Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 99

1.

Differences in pain management between hematologists and hospitalists caring for patients with sickle cell disease hospitalized for vasoocclusive crisis.

Shah N, Rollins M, Landi D, Shah R, Bae J, De Castro LM.

Clin J Pain. 2014 Mar;30(3):266-8. doi: 10.1097/AJP.0b013e318295ec04.

2.

Hospitalist management of vaso-occlusive pain crisis in patients with sickle cell disease using a pathway of care.

Allen Liles E, Kirsch J, Gilchrist M, Adem M.

Hosp Pract (1995). 2014 Apr;42(2):70-6. doi: 10.3810/hp.2014.04.1105.

PMID:
24769786
3.

Comparison of processes and outcomes of pneumonia care between hospitalists and community-based primary care physicians.

Rifkin WD, Conner D, Silver A, Eichorn A.

Mayo Clin Proc. 2002 Oct;77(10):1053-8.

PMID:
12374249
4.

Patient-controlled analgesia versus continuous infusion of morphine during vaso-occlusive crisis in sickle cell disease, a randomized controlled trial.

van Beers EJ, van Tuijn CF, Nieuwkerk PT, Friederich PW, Vranken JH, Biemond BJ.

Am J Hematol. 2007 Nov;82(11):955-60.

5.

IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studies.

Dampier CD, Smith WR, Wager CG, Kim HY, Bell MC, Miller ST, Weiner DL, Minniti CP, Krishnamurti L, Ataga KI, Eckman JR, Hsu LL, McClish D, McKinlay SM, Molokie R, Osunkwo I, Smith-Whitley K, Telen MJ; Sickle Cell Disease Clinical Research Network (SCDCRN).

Clin Trials. 2013 Apr;10(2):319-31. doi: 10.1177/1740774513475850.

PMID:
23539110
6.

Impact of PCA strategies on pain intensity and functional assessment measures in adults with sickle cell disease during hospitalized vaso-occlusive episodes.

Dampier CD, Wager CG, Harrison R, Hsu LL, Minniti CP, Smith WR; Investigators of the Sickle Cell Disease Clinical Research Network (SCDCRN).

Am J Hematol. 2012 Oct;87(10):E71-4. doi: 10.1002/ajh.23302. Epub 2012 Aug 7. No abstract available.

7.

Outcomes of care by hospitalists, general internists, and family physicians.

Lindenauer PK, Rothberg MB, Pekow PS, Kenwood C, Benjamin EM, Auerbach AD.

N Engl J Med. 2007 Dec 20;357(25):2589-600.

8.

Variation in length of stay and outcomes among hospitalized patients attributable to hospitals and hospitalists.

Goodwin JS, Lin YL, Singh S, Kuo YF.

J Gen Intern Med. 2013 Mar;28(3):370-6. doi: 10.1007/s11606-012-2255-6. Epub 2012 Nov 6.

9.

A comparison of two regimens of patient-controlled analgesia for children with sickle cell disease.

Trentadue NO, Kachoyeanos MK, Lea G.

J Pediatr Nurs. 1998 Feb;13(1):15-9.

PMID:
9503762
10.

Frequently asked questions by hospitalists managing pain in adults with sickle cell disease.

Smith WR, Jordan LB, Hassell KL.

J Hosp Med. 2011 May;6(5):297-303. doi: 10.1002/jhm.933. Review.

PMID:
21661104
11.

Clinical and Geographic Characterization of 30-Day Readmissions in Pediatric Sickle Cell Crisis Patients.

McMillan JE, Meier ER, Winer JC, Coco M, Daymont M, Long S, Jacobs BR.

Hosp Pediatr. 2015 Aug;5(8):423-31. doi: 10.1542/hpeds.2014-0184.

PMID:
26231632
12.

Opioid selection during sickle cell pain crisis and its impact on the development of acute chest syndrome.

Buchanan ID, Woodward M, Reed GW.

Pediatr Blood Cancer. 2005 Oct 15;45(5):716-24.

PMID:
15926170
13.

[Postoperative pain management after minimally invasive hysterectomy: thoracic epidural analgesia versus intravenous patient-controlled analgesia].

Hensel M, Frenzel J, Späker M, Keil E, Reinhold N.

Anaesthesist. 2013 Oct;62(10):797-807. doi: 10.1007/s00101-013-2234-2. Epub 2013 Sep 22. German.

PMID:
24057760
14.

Inpatient management of sickle cell pain: a 'snapshot' of current practice.

Miller ST, Kim HY, Weiner D, Wager CG, Gallagher D, Styles L, Dampier CD; Investigators of the Sickle Cell Disease Clinical Research Network (SCDCRN).

Am J Hematol. 2012 Mar;87(3):333-6. doi: 10.1002/ajh.22265. Epub 2012 Jan 9.

15.

The management of sickle cell pain in the emergency department: a priority for health systems.

Po' C, Colombatti R, Cirigliano A, Da Dalt L, Agosto C, Benini F, Zanconato S, Sainati L.

Clin J Pain. 2013 Jan;29(1):60-3. doi: 10.1097/AJP.0b013e318245764b.

PMID:
22751027
16.

A retrospective review of acupuncture use for the treatment of pain in sickle cell disease patients: descriptive analysis from a single institution.

Lu K, Cheng MC, Ge X, Berger A, Xu D, Kato GJ, Minniti CP.

Clin J Pain. 2014 Sep;30(9):825-30. doi: 10.1097/AJP.0000000000000036.

17.
18.

Day hospital versus inpatient management of uncomplicated vaso-occlusive crises in children with sickle cell disease.

Raphael JL, Kamdar A, Wang T, Liu H, Mahoney DH, Mueller BU.

Pediatr Blood Cancer. 2008 Sep;51(3):398-401. doi: 10.1002/pbc.21537.

PMID:
18300322
19.

Does e-pain plan improve management of sickle cell disease associated vaso-occlusive pain crisis? a mixed methods evaluation.

Kato-Lin YC, Krishnamurti L, Padman R, Seltman HJ.

Int J Med Inform. 2014 Nov;83(11):814-24. doi: 10.1016/j.ijmedinf.2014.08.003. Epub 2014 Aug 17.

PMID:
25179666
20.

The effect of full-time faculty hospitalists on the efficiency of care at a community teaching hospital.

Diamond HS, Goldberg E, Janosky JE.

Ann Intern Med. 1998 Aug 1;129(3):197-203.

PMID:
9696727
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk