients resuscitated from ventricular arrhythmias; use of implantable cardioverter-defibrillators (ICD) in reducing mortality17 | ICD vs. antiarrhythmic drug therapy | All-cause mortality | 18 months | 24 | 16 | 13 (8 to 30) |
Myocardial infarction with cardiogenic shock18 | Immediate revascularization (angioplasty or bypass surgery to be done as soon as possible and within 6 hours of randomization) vs. medical stabilization (intraaortic balloon counterpulsation and thrombolytic therapy with delayed revascularization – minimum 54 hours after randomization) | All-cause mortality | 6 months | 63 | 50 | 8 (5 to 66) |
Coronary artery disease (CAD) and low levels of high density lipoprotein cholesterol19 | Gemfibrozil vs. placebo | Nonfatal myocardial infarction or CAD death | 5 years | 21.7 | 17.3 | 23 (13 to 74) |
Stroke | 6.9 | 5.1 | 56 (27 to 725) | |||
Acute myocardial infraction (MI)20 | Aspirin and heparin plus angioplasty vs. aspirin and heparin plus streptokinase (control) | All-cause mortality | 5 years | 24 | 13 | 10 (6 to 35) |
Cardiac mortality | 20 | 7 | 8 (5 to 15) | |||
Death and nonfatal MI | 22 | 6 | 6 (4 to 11) | |||
Unstable coronary artery disease21 | Dalteparin vs. placebo | Death, MI or both at 1 month | 6 months | 5.8 | 3.1 | 37 (23 to 102) |
Death, MI or need for revascularization at 3 months | 33 | 29 | 27 (13 to 208) | |||
Unstable coronary artery disease22 | Invasive strategy vs. noninvasive strategy | Death, MI or both | 6 months | 12 | 9 | 37 (20 to 398) |
Medically refractory angina23 | Transmyocardial revascularization (TMR - consisted of a limited muscle-sparingleft thoracotomy and the creation of transmyocardial laser channels) and continued medication vs. continued medication alone | Reduction of ≥ 2 angina cases | 12 months | 11 | 61 | 2 (2 to 3) |
Congestive heart failure (CHF)24 | Usual CHF medicine plus low dose of lisinopril (2.5 or 5.0 mg/d-control) vs. usual CHF medicine plus high dose of lisinopril (30 mg/d) | Mortality plus hospitalization | 3 years | 83.8 | 79.7 | 26 (16 to 82) |
Mortality plus cardiovascular (CV) hospitalization | 74.1 | 71.1 | 34 (17 to 264) | |||
Mortality Plus CHF hospitalization | 60.4 | 55.1 | 17 (12 to 37) | |||
CV mortality plus CV hospitalization | 72.7 | 69.4 | 30 (16 to 281) | |||
Recent-onset atrial fibrillation25 | Oral amiodarone vs. placebo | Rates of conversion to sinus rhythm (verified by Holter monitoring) | 24 hours | 35 | 87 | 2 (1 to 4) |
Chronic heart failure26 | Metroprolol vs. placebo | All-cause death or hospital admission | 1 year | 38 | 32 | 17 (12 to 32) |
Hospitalization for worsening heart failure | 15 | 10 | 22 (15 to 39) | |||
Atrial fibrillation (AF)27 | Amiodarone (10 mg/kg of body weight) vs. sotalol or propafenone (control) | Time to first recurrence of AF confirmed on ECG | 468 days | 63 | 35 | 4 (3 to 6) |
Balloon angioplasty28 | Routine stent implantation vs. optimal balloon angioplasty with provisional stent | Composite end point | 6 months | 14.9 | 6.1 | 11 (7 to 30) |
Target vessel Revascularization or surgery | 10.1 | 3.9 | 16 (9 to 62) | |||
Revascularization or surgery | 12.9 | 5.2 | 13 (8 to 309) | |||
Unstable coronary artery disease29 | Invasive strategy (immediate angioplasty and revascularization) vs. non-invasive strategy | Death or myocardial infraction (MI) | 1 year | 14 | 10 | 27 (16 to 92) |
Death | 3.9 | 2.2 | 60 (32 to 306) | |||
Readmission | 57 | 37 | 5 (4 to 6) | |||
Cardiac intervention after discharge | 31 | 8 | 5 (4 to 5) | |||
Acute myocardial infarction30 | Coronary stenting plus abciximab vs. intravenous alteplase (control) | Composite of death, reinfarction or stroke | 6 months | 23 | 9 | 7 (5 to 36) |
Angina and percutaneous transluminal coronary angioplasty31 | Coumarin and aspirin vs. aspirin alone | Composite end point of death, myocardial infarction, target-lesion revascularization and stoke at 30 days | 1 year | 6.4 | 3.4 | 33 (17 to 222) |
Composite at 1 year | 20 | 14 | 17 (10 to 73) | |||
Atrial fibrillation (AF)32 | Amiodarone vs. placebo | Rates and time to AF or intolerable adverse effects | 22 months | 88 | 48 | 3 (2 to 4) |
Sotalol vs. placebo | Rates and time to AF or intolerable adverse effects | 88 | 77 | Not significant | ||
Patients with cardiovascular disease (CVD) receiving long-term hemodialysis33 | Vitamin E vs. placebo | CDV events | 512 days | 34 | 19 | 6 (4 to 29) |
Myocardial infraction | 18 | 8 | 10 (5 to 230) | |||
CAD and hypertension34 | Acarbose vs placebo | Major CV events | 3.3 years | 4.7 | 2.2 | 44 (30 to 436) |
Myocardial infaraction35 | Warfarin + aspirin, warfarin vs aspirin | Composite outcomes | 1445 days | 15% vs 20%, 17% vs 20% | 20 (12 to 51), 30 (16 to 483) | |
Atrial fibrillation36 | Anterior-posterior versus anterior-lateral electrode position | Successful cardioversion | 24 hours | 78 | 96 | 6 (4 to 19) |
chronic heart failure37 | Candesartan 4 or 8 mg vs placebo | All-cause mortality | 37.7 months | 25 | 23 | 46 (26 to 463) |
acute myocardial infarction38 | Coronary angioplasty vs fibrinolytic therapy | Composite endpoint | 30 day | 13.7 | 8.0 | 18 (12 to 38) |
CAD39 | Perindopril vs placebo | Large MI or death | 4.2 years | 9.9 | 8.0 | 54 (35 to 115) |
References
- Circulation 1998; 97:2202-12
- Circulation 1998; 98:1184-91
- N Engl J Med 1999 Sep 2;341(10):709-17
- N Engl J Med 1997 Aug 14;337(7):447-52
- JAMA 1998 May 27;279(20):1615-22
- Lancet 1998 Jun 13;351(9118):1755-62
- Ann Intern Med 1998 Nov 1;129(9):681-9
- Circulation 1999 Mar 9;99(9):1173-82
- J Am Coll Cardiol 1999 Jan;33(1):16-20
- Arch Intern Med 1999 Feb 8;159(3):257-61
- BMJ. 9 May 1998; 316: 1434-7
- N Engl J Med. 20 Jan 2000; 342: 145-53
- J Am Coll Cardiol. 1 Nov 1992; 20: 1056-62
- Ann Intern Med. 15 Apr 1997; 126: 621-5
- N Engl J Med. 27 Nov 1997; 337: 1576-83
- N Engl J Med. 27 Nov 1997; 337: 1576-83
- N Engl J Med. 27 Nov 1997; 337: 1576-83
- N Engl J Med. Aug 26, 1999; 341: 625-34
- N Engl J Med. Aug 5, 1999; 341: 410-8
- N Engl J Med. Nov 4, 1999; 341: 1413-9
- Lancet. Aug 28, 1999; 354: 701-7
- Lancet. Aug 28, 1999; 354: 708-15
- Lancet. Sept 11, 1999; 354: 885-90
- Circulation. Dec 7, 1999; 100: 2312-8
- Am J Cardiol. Feb 15, 2000; 85: 462-5
- JAMA. Mar 8, 2000; 283: 1295-1302
- N Engl J Med. Mar 30, 2000; 342: 913-20
- Lancet. Jun 24, 2000; 355:2199-203
- Lancet. Jul 1, 2000; 356:9-16
- N Engl J Med. Ayg 10, 2000; 343: 385-91
- Circulation. Jul 25 2000; 102: 386-91
- Heart. Sept 2000; 84: 251-7
- Lancet. Oct 7, 2000; 356: 1213-8
- JAMA 2003;5290:486-94
- NEJM 2002;347:969-74.5290:486-9
- Lancet 2002;360:1275-6.
- Lancet 2003;362:759-66.
- N Engl J Med. 2003;349:733-42.
- Lancet. 2003;362:782-8.
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Intravenous skin antisepsis1 | 0.5% chlorohexidine gluconate (CHG) vs. 70% isopropyl alcohol swab followed by povidone-iodine swab (control) | Local catheter related infection | 72 hours | 12.5 | 1.2 | 9 (5 to 23) |
CHG vs. povidone-iodine swab followed by 70% isopropyl alcohol swab (control) | 9.9 | 1.2 | 12 (6 to 48) |
References
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Graves Hyperthyroidism1 | Radioiodine and prednisone vs. radioiodine therapy | Development and improvement of opthalmopathy | 1 year | 15 | 0 | 7 (5 to 11) |
Type 2 diabetes mellitus in overweight patients2 | Radioiodine and prednisone vs. radioiodine therapy | Diabetes related end point | 10 years | 39 | 29 | 10 (6 to 29) |
Deaths from diabetes | 13 | 8> | 19 (10 to 138) | |||
All cause mortality | 22 | 15 | 14 (8 to 67) | |||
MI | 18 | 11 | 16 (9 to 78) | |||
Diabetic men with erectile dysfunction3 | Sildenafil vs. placebo | Improved erections | 12 weeks | 10.2 | 56.5 | 3 (2 to 3) |
"Insulin requiring" diabetes4 | Regular telephone contact with a diabetes nurse educator for advice about adjustment of insulin therapy vs. regular clinic visits and usual contact with the endocrinologist for insulin adjustment | Mean HbAlc level and proportion of patients who achieved a reduction in HbAlc level ≥ 10% | 6 months | 35 | 87 | 2 (1 to 4) |
References
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Endoscopic re-treatment of bleeding peptic ulcer1 | Endoscopy vs. surgery | Mortality at 30 days, duration of hospitalization after treatment, ICU stay, need for blood transfusion and treatment-related complications | 6 weeks | 36 | 15 | 5 (3 to 25) |
Remission rates in active Crohn disease2 | Budesonide vs. mesalamine | Remission | 16 weeks | 36 | 62 | 4 (3 to 10) |
Endoscopic gastroduodenal ulcers in osteoarthritis3 | Rofecoxib vs. Ibuprofen | Endoscopic gastroduodenal ulcers ≥ 3 mm at 12 weeks | 24 weeks | 7 | 25 | 5 (4 to 9) |
Women with irritable bowel syndrome4 | Alosetron vs. placebo | Relief of abdominal symptoms | 1 month | 29 | 41 | 8 (5 to 22) |
Constipation | 3 | 30 | 4 (3 to 5) | |||
Bleeding peptic ulcer5 | Omeprazole vs. placebo | Recurrent bleeding | 8 weeks | 22.5 | 6.7 | 6 (4 to 14) |
Hospital stay < 5 days | 31.7 | 46.7 | 7 (4 to 38) | |||
H pylori infection6 | Clarithromycin. Iansoprazole, metronidazole vs clarithromycin, Iasoprazole, amoxicillin | Eradication of H pylori | 6 weeks | 84 | 66 | 6 (3 to infinity) |
References
- Gastroenterology. Oct 1999; 117: 776-83
- N Engl J Med. 6 Aug 1998; 339: 370-4
- N Engl J Med. 6 Aug 1998; 339: 370-4
- Lancet. Mar 25, 2000; 355:1035-40
- N Engl J Med. Aug 3, 2000; 343: 310-6
- JAMA. 2003;290:1593-9
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Hip and knee arthroplasty1 | Patients were allocated to a clinical pathway group (received "proactive" treatment where specific daily goals were set for the patient) vs. control group (received "reactive" treatment where the healthcare team provided care in response to the patient's conditions and wants) | Complications (wound infection, chest infections deep venous thrombosis, joint dislocation, decubitus pressure areas, failure to cope at home and decreased range of motion after discharge) | 3 months | 28.2 | 10.9 | 6 (4 to 19) |
Postoperative abdominal wound infection2 | Impervious wound-edge protector vs. no wound edge protector (control) | All wounds | 30 days | 30 | 14 | 7 (4 to 13) |
Clean-contaminated wounds (minor interruption in aseptic technique or minor spillage from the gastrointestina1 tract) | 13 | 7 | Not significant | |||
Contaminated wounds (major interruption in aseptic technique or subsequent spillage | 67 | 24 | 3 (2 to 6) | |||
Dirty wounds (gross fecal spillage) | 94 | 75 | Not significant | |||
Hip surgery3 | Aspirin vs. placebo | Symptomatic deep venous thrombosis | 35 days | 1.5 | 1 | 232 (140 to 2239) |
Pulmonary embolism | 1.2 | 0.7 | 195 (140 to 466) |
References
- Med J Aust. 18 Jan 1999; 170: 59-62
- Lancet. May 8, 1999; 353: 1585
- Lancet. Apr 15, 2000; 355: 1295-302
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Nonvertebral fractures in community living elderly persons1 | Calcium and Vitamin D Supplementation vs.placebo | Nonvertebral fractures | 3 years | 13 | 6 | 15 (8 to 12) |
Nonvertebral fractures and bone loss2 | Calcium and vitamin D vs.placebo | Nonvertebral fractures | 3 years | 13 | 6 | 15 (8 to 12) |
Alzheimer disease3 | Donepezil vs.placebo | Nausea | 12 weeks | 8 | 22 | 8 (5 to 17) |
Insomnia | 5 | 18 | 9 (6 to 18) | |||
Diarrhea | 3 | 13 | 10 (6 to 20) | |||
Non-vertebral fractures and bone loss in the elderly4 | Elemental calcium+vitamin D vs. placebo | Non-vertebral fractures verified by radiographs or hospital records | 3 years | 12.9 | 5.9 | 15 (8 to 12) |
Hip fractures in nursing home patients55 | External hip protectors vs. control(no hip protector) | Hip fracture | 1 month | 7.4 | 3.2 | 24 (13 to 183) |
New fractures in postmenopausal women who had low bone-mineral density and existing vertebral fractures6 | Alendronate sodium vs. placebo | New vertebral fractures confirmed by radiography | 3 years | < 75 years of age: 13 | < 75 years of age: 6 | < 75 years of age: 15 (11 to 27) |
≥75 years of age: 18 | ≥75 years of age: 11 | ≥75 years of age: 15 (8 to 21) | ||||
Postmenopausal77 | Alendronate sodium vs. placebo | ≥1 day of bed rest | 3 years | 15 | 11 | 23 (15 to 56) |
≥7 days of bed rest | 9 | 4 | 21 (17 to 32) | |||
≥7 days of limited activity | 44 | 41 | 23 (12 to 308) | |||
Postmenopausal women with osteoporosis8 | Oral risedronate vs. placebo | New vertebral fractures | 3 years | 16 | 11 | 20 (11 to 111) |
Non-vertebral fractures | 8 | 5 | 32 (17 to 250) | |||
Residents in nursing homes9 | Pharmacist medication review vs. no review | Deaths from 5 to 8 months (intervention phase) | 8 months | 9 | 4 | 17 (9 to 213) |
Hip fracture patients with mild to moderate dementia10 | Intensive geriatric rehabilitation (advice, training, drug treatment, physiotherapy, occupational and speech therapy) vs. control group (discharge to a local hospital) | Independent living at 3 months-mild dementia | 1 year | 67 | 91 | 5 (3 to 16) |
Independent living at 3 months -moderate dementia | 1 year | 17 | 63 | 3 (2 to 9) | ||
Vertebral fractures in men with osteoporosis11 | Alendronate vs. placebo | Incidence of vertebral fractures | 2 years | 7 | 1 | 16 (7 to 56) |
- N Engl J Med 1997; 337:670-6
- N Engl J Med 1997 Sep 4;337(10):670-6
- Arch Intern Med 1998 May 11;158(9):1021-31
- N Engl J Med. 4 Sept 1997; 337: 670-6
- Lancet. 2 Jan 1993; 341: 11-3
- Arch Intern Med. 8/22 Dec 1997; 157: 2617-24
- Arch Intern Med. Jan 10, 2000; 160: 77-85
- JAMA. Oct 13, 1999; 282: 1344-52
- Br J Psychiatry. Jun 2000; 176: 563-7
- BMJ. Nov 4, 2000; 321: 1107-11
- N Engl J Med. Aug 31 2000: 343: 604-10
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Reducing venous thromboembolism after elective neurosurgery1 | Enoxaparin vs. placebo | Pulmonary embolism (PE) or deep venous Thrombosis (DVT) | 8 days | 33 | 17 | 7 (4 to 18) |
PE or proximal DVT | 14 | 5 | 12 (6 to 73) | |||
Overall DVT | 32 | 17 | 7 (4 to 20) | |||
Proximal DVT | 13 | 5 | 13 (7 to 143) | |||
Stroke in children with sickle-cell anaemia; periodic blood transfusions2 | Transfusion vs. standard care | All strokes | 20 months | 16 | 2 | 7 (4 to 18) |
Cerebral infarction | 15 | 2 | 8 (5 to 22) | |||
Idiopathic venous thromboembolism3 | Warfarin vs. placebo | Recurrent venous thromboembolism | 3 months | 20.5 | 1.3 | 6 (3 to 9) |
Total bleeding | 1.2 | 11.4 | 10 (5 to 30) | |||
Pulmonary embolism and proximal deep venous thrombosis (DVT)4 | Subcutaneous low-molecular-weight heparin (tinzaparin sodium) vs. unfractionated heparin (control) | Recurrent venous thromboembolism | 3 months | 6.8 | 0 | 15 (8 to 36) |
Major bleeding | 1.9 | 1.0 | Not significant | |||
Minor bleeding | 2.9 | 1.0 | Not significant | |||
Death | 8.7 | 6.2 | Not significant |
References
- N Engl J Med 1998 Jul 9;339(2):80-5
- N Engl J Med 1998 Jul 30;339(5):339-40
- N Engl J Med 1999 Mar 25;340(12):901-7
- Arch Intern Med. Jan 24, 2000; 160: 229-36
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
AIDS1 ; Patients with HIV-1 infection and CD4+ lymphocyte count ≤ 100/mL | Ritonavir vs. placebo | AIDS-defining illness or death | Median 28.9 weeks | 37.5 | 21.9 | 6 (5 to 10) |
AIDS1; as above | Ritonavir vs. placebo | Death from any cause | Median 51 weeks | 23 | 16 | 14 (9 to 43) |
Herpetic gingivostomatitis2 | Acyclovir vs. placebo | Oral lesions | 8 days | 70 | 6.5 | 2 (1 to 2) |
Eating difficulties | 47 | 6.5 | 3 (2 to 5) | |||
Drinking difficulties | 30 | 3.2 | 4 (2 to 11) | |||
HIV infected persons with previous antiretroviral treatment3 | Indinavir, zidovudine + lamivudine vs. zidovudine + lamivudine | Changes in HIV RNA levels and CD4+ cell counts. | 24 weeks | 0 | 90 | 2 |
Shigellosis in Bangladeshi children4 | Vitamin A vs. no vitamin A | Clinical cure by day 5 | 5 days | 20 | 45 | 4 (2 to 18) |
Bacteriological cure from day 3 | 39 | 38 | Not significant | |||
HIV infection; breast-fed infants5 | Zidovudine vs. placebo | HIV-1 infection in the live-born children of women in the study | 6 months | 27.5 | 18 | 11 (6 to 100) |
Sexually transmitted diseases in minority women6 | Behavioral intervention (3 weekly group sessions in which recognition of risk, commitment to change and acquisition of skills were discussed) vs. control group (received 15 minutes of standard individualized counseling by nurse clinicians according to guidelines from the US Centers for Disease Control and Prevention) | Subsequent infection with Chlamydia trachomatis or Neisseria gonorrhoeae, assessed by testing endocervical samples with DNA probes | 6 and 12 months | 26.9 | 16.8 | 10 (6 to 32) |
HIV-1-infected patients with tuberculosis7 | Trimethoprim-sulfamethoxazole (co-trimoxazole) vs. placebo | Death | 10.5 months | 22.6 | 13.3 | 11 (7 to 26) |
≥ hospitalization | 12.4 | 7.6 | 21 (11 to 172) | |||
HIV-1-infection8 | Efavirenz plus zidovudine and lamivudine vs. indinavir plus zidovudine and lamivudine | Percentage of patients with suppression of plasma HIV-1 RNA to < 400 copies/mL | 48 weeks | 48 | 70 | 5 (4 to 10) |
meningitis9 | Dexamethasone vs placebo | death | 8 weeks | 25 | 15 | 1 (5 to 73) |
References
- Lancet 1998; 351:543-9
- BMJ 1997 Jun 21;314(7097):1800-3
- N Engl J Med 1997 Sep 11;337(11):734-9
- BMJ. 7 Feb 1998; 316: 422-6
- Lancet 1999 Mar 6;353(9155):786-92
- N Engl J Med. 14 Jan 1999; 340: 93-100
- Lancet. May 1, 1999; 353: 1469-75
- N Engl J Med. Dec16, 1999; 341:1865-73
- NEJM. 2002;347:1549-56
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Major depression1 | Repetitive transcranial magnetic stimulation (rTMS) vs. sham rTMS | ≥50% reduction in scores on the Hamilton Depression Rating Scale or Montgomery-Asberg Depression Rating Scale | 2 weeks | 25 | 49 | 5 (3 to 466) |
Children and adolescents with non-psychotic major depressive disorder2 | Fluoxetine vs. placebo | Improvement | 8 weeks | 33 | 56 | 5 (3 to 33) |
Bipolar disorder; manic relapse3 | Training plus routine care vs. routine care alone | Manic relapse | 18 months | 57 | 27 | 3 (2 to 16) |
Major depression4 | Slow, repetitive transcranial magnetic stimulation (rTMS) vs. Sham rTMS | Severity of depression | 2 weeks | 25 | 49 | 5 (3 to 466) |
Social phobia5 | Paroxetine vs. placebo | Treatment response (mean change in scores on the Liebowitz Social Anxiety Scale and the proportion of responders on the Clinical Global Impression scale) | 12 weeks | 32 | 66 | 4 (3 to 5) |
Engaging unmotivated problem drinkers into treatment6 | Concerned significant others (CSO) were allocated to Community reinforcement and family training (CRAFT- teaching behavior changing skills to use at home) or Johnson Institute (JI) intervention (to prepare for confrontational family meetings) or Al-Anon (a 12 step program) | Number of problem drinkers engaged in treatment at follow up, change in concerned significant other functioning and relationship quality | 1 year | CRAFT: 67 | vs. Al-A: 20 | 3 (2 to 4) |
CRAFT: 67 | vs. JI: 35 | 4 (2 to 10) | ||||
Al-A: 35 | vs. JI: 20 | Not significant | ||||
Relapse in residual depression7 | Clinical management + cognitive therapy (CT) vs. clinical management alone | Relapse | 1 year | 47 | 29 | 6 (4 to 42) |
Non-chronic treatment resistant depression8 | Venlafaxine vs. paroxetine (control) | Therapeutic response | 4 weeks | 33 | 52 | 6 (3 to 254) |
Remission | 20 | 42 | 5 (3 to 21) | |||
Alcohol related illness in ongoing drinkers 9 | Integrated outpatient treatment (IOT-inpatient evaluation, treatment plan, monthly primary care visits to measure biological indicators of heavy drinking and offer help and efforts to involve family members) vs. standard care | Drinking in previous 30 days | 2 years | 70 | 81 | 4 (3 to 35) |
Social Phobia10 | Paroxetine vs. placebo | Mean change in scores on the Liebowitz Social Anxiety Scale and the proportion of responders on the Clinical Global Impression Scale | 12 weeks | 32 | 66 | 4 (3 to 5) |
Relapse in residual depression11 | Antidepressants plus cognitive therapy vs. clinical management alone | Relapse and symptom ratings | 1 year | 47 | 29 | 6 (4 to 42) |
Depression12 | Fluozetine vs. desipramine (control) | Continuing initial medication | 12 months | 20 | 42 | 5 (4 to 10) |
Fluozetine vs. imipramine (control) | 27 | 42 | 7 (4 to 25) | |||
Moderate depression13 | Hypericum extract vs. placebo | ≥50% improvement in the Hamilton Depression Rating Scale | 8 weeks | 48 | 67 | 6 (3 to 50) |
Hypericum extract vs. imipramine | 67 | 76 | Not significant | |||
Opioid dependance14 | Methadone maintenance for 14 months vs. 120 days of methadone-assisted maintenance and 60 days of methadone-assited detoxification with intensivepsychosocial serivces and 8 months of aftercare (control) | Treatment retention | 12 months | 55 | 74 | 6 (4 to 20) |
Depression15 | Fluoxetine plue folic acid vs. fluoxetine plus placebo | Clinical response (>50% improvement on the Hamilton Depression Rating Scale) | 10 weeks | 62 | 82 | 5 (3 to 30) |
Depression16 | Nurse telehealth care (12-14 calls to each patient during treatment in which the clinic nurse answered questions, offered support and discussed the patient's mental and overall health vs. usual physician care (counselling and treatment with a selective serotonin reuptake inhibitor) | ≥50% improvement on the Hamilton Depression Rating Scale | 6 weeks | 37 | 50 | 8 (4 to 90) |
6 months | 38 | 57 | 6 (4 to 18) | |||
≥50% improvement on Beck Depression Inventory | 6 weeks | 33 | 38 | Not significant | ||
6 months | 37 | 48 | Not significant | |||
Alzheimer's disease17 | Family intervention, which comprised 3 sessions of caregiver education, 6 sessions of stress management and 5 sessions of coping skills management vs. interview control group, which comprised of a1 session cathartic interview | Caregiver psychiatric morbidity and depression | 3 months | 85 | 23 | 2 (2 to 5) |
Family intervention vs. no interview | 77 | 23 | 2 (2 to 7) | |||
Postpartum depression18 | Support group (7 psychoeducation a1 visits in which partners participated in 4 out of the 7 visits) vs. control group (7 sessions without partner) | Depression status established by the Mini International Neuropsychiatric Instrument | 10 weeks | 62 | 19 | 3 (2 to 15) |
Fear of flying19 | Virtual reality exposure (8 sessions, 4 of which involved information gathering, treatment planning, brief breathing training and cognitive restructuring) vs. waiting list control | Proportion of patients who went on a round trip flight at 6 weeks and changes in symptoms (determined from questionnaire) | 12 months | 7 | 53 | 3 (2 to 7) |
Standard exposure (8 sessions done at the airport with exposure to pre-flight stimuli and sitting on a stationary airplane with imaginal exposure to takeoffs, cruising and landing) vs. waiting list control | 7 | 67 | 2 (2 to 4) | |||
Aggression and conduct disorder20 | Lithium vs. placebo | Responders on the Global Clinical Judgments (Consensus Scale) | 4 weeks | 30 | 80 | 2 (2 to 6) |
Responders on the Clinical Global Impressions | 70 | 20 | 2 (2 to 6) | |||
Bulimia nervosa21 | Cognitive behavioural therapy vs. interpersonal therapy (control) | Recovery at 20 weeks | 1 year | 6 | 29 | 4 (3 to 8) |
Remission at 20 weeks | 28 | 48 | 5 (3 to 14) | |||
Normal eating attitudes and behaviours at 20 weeks | 27 | 41 | 7 (4 to 92) | |||
Post-traumatic stress disorder (PTSD)22 | Sertraline vs. placebo | Response rate (≥ 30% reduction from baseline in Clinician Administered PTSD Scale, Part 2 total severity score and Clinical Global Improvement - Improvement (CGI - I) score of 1 or 2) | 12 weeks | 32 | 53 | 5 (3 to 17) |
Schizophrenia or schizoaffective disorder23 | Programme for relapse prevention (education about relapse and how to recognise prodromal symptoms and behaviour, active monitoring, clinical intervention when prodromal episodes were detected and 90 minuets of multifamily psychoeducation groups) vs. usual care | Relapse free survival | 18 months | 66 | 83 | 1 (1 to 5) |
No hospital admission | 61 | 78 | 1 (1 to 3) | |||
Chronic depression24 | Nefazodone and psychotherapy vs. nefazodone or psychotherapy (control) | Remission (a score of 8 or less on the Hamilton Rating Scale for Depression) or satisfactory response (a reduction in the HRDS by at least 50% from baseline and a score of 15 or less) | 12 weeks | 48 | 73 | 4 (3 to 7) |
Acute mania25 | Valproate vs. placebo | ≥ 50% improvement on the Young Mania Rating Scale | 21 days | 46 | 70 | 5 (3 to 15) |
Moderate to marked improvement on the Clinical Global Impression Scale | 50 | 68 | 6 (4 to 74) | |||
Major depressive disorder (MDD)26 | Titrated right unilateral electroconvulsive therapy (RUL ECT) vs. fixed dose RUL ECT (control) | Cognitive disturbance (decreased ≥ 5 points on the Mini-Mental State Examination) | 1-2 days | 30 | 6.7 | 5 (3 to 22) |
Secondary insomnia27 | Treatment group (4 weekly 1 hour sessions with a therapist involving sleep hygiene instructions, stimulus control and relaxation) vs. control group | Clinical improvement (measured by sleep efficiency percentage) | 3 months | 19 | 57 | 3 (2 to 12) |
Secondary insomnia28 | Naltrexone plus cognitive behavioural therapy (CBT) vs. placebo plus CBT | Drinking relapse (≥ 5 drinks/day for men and ≥ 4 drinks/day for women) | 12 weeks | 60 | 38 | 5 (3 to 21) |
Secondary insomnia29 | Risperidone vs. haloperidol (control) | Need for antiparkinsonian drugs | 6 weeks | 75 | 50 | 5 (3 to 10) |
Moderate depression30 | Hypericum extract vs. placebo | ≥ 50% improvement in Hamilton Depression Rating Scale score | 8 weeks | 48 | 67 | 6 (3 to 50) |
Hypericum extract vs. imipramine (control) | 67 | 76 | Not significant | |||
Drug refractory schizophrenia31 | Cognitive behavioural therapy (attaining a collaborative understanding of the development of symptoms and working towards reducing distress and disability) vs. befriending (control - sessions focused on neutral topics) | ≥ 50% improvement in Comprehensive Psychiatric Rating Scale (CPRS) total score | 9 months | 39 | 63 | 5 (3 to 28) |
≥ 0% improvement in CPRS schizophrenia change scores | 50 | 70 | Not significant |
References
- Arch Gen Psychiatry 1999; 56:315-20
- Arch Gen Psychiatry 1997 Nov;54(11):1031-7
- BMJ 1999 Jan 16;318(7177):149-53
- Arch Gen Psychiatry. Apr 1999; 56: 15-20
- Br J Psychiatry. Aug 1999; 175: 120-6
- J Consult Clin Psychol. Oct 1999; 67: 688-97
- Arch Gen Psychiatry. Sept 1999; 56: 829-35
- Br J Psychiatry. Jul 1999; 175: 12-6
- Arch Intern Med. 13 Sept 1999; 159: 1946-52
- Br J Psychiatry. Aug 1999; 175: 120-6
- Arch Gen Psychiatry. Sept 1999; 56: 829-94
- Arch Fam Med. Jul/Aug 1999; 8: 319-25
- BMJ. Dec 11, 1999; 319: 1534-9
- JAMA. Mar 8, 2000; 283: 1303-10
- Affect Disord. Nov 2000; 60: 121-30
- Arch Fam Med. Aug 2000; 9:700-8
- Br J Psychiatry. Jun 2000; 176: 557-62
- Can J Psychiatry. Aug 2000; 45: 554-8
- J Consult Clin Psychol. Dec 2000; 68: 1020-6
- Arch Gen Psychiatry. Jul 2000; 57: 649-54
- Arch Gen Psychiatry. May 2000; 57: 459-66
- JAMA. Apr 12, 2000; 283: 1837-44
- Arch Gen Psychiatry. Mar 2000; 57:277-83
- N Engl J Med. May 18, 2000. 342; 1462-70
- J Clin Psychopharmacol. Apr 2000; 20: 195-203
- Arch Gen Psychiatry. May 2000; 57: 438-44
- Psychol Aging. Jun 2000; 15: 232-40/a>
- Am J Psychiatry. Nov 1999; 156: 1758-64
- Am J Psychiatry. Nov 1999; 156: 1758-64
- Schizophr Bull. 1999; 25: 721-9
- BMJ. Dec 1999; 319: 1534-9
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Alcohol-related seizures1 | Lorazepam vs. placebo | Occurrence of a second seizure | 6 hours | 24 | 3 | 5 (4 to 9) |
Care for acute stroke victims2 | Patients were allocated to a Stroke unit or to Ward care | Proportion of patients living at home | 5 years | 18.2 | 34.5 | 6 (4 to 21) |
Migraine headaches3 | Riboflavin vs. placebo | Frequency of headaches | 3 months | 19 | 54 | 3 (2 to 11) |
Headache days | 15 | 57 | 3 (2 to 6) | |||
Acute stroke unit care4 | Stroke unit vs. general ward care | Quality of life measured by the Frenchay Activity index ≥ 30 points | 5 years | 40.6 | 5 (2 to 80) | |
Non-disabling stroke; carotid endarterectomy5 | Carotid endarterectomy vs. medical care | Ipsolateral stroke | 5 years | 18.7 | 13.1 | 18 (10 to 186) |
Any stroke | 26.4 | 19.8 | 15 (8 to 100) | |||
Stroke or death | 36.4 | 27.9 | 12 (7 to 44) | |||
Disabling stroke or death | 20.1 | 14.9 | 19 (10 to 783) | |||
Multiple sclerosis attacks6 | Methylpredni-solone vs. placebo | ≥ 1 point improvement on Kurtzke Expanded Disability Status Scale | 1 year | 22 | 50 | 4 (2 to 105) |
Secondary progressive multiple sclerosis7 | Interferon-b1b vs. placebo | Progression | 33 months | 49.7 | 39.1 | 9 (6 to 30) |
Acute Stroke7 | Intra-arterial recombinant prourokinase plus intravenous heparin vs. intravenous heparin alone | Proportion of patients with a modified Rankin score ≤ 2 | 90 days | 25 | 40 | 7 (3 to 268) |
Episodic cluster headache8 | Verapamil vs. placebo | Non-response (= having ≤ 50% reduction in cluster headache attack frequency) | 2 weeks | 100 | 20 | 1 (1 to 2) |
Multiple sclerosis (MS)9 | Interferon β-1a vs. placebo | Mean change in scores on the Liebowitz Social Anxiety Scale and the proportion of responders on the Clinical Global Impression Scale | 12 weeks | 32 | 66 | 4 (3 to 5) |
References
- N Engl J Med 1999 Mar 25;340(12):915-9
- Stroke 1997 Oct;28(10):1861-6
- Neurology 1998 Feb;50(2):466-70
- Stroke 1998 May;29(5):895-9
- N Engl J Med 1998 Nov 12;339(20):1415-25
- Neurology 1998 Aug;51(2):529-34
- BMJ 1998 Jul 25;317(7153):235-40
- Neurology. Mar 2000; 54: 1382-5
- N Engl J Med. Sept 28, 2000; 343: 898-904
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Excessive uterine bleeding1 | Levonorgestrel intrauterine system vs. control group | Number of women canceling their decision to have a hysterectomy | 6 months | 14 | 64 | 2 (1 to 4) |
First-stage labor pain2 | Intracutaneous injections of sterile water vs. placebo | Labor pain was measured with a 10-cm visual analog scale (0 cm = no pain; 10 cm = worst conceivable pain) | 90 minutes | 25 | 59 | 3 (2 to 13) |
Subcutaneous injections of sterile water vs. placebo | 25 | 52 | 4 (3 to 82) | |||
Breech presentation3 | Planned cesarean section vs. planned vaginal birth (control) | Perinatal or neonatal mortality or serious neonatal morbidity | 6 weeks | 5.0 | 1.6 | 30 (20 to 54) |
Perinatal or neonatal mortality | 1.3 | 0.3 | 104 (54 to 416) | |||
Serious neonatal morbidity | 3.8 | 1.4 | 41 (26 to 90) |
References
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Breast cancer1; Postmenopausal women with breast cancer | Radiotherapy plus tamoxifen vs. tamoxifen alone | Recurrence (both locoregional recurrence and distant metastasis) | 10 years | 60 | 47 | 8 (6 to 13) |
Stages II and III breast cancer2 | Adjuvant chemotherapy + radiotherapy vs. chemotherapy alone | Locoregional recurrence | 10 years | 26 | 5 | 5 (4 to 6) |
Locally advanced prostate cancer3 | Radiotherapy + goserelin vs. radiotherapy alone | Death | 5 years | 28 | 17 | 10 (5 to 34) |
Acute myeloid leukemia; autologous bone-marrow transplantation after intensive chemotherapy4 | Bone-marrow transplantation vs. no further treatment | Relapse | 7 years | 53 | 34 | 5 (3 to 11) |
Relapse or cancer-specific death | 57 | 45 | 9 (5 to 80) | |||
Death | 49 | 40 | Not significant | |||
Breast cancer; preservation of the intercostobrachial nerve during axillary node clearance5 | Preservation vs. sacrifice of the intecostobrachial nerve | Some sensory deficit | 3 months | 84 | 63 | 5 (3 to 24) |
Breast cancer6 | Radiotherapy plus tamoxifen vs. tamoxifen alone | All recurrences | 10 years | 60 | 47 | 8 (6 to 13) |
Locoregional recurrence with or without distant metastases | 35 | 8 | 4 (4 to 5) | |||
Node-positive prostate cancer7 | Antiandrogen therapy immediately after surgery vs. observation | Death | 7.1 years | 35 | 15 | 5 (3 to 34) |
Death from prostate cancer | 31 | 6.4 | 4 (3 to 10) | |||
Any recurrence | 82 | 15 | 2 (2 to 2) | |||
Prostate cancer8 | Pelvic floor re-education program (included education about the anatomy and function of the bladder and pelvic floor, active pelvic-floor muscle exercises and biofeedback) vs. placebo program (information about the origin of their incontinence and placebo electrotherapy applied to the abdomen and thighs, but that could not affect pelvic floor function) | Incontinence rate at 3 months (continence was defined as a loss of ≤ 2g of urine on both the 24-hour and 1-hour pad test | 1 year | 44 | 10 | 3 (2 to 6) |
Incontinence at 1 year | 17 | 4 | 8 (4 to 72) |
References
- Lancet 1999; 353:1641-8
- N Engl J Med 1997 Oct 2;337(14):949-55
- N Engl J Med 1997 Jul 31;337(5):295-300
- Lancet 1998 Mar 7;351(9104):700-8
- Br J Surg 1998 Oct;85(10):1443-5
- Lancet 1999 May 15;353(9165):1641-8
- N Engl J Med. Dec 9, 1999; 341: 1781-8
- Lancet. Jan 8 2000; 355: 98-102
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Second-eye cataract surgery1 | Surgery vs. control | Difficulty reading normal print | 6 months | 35 | 6 | 4 (3 to 6) |
Eyesight prevented most activities | 11 | 0 | 10 (6 to 23) | |||
Below-average overall vision | 18 | 0 | 6 (4 to 10) | |||
Eyesight interfered greatly in life | 26 | 1 | 5 (3 to 7) | |||
Stereoacuity worse than 3000-sec arc | 70 | 12 | 2 (2 to 3) |
References
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Painful stiff shoulder1 | Corticosteroid injections vs. physiotherapy | Treatment success | 1 year | 46 | 77 | 3 (2 to 8) |
Subacute or chronic low back pain2 | Exercise program (8 one hour sessions over 4 weeks which consisted of stretching, low impact aerobics and strengthening exercises) vs. control (standard care from GPs) | Functional limitation (24 point Roland back pain disability questionnaire) | 1 year | 35 | 64 | 4 (3 to 8) |
Lateral epicondylitis (tennis elbow)3 | Local corticosteroid injection of methylprednisolone and lignocaine vs. enteric-coated naproxen | Complete recovery at 4 weeks | 12 months | 5.7 | 42 | 3 (2 to 5) |
Local corticosteroid injection of methylprednisolone and lignocaine vs. placebo | Pain scores ≤ 3 at 4 weeks (on 10 point Likert scale) | 50 | 82 | 4 (3 to 8) | ||
Osteoarthritis of the knee4 | Manual physical therapy and exercise vs. placebo (ultrasonography at a sub-therapeutic intensity) | Knee surgery | 1 year | 20 | 5 | 7 (4 to 134) |
Acute whiplash injuries5 | Active treatment (gentle, active, small-range and small-amplitude rotational movements of the neck) vs. standard treatment (leaflet providing information about injury mechanisms, advice on suitable activities and instruction on postural correction) | No pain | 6 months | 11 | 30 | 6 (3 to 45) |
No or low pain | 20 | 44 | 5 (3 to 22) |
References
- N Engl J Med. 12 Nov 1998; 339: 1415-25
- BMJ. 31 Jul 1999; 319: 279-83
- BMJ. Oct 9, 1999; 319: 964-8
- Ann Intern Med. Feb 1 2000; 132: 173-81
- Spine. Jul 15, 2000; 25: 1782-7
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Acute otitis media (AOM)1 | Xylitol syrup vs. control syrup | Incidence of AOM | 3 months | 41 | 29 | 8 (4 to 53) |
Xylitol gum vs. control gum | 28 | 16 | 9 (5 to 36) | |||
Xylitol lozenges vs. control gum | 28 | 22 | Not significant | |||
Diarrhea incidence in children treated with antibiotics2 | Lctobacillus GG vs. placebo | Incidence of diarrhea | 10 days | 26 | 8 | 6 (4 to 13) |
Stool consistency < 4§ | 48 | 17 | 4 (3 to 6) | |||
Acute otitis media3 | Amoxicillin suspension vs. placebo | Persistent symptoms at 4 days | 6 weeks | 72 | 59 | 8 (4 to 72) |
Clinical treatment failure at 11 days (persistent fever, earache, crying, irritability or no improvement in appearance of the tympanic membrane) | 70 | 60 | Not significant | |||
Constipation in children4 | Cisapride vs. placebo | clinical response (>3 spontaneous bowel movements/week with no fecal soiling and no use of other laxtives for ≥ 2 weeks) | 12 weeks | 42 | 76 | 3 (2 to 60) |
Routine primary immunisation5 | Longer needle vs. shorter needle (control) | Any local reaction up to 3 days | 3 days | 84 | 62 | 5 (3 to 19) |
Redness at 6 hours | 66 | 40 | 5 (3 to 81) | |||
Redness at 1 day | 63 | 28 | 3 (2 to 7) | |||
Redness at 2 days | 39 | 9 | 4 (3 to 8) | |||
Redness at 3 days | 28 | 4 | 5 (3 to 9) | |||
Swelling at 6 hours | 58 | 23 | 3 (3 to 6) | |||
Swelling at 1 day | 63 | 28 | 3 (2 to 7) | |||
Swelling at 2 days | 51 | 19 | 4 (3 to 7) | |||
Swelling at 3 days | 40 | 13 | 4 (3 to 10) | |||
Children with asthma exacerbations6 | Ward care based on a clinical pathway (comprised a nurse driven protocol for weaning bronchodilators, regular peak flow measurements, asthma teaching, prescriptions for home treatments and coordination of care between the attending physician and private medical doctors) vs. usual ward care | Discharge within 24 hours of admission | 2 weeks | 38 | 15 | 5 (3 to 14) |
Acute diarrhea in children7 | Oral rehydration solution (ORS) vs. standard care | Unscheduled follow up visit | 10 days | 17 | 11 | 16 (8 to 481) |
ORS use | 71 | 85 | 8 (5 to 17) | |||
Head lice in children8 | Malathion lotion vs. bug busting (control) | Live lice at 7 days after treatment | 7 days | 63 | 23 | 2 (2 to 6) |
Severe watery diarrhea in children9 | Racecadotril vs. placebo | 5 day cure rate | 5 days | 66 | 84 | 6 (4 to 29) |
References
- Pediatrics 1998 Oct;102(4 Pt 1):879-84
- J Pediatr. Nov 1999; 135: 564-8
- BMJ. Feb 5, 2000; 320: 350-4
- J Pediatr. Jan 2000;136: 35-40
- BMJ. Oct 14, 2000; 321: 931-3
- Pediatrics. Nov 2000; 106: 1006-12
- Pediatrics. Sep 1999; 104: e29
- Br J gen Pract. Oct 2000; 50: 817-20
- N Engl J Med. Aug 17, 2000; 343: 463-7
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Acute arterial leg occlusion1 | Thrombolysis vs. surgery | Amputation- free survival at 6 and 12 months | 6 and 12 months | 6 months: 25.2 12 months: 30.1 |
6 months: 28.2 12 months: 35 |
Not significant |
Hemorrhagic complications | 5.5 | 12.5 | 14 (8 to 47) |
References
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Chronic fatigue syndrome1; Patients reporting fatigue (medically unexplained, lasting ≥6 months) | Cognitive behaviour therapy vs. orthodox medical care | Improved function | 6-7 months | 26.7 | 73.3 | 3 (2 to 5) |
Head lice2; Patients of any infected with live lice | Pediculicides (e.g., permethrin) vs. placebo | Freedom from viable lice or eggs | 14 days | 5.9 | 97 | 2 (1 to 2) |
Nosocomial pneumonia3 | Semirecumbent body position (45° from the horizontal) vs. supine body position | Clinically suspected nosocomial pneumonia | 72 hours | 34 | 8 | 4 (3 to 11) |
Microbiologically confirmed nosocomial pneumonia (by bronchoalveolar lavage or protected specimen-brush cultures | 23 | 5 | 6 (4 to 29) | |||
Influenza4 | Oral oseltamivir once daily vs. placebo | Laboratory-confirmed influenza-like illness | 6 weeks | 4.8 | 1.2 | 27 (17 to 59) |
Oral oseltamivir twice daily vs. placebo | 4.8 | 1.3 | 29 (17 to 69) | |||
Ventilator-associated5 | Invasive management strategy (fiberoptic bronchoscopy to obtain protected specimen-brush samples or bronchoalveolar lavage samples to guide treatment vs. Clinical management strategy (control-clinical evaluation, examination of Gram-stained endotracheal aspirates and adherence to the American Thoracic Society guideline recommendations for choosing antiboitics) | All-cause mortality | 28 days | 26 | 16 | 11 (6 to 56) |
Dissolving earwax6 | Docusate sodium vs. triethanolamine polypeptide (control) | Complete visualisation of the tympanic membrane (with or without irrigation) | 35 | 81 | 3 (2 to 6) | |
Sepsis7 | Immune enhancing enteral feeding formula vs. control formula | Mortality | 32 | 19 | 8 (4 to 637) | |
Acquired bacteraemia | 22 | 8 | 8 (4 to 28) | |||
≥1 acquired nosocomial infection | 20 | 6 | 8 (5 to 23) | |||
Influenza8 | Influenza vaccine vs. placebo | Patients reports of fever plus cough or sore throat and associated physician visits and lost work days during influenza period during flu season of 1998-99 | After flu season was finished | 10.2 | 1.4 | 12 (7 to 27) |
References
- Price JR, Couper J. Cognitive behaviour therapy for adults with chronic fatigue syndrome. Cochrane Review, 24 Aug 1998. In: The Cochrane Library. Oxford: Update Software.
- Interventions for treating headlice. Cochrane Review, 14 Jan 1999. In: The Cochrane Library. Oxford:Update Software.
- Lancet. Nov 27, 1999; 354: 1851-8
- N Engl J Med. Oct 28, 1999; 341:1336-43
- Ann Intern Med. Apr 18, 2000; 132: 621-30
- Ann Emerg Med. Sep 2000; 36: 228-32
- Crit Care Med. Mar 2000; 28: 643-8
- JAMA. Oct 4, 2000; 284: 1655-63
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Acute asthma1 | Budesonide vs. placebo | Relapse | 21 days | 25 | 13 | 9 (5 to 179) |
Chronic obstructive pulmonary disease (COPD)2 | Glucocorticoids vs. placebo | First treatment failure (death, need for intubation and mechanical ventilation, readmission for COPD, or intensification of drug therapy) | 1 and 3 months | 1 month: 33 | 1 month: 23 | 10 (5 to infinity) |
3 months: 48 | 3 months: 37 | 9 (4 to infinity) | ||||
Children with asthma3 | Structured discharge packages vs. usual discharge packages at the time of discharge | Readmission to hospital | 6 months | 38 | 15 | 5 (3 to 12) |
Smoking cessation; using a nicotine inhaler4 | Nicotine inhalers vs. placebo | Self reported abstinence from smoking (verified by laboratory measurements) | 1 year | 18 | 29 | 10 (5 to 483) |
Smoking cessation rates5 | Intensive intervention (which includes a 30 minute behavioral counseling session given by nurses, a videotape from the American Heart Association and an audiotape of relaxation exercises vs. usual care (which includes printed material and a list of partially subsidized outpatient cessation programs) | Confirmed smoking cessation | 12 months | 20 | 27 | 16 (9 to 25) |
asthma; effectiveness in treating inner city patients6 | Educational program vs. conventional asthma care and routine follow-up | Attendance at follow up appointments, subsequent ED visits and hospitalization | 6 months | 27 | 59 | 3 (2 to 11) |
Asthma7 | Asthma clinic vs. standard treatment group | Owning a peak flow meter | 6 months | 56 | 73 | 6 (3 to 31) |
Waking at night because of asthma | 20 | 7.0 | 8 (4 to 29) | |||
Acute-on-chronic obstructive pulmonary disease8 | Standard treatment plus pressure supported ventilation through a face or nasal mask vs. standard treatment alone | Need for intubation | After discharge | 27 | 15 | 9 (5 to 69) |
Death | 20 | 10 | 10 (6 to 98) | |||
Acute respiratory distress syndrome9 | Lower tidal volumes vs. traditional tidal volumes (control) | Death | 180 days | 40 | 31 | 12 (7 to 41) |
Pulmonary infiltrates10 | Ciprofloxacin vs. control (physician-directed antibiotics) | Mortality | 30 days | 31 | 13 | Not significant |
Resistance or superinfection | 38 | 14 | 5 (3 to 22) |
References
- JAMA. 9 Jun 1999; 281: 2119-26
- N Engl J Med. 24 Jun 1999; 340:1941-7
- Arch Dis Child. Feb 1999; 80: 110-4
- Arch Intern Med. 11/25 Aug 1997; 157: 1721-8
- Arch Intern Med. 24 Feb 1997; 157: 409-15
- Arch Intern Med. 9/23 Aug 1999; 159: 1710-6
- Med J Aust. Jul 19, 1999; 171: 68-71
- Lancet. Jun 3, 2000; 355: 1931-5
- N Engl J Med. May 4, 2000; 342: 1301-8
- Am J Respir Crit Care Med. Aug 2000; 162: 505-11
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Calcific shoulder tendinitis1 | Pulsed ultrasound vs. sham therapy | Changes from baseline in shoulder calcium deposits on radiography, pain, active range of motion and power of shoulder and activities of daily living were assessed. | 9 months | 8 | 42 | 3 (2 to 9) |
Carpal tunnel syndrome2 | Injection of methylprednisolone and lignocaine vs. lignocaine alone (control) | Symptom improvement-defined as having no symptoms or minor symptoms requiring no further treatment | 1 year | 7 | 50 | 3 (2 to 9) |
Rheumatoid arthritis3 | Intravenous infusion of infliximab, 3mg/kg of body weight every 4 weeks vs. placebo | Response rate (defined as 20% improvement from baseline according to the 1987 American College of Rheumatology criteria) | 30 weeks | 20 | 53 | 4 (3 to 6) |
Intravenous infusion of infliximab, 3mg/kg every 8 weeks vs. placebo | 20 | 50 | 4 (3 to 6) | |||
Intravenous infusion of infliximab, 10mg/kg every 4 weeks vs. placebo | 20 | 58 | 3 (2 to 5) | |||
Intravenous infusion of infliximab, 10mg/kg every 8 weeks vs. placebo | 20 | 52 | 4 (3 to 6) |
References
- N Engl J Med. 20 May 1999; 340: 1533-8
- Can J Infect Con. 2000; Spring: 9-14
- Lancet. Dec 4, 1999; 354: 1932-9
Condition or Disorder | Intervention vs. Control | Outcome | Follow-up Duration | Event Rates % | NNT (95% CI) | |
---|---|---|---|---|---|---|
CER | EER | |||||
Benign prostatic hyperplasia1 | Finasteride vs. placebo | Surgery for BPH | 4 years | 10.1 | 4.6 | 18 (13 to 27) |
Acute urine retention | 6.6 | 2.8 | 27 (19 to 43) | |||
Urinary incontinence in women2 | Bladder training or pelvic muscle exercises with biofeedback assisted instruction vs. combined bladder training plus pelvic muscle exercises | Frequency of self reported incontinence | 3 months | 13 | 31 | 5 (3 to 23) |
Perceived symptom improvement | 30 | 52 | 4 (3 to 20) |